Background: Natural products acquire vast and intriguing structural diversity and have been recognized as a tremendously diverse source of new lead compounds. Numerous bioactive secondary metabolites are present in the form of glycosylated molecules in which the sugar parts are normally associated with the interaction along with molecular recognition of the cellular target. Scope and approach: The presence of sugar entities are crucial as well as in some cases necessary, for therapeutic effects. Establishing novel and potent glycosylated secondary metabolites has formed a main goal in the natural product field from fungi and bacteria. These compounds possess a diverse range of sugar units. Key findings and conclusions: Fungi is considered one of the important sources for approved drugs with a diverse range of mode of action. The sugar part in numerous pharmacologically active natural products enhances bioavailability, biological potential, reduce toxicity, and improve stability. The vast majority of glyocosides showed antimicrobial effects, cytotoxic, antiviral and antiinflammatory effects. Notably, numerous fungal glycosides presented in this review illustrate significant antimicrobial effects towards various microorganisms especially against plant pathogens. The antimicrobial effects of these fungal glycosides indicate that these metabolites could be employed as natural preservatives in food in order to abolish or control the growth of pathogenic and spoilage microorganisms.
- Compound ID: 15956
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b-D-Olip-(1-4)-b-Rhop-(1-4)-a-L-Rhap-(1-4')-Subst
Subst = fulicinerine = SMILES CC[C@H]({111}[C@@H](O)[C@H]1[C@H](C[C@@H](/C=C/C=C(C2=C{1}C(O)=C3C(OC4=C3{9}C(O)=C(CC[C@H]({54}CO)C)C=C4)=C2)\C)C)O1)C |
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Structure type: monomer
Trivial name: fulicineroside
Compound class: glycoside
- Compound ID: 19941
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b-D-Glcp-(1-1)-+
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R-2HOC16={t3}-(1-2)-Subst
Subst = (2S,3R,4E,8E)-2-amino-9-methylicosa-4,8-diene-1,3-diol = SMILES CCCCCCCCCCC/C(C)=C/CC/C=C/{3}[C@@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
C11H81NO8
Trivial name: asperamide B
Compound class: glycolipid, glycoside
- Compound ID: 21175
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a-L-Rhap-(1-7)-Subst
Subst = 3,5,7-trihydroxy-coumarin = SMILES O=c2oc1c{7}c(O)cc(O)c1cc2O |
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Structure type: monomer
Compound class: glycoside, coumarin glycoside
- Compound ID: 23039
Structure type: monomer
Compound class: glycoside
- Compound ID: 23040
Structure type: monomer
Compound class: glycoside
- Compound ID: 23041
Structure type: monomer
Compound class: glycoside
- Compound ID: 20119
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b-D-Glcp-(1-1)-+
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R-2HOC18={t3}-(1-2)-Subst
Subst = (2S,3S,4E,9E)-2-amino-10-methyloctadeca-4,9-diene-1,3-diol = SMILES CCCCCCCC/C(C)=C/CCC/C=C/{3}[C@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: flavuside A, flavuside B
Compound class: glycosphingolipid, glycoside, cerebroside
- Compound ID: 23049
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R-2HOSte-(1-2)-+
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b-D-Glcp-(1-1)-Subst
Subst = (2S,3S,4E,9E)-2-amino-10-methyloctadeca-4,9-diene-1,3-diol = SMILES CCCCCCCC/C(C)=C/CCC/C=C/{3}[C@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: flavuside B
Compound class: glycoside
- Compound ID: 18694
Structure type: monomer
C43H81O9N
Trivial name: cerebroside C, cerebroside D
Compound class: glycolipid, glycosphingolipid, glycoside, cerebroside, ceramide
- Compound ID: 23031
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b-D-Glcp-(1-1)-+
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R-2HOC18={t3}-(1-2)-Subst
Subst = (2R,3S,4E,8E)-9-methyl-4,8-sphingadienine-C18 = SMILES CCCCCCCCC/C(C)=C/CC/C=C/{3}[C@@H]({2}[C@@H]({1}CO)N)O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23067
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Subst-(1-2)-+
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b-D-Glcp-(1-1)-Subst1
Subst = 2R-hydroxytrideca-3E,5E,7E,9E-tetraenoic acid = SMILES CCC/C=C/C=C/C=C/C=C/{2}[C@@H](O){1}C(O)=O;
Subst1 = (2S)-sphinganine-C23 = SMILES O{1}C{2}[C@H](N){3}C(O)CCCCCCCCCCCCCCCCCCCC |
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Structure type: monomer
Trivial name: asperiamide B
Compound class: glycoside
- Compound ID: 23068
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b-D-Glcp-(1-1)-+
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R-2HOC16={t3}-(1-2)-Subst
Subst = (2S,3R,4E,8E)-2-amino-9-methyldocosa-4,8-diene-1,3-diol = SMILES CCCCCCCCCCCCC/C(C)=C/CC/C=C/{3}[C@@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: asperiamide C
Compound class: glycoside
- Compound ID: 23060
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Subst-(1-2)-+
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b-D-Glcp-(1-1)-Subst1
Subst = 2R-hydroxy-heptadec-3E-enoic acid = SMILES CCCCCCCCCCCCC/C=C/{2}[C@@H](O){1}C(O)=O;
Subst1 = (2S,4E,17E,19E)-18-methyl-4,17,19-sphingatrienine-C32 = SMILES O{3}C({2}[C@H]({1}CO)N)/C=C/CC/C=C/CCCCCCC/C=C(C)/C=C/CCCCCCCCCCCC |
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Structure type: monomer
Trivial name: asperiamide A
Compound class: glycoside
- Compound ID: 23144
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a-D-Ribf-(1-3)-Subst
Subst = diorcinol = SMILES CC1=CC(OC2=C{3}C(O)=CC(C)=C2)=C{53}C(O)=C1 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 20874
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Subst1-(1-3)-b-D-6dAltp4Me-(1-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4;
Subst1 = hexa-2Z,4E-dienoic acid = SMILES C/C=C/C=C\{1}C(=O)O |
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Structure type: monomer
Trivial name: zofimarin
Compound class: glycoside
Reference(s) to other database(s): GenDB:FJ175179
- Compound ID: 22994
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a-D-Glcp6Me-(1-9)-Subst3Me16Me
Subst = dongtingnoid A aglycon = SMILES CC(C)/C3=C/2{9}[C@@H](O){8}[C@H](O)[C@H](C)[C@@H]/1CC{3}[C@](O)({16}CO)C1=C\[C@@]2(C)CC3 |
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Structure type: monomer
Trivial name: dongtingnoid A
Compound class: glycoside
- Compound ID: 22995
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a-D-Glcp6Me-(1-9)-Subst3Me16Me
Subst = dongtingnoid B aglycon = SMILES CC(C)/C3=C/2{9}[C@@H](O){8}[C@H](O)[C@H](C)[C@@H]/1CC{3}[C@@](O)({16}CO)C1=C\[C@@]2(C)CC3 |
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Structure type: monomer
Trivial name: dongtingnoid B
Compound class: glycoside
- Compound ID: 22996
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a-D-Glcp6Me-(1-9)-Subst
Subst = dongtingnoid C aglycon = SMILES CC(C)/C3=C/2{9}[C@@H](O){8}[C@H](O)[C@H](C)/C1=C(C(=O)CC1)\{1}[C@H](O)[C@@]2(C)CC3 |
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Structure type: monomer
Trivial name: dongtingnoid C
Compound class: glycoside
- Compound ID: 22997
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a-D-Glcp6Me-(1-9)-Subst16Me
Subst = dongtingnoid D aglycon = SMILES CC(C)/C3=C/2{9}[C@@H](O){8}[C@H](O)[C@H](C)[C@@H]1CC/C({16}CO)=C1/{1}[C@H](O)[C@@]2(C)CC3 |
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Structure type: monomer
Trivial name: dongtingnoid D
Compound class: glycoside
- Compound ID: 22998
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a-D-Glcp6Me-(1-9)-Subst16Me
Subst = dongtingnoid E aglycon = SMILES CC(C)/C3=C/2{9}[C@@H](O){8}[C@H](O)[C@H](C)[C@@H]/1C/C=C({16}CO)\C1=C\[C@@]2(C)CC3 |
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Structure type: monomer
Trivial name: dongtingnoid E
Compound class: glycoside
- Compound ID: 23021
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b-D-Glcp-(1-8)-Subst
Subst = 8-hydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylic acid = SMILES O{10}C(C1=CC=CC(OC2=C3{8}C(O)=CC(C)=C2)=C1C3=O)=O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23028
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a-D-Glcp-(1-4')-Subst
Subst = mycophenolic acid = SMILES COC1=C(C(CO2)=C({7}C(O)=C1C/C=C({54}C(C{56}C(O)=O)O)\C)C2=O)C |
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Structure type: monomer
Trivial name: penicacid B
Compound class: glycoside
- Compound ID: 23055
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Subst-(1-2)-+
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a-D-Glcp-(1-1)-SphC16
Subst = (2S,7E)-7-sphingenine-C16 = SMILES O{3}C({2}[C@H]({1}CO)N)CCC/C=C/CCCCCCCC |
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Structure type: monomer
Trivial name: penicilloside A
Compound class: glycoside
- Compound ID: 23056
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Subst-(1-2)-+
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a-D-Glcp-(1-1)-Subst1
Subst = (2R,3E)-2-hydroxy-3-decenoic acid = SMILES CCCCCC/C=C/{2}[C@@H](O){1}C(O)=O;
Subst1 = (2S,3R,7E)-7-methyl-7-sphingenine-C11 = SMILES CCC/C=C(C)/CCC{3}[C@H]({2}[C@H]({1}CO)N)O |
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Structure type: monomer
Trivial name: penicilloside B
Compound class: glycoside
- Compound ID: 23115
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b-D-Galp-(1-4')-Subst
Subst = djalonensone = SMILES COC1=CC(OC(C2=C3C={54}C(O)C={52}C2O)=O)=C3C(C)=C1 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23030
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b-D-Glcp-(1-1)-+
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R-2HOC16={t3}-(1-2)-Subst
Subst = (2R,3S,4E)-4-sphingenine-C18 = SMILES CCCCCCCCCCCCC/C=C/{3}[C@@H]({2}[C@@H]({1}CO)N)O |
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Structure type: monomer
Trivial name: cerebroside D
Compound class: glycoside
- Compound ID: 17903
Structure type: monomer
C41H77O9N
Trivial name: cerebroside B
Compound class: glycolipid, glycosphingolipid, glycoside, cerebroside
- Compound ID: 22682
Structure type: monomer
Trivial name: cerebroside A, cerebroside C
Compound class: glycolipid, glycoside, cerebroside
Reference(s) to other database(s): GenDB:MN692190
- Compound ID: 23029
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b-D-Glcp-(1-1)-+
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R-2HOC16={t3}-(1-2)-Subst
Subst = (2R,3S,4E,8E)-9-methyl-4,8-sphingadienine-C18 = SMILES CCCCCCCCC/C(C)=C/CC/C=C/{3}[C@@H]({2}[C@@H]({1}CO)N)O |
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Structure type: monomer
Trivial name: cerebroside A
Compound class: glycoside
- Compound ID: 23052
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R-2HOPam-(1-2)-+
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b-D-Glcp-(1-1)-Subst
Subst = (2S,3S,4E,9E)-10-methyl-4,9-sphingadienine-C19 = SMILES O{1}C{2}[C@@H]({3}[C@H](/C=C/CCC/C=C(CCCCCCCCC)\C)O)N |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23064
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2HOLig-(1-2)-+
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b-D-Glcp-(1-1)-Subst
Subst = (2S,4E,8E)-9-methyl-4,8-sphingadienine-C18 = SMILES CCCCCCCCC/C(C)=C/CC/C=C/{3}C(O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: Sch V
Compound class: glycoside
- Compound ID: 23125
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a-L-Rhap-(1-2)-b-D-Glcp-(1-3)-Subst
Subst = solasodine = SMILES [H][C@]1(O[C@@]2(NC[C@H](C)CC2)[C@H]3C)C[C@@]4([H])[C@]5([H])CC=C6C{3}[C@@H](O)CC[C@]6(C)[C@@]5([H])CC[C@]4(C)[C@]13[H] |
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Structure type: oligomer
Trivial name: β-1-solamargine, β-1-Solamargine
Compound class: saponin glycoside, glycoside
Reference(s) to other database(s): CCSD:
41748, CBank-STR:3412
- Compound ID: 23126
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b-D-Glcp-(1-3)-Subst
Subst = solasodine = SMILES [H][C@]1(O[C@@]2(NC[C@H](C)CC2)[C@H]3C)C[C@@]4([H])[C@]5([H])CC=C6C{3}[C@@H](O)CC[C@]6(C)[C@@]5([H])CC[C@]4(C)[C@]13[H] |
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Structure type: monomer
Compound class: glycoside, alkaloid
- Compound ID: 23127
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b-D-Glcp-(1-4)-+
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a-L-Rhap-(1-2)-b-D-Glcp-(1-3)-Subst
Subst = 25R-furost-5-en-3β,22α,26-triol = SMILES C[C@H]1[C@H]2[C@H](C[C@@H]3[C@@]2(CC[C@H]4[C@H]3CC=C5[C@@]4(CC{3}[C@@H](C5)O)C)C)O{22}[C@@]1(CC[C@@H](C){26}[CH2]O)O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23128
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a-L-Arap-(1-3)-+
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a-L-Rhap-(1-2)-b-D-Glcp-(1-3)-Subst
Subst = 25R-furost-5-en-3β,22α,26-triol = SMILES C[C@H]1[C@H]2[C@H](C[C@@H]3[C@@]2(CC[C@H]4[C@H]3CC=C5[C@@]4(CC{3}[C@@H](C5)O)C)C)O{22}[C@@]1(CC[C@@H](C){26}[CH2]O)O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23129
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b-D-Xylp-(1-3)-+
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a-L-Rhap-(1-2)-b-D-Glcp-(1-3)-Subst
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b-D-Glcp-(1-4)-+
Subst = 25R-furost-5-en-3β,22α,26-triol = SMILES C[C@H]1[C@H]2[C@H](C[C@@H]3[C@@]2(CC[C@H]4[C@H]3CC=C5[C@@]4(CC{3}[C@@H](C5)O)C)C)O{22}[C@@]1(CC[C@@H](C){26}[CH2]O)O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 19140
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b-D-1,4dxylHexp-(1C-3)-Subst
Subst = deoxyneofusapyrone aglycon = SMILES CCCCCCC(C/C(C)=C\C(/C=C(/C=C/{8}C(O)C(C)(C1=C{4}C(O)={3}CC(O1)=O)C)C)C)C |
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Structure type: monomer
Trivial name: deoxyfusapyrone
Compound class: glycoside
- Compound ID: 22779
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Subst-(1-4)-a-D-Glcp-(1-1)-a-D-Glcp
Subst = 2,2-dimethyl-3-oxoicosa-4E,11E,13E,18E-tetraenoic acid = SMILES C/C=C/CCC/C=C/C=C/CCCCC/C=C/C(=O)C(C)(C){1}C(=O)O |
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Structure type: oligomer
Trivial name: fusaroside
Compound class: glycolipid, glycoside
- Compound ID: 22899
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b-D-1,4dxylHexp-(1C-3)-Subst
Subst = fusapyrone aglycon = SMILES CCCCCCC(C/C(C)=C\C(/C=C(/C=C/{8}C(O)C(C)(C1=CC({3}C={2}C(O)O1)=O)C)C){27}CO)C |
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Structure type: monomer
Trivial name: fusapyrone, neofusapyrone
Compound class: glycoside
- Compound ID: 23002
|
b-D-Glcp-(1-12)-Subst
Subst = (2S,5S,10R)-2-((R)-1,2-dihydroxypropan-2-yl)-6,10-dimethylspiro[4.5]dec-6-en-8-one = SMILES O=C1C[C@@H](C)[C@@]2(CC[C@H]({11}[C@@](C)(O){12}CO)C2)C(C)=C1 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23054
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R-2HOPam-(1-2)-+
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b-D-Glcp-(1-1)-Subst
Subst = (2S,3R,4E,8E,10E)-9-methyl-4,8,10-sphingatrienine-C18 = SMILES O{3}[C@@H]({2}[C@H]({1}CO)N)/C=C/CC/C=C(C)/C=C/CCCCCCC |
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Structure type: monomer
Trivial name: phalluside-1
Compound class: glycoside
- Compound ID: 23078
|
Subst-(1-6)-b-D-Galp-(1-4)-a-D-Sugp-(3-1)-Subst1
Subst = stillingic acid = SMILES CCCCC/C=C\C=C\{1}C(=O)O;
Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O;
Subst1 = 7-hydroxytetradeca-2E,4E,8E,10E-tetraenoic acid = SMILES CCC/C=C/C=C/{7}C(O)C/C=C/C=C/{1}C(=O)O |
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Structure type: oligomer
Trivial name: PF-1042
Compound class: glycoside
- Compound ID: 23079
|
Cin-(9-6)-b-D-Galp-(1-4)-a-D-Sugp-(3-1)-Subst1
Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O;
Subst1 = 7-hydroxytetradeca-2E,4E,8E,10E-tetraenoic acid = SMILES CCC/C=C/C=C/{7}C(O)C/C=C/C=C/{1}C(=O)O |
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Structure type: oligomer
Trivial name: saricandin
Compound class: glycoside
- Compound ID: 22986
|
b-D-Sugf2Me-(6-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4;
Subst1 = 2-methylhexa-2Z,4Z-dienoic acid = SMILES C\C=C/C=C(/C)\{1}C(=O)O;
Sug = tricyclic uronic acid = SMILES O{6}[C@]1([C@@H]([C@H]2O[C@H]3O1)C)O[C@@H]3{2}[C@H]2O |
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Structure type: monomer
Trivial name: xylarin
Compound class: glycoside
- Compound ID: 23044
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b-D-Glcp-(1-1)-+
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R-2HOC18={t3}-(1-2)-Subst
Subst = (2S,3R,5E,9Z)-5,9-sphingadienine-C19 = SMILES O{3}[C@@H]({2}[C@H]({1}CO)N)C/C=C/CC/C=C\CCCCCCCCC |
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Structure type: monomer
Trivial name: chrysogeside A, alternaroside C
Compound class: glycoside
- Compound ID: 23045
|
Subst-(1-2)-+
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b-D-Glcp-(1-1)-Subst1
Subst = cerebronic acid = SMILES CCCCCCCCCCCCCCC/C=C/{2}[C@@H](O){1}C(O)=O;
Subst1 = (2S,3R,4E,8E)-9-methyl-4,8-sphingadienine-C14 = SMILES C/C(CCCCC)=C\CC/C=C/{3}[C@@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: chrysogeside B
Compound class: glycoside
- Compound ID: 23046
|
Subst-(1-2)-+
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b-D-Glcp-(1-1)-Subst1
Subst = cerebronic acid = SMILES CCCCCCCCCCCCCCC/C=C/{2}[C@@H](O){1}C(O)=O;
Subst1 = (2S,3R,4E,8E)-9-methyl-4,8-sphingadienine-C13 = SMILES CCCC/C(C)=C/CC/C=C/{3}[C@@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: chrysogeside C
Compound class: glycoside
- Compound ID: 23047
|
Subst-(1-2)-+
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b-D-Glcp-(1-1)-Subst1
Subst = cerebronic acid = SMILES CCCCCCCCCCCCCCC/C=C/{2}[C@@H](O){1}C(O)=O;
Subst1 = (2S,3R,4E,8E)-9-methyl-4,8-sphingadienine-C16 = SMILES C/C(CCCCCCC)=C\CC/C=C/{3}[C@@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: chrysogeside D
Compound class: glycoside
- Compound ID: 23048
|
Subst-(1-2)-+
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b-D-Glcp-(1-1)-Subst1
Subst = 2R-hydroxynonadecanoic acid = SMILES CCCCCCCCCCCCCCCCC{2}[C@@H](O){1}C(O)=O;
Subst1 = (2S,3R,4E,8E)-9-methyl-4,8-sphingadienine-C14 = SMILES C/C(CCCCC)=C\CC/C=C/{3}[C@@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: chrysogeside E
Compound class: glycoside
- Compound ID: 23164
Structure type: monomer
Compound class: glycoside
- Compound ID: 22900
|
b-D-1,4dxylHexp-(1C-3)-Subst
Subst = 7-desmethyldeoxyneofusapyrone aglycon = SMILES CCCCCCC(C/C(C)=C\C(/C=C(/C=C/{8}C(O)C(C1=C{4}C(O)={3}CC(O1)=O)C)C)C)C |
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Structure type: monomer
Trivial name: 7-desmethyldeoxyneofusapyrone
Compound class: glycoside
- Compound ID: 17549
|
b-D-Glcp-(1-10)-Subst
Subst = egonol = SMILES COC1=C2C(=CC(=C1)CC{10}CO)C=C(O2)C3=CC4=C(C=C3)OCO4 |
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Structure type: monomer
Trivial name: egonol glucoside
Compound class: glycoside
- Compound ID: 23113
|
b-D-Xylp-(1-6)-b-D-Glcp-(1-10)-Subst
Subst = egonol = SMILES COC1=C2C(=CC(=C1)CC{10}CO)C=C(O2)C3=CC4=C(C=C3)OCO4 |
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Structure type: monomer
Trivial name: masutakeside I
Compound class: glycoside
- Compound ID: 23114
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-10)-Subst
Subst = egonol = SMILES COC1=C2C(=CC(=C1)CC{10}CO)C=C(O2)C3=CC4=C(C=C3)OCO4 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23130
|
b-D-Manp-(1-29)-Subst
Subst = colletotrichamide A aglycon = SMILES CC[C@@H](C1C(O[C@@H](C{21}[C@H]([C@H](C(N[C@@H](C(N1C)=O)CC2=CC=CC=C2)=O)C)O)[C@H](CCCC{29}[C@H](O)C)C)=O)C |
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Structure type: monomer
Trivial name: colletotrichamide A
Compound class: glycoside
- Compound ID: 23131
|
b-D-Manp-(1-29)-Subst
Subst = colletotrichamide B aglycon = SMILES CCC(C1C(OC(C{21}C(C(C(NC(C(N1C)=O)CC2=CC=CC=C2)=O)C)O)C(C/C=C/C{29}[C@H](O)C)C)=O)C |
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Structure type: monomer
Trivial name: colletotrichamide B
Compound class: glycoside
- Compound ID: 23132
|
b-D-Manp-(1-29)-Subst
Subst = colletotrichamide C aglycon = SMILES CCC(C1C(OC(C{21}C(CC(NC(C(N1C)=O)CC2=CC=CC=C2)=O)O)C(CCCC{29}[C@H](O)C)C)=O)C |
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Structure type: monomer
Trivial name: colletotrichamide C
Compound class: glycoside
- Compound ID: 23133
|
b-D-Manp-(1-29)-Subst
Subst = colletotrichamide D aglycon = SMILES CC(C[C@H]1C(O[C@@H](C{21}[C@H](C(C(N[C@@H](C(N1C)=O)CC2=CC=CC=C2)=O)C)O)C(CCCC{29}[C@H](O)C)C)=O)C |
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Structure type: monomer
Trivial name: colletotrichamide D
Compound class: glycoside
- Compound ID: 23134
|
b-D-Manp-(1-29)-Subst
Subst = colletotrichamide E aglycon = SMILES C{29}[C@@H](O)CCCCC(C)[C@@H]1C{21}C(O)C(C)C(NC(CC2=CC=CC=C2)C(N(C)[C@@H](C(C)C)C(O1)=O)=O)=O |
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Structure type: monomer
Trivial name: colletotrichamide E
Compound class: glycoside
- Compound ID: 18968
|
b-D-Manp-(1-21)-Subst
Subst = epicoccamide A, B, C aglycon = SMILES CC1C(/C(C(N1C)=O)={6}C(O)\C(CCCCCCCCCCCCC{21}CO)C)=O |
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Structure type: monomer
Trivial name: epicoccamide A
Compound class: glycoside
Reference(s) to other database(s): PubChem:54719804
- Compound ID: 22323
|
a-D-Galf-(1C-3)-Subst
Subst = epipyrone aglycon = SMILES CCC(CC(/C=C({28}C(O)=O)/C=C(/C=C/C=C/C=C/C=C/C=C/C1=C{4}C(O)={3}C(C(O1)=O))C)C)C |
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Structure type: monomer
Trivial name: epipyrone B
Compound class: glycoside
- Compound ID: 22324
|
b-D-Galf-(1C-3)-Subst
Subst = epipyrone aglycon = SMILES CCC(CC(/C=C({28}C(O)=O)/C=C(/C=C/C=C/C=C/C=C/C=C/C1=C{4}C(O)={3}C(C(O1)=O))C)C)C |
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Structure type: monomer
Trivial name: epipyrone C
Compound class: glycoside
- Compound ID: 22894
|
b-D-Galp-(1C-3)-Subst
Subst = epipyrone aglycon = SMILES CCC(CC(/C=C({28}C(O)=O)/C=C(/C=C/C=C/C=C/C=C/C=C/C1=C{4}C(O)={3}C(C(O1)=O))C)C)C |
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Structure type: monomer
Trivial name: epipyrone A, orevactaene
Compound class: glycoside
- Compound ID: 17643
|
b-D-Altp-(1-19)-Subst
Subst = isopimara-7,15-diene-2α,3β,19-triol = SMILES C[C@@]1(CCC2[C@@](C)(C[C@@H](O)[C@@H]([C@@]3({19}CO)C)O)C3CC=C2C1)C=C |
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Structure type: monomer
Trivial name: virescenoside A
Compound class: glycoside
- Compound ID: 17644
|
b-D-Altp-(1-19)-Subst
Subst = isopimara-7,15-diene-3β,19-diol = SMILES C[C@](C1)(C=C)CCC2C1=CCC3[C@]2(C)CC{3}C(O)[C@]3(C){19}CO |
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Structure type: monomer
Trivial name: virescenoside B
Compound class: glycoside
- Compound ID: 17645
|
b-D-Altp-(1-19)-Subst
Subst = 3-oxo-isopimara-7(8),15-diene-19-ol = SMILES C[C@@]1(CCC2[C@@](C)(CCC([C@@]3({19}CO)C)=O)C3CC=C2C1)C=C |
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Structure type: monomer
C26H40O7
Trivial name: virescenoside C
Compound class: glycoside
- Compound ID: 22947
|
a-D-Glcp-(1-6)-b-D-Altp-(1-19)-Subst
Subst = virescenoside R1 aglycon = SMILES C[C@]1(C=C)CC[C@H]2C(C=C[C@@H]3[C@]2(C)C{2}[C@@H](O){3}[C@H](O)[C@@]3({19}CO)C)=C1 |
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Structure type: oligomer
Trivial name: virescenoside R1
Compound class: glycoside
- Compound ID: 22948
|
a-D-Glcp-(1-6)-b-D-Altp-(1-19)-Subst
Subst = virescenoside V, Z14 aglycon = SMILES C=C[C@]3(C)/C=C\2C(=O)C[C@H]1[C@@](C)({19}CO){3}[C@@H](O){2}[C@H](O)C[C@]1(C)[C@H]2CC3 |
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Structure type: oligomer
Trivial name: virescenoside R2
Compound class: glycoside
- Compound ID: 22949
|
a-D-Glcp-(1-6)-b-D-Altp-(1-19)-Subst
Subst = virescenoside R3 aglycon = SMILES C[C@]1(C=C)CC[C@@]2(C)C(C1)=CC[C@@H]3[C@]2(C)C{2}[C@@H](O){3}[C@H](O)[C@@]3({19}CO)C |
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Structure type: oligomer
Trivial name: virescenoside R3
Compound class: glycoside
- Compound ID: 22950
|
a-D-Glcp-(1-6)-b-D-Altp-(1-19)-Subst
Subst = virescenoside R4 aglycon |
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Structure type: oligomer
Trivial name: virescenoside Z
Compound class: glycoside
- Compound ID: 22943
|
b-D-Sugp-(1-19)-Subst
Subst = 3-oxo-isopimara-7(8),15-diene-19-ol = SMILES C[C@@]1(CCC2[C@@](C)(CCC([C@@]3({19}CO)C)=O)C3CC=C2C1)C=C;
Sug = bD4dthrHexp4enodialdose = SMILES O{1}[C@@H]1OC(C=O)=C{3}[C@@H](O){2}[C@@H]1O |
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Structure type: monomer
Trivial name: virescenoside D
Compound class: glycoside
- Compound ID: 22944
|
b-D-Sugp-(1-19)-Subst
Subst = isopimara-7,15-diene-2α,3β,19-triol = SMILES C[C@@]1(CCC2[C@@](C)(C[C@@H](O)[C@@H]([C@@]3({19}CO)C)O)C3CC=C2C1)C=C;
Sug = bD4dthrHexp4enodialdose = SMILES O{1}[C@@H]1OC(C=O)=C{3}[C@@H](O){2}[C@@H]1O |
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Structure type: monomer
Trivial name: virescenoside E
Compound class: glycoside
- Compound ID: 22945
|
b-D-4dthrHexp4en-(1-19)-Subst
Subst = isopimara-7,15-diene-3β,19-diol = SMILES C[C@](C1)(C=C)CCC2C1=CCC3[C@]2(C)CC{3}C(O)[C@]3(C){19}CO |
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Structure type: monomer
Trivial name: virescenoside H
Compound class: glycoside
- Compound ID: 17649
|
a-D-Glcp-(1-1)-+
|
Subst-(1-17)-17HOBeh-(1-3)-a-D-Glcp
l?17HOBeh = 17-hydroxybehenic acid;
Subst = oxalic acid = SMILES O=C(O){1}C(=O)O |
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Structure type: oligomer
Trivial name: emmyguyacin B
Compound class: glycoside
- Compound ID: 23088
|
a-D-Galp-(1-1)-+
|
Subst-(1-17)-17HOBeh-(1-3)-a-D-Glcp
l?17HOBeh = 17-hydroxybehenic acid;
Subst = oxalic acid = SMILES O=C(O){1}C(=O)O |
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Structure type: oligomer
Trivial name: emmyguyacin A
Compound class: glycoside
- Compound ID: 23089
|
a-L-Rhap-(1-3)-Subst-(1-1)-Me
Subst = (S)-3-hydroxyundecanoic acid = SMILES CCCCCCCC{3}[C@H](O)C{1}C(O)=O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 20865
|
a-D-Glcp-(1-8)-Subst6Me
Subst = halorosellin B aglycon = SMILES O=C3O/C(=C)C(c2c3{8}c(O)c{6}c(O)c2C)C |
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Structure type: monomer
Trivial name: halorosellin A
Compound class: glycoside
- Compound ID: 20866
|
a-D-Glcp-(1-8)-Subst
Subst = halorosellin B aglycon = SMILES O=C3O/C(=C)C(c2c3{8}c(O)c{6}c(O)c2C)C |
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Structure type: monomer
Trivial name: halorosellin B
Compound class: glycoside
- Compound ID: 23032
|
R-2HOPam-(1-2)-+
|
b-D-Glcp-(1-1)-Subst
Subst = (2S,3R,4E)-8-hydroxy-9-methylene-4-sphingenine-C18 = SMILES CCCCCCCCCC({8}C(O)CC/C=C/{3}[C@H]({2}[C@H]({1}CO)N)O)=C |
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Structure type: monomer
Trivial name: termitomycesphin A
Compound class: glycoside
- Compound ID: 23033
|
R-2HOSte-(1-2)-+
|
b-D-Glcp-(1-1)-Subst
Subst = (2S,3R,4E)-8-hydroxy-9-methylene-4-sphingenine-C18 = SMILES CCCCCCCCCC({8}C(O)CC/C=C/{3}[C@H]({2}[C@H]({1}CO)N)O)=C |
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Structure type: monomer
Trivial name: termitomycesphin B
Compound class: glycoside
- Compound ID: 23034
|
R-2HOPam-(1-2)-+
|
b-D-Glcp-(1-1)-Subst
Subst = (2S,3R,4E,7E)-2-amino-9-methyloctadeca-4,7-diene-1,3,9-triol = SMILES CCCCCCCCC{9}C(O)(C)/C=C/C/C=C/{3}[C@@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: termitomycesphin C
Compound class: glycoside
- Compound ID: 23035
|
R-2HOSte-(1-2)-+
|
b-D-Glcp-(1-1)-Subst
Subst = (2S,3R,4E,7E)-2-amino-9-methyloctadeca-4,7-diene-1,3,9-triol = SMILES CCCCCCCCC{9}C(O)(C)/C=C/C/C=C/{3}[C@@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: termitomycesphin D
Compound class: glycoside
- Compound ID: 23036
|
R-2HOPam-(1-2)-+
|
b-D-Glcp-(1-1)-Subst
Subst = (2S,3R,E)-2-amino-9-methyloctadec-4-ene-1,3,8-triol = SMILES CCCCCCCCCC(C){8}C(O)CC/C=C/{3}[C@@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: termitomycesphin E
Compound class: glycoside
- Compound ID: 23037
|
R-2HOSte-(1-2)-+
|
b-D-Glcp-(1-1)-Subst
Subst = (2S,3R,E)-2-amino-9-methyloctadec-4-ene-1,3,8-triol = SMILES CCCCCCCCCC(C){8}C(O)CC/C=C/{3}[C@@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: termitomycesphin F
Compound class: glycoside
- Compound ID: 23042
Structure type: monomer
Trivial name: flavicerebroside A
Compound class: glycoside
- Compound ID: 23043
Structure type: monomer
Trivial name: flavicerebroside B
Compound class: glycoside
- Compound ID: 23050
|
b-D-Glcp-(1-1)-+
|
R-2HOC18={t3}-(1-2)-Subst
Subst = (2S,3S,4E,8E,10E)-9-methyl-4,8,10-sphingatrienine-C19 = SMILES CC(/C=C/CCCCCCCC)=C\CC/C=C/{3}[C@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: fusaruside
Compound class: glycoside
- Compound ID: 23051
|
b-D-Glcp-(1-1)-+
|
R-2HOC18={t3}-(1-2)-Subst
Subst = (2S,3S,4E,8E)-9-methyl-4,8-sphingadienine-C19 = SMILES C/C(CCCCCCCCCC)=C\CC/C=C/{3}[C@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 20860
|
b-D-Altp-(1-19)-Subst
Subst = virescenoside M aglycon = SMILES C[C@]1(C=C)CCC([C@@](C{3}[C@H]({2}[C@H](O)[C@]2(C){19}CO)O)(C2CC3=O)C)=C3C1 |
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Structure type: monomer
Trivial name: virescenoside M
Compound class: glycoside
- Compound ID: 20861
|
b-D-Altp-(1-19)-Subst
Subst = virescenoside N aglycon = SMILES C[C@]1(C=C)CCC2[C@@](C{3}[C@H]({2}[C@H](O)[C@]3(C){19}CO)O)(C3{6}[C@@H](C=C2C1)O)C |
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Structure type: monomer
Trivial name: virescenoside N
Compound class: glycoside
- Compound ID: 20862
|
b-D-Altp-(1-19)-Subst
Subst = sandaracopimara-8(14),15-diene-3β,7α,19-triol = SMILES C[C@@]1(CCC(C2=C1)[C@@](C)(CCC([C@@]3({19}CO)C)O)C3C[C@H]2O)C=C |
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Structure type: monomer
Trivial name: virescenoside O
Compound class: glycoside
- Compound ID: 20863
|
b-D-Altp-(1-19)-Subst
Subst = 7-oxoisopimara-8(9),15-diene-3β,19β-diol = SMILES C[C@](C1)(C=C)CCC([C@@](C2C3)(C)CC{3}C(O)[C@]2(C){19}CO)=C1C3=O |
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Structure type: monomer
Trivial name: virescenoside P
Compound class: glycoside
- Compound ID: 20864
|
b-D-Manp-(1-19)-Subst
Subst = isopimara-7,15-diene-3β,19-diol = SMILES C[C@](C1)(C=C)CCC2C1=CCC3[C@]2(C)CC{3}C(O)[C@]3(C){19}CO |
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Structure type: monomer
Trivial name: virescenoside Q
Compound class: glycoside
- Compound ID: 20878
|
a-D-Glcp-(1-6)-b-D-Altp-(1-19)-Subst
Subst = isopimara-7,15-diene-2α,3β,19-triol = SMILES C[C@@]1(CCC2[C@@](C)(C[C@@H](O)[C@@H]([C@@]3({19}CO)C)O)C3CC=C2C1)C=C |
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Structure type: oligomer
Trivial name: virescenoside R
Compound class: glycoside
- Compound ID: 20879
|
b-D-Altp-(1-19)-Subst
Subst = virescenoside W aglycon = SMILES C[C@]1(C=C)CCC2[C@@](C{3}[C@H]({2}[C@H](O)[C@]3(C){19}CO)O)(C3{6}[C@H](C=C2C1)O)C |
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Structure type: monomer
Trivial name: virescenoside W
Compound class: glycoside
- Compound ID: 20880
|
b-D-Altp-(1-19)-Subst
Subst = virescenoside V, Z14 aglycon = SMILES C=C[C@]3(C)/C=C\2C(=O)C[C@H]1[C@@](C)({19}CO){3}[C@@H](O){2}[C@H](O)C[C@]1(C)[C@H]2CC3 |
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Structure type: monomer
Trivial name: virescenoside V
Compound class: glycoside
- Compound ID: 20881
|
b-D-Altp-(1-19)-Subst
Subst = 3-oxo-isopimara-8(14),15-diene-7α,19-diol = SMILES C[C@]1(C=C)CCC2[C@@](CCC([C@]3(C){19}CO)=O)(C3C[C@@H](O)C2=C1)C |
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Structure type: monomer
Trivial name: virescenoside S
Compound class: glycoside
- Compound ID: 20882
|
b-D-Altp-(1-19)-Subst
Subst = 3,7-dioxo-isopimara-8(14),15-diene-19-ol = SMILES C[C@@]({19}CO)(C1C2)C(CC[C@]1(C)C3CC[C@](C)(C=C)C=C3C2=O)=O |
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Structure type: monomer
Trivial name: virescenoside U
Compound class: glycoside
- Compound ID: 20883
|
b-D-Altp-(1-19)-Subst
Subst = 3,7-dioxo-isopimara-8(9),15-diene-19-ol = SMILES C[C@@]({19}CO)(C1C2)C(CC[C@]1(C)C3=C(C[C@@](C=C)(CC3)C)C2=O)=O |
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Structure type: monomer
Trivial name: virescenoside T
Compound class: glycoside
- Compound ID: 20884
|
b-D-Altp-(1-19)-Subst
Subst = virescenoside X aglycon = SMILES C[C@@](CC1)(C=C)CC2=C1[C@]3(C)C(C{7}[C@H]2O)[C@@](C)({19}CO){3}[C@@H](O){2}[C@H](O)C3 |
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Structure type: monomer
Trivial name: virescenoside X
Compound class: glycoside
- Compound ID: 20889
|
b-D-AltpA-(1-19)-Subst
Subst = isopimara-7,15-diene-2α,3β,19-triol = SMILES C[C@@]1(CCC2[C@@](C)(C[C@@H](O)[C@@H]([C@@]3({19}CO)C)O)C3CC=C2C1)C=C |
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Structure type: monomer
C26H40O9
Trivial name: virescenoside F
Compound class: glycoside, diterpene glycoside
- Compound ID: 20890
|
b-D-AltpA-(1-19)-Subst
Subst = isopimara-7,15-diene-3β,19-diol = SMILES C[C@](C1)(C=C)CCC2C1=CCC3[C@]2(C)CC{3}C(O)[C@]3(C){19}CO |
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Structure type: monomer
C26H40O8
Trivial name: virescenoside G
Compound class: glycoside, diterpene glycoside
- Compound ID: 22724
|
b-D-AltpA-(1-19)-Subst
Subst = virescenoside Z6 aglycon = SMILES C[C@]12CC{3}[C@H](O)[C@@]({19}CO)(C)C1C{7}[C@@H](O)C3=C[C@](C=C)(C)CCC32 |
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Structure type: monomer
Trivial name: virescenoside Z6
Compound class: glycoside, diterpene glycoside
- Compound ID: 22725
|
b-D-AltpA-(1-19)-Subst
Subst = virescenoside Z7 aglycon = SMILES C[C@]12C{2}[C@@H](O){3}[C@H](O)[C@@]({19}CO)(C)C1C(C=C3C2CC[C@@]({15}[C@@H](O)CCl)(C)C3)O |
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Structure type: monomer
Trivial name: virescenoside Z7
Compound class: glycoside, diterpene glycoside
- Compound ID: 22726
|
b-D-AltpA-(1-19)-Subst
Subst = virescenoside Z8 aglycon = SMILES C[C@]12C{2}[C@@H](O){3}[C@H](O)[C@@]({19}CO)(C)C1{6}C(O)=CC3=C[C@](C=C)(C)CCC32 |
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Structure type: monomer
Trivial name: virescenoside Z8
Compound class: glycoside, diterpene glycoside
- Compound ID: 22946
|
b-D-4dthrHexp4en-(1-19)-Subst
Subst = isopimara-7,15-diene-2α,3β,19-triol = SMILES C[C@@]1(CCC2[C@@](C)(C[C@@H](O)[C@@H]([C@@]3({19}CO)C)O)C3CC=C2C1)C=C |
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Structure type: monomer
Trivial name: virescenoside L
Compound class: glycoside
- Compound ID: 22951
|
b-D-AltpA-(1-19)-Subst
Subst = 3-oxo-isopimara-7(8),15-diene-19-ol = SMILES C[C@@]1(CCC2[C@@](C)(CCC([C@@]3({19}CO)C)=O)C3CC=C2C1)C=C |
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Structure type: monomer
Trivial name: virescenoside Z4
Compound class: glycoside
- Compound ID: 22952
|
b-D-AltpA-(1-19)-Subst
Subst = virescenoside Z5 aglycon = SMILES C[C@@]1(C(CC=C2C1CC[C@@]({20}[C@@H](O)CCl)(C)C2)[C@@]3(C){19}CO)CCC3=O |
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Structure type: monomer
Trivial name: virescenoside Z5
Compound class: glycoside
- Compound ID: 22916
|
b-D-Glcp4Me-(1-11)-Subst6Me
Subst = decarboxyhydroxycitrinone = SMILES CC1={6}C(O)C={8}C(O)C2=C1C(C)=C({11}CO)OC2=O |
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Structure type: monomer
Trivial name: acremonone H
Compound class: glycoside
- Compound ID: 23098
|
b-D-Galp-(1-6)-Subst-(7-4)-Subst
Subst = 2-octyl-4,6-dihydroxybenzoic acid = SMILES O{6}C1={5}C{4}C(O)=CC(CCCCCCCC)=C1{7}C(O)=O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23099
|
b-D-Galp-(1-6)-b-D-Galp-(1-6)-Subst-(7-4)-Subst
Subst = 2-octyl-4,6-dihydroxybenzoic acid = SMILES O{6}C1={5}C{4}C(O)=CC(CCCCCCCC)=C1{7}C(O)=O |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 23140
|
b-D-Glcp-(1-3)-+
|
b-D-Glcp-(1-1)-Subst
Subst = 4-(2-methylbut-3-en-2-yl)benzene-1,3-diol = SMILES CC(C=C)(C)C1=CC={1}C(O)C={3}C1O |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 23141
|
b-D-Glcp-(1-3)-Subst
Subst = 4-(2-methylbut-3-en-2-yl)benzene-1,3-diol = SMILES CC(C=C)(C)C1=CC={1}C(O)C={3}C1O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23156
|
b-D-Glcp4Me-(1-1)-Subst
Subst = 5-heptylresorcinol = SMILES O{1}C1=CC(CCCCCCC)=C{3}C(O)=C1 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23061
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Subst-(1-2)-+
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b-D-Glcp-(1-1)-S,R-9b1SphdC19
Subst = 2R-hydroxy-tetracos-17Z-enoic acid = SMILES O={1}C(O){2}[C@H](O)CCCCCCCCCCCCCC/C=C\CCCCCC |
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Structure type: monomer
Trivial name: catacerebroside A
Compound class: glycoside
- Compound ID: 23062
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Subst-(1-2)-+
|
b-D-Glcp-(1-1)-Subst1
Subst = 2R-hydroxy-tetracos-17Z-enoic acid = SMILES O={1}C(O){2}[C@H](O)CCCCCCCCCCCCCC/C=C\CCCCCC;
Subst1 = (2S,3R,4R)-4-hydroxysphinganine-C18 = SMILES CCCCCCCCCCCCCC{4}[C@@H](O){3}[C@@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: catacerebroside B
Compound class: glycoside
- Compound ID: 23063
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Subst-(1-2)-+
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b-D-Glcp-(1-1)-Subst1
Subst = 2R,3-dihydroxy-tetracos-17Z-enoic acid = SMILES O={1}C(O){2}[C@H](O){3}C(O)CCCCCCCCCCCCC/C=C\CCCCCC;
Subst1 = (2S,3R,4R)-4-hydroxysphinganine-C18 = SMILES CCCCCCCCCCCCCC{4}[C@@H](O){3}[C@@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: catacerebroside C
Compound class: glycoside
- Compound ID: 23121
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b-D-Sugf-(1C-9)-Subst
Sug = SMILES O[C@@H]1{1}[C@@H]O[C@@H](C)[C@@H]1O;
Subst = (2-methoxy-6-vinylphenyl)methanol = SMILES COC1=CC=CC(C={9}C)=C1{7}CO |
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Structure type: monomer
Trivial name: (+)-varitriol
Compound class: glycoside
- Compound ID: 20235
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a-D-Ribf-(1-3)-Subst
Subst = asperflavin = SMILES COC1=C{3}C(O)=CC(C=C2C{6}[C@@](C)(C3)O)=C1{9}C(O)=C2C3=O |
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Structure type: monomer
Compound class: glycoside
Reference(s) to other database(s): GenDB:JQ743649
- Compound ID: 23091
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b-D-Galf-(1-2)-Subst
Subst = 3-heptyl-5-hydroxyphenyl 6-heptyl-2,6-dihydroxybenzoate = SMILES O{53}C1=CC(OC(C2=C(CCCCCCC)C={4}C(O)C={2}C2O)=O)=CC(CCCCCCC)=C1 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23092
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b-D-Galf-(1-6)-Subst-(7-4)-Subst
Subst = 2-heptyl-4,6-dihydroxybenzoic acid = SMILES O{6}C1={5}C{4}C(O)=CC(CCCCCCC)=C1{7}C(O)=O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22873
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b-D-Manp-(1-27)-Subst
Subst = virgineone aglycon = SMILES CC(C(C1={3}C([C@@H](NC1=O)CC2=CC={54}C(C=C2)O)O)=O)CCCCCCCCC(CCCCCCCCC{26}[C@H]({27}CO)O)=O |
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Structure type: monomer
Trivial name: virgineone
Compound class: glycoside
- Compound ID: 22874
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b-D-Manp-(1-27)-Subst
Subst = 1,2-dehydrovirgineone aglycon = SMILES CC(C(C1={3}C(C(CC2=CC={54}C(C=C2)O)=NC1=O)O)=O)CCCCCCCCC(CCCCCCCCC{26}[C@H]({27}CO)O)=O |
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Structure type: monomer
Trivial name: 1,2-dehydrovirgineone
Compound class: glycoside
- Compound ID: 22883
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b-D-Manp-(1-13)-Subst-(1-5)-D-Lyx-ol
Subst = SMILES CCC(CC(/C=C({13}[C@H]([C@H](/C=C([C@H]([C@H](/C=C([C@H]([C@H](/C=C({1}C(O)=O)\C)C)O)\C)C)O)\C)C)O)\C)C)C |
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Structure type: oligomer
Trivial name: bionectriol A
Compound class: glycoside
- Compound ID: 22885
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b-D-Manp4Me-(1-5)-Subst
Subst = myrothecoside aglycon = SMILES [H][C@]12/C=C\[C@@H](C)[C@@H](/C=C/{5}[C@H](O)C{3}[C@@H](O)CC(N)=O)[C@@]1([H])[C@@H](C)C[C@H](C)C2 |
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Structure type: monomer
Trivial name: myrothecoside
Compound class: glycoside
- Compound ID: 23065
|
b-D-Glcp-(1-1)-+
|
R-2HOC16={t3}-(1-2)-Subst
Subst = sphinga-4E,8E-dienine = SMILES CCCCCCCCC/C=C/CC/C=C/{3}[C@@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: soyacerebroside I
Compound class: glycoside
- Compound ID: 21246
Structure type: monomer
Compound class: glucoside, glycoside
- Compound ID: 20232
|
a-D-Ribf-(1-3)-Subst
Subst = questin = SMILES COC1=C{3}C(O)=CC(C(C2=C3{8}C(O)=CC(C)=C2)=O)=C1C3=O |
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Structure type: monomer
Compound class: glycoside
Reference(s) to other database(s): GenDB:JQ743649
- Compound ID: 23014
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a-D-Ribf-(1-4)-Subst2Me
Subst = 9-dehydroxyeurotinone = SMILES O=C1C2=C(CC(C={4}C(C={2}C3O)O)=C3O1)C=C(C)C={11}C2O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22364
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b-D-Manp3Ac-(1-21)-Subst
Subst = epicoccamide A, B, C aglycon = SMILES CC1C(/C(C(N1C)=O)={6}C(O)\C(CCCCCCCCCCCCC{21}CO)C)=O |
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Structure type: monomer
Trivial name: epicoccamide B
Compound class: glycoside
- Compound ID: 22365
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b-D-Manp6Ac-(1-21)-Subst
Subst = epicoccamide A, B, C aglycon = SMILES CC1C(/C(C(N1C)=O)={6}C(O)\C(CCCCCCCCCCCCC{21}CO)C)=O |
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Structure type: monomer
Trivial name: epicoccamide C
Compound class: glycoside
- Compound ID: 22872
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b-D-Manp-(1-24)-Subst
Subst = epicoccamide D aglycon = SMILES CC1C(/C(C(N1C)=O)={7}C(O)\C(CCCCCCCCCCCCCCC{24}CO)C)=O |
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Structure type: monomer
Trivial name: epicoccamide D
Compound class: glycoside
- Compound ID: 22901
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b-D-1dGalp-(1C-3)-Subst
Subst = (2Z,3Z,5E,7E,9E,11E,13E)-14-(4-hydroxy-2-oxo-2H-pyran-6-yl)-2-(4,6-dimethyloctylidene)-4-methyltetradeca-3,5,7,9,11,13-hexaenoic acid = SMILES CCC(C)CC(C)CC/C=C({29}C(O)=O)/C=C(\C=C\C=C\C=C\C=C\C=C\C(O1)=C{4}C(O)={3}CC1=O)C |
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Structure type: monomer
Trivial name: iso-D8646-2-6
Compound class: glycoside
- Compound ID: 20509
|
b-D-Glcp4Me-(1-3)-Subst
Subst = diorcinol = SMILES CC1=CC(OC2=C{3}C(O)=CC(C)=C2)=C{53}C(O)=C1 |
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Structure type: monomer
Trivial name: cordyol A
Compound class: glycoside, diphenyl ether glycoside, phenolic glycoside
- Compound ID: 23143
|
b-D-Glcp4Me-(1-3)-Subst-(1-4)-Ors7Me
Subst = 3-hydroxy-5-methyl phenol = SMILES O{1}C1=CC(C)=C{3}C(O)=C1 |
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Structure type: monomer
Trivial name: cordyol B
Compound class: glycoside
- Compound ID: 22935
|
a-D-Glcp4Me-(1-8)-+
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a-D-Glcp4Me-(1-1)-Subst
Subst = naphthalene-1,8-diol = SMILES O{8}c1cccc2ccc{1}c(O)c12 |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 23152
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b-D-Glcp4Me-(1-4)-Subst
Subst = SMILES O{4}C1=CC={1}C(O)C(OC)=C1 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23153
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b-D-Glcp4Me-(1-1)-Subst
Subst = SMILES O{4}C1=CC={1}C(O)C(OC)=C1 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23154
|
b-D-Glcp4Me-(1-4)-Subst
Subst = vanillic acid = SMILES COC1=CC({7}C(O)=O)=CC={4}C1O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23155
|
b-D-Glcp4Me-(1-3)-Subst
Subst = SMILES O{3}C1=CC(/C=C/{9}C(O)=O)=CC(OC)=C1 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23157
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b-D-Glcp-(1-4)-Subst
Subst = glyscavin A aglycon = SMILES O{1}C1=CC={4}C(O)C(/C=C/C=C/C)=C1{7}CO |
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Structure type: monomer
Trivial name: glyscavin A
Compound class: glycoside
- Compound ID: 23158
|
b-D-Glcp-(1-4)-Subst
Subst = glyscavin B aglycon = SMILES O{1}C1=CC={4}C(O)C(/C=C/CCC)=C1{7}CO |
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Structure type: monomer
Trivial name: glyscavin B
Compound class: glycoside
- Compound ID: 23159
|
b-D-Glcp-(1-4)-Subst
Subst = glyscavin C = SMILES O{1}C1=CC={4}C(O)C(CCCCC)=C1{7}CO |
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Structure type: monomer
Trivial name: glyscavin C
Compound class: glycoside
- Compound ID: 22941
|
b-D-Glcp4Me-(1-6)-Subst
Subst = 5,6,8-trihydroxy-2,7-dimethyl-4H-chromen-4-one = SMILES O=C(C=C(C)O1)C2=C1{8}C(O)=C(C){6}C(O)={5}C2O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23038
|
2HOPam-(1-2)-+
|
b-D-Glcp-(1-1)-Subst
Subst = (2S,3R,5E,9Z)-5,9-sphingadienine-C19 = SMILES O{3}[C@@H]({2}[C@H]({1}CO)N)C/C=C/CC/C=C\CCCCCCCCC |
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Structure type: monomer
Trivial name: deformin
Compound class: glycoside
- Compound ID: 22927
|
b-D-Glcp4Me-(1-6)-Subst
Subst = 5-methoxy-6,8-dihydroxy-3-methylisochromen-1-one = SMILES O=c1oc(C)cc2c(OC){6}c(O)c{8}c(O)c12 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23148
|
b-D-Galp-(1-1)-Subst
Subst = stemphol = SMILES CCCCCC1=C{1}C(O)=C({3}C(O)={4}C1)CCCC |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22908
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b-D-Glcp4Me-(1-6)-Subst
Subst = 6,8-dihydroxy-3-methylisocoumarin = SMILES Cc2cc1c{6}c(O)cc(O)c1c(=O)o2 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22909
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b-D-Glcp4Me-(1-9)-Subst
Subst = 6,8-dihydroxy-3-hydroxymethylisocoumarin = SMILES O=c1oc({9}CO)cc2cc(O)cc(O)c12 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22910
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b-D-Glcp4Me-(1-6)-Subst
Subst = 6,8-dihydroxy-3-hydroxymethylisocoumarin = SMILES O=c1oc(CO)cc2c{6}c(O)cc(O)c12 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22931
|
a-D-Glcp-(1-1)-Subst
Subst = naphthalene-1,8-diol = SMILES Oc1cccc2ccc{1}c(O)c12 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23135
|
a-L-Rhap-(1-1)-Subst
Subst = phenylethanol = SMILES O{1}CCC1=CC=CC=C1 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 18785
|
b-D-Glcp4Me-(1-7)-Subst
Subst = indigotide A aglycon = SMILES C/C=C/C=C/C1=CC2=C(CO1){8}C(O)={7}C(O){6}C(O)=C2 |
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Structure type: monomer
C21H26O9
Trivial name: indigotide A
Compound class: glycoside, polyketide glycoside
- Compound ID: 17658
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Subst-(2-6)-a-D-Glcp3Ac-(1-9)-Subst1
Subst = 2-methylbut-3-en-2-ol = SMILES C=C{2}C(C)(C)O;
Subst1 = fusicoccin A aglycon = SMILES COC[C@]1(CC[C@]2([H])/C1=C\[C@]3({12}[C@@H](O)CC([C@](COC(C)=O)([H])C)=C3{9}[C@H]({8}[C@@H]([C@@H]2C)O)O)C)[H] |
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Structure type: monomer
Trivial name: fusicoccin A
Compound class: glycoside, diterpene glycoside
Reference(s) to other database(s): GTC:G97099AY
- Compound ID: 18826
|
Subst-(2-6)-a-D-Glcp-(1-9)-Subst1
Subst = 2-methylbut-3-en-2-ol = SMILES C=C{2}C(C)(C)O;
Subst1 = 16-O-demethyl 3-epifusicoccin J aglycon = SMILES CC(C)/C3=C/2{9}[C@@H](O){8}[C@H](O)[C@H](C)[C@@H]/1CC[C@@H]({16}CO)C1=C\[C@@]2(C){12}[C@@H](O)C3 |
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Structure type: monomer
Trivial name: 16-O-demethyl 3-epifusicoccin J, 16-O-demethyl-3-epifusicoccin J
Compound class: glycoside
- Compound ID: 19042
|
b-D-Glcp-(1-9)-Subst-(16-1)-Me
Subst = fusicoccin Q aglycon = SMILES CC(C)/C3=C/2{9}[C@@H](O){8}[C@H](O)[C@H](C)[C@@H]/1CC[C@H]({16}CO)C1=C\[C@@]2(C){12}[C@@H](O)C3 |
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Structure type: monomer
Trivial name: fusicoccin P
Compound class: glycoside
- Compound ID: 19043
|
Subst-(2-6)-b-D-Glcp-(1-9)-Subst1-16Me
Subst = 2-methylbut-3-en-2-ol = SMILES C=C{2}C(C)(C)O;
Subst1 = fusicoccin Q aglycon = SMILES CC(C)/C3=C/2{9}[C@@H](O){8}[C@H](O)[C@H](C)[C@@H]/1CC[C@H]({16}CO)C1=C\[C@@]2(C){12}[C@@H](O)C3 |
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Structure type: monomer
Trivial name: fusicoccin J
Compound class: glycoside
- Compound ID: 19046
|
b-D-Glcp-(1-9)-Subst
Subst = fusicoccin Q aglycon = SMILES CC(C)/C3=C/2{9}[C@@H](O){8}[C@H](O)[C@H](C)[C@@H]/1CC[C@H]({16}CO)C1=C\[C@@]2(C){12}[C@@H](O)C3 |
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Structure type: monomer
Trivial name: fusicoccin Q
Compound class: glycoside
- Compound ID: 19048
|
Subst-(2-6)-b-D-Glcp-(1-9)-Subst1
Subst = 2-methylbut-3-en-2-ol = SMILES C=C{2}C(C)(C)O;
Subst1 = deacetylfusicoccin A aglycon = SMILES COC[C@]1(CC[C@]2([H])/C1=C\[C@]3({12}[C@@H](O)CC([C@]({15}CO)([H])C)=C3{9}[C@H]({8}[C@@H]([C@@H]2C)O)O)C)[H] |
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Structure type: monomer
Trivial name: fusicoccin D
Compound class: glycoside
- Compound ID: 22964
|
Subst-(2-6)-a-D-Glcp4Ac-(1-9)-Subst1
Subst = 2-methylbut-3-en-2-ol = SMILES C=C{2}C(C)(C)O;
Subst1 = fusicoccin A aglycon = SMILES COC[C@]1(CC[C@]2([H])/C1=C\[C@]3({12}[C@@H](O)CC([C@](COC(C)=O)([H])C)=C3{9}[C@H]({8}[C@@H]([C@@H]2C)O)O)C)[H] |
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Structure type: monomer
Trivial name: fusicoccin B
Compound class: glycoside
- Compound ID: 22965
|
Subst-(2-6)-a-D-Glcp-(1-9)-Subst1
Subst = 2-methylbut-3-en-2-ol = SMILES C=C{2}C(C)(C)O;
Subst1 = fusicoccin A aglycon = SMILES COC[C@]1(CC[C@]2([H])/C1=C\[C@]3({12}[C@@H](O)CC([C@](COC(C)=O)([H])C)=C3{9}[C@H]({8}[C@@H]([C@@H]2C)O)O)C)[H] |
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Structure type: monomer
Trivial name: fusicoccin C
Compound class: glycoside
- Compound ID: 22966
|
b-D-Glcp-(1-9)-Subst
Subst = fusicoccin F aglycon O{18}C[C@]1(CC[C@]2([H])/C1=C\[C@]3({12}[C@@H](O)CC([C@]({16}CO)([H])C)=C3{9}[C@H]({8}[C@@H]([C@@H]2C)O)O)C)[H] |
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Structure type: monomer
Trivial name: fusicoccin F
Compound class: glycoside
- Compound ID: 22967
|
b-D-Glcp-(1-9)-Subst16Me
Subst = fusicoccin H aglycon = SMILES CC(C)/C3=C/2{9}[C@@H](O){8}[C@H](O)[C@H](C)[C@@H]/1CC[C@H]({16}CO)C1=C\[C@@]2(C)CC3 |
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Structure type: monomer
Trivial name: fusicoccin H
Compound class: glycoside
- Compound ID: 22968
|
Subst-(2-6)-b-D-Glcp4Ac-(1-9)-Subst1-16Me
Subst = 2-methylbut-3-en-2-ol = SMILES C=C{2}C(C)(C)O;
Subst1 = fusicoccin Q aglycon = SMILES CC(C)/C3=C/2{9}[C@@H](O){8}[C@H](O)[C@H](C)[C@@H]/1CC[C@H]({16}CO)C1=C\[C@@]2(C){12}[C@@H](O)C3 |
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Structure type: monomer
Trivial name: isofusicoccin A
Compound class: glycoside
- Compound ID: 22969
|
b-D-Glcp-(1-9)-Subst
Subst = epifusicoccin H aglycon = SMILES CC(C)/C3=C/2{9}[C@@H](O){8}[C@H](O)[C@H](C)[C@@H]/1CC[C@@H]({16}CO)C1=C\[C@@]2(C)CC3 |
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Structure type: monomer
Trivial name: 3-epifusicoccin H
Compound class: glycoside
- Compound ID: 22970
|
b-D-Glcp-(1-9)-Subst
Subst = 16-O-demethyl 3-epifusicoccin J aglycon = SMILES CC(C)/C3=C/2{9}[C@@H](O){8}[C@H](O)[C@H](C)[C@@H]/1CC[C@@H]({16}CO)C1=C\[C@@]2(C){12}[C@@H](O)C3 |
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Structure type: monomer
Trivial name: 3-epifusicoccin Q
Compound class: glycoside
- Compound ID: 22971
|
Subst-(2-6)-a-D-Glcp-(1-9)-Subst1
Subst = 2-methylbut-3-en-2-ol = SMILES C=C{2}C(C)(C)O;
Subst1 = 3-α-hydroxyfusicoccin J aglycon = SMILES CC(C)/C3=C/2{9}[C@@H](O){8}[C@H](O)[C@H](C)[C@@H]/1CC[C@](O)({16}CO)C1=C\[C@@]2(C){12}[C@@H](O)C3 |
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Structure type: monomer
Trivial name: 3-α-hydroxyfusicoccin J
Compound class: glycoside
- Compound ID: 22972
|
Subst-(2-6)-a-D-Glcp-(1-9)-Subst1
Subst = 2-methylbut-3-en-2-ol = SMILES C=C{2}C(C)(C)O;
Subst1 = fusicoccin R aglycon = SMILES C[C@@H]({17}CO)/C3=C/2{9}[C@@H](O){8}[C@H](O)[C@H](C)[C@@H]/1CC[C@](O)({16}CO)C1=C\[C@@]2(C){12}[C@@H](O)C3 |
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Structure type: monomer
Trivial name: fusicoccin R
Compound class: glycoside
- Compound ID: 22973
|
a-D-Glcp-(1-9)-Subst
Subst = fusicoccin S aglycon = SMILES CC(C1=C2{8}[C@H]({9}[C@@H]([C@@H]([C@@H]3CC{3}[C@@](/C3=C/[C@]2({12}[C@H](C1)O)C)(O){19}CO)C)O)O)C |
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Structure type: monomer
Trivial name: fusicoccin S
Compound class: glycoside
- Compound ID: 18824
|
a-D-Sugp6Me-(1-6)-Subst
Sug = xylo-hexos-4-ulose derivative = SMILES CC2([C@H]1CO1)O[C@@]34OC2O[C@@H]3[C@@H](O){1}[C@@H](O)O[C@@H]4{6}CO;
Subst = cotylenol = SMILES COC{1}[C@@]1(O)CC[C@H]2/C1=C\[C@@]3(C)CCC(C(C)C)=C3{6}[C@@H](O){5}[C@H](O)[C@@H]2C |
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Structure type: monomer
Trivial name: cotylenin A
Compound class: glycoside
Reference(s) to other database(s): GTC:G30893DQ
- Compound ID: 21908
|
a-D-Glcp6Me-(1-6)-Subst
Subst = cotylenol = SMILES COC{1}[C@@]1(O)CC[C@H]2/C1=C\[C@@]3(C)CCC(C(C)C)=C3{6}[C@@H](O){5}[C@H](O)[C@@H]2C |
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Structure type: monomer
Trivial name: cotylenin E
Compound class: glycoside
Reference(s) to other database(s): GenDB:MH458525
- Compound ID: 21909
|
a-D-Glcp6Me-(1-6)-Subst
Subst = cotylenol epimer = SMILES COC{1}[C@]1(O)CC[C@H]2/C1=C\[C@@]3(C)CCC(C(C)C)=C3{6}[C@@H](O){5}[C@H](O)[C@@H]2C |
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Structure type: monomer
Trivial name: cotylenin J
Compound class: glycoside
Reference(s) to other database(s): GenDB:MH458525
- Compound ID: 22974
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a-D-Sugp6Me-(1-6)-Subst
Sug = xylo-hexos-4-ulose derivative = SMILES CC1(O[C@@]23OC1O[C@@H]2[C@H]({1}[C@H](O[C@@H]3{6}CO)O)O)CCCl;
Subst = cotylenol = SMILES COC{1}[C@@]1(O)CC[C@H]2/C1=C\[C@@]3(C)CCC(C(C)C)=C3{6}[C@@H](O){5}[C@H](O)[C@@H]2C |
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Structure type: monomer
Trivial name: cotylenin B
Compound class: glycoside
- Compound ID: 22975
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Subst1-(1-3:2-4)-a-D-Glcp6Me-(1-6)-Subst
Subst = cotylenol = SMILES COC{1}[C@@]1(O)CC[C@H]2/C1=C\[C@@]3(C)CCC(C(C)C)=C3{6}[C@@H](O){5}[C@H](O)[C@@H]2C;
Subst1 = 2-((S)-oxiran-2-yl)propane-1,2-diol = SMILES C{2}C(O)([C@H]1OC1){1}CO |
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Structure type: monomer
Trivial name: cotylenin C
Compound class: glycoside
- Compound ID: 22976
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a-D-Sugp6Me-(1-6)-Subst
Sug = xylo-hexos-4-ulose derivative = SMILES CC1(O[C@@]23OC1O[C@@H]2[C@H]({1}[C@H](O[C@@H]3{6}CO)O)O)CCO;
Subst = cotylenol = SMILES COC{1}[C@@]1(O)CC[C@H]2/C1=C\[C@@]3(C)CCC(C(C)C)=C3{6}[C@@H](O){5}[C@H](O)[C@@H]2C |
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Structure type: monomer
Trivial name: cotylenin D
Compound class: glycoside
- Compound ID: 22977
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Subst1-(2-4)-a-D-Glcp6Me-(1-6)-Subst
Subst = cotylenol = SMILES COC{1}[C@@]1(O)CC[C@H]2/C1=C\[C@@]3(C)CCC(C(C)C)=C3{6}[C@@H](O){5}[C@H](O)[C@@H]2C;
Subst1 = 2-((S)-oxiran-2-yl)propane-1,2-diol = SMILES C{2}C(O)([C@H]1OC1){1}CO |
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Structure type: monomer
Trivial name: cotylenin F
Compound class: glycoside
- Compound ID: 22978
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Subst1-(2-4:3-3)-a-D-Glcp6Me-(1-6)-Subst
Subst = cotylenol = SMILES COC{1}[C@@]1(O)CC[C@H]2/C1=C\[C@@]3(C)CCC(C(C)C)=C3{6}[C@@H](O){5}[C@H](O)[C@@H]2C;
Subst1 = (2R,3R)-2-methylbutane-1,2,3-triol = SMILES C{3}[C@H]({2}[C@@](O)(C){1}CO)O |
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Structure type: monomer
Trivial name: cotylenin G
Compound class: glycoside
- Compound ID: 22979
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a-D-Sugp6Me-(1-6)-Subst
Subst = cotylenol = SMILES COC{1}[C@@]1(O)CC[C@H]2/C1=C\[C@@]3(C)CCC(C(C)C)=C3{6}[C@@H](O){5}[C@H](O)[C@@H]2C;
Sug = SMILES O=C1{4}[C@H](O){5}[C@@H]({6}CO)O{1}[C@H](O){2}[C@@H]1O |
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Structure type: monomer
Trivial name: cotylenin H
Compound class: glycoside
- Compound ID: 22980
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Subst1-(2-4)-a-D-Glcp6Me-(1-6)-Subst
Subst = cotylenol = SMILES COC{1}[C@@]1(O)CC[C@H]2/C1=C\[C@@]3(C)CCC(C(C)C)=C3{6}[C@@H](O){5}[C@H](O)[C@@H]2C;
Subst1 = 2-methylbut-3-en-2-ol = SMILES C{2}C(C=C)(C)O |
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Structure type: monomer
Trivial name: cotylenin I
Compound class: glycoside
- Compound ID: 19231
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a-D-Ribf-(1-4)-Subst
Subst = 2,2-dimethylchromen-6-ol = SMILES CC1(C=CC2=C(O1)C=C{4}C(O)=C2)C |
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Structure type: monomer
Trivial name: sterin A
Compound class: glycoside
- Compound ID: 19222
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b-D-Manp-(1-5)-D-Man-onic-(1-23)-Subst
Subst = caloporoside aglycon = SMILES C{23}[C@H](CCCCCCCCCCCCCCCC1=C({1}C(O)=O){3}C(O)=CC=C1)O |
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Structure type: oligomer
Trivial name: bis-deacetyl caloporoside, caloporoside A
Compound class: glycoside
- Compound ID: 23104
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b-D-Manp2Ac3Ac-(1-23)-Subst
Subst = caloporoside aglycon = SMILES C{23}[C@H](CCCCCCCCCCCCCCCC1=C({1}C(O)=O){3}C(O)=CC=C1)O |
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Structure type: monomer
Trivial name: caloporoside G
Compound class: glycoside
- Compound ID: 23105
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Mal3Me-(1-6)-+
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b-D-Manp2Ac-(1-5)-D-Man2Ac-onic-(1-23)-Subst
Subst = caloporoside aglycon = SMILES C{23}[C@H](CCCCCCCCCCCCCCCC1=C({1}C(O)=O){3}C(O)=CC=C1)O |
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Structure type: oligomer
Trivial name: caloporoside H
Compound class: glycoside
- Compound ID: 23106
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Mal-(1-6)-+
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b-D-Manp2Ac-(1-5)-D-Man2Ac-onic-(1-23)-Subst
Subst = caloporoside aglycon = SMILES C{23}[C@H](CCCCCCCCCCCCCCCC1=C({1}C(O)=O){3}C(O)=CC=C1)O |
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Structure type: oligomer
Trivial name: F-16438G
Compound class: glycoside
- Compound ID: 23107
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b-D-Manp-(1-5)-D-Man-onic-(1-23)-Subst
Subst = F-16438 A aglycon = SMILES C{23}[C@H](CCCCCCCCCCCCCC(=O)CC1=C({1}C(O)=O){3}C(O)=CC=C1)O |
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Structure type: oligomer
Trivial name: F-16438 A
Compound class: glycoside
- Compound ID: 23108
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b-D-Manp2Ac-(1-5)-D-Man-onic-(1-23)-Subst
Subst = F-16438 A aglycon = SMILES C{23}[C@H](CCCCCCCCCCCCCC(=O)CC1=C({1}C(O)=O){3}C(O)=CC=C1)O |
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Structure type: oligomer
Trivial name: caloporoside B
Compound class: glycoside
- Compound ID: 23109
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Mal3Me-(1-6)-+
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b-D-Manp2Ac-(1-5)-D-Man2Ac-onic-(1-23)-Subst
Subst = F-16438 A aglycon = SMILES C{23}[C@H](CCCCCCCCCCCCCC(=O)CC1=C({1}C(O)=O){3}C(O)=CC=C1)O |
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Structure type: oligomer
Trivial name: caloporoside E
Compound class: glycoside
- Compound ID: 23110
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Mal-(1-6)-+
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b-D-Manp2Ac-(1-5)-D-Man2Ac-onic-(1-23)-Subst
Subst = F-16438 A aglycon = SMILES C{23}[C@H](CCCCCCCCCCCCCC(=O)CC1=C({1}C(O)=O){3}C(O)=CC=C1)O |
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Structure type: oligomer
Trivial name: caloporoside F
Compound class: glycoside
- Compound ID: 23111
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Mal-(1-6)-+
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b-D-Manp2Ac-(1-5)-D-Man-onic-(1-23)-Subst1Ac
Subst = caloporoside aglycon = SMILES C{23}[C@H](CCCCCCCCCCCCCCCC1=C({1}C(O)=O){3}C(O)=CC=C1)O |
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Structure type: monomer
Trivial name: caloporoside C
Compound class: glycoside
- Compound ID: 23112
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Mal-(1-6)-+
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b-D-Manp2Ac-(1-5)-D-Man-onic-(1-23)-Subst
Subst = caloporoside aglycon = SMILES C{23}[C@H](CCCCCCCCCCCCCCCC1=C({1}C(O)=O){3}C(O)=CC=C1)O |
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Structure type: monomer
Trivial name: caloporoside D
Compound class: glycoside
- Compound ID: 19284
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b-D-Glcp-(1-1)-Subst
Subst = 2-methylbenzene-1,4-diol = SMILES Cc1cc(O)cc{1}c1O |
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Structure type: monomer
Trivial name: iso-homoarbutin, isohomoarbutin
Compound class: glycoside, phenolic glycoside
- Compound ID: 21952
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b-D-Glcp-(1-1)-Subst
Subst = acremonin A = SMILES C=C(C)[C@H]2Cc1{1}c(O)ccc(O)c12 |
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Structure type: monomer
Compound class: glycoside, phenolic glycoside
Reference(s) to other database(s): GenDB:KY171948
- Compound ID: 23138
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b-D-Glcp6Ac-(1-1)-Subst
Subst = 2-methylbenzene-1,4-diol = SMILES Cc1cc(O)cc{1}c1O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23139
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b-D-Glcp-(1-1)-Subst
Subst = (S)-1,1-dimethyl-2,3-dihydro-1H-indene-2,4,7-triol = SMILES CC2(C)c1c(O)cc{1}c(O)c1C[C@@H]2O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23149
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b-D-Glcp-(1-2)-Subst
Subst = 4-(3-hydroxy-5-methylphenoxy)-5-methylbenzene-1,3-diol = SMILES O{53}C1=CC(C)=C(OC2=C{2}C(O)=CC(C)=C2){4}C(O)=C1 |
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Structure type: monomer
Trivial name: phomaether A
Compound class: glycoside
- Compound ID: 23150
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a-D-Ribf-(1-3')-Subst
Subst = 4-(3-hydroxy-5-methylphenoxy)-5-methylbenzene-1,3-diol = SMILES O{53}C1=CC(C)=C(OC2=C{2}C(O)=CC(C)=C2){4}C(O)=C1 |
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Structure type: monomer
Trivial name: phomaether B
Compound class: glycoside
- Compound ID: 22912
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b-D-Glcp-(1-8)-Subst
Subst = R-(-)-mellein = SMILES C[C@@H]1CC2=CC=C{8}C(O)=C2C(O1)=O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 18714
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a-D-Manp-(1-16)-Subst
Subst = 16-hydroxyisopimar-7-en-19-oic acid = SMILES C[C@]1({19}C(O)=O)CCC[C@@]2(C)[C@H]1CC=C3[C@@H]2CC[C@](C)(C{16}CO)C3 |
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Structure type: monomer
Compound class: glycoside, isopimarane diterpene glycoside, diterpene glycoside
- Compound ID: 18715
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a-D-Glcp-(1-16)-Subst
Subst = 16-hydroxyisopimar-7-en-19-oic acid = SMILES C[C@]1({19}C(O)=O)CCC[C@@]2(C)[C@H]1CC=C3[C@@H]2CC[C@](C)(C{16}CO)C3 |
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Structure type: monomer
Compound class: glycoside, isopimarane diterpene glycoside
- Compound ID: 22959
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a-D-Manp-(1-16)-Subst
Subst = 15,16-dihydroxyisopimar-7-en-19-oic acid = SMILES C[C@]1({19}C(O)=O)CCC[C@@]2(C)[C@H]1CC=C3[C@@H]2CC[C@](C)({15}C(O){16}CO)C3 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 19653
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b-D-Altp4Me-(1-17)-Subst
Subst = sordarin C aglycon = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@H]4C[C@@](C=O)2[C@]({13}[C@](O)=O)3C(C({19}CO)C)=C4 |
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Structure type: monomer
Trivial name: sordarin C
Compound class: glycoside, diterpene glycoside
- Compound ID: 20244
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b-D-6dAltp4Me-(1-17)-Subst
Subst = sordarin D aglycon = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@H]4C[C@@](C=O)2[C@]({13}[C@](O)=O)3/C(C4=O)=C(C)\C |
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Structure type: monomer
Trivial name: sordarin D
Compound class: glycoside
- Compound ID: 20245
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b-D-6dAltp4Me-(1-17)-Subst
Subst = sordarin E aglycon = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@H]4C[C@@](C=O)2[C@]({13}[C@](O)=O)3C5(C(C)C5)C4=O |
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Structure type: monomer
Trivial name: sordarin E
Compound class: glycoside
- Compound ID: 20246
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b-D-6dAltp4Me-(1-17)-Subst
Subst = sordarin F aglycon = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@H]4C[C@@](C=O)2[C@]({13}[C@](O)=O)3/C(C4=O)=C\CC |
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Structure type: monomer
Trivial name: sordarin F
Compound class: glycoside
- Compound ID: 22923
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b-D-Glcp-(1-8)-Subst
Subst = (3S,11E,13E)-5-acetyl-6,8-dihydroxy-3-(oxopentadienyl)isochroman-1-one = SMILES CC(=O)c1{6}c(O)c{8}c(O)c2C(=O)O[C@H](/C=C/C=C/C=O)Cc12 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22924
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b-D-Glcp-(1-8)-Subst-(6-1)-Me
Subst = (3S,11E,13E)-5-acetyl-6,8-dihydroxy-3-(oxopentadienyl)isochroman-1-one = SMILES CC(=O)c1{6}c(O)c{8}c(O)c2C(=O)O[C@H](/C=C/C=C/C=O)Cc12 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22925
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b-D-Glcp-(1-8)-Subst
Subst = (S)-3-[(1E,3E,5E)-hepta-1,3,5-trienyl]-3,4-dihydro-6,8-dihydroxy-5-methyl-1H-2-benzopyran-1-one = SMILES C/C=C/C=C/C=C/[C@@H]1CC2=C({8}C(O)=C{6}C(O)=C2C(O1)=O)C |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22926
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b-D-Glcp6Ac-(1-8)-Subst-(6-1)-Me
Subst = (S)-3-[(1E,3E,5E)-hepta-1,3,5-trienyl]-3,4-dihydro-6,8-dihydroxy-5-methyl-1H-2-benzopyran-1-one = SMILES C/C=C/C=C/C=C/[C@@H]1CC2=C({8}C(O)=C{6}C(O)=C2C(O1)=O)C |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22963
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b-D-Galp-(1-1)-Subst
Subst = 1α-hydroxy-ent-13-epi-manoyl oxide = SMILES C=C[C@@]3(C)CC[C@@H]2[C@](C)(CC[C@@H]1C(C)(C)CC{1}[C@H](O)[C@]12C)O3 |
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Structure type: monomer
Trivial name: phaeoside
Compound class: glycoside
- Compound ID: 20136
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Hxo-(1-6)-+
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Hxo-(1-3)-+ |
| |
Oco-(1-2)-b-D-Manp-(1-1)-D-Man-ol
|
Hxo-(1-4)-+ |
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Structure type: oligomer
C38H68O15
Trivial name: acremomannolipin A
Compound class: glycolipid, glycoside
- Compound ID: 22001
|
b-D-Glcp-(1C-3)-Subst7Et
Subst = carnemycin A, B, C aglycon = SMILES CC/C=C/C=C/CCC1=C({7}C(O)=O){2}C(O)={3}C{4}C(O)=C1 |
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Structure type: monomer
Trivial name: carnemycin A
Compound class: glycoside
- Compound ID: 23142
|
b-D-Glcp-(1C-3)-Subst7Me
Subst = carnemycin A, B, C aglycon = SMILES CC/C=C/C=C/CCC1=C({7}C(O)=O){2}C(O)={3}C{4}C(O)=C1 |
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Structure type: monomer
Trivial name: carnemycin B
Compound class: glycoside
- Compound ID: 19655
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b-D-Altp4Me-(1-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4 |
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Structure type: monomer
Trivial name: hydroxysordarin
Compound class: glycoside, diterpene glycoside
- Compound ID: 20247
|
b-D-6dAltp4Me-(1-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4 |
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Structure type: monomer
C27H40O8
Trivial name: sordarin
Compound class: glycoside
Reference(s) to other database(s): GenDB:AJ302438
- Compound ID: 20859
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Subst1-(1-3)-b-D-6dAltp4Me-(1-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4;
Subst1 = (Z)-2-methyl-3-((2'S,3S,3'S)-3'-methyl-[2,2'-bioxiran]-3-yl)acrylic acid = SMILES C/C(=C/[C@@H]1OC1[C@H]2O[C@H]2C){1}C(=O)O |
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Structure type: monomer
Trivial name: hypoxysordarin, hypoxysordarin, FR231956
Compound class: glycoside
- Compound ID: 20869
|
Subst1-(1-3)-b-D-6dAltp4Me-(1-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4;
Subst1 = (2Z,5E)-7-hydroxy-2-methyl-4-oxoocta-2,5-dienoic acid = SMILES C/C(=C/C(=O)/C=C/C(C)O){1}C(=O)O |
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Structure type: monomer
Trivial name: neosordarin
Compound class: glycoside
- Compound ID: 23020
|
a-L-Arap-(1-6)-b-D-Glcp-(1-3)-Subst
Subst = 3-hydroxy-1,4-dimethoxy-9H-xanthen-9-one = SMILES O=C1C(C=CC=C2)=C2OC3=C1C(OC)=C{3}C(O)=C3OC |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 20848
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a-D-Ribf-(1-6)-Subst
Subst = orthosporin = SMILES C{10}[C@@H](CC1=CC2=C(C(O1)=O){8}C(O)=C{6}C(O)=C2)O |
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Structure type: monomer
Trivial name: daldiniside C
Compound class: glycoside
Reference(s) to other database(s): GenDB:KF030724 and GenDB:KF030725
- Compound ID: 22915
|
a-D-Ribf-(1-6)-Subst
Subst = isocoumarin moiety = SMILES OC1=C2C(C=C(C)OC2=O)=C{6}C(O)=C1 |
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Structure type: monomer
Trivial name: daldiniside B
Compound class: glycoside
- Compound ID: 22942
|
a-D-Ribf-(1-5)-Subst
Subst = chromane moiety = SMILES O{5}C1=C([C@H](O)C[C@@H](C)O2)C2=CC=C1 |
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Structure type: monomer
Trivial name: daldiniside A
Compound class: glycoside
- Compound ID: 17811
|
b-D-Manp6Ac-(1-13)-Subst-(1-1)-D-Ara-ol
Subst = 2,4,6,8,10,12,14,16,18-nonamethyl-5,9,13-trihydroxy-2E,6E,10E-icosatrienoic acid = SMILES CC[C@H](C)C[C@H](C)C[C@H](C){13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(O)=O |
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Structure type: oligomer
Trivial name: roselipin 2A
Compound class: glycolipid, glycoside
- Compound ID: 17812
|
b-D-Manp6Ac-(1-13)-Subst-(1-1)-D-Lyx-ol
Subst = 2,4,6,8,10,12,14,16,18-nonamethyl-5,9,13-trihydroxy-2E,6E,10E-icosatrienoic acid = SMILES CC[C@H](C)C[C@H](C)C[C@H](C){13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(O)=O |
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Structure type: oligomer
Trivial name: roselipin 2B
Compound class: glycolipid, glycoside
- Compound ID: 21193
|
b-D-Manp4Me-(1-13)-Subst-(1-1)-D-Ara-ol
Subst = rogerson aglycon = SMILES CC[C@H](C)C[C@H](C)/C=C(C)/{13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(=O)O |
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Structure type: oligomer
Trivial name: TMC-154
Compound class: glycolipid, glycoside
- Compound ID: 21431
|
b-D-Manp-(1-13)-Subst-(1-1)-D-Ara-ol
Subst = 2,4,6,8,10,12,14,16,18-nonamethyl-5,9,13-trihydroxy-2E,6E,10E-icosatrienoic acid = SMILES CC[C@H](C)C[C@H](C)C[C@H](C){13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(O)=O |
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Structure type: oligomer
Trivial name: roselipin 1A, roselipin 1A, TMC-151 D
Compound class: glycolipid, glycoside
- Compound ID: 21432
|
b-D-Manp-(1-13)-Subst-(1-1)-D-Lyx-ol
Subst = 2,4,6,8,10,12,14,16,18-nonamethyl-5,9,13-trihydroxy-2E,6E,10E-icosatrienoic acid = SMILES CC[C@H](C)C[C@H](C)C[C@H](C){13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(O)=O |
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Structure type: oligomer
Trivial name: roselipin 1B
Compound class: glycolipid, glycoside
- Compound ID: 22880
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b-D-Manp-(1-13)-Subst-(1-3)-D-Man-ol
Subst = rogerson aglycon = SMILES CC[C@H](C)C[C@H](C)/C=C(C)/{13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(=O)O |
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Structure type: monomer
Trivial name: TMC-171 A
Compound class: glycoside
- Compound ID: 22881
|
b-D-Manp-(1-13)-Subst-(1-2)-D-Man-ol
Subst = rogerson aglycon = SMILES CC[C@H](C)C[C@H](C)/C=C(C)/{13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(=O)O |
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Structure type: oligomer
Trivial name: TMC-171 B
Compound class: glycoside
- Compound ID: 22882
|
b-D-Manp-(1-13)-Subst-(1-1)-D-Man-ol
Subst = rogerson aglycon = SMILES CC[C@H](C)C[C@H](C)/C=C(C)/{13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(=O)O |
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Structure type: oligomer
Trivial name: TMC-171 C
Compound class: glycoside
- Compound ID: 22932
|
a-L-Rhap-(1-1)-Subst
Subst = naphthalene-1,8-diol = SMILES Oc1cccc2ccc{1}c(O)c12 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22914
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a-D-Glcp6Ac-(1-5)-Subst
Subst = R-(-)-5-hydroxymellein = SMILES C[C@@H]1CC2={5}C(O)C=C{8}C(O)=C2C(O1)=O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23090
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Suga-(1-4)-b-D-Glcp
Sug = glucitol diacetal = SMILES O{1}C(O)[C@@H]([C@H]([C@@H]([C@@H](CO)O)O)O)O |
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Structure type: oligomer
Trivial name: diglucotol
Compound class: glycoside
- Compound ID: 23053
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b-D-Glcp-(1-1)-+
|
R-2HOC18={t3}-(1-2)-Subst
Subst = (2S,3S,4E)-8-oxo-9-methylene-4-sphingenine C18 = SMILES O{3}[C@H]({2}[C@H]({1}CO)N)/C=C/CCC(C(CCCCCCCCC)=C)=O |
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Structure type: monomer
Trivial name: alternaroside A
Compound class: glycoside
- Compound ID: 22907
|
b-D-Glcp-(1-8)-Subst
Subst = 3-(3,3-dichloro-2-hydroxypropyl)-6-methoxy-8-hydroxy-1H-2-benzopyran-1-one = SMILES O{8}C1=C2C(C=C(C{10}C(O)C(Cl)Cl)OC2=O)=CC(OC)=C1 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22928
|
b-D-Glcp-(1-1)-Subst
Subst = 3-methoxy-8-methylnaphthalene-1,2-diol = SMILES CC1=CC=CC2=C1{1}C(O)={2}C(O)C(OC)=C2 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22929
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b-D-Glcp-(1-2)-Subst
Subst = 3-methoxy-8-methylnaphthalene-1,2-diol = SMILES CC1=CC=CC2=C1{1}C(O)={2}C(O)C(OC)=C2 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 20764
|
Subst-(1-6)-b-D-Galp-(1-4)-a-D-Sugp-(3-1)-Subst1
Subst = 2E,4E-decadienoic acid = SMILES CCCCC/C=C/C=C/{1}C(=O)O;
Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O;
Subst1 = 7-hydroxy-8,14-dimethylhexadeca-2E,4E,8E,10E-tetraenoic acid = SMILES CCC(C)CC/C=C/C=C(C)/{7}C(O)C/C=C/C=C/{1}C(=O)O |
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Structure type: oligomer
Trivial name: papulacandin A
Compound class: glycoside, papulacandin
- Compound ID: 20765
|
Subst-(1-6)-b-D-Galp-(1-4)-a-D-Sugp-(3-1)-Subst1
Subst = (2E,4Z,6E)-8-hydroxydeca-2,4,6-trienoic acid = SMILES CCC(O)/C=C/C=C\C=C\{1}C(=O)O;
Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O;
Subst1 = 7-hydroxy-8,14-dimethylhexadeca-2E,4E,8E,10E-tetraenoic acid = SMILES CCC(C)CC/C=C/C=C(C)/{7}C(O)C/C=C/C=C/{1}C(=O)O |
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Structure type: oligomer
Trivial name: papulacandin B
Compound class: glycoside, papulacandin
- Compound ID: 20766
|
Subst-(1-6)-b-D-Galp-(1-4)-a-D-Sugp-(3-1)-Subst1
Subst = (2E,4E,6E)-8-hydroxydeca-2,4,6-trienoic acid = SMILES CCC(O)/C=C/C=C/C=C/{1}C(=O)O;
Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O;
Subst1 = 7-hydroxy-8,14-dimethylhexadeca-2E,4E,8E,10E-tetraenoic acid = SMILES CCC(C)CC/C=C/C=C(C)/{7}C(O)C/C=C/C=C/{1}C(=O)O |
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Structure type: oligomer
Trivial name: papulacandin C
Compound class: glycoside, papulacandin
- Compound ID: 20767
|
a-D-Sugp-(3-1)-Subst
Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O;
Subst = 7-hydroxy-8,14-dimethylhexadeca-2E,4E,8E,10E-tetraenoic acid = SMILES CCC(C)CC/C=C/C=C(C)/{7}C(O)C/C=C/C=C/{1}C(=O)O |
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Structure type: monomer
Trivial name: papulacandin D
Compound class: glycoside, papulacandin
- Compound ID: 23084
|
Subst1-(1-3)-+
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Subst-(1-6)-b-D-Galp-(1-4)-b-D-1dGlcp-(1C-6)-Subst2
Subst = stillingic acid = SMILES CCCCC/C=C\C=C\{1}C(=O)O;
Subst1 = (2E,4E,8E,10E)-7-hydroxy-8-methyltetradeca-2,4,8,10-tetraenoic acid = SMILES CCC/C=C/C=C(C)/{7}C(O)C/C=C/C=C/{1}C(=O)O;
Subst2 = 5-(hydroxymethyl)benzene-1,3-diol = SMILES O{1}C1=C{3}C(O)=CC({7}CO)={6}C1 |
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Structure type: oligomer
Trivial name: chaetiacandin
Compound class: glycoside
- Compound ID: 23025
|
b-D-Glcp-(1-4)-Subst
Subst = (Z)-4,6-dihydroxy-7-methoxy-2-(4-methoxybenzylidene)benzofuran-3(2H)-one = SMILES COC1=CC=C(C=C1)/C=C(O2)/C(C3=C2C(OC)={6}C(O)C={4}C3O)=O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23163
Structure type: monomer
Trivial name: penicitriketo
Compound class: glycoside
- Compound ID: 23165
|
b-D-Glcp-(1-4)-Caf-(9-4)-Subst
Subst = SMILES O[C@@]1(C(O)=O)C[C@@H](O){4}[C@@H](O)[C@@H](O)C1 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 20857
|
b-D-Fruf-(2-3)-+
|
L-Ala-(1-2)-L-Thr-(1-2)-L-Thr2Me-(1-2)-L-Val2Me-(1-2)-L-Val-(1-2)-L-Val2Me-(1-2)-L-Val2Me-(1-2)-L-Val2Me-(1-2)-L-Ile-(1-2)-L-Val2Me-(1-2)-Gly2Me-(1-2)-2NBz |
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Structure type: monomer
Trivial name: dictyonamide B
Compound class: glycopeptide, glycoside
- Compound ID: 20887
|
b-D-Glcp4Me-(1-4')-Subst
Subst = 4',5'-dihydro-4'-hydroxyascochlorin = SMILES C[C@@H]1CCC([C@H](C)[C@]1(C{54}[C@@H](O)/C(C)=C/CC2=C(O)C(C=O)=C(C)C(Cl)=C2O)C)=O |
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Structure type: monomer
Trivial name: vertihemipterin A
Compound class: glycoside
- Compound ID: 23145
|
b-D-Galp-(1-4)-Subst
Subst = 2,4-dihydroxy-6-pentadecanoylbenzoic acid = SMILES CCCCCCCCCCCCCCCC1=C({7}C(O)=O){2}C(O)=C{4}C(O)=C1 |
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Structure type: monomer
Trivial name: aquastatin C
Compound class: glycoside
- Compound ID: 20870
|
b-D-Rhap4Me-(1-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4 |
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Structure type: monomer
Trivial name: sordarin B
Compound class: glycoside
- Compound ID: 23019
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CineruloseAp-(1-4)-b-D-Quip-(1-4)-a-D-Rhonp-(1-5)-Subst
Subst = 5-hydroxy-9,10-dioxo-9,10-dihydroanthracene-1,3-dicarboxylic acid = SMILES O=C1C2=C(C(C3=C1C(C(O)=O)=CC(C(O)=O)=C3)=O){5}C(O)=CC=C2;
CineruloseA = 2,3,6-trideoxy-L-glycero-hexos-4-ulose = SMILES C[C@H]1C(=O)CC{1}[CH](O1)O |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 21196
|
b-D-Manp6Ac-(1-15)-Subst-(1-1)-D-Ara-ol
Subst = 3,7,11,15-tetrahydroxy-2,4,6,8,10,12,14,16,18,20-decamethyldocosa-4E,8E,12E-trienoic acid = SMILES CCC(C)CC(C)CC(C){15}C(O)C(C)/C=C(C)/{11}C(O)C(C)/C=C(C)/{7}C(O)C(C)/C=C(C)/{3}C(C(C){1}C(O)=O)O |
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Structure type: oligomer
Trivial name: cladionol A
Compound class: glycolipid, glycoside
- Compound ID: 23137
|
b-D-Glcp-(1-4)-Subst4'Me4"Me
Subst = gliocladinin C aglycon = SMILES O{4}C1=CC=C(C2=C{52}C(O)=C({54}C(O)={55}C2O)C3=CC={104}C(O)C=C3)C=C1 |
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Structure type: monomer
Trivial name: gliocladinin B
Compound class: glycoside
- Compound ID: 22875
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b-D-Manp-(1-13)-Subst-(1-3)-D-Man-ol
Subst = 2,4,6,8,10,12,14,16,18-nonamethyl-5,9,13-trihydroxy-2E,6E,10E-icosatrienoic acid = SMILES CC[C@H](C)C[C@H](C)C[C@H](C){13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(O)=O |
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Structure type: oligomer
Trivial name: TMC-151 A
Compound class: glycoside
- Compound ID: 22876
|
b-D-Manp-(1-13)-Subst-(1-2)-D-Man-ol
Subst = 2,4,6,8,10,12,14,16,18-nonamethyl-5,9,13-trihydroxy-2E,6E,10E-icosatrienoic acid = SMILES CC[C@H](C)C[C@H](C)C[C@H](C){13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(O)=O |
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Structure type: oligomer
Trivial name: TMC-151 B
Compound class: glycoside
- Compound ID: 22877
|
b-D-Manp-(1-13)-Subst-(1-1)-D-Man-ol
Subst = 2,4,6,8,10,12,14,16,18-nonamethyl-5,9,13-trihydroxy-2E,6E,10E-icosatrienoic acid = SMILES CC[C@H](C)C[C@H](C)C[C@H](C){13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(O)=O |
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Structure type: oligomer
Trivial name: TMC-151 C
Compound class: glycoside
- Compound ID: 22878
|
b-D-Manp2Ac-(1-13)-Subst-(1-1)-D-Man-ol
Subst = 2,4,6,8,10,12,14,16,18-nonamethyl-5,9,13-trihydroxy-2E,6E,10E-icosatrienoic acid = SMILES CC[C@H](C)C[C@H](C)C[C@H](C){13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(O)=O |
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Structure type: oligomer
Trivial name: TMC-151 E
Compound class: glycoside
- Compound ID: 22879
|
b-D-Manp2Ac-(1-13)-Subst-(1-1)-D-Ara-ol
Subst = 2,4,6,8,10,12,14,16,18-nonamethyl-5,9,13-trihydroxy-2E,6E,10E-icosatrienoic acid = SMILES CC[C@H](C)C[C@H](C)C[C@H](C){13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(O)=O |
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Structure type: oligomer
Trivial name: TMC-151 F
Compound class: glycoside
- Compound ID: 18820
|
b-D-Glcp-(1-8)-Subst
Subst = tyrosol = SMILES O{8}CCC1=CC={4}C(O)C=C1 |
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Structure type: monomer
Trivial name: salidroside
Compound class: saponin glycoside, glycoside, phenolic glycoside, flavonol glycoside, phenylethanoid glycoside
Reference(s) to other database(s): CCSD:
49805, CBank-STR:1101
- Compound ID: 23151
|
b-D-Xylp-(1-6)-b-D-Glcp-(1-4)-Subst
Subst = piceol = SMILES CC(C1=CC={4}C(O)C=C1)=O |
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Structure type: oligomer
Trivial name: asterbatanoside A
Compound class: glycoside
- Compound ID: 23086
|
Subst-(1-6)-+
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b-D-Galp-(1-2)-b-D-Galp-(1-4)-b-D-1dGlcp-(1C-6)-Subst1
Subst = stillingic acid = SMILES CCCCC/C=C\C=C\{1}C(=O)O;
Subst1 = 5-(hydroxymethyl)benzene-1,3-diol = SMILES O{1}C1=C{3}C(O)=CC({7}CO)={6}C1 |
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Structure type: oligomer
Trivial name: fusacandin A
Compound class: glycoside
- Compound ID: 23087
|
b-D-Galp-(1-2)-b-D-Galp-(1-4)-b-D-1dGlcp-(1C-6)-Subst
Subst = 5-(hydroxymethyl)benzene-1,3-diol = SMILES O{1}C1=C{3}C(O)=CC({7}CO)={6}C1 |
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Structure type: oligomer
Trivial name: fusacandin B
Compound class: glycoside
- Compound ID: 21794
|
b-D-Glcp4Me-(1-9)-Subst
Subst = cytogenin = SMILES O=c1oc({9}CO)cc2cc(O)cc(O)c12 |
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Structure type: monomer
C18H22O10
Compound class: glycoside
- Compound ID: 22911
|
b-D-Glcp4Me-(1-9)-Subst
Subst = cytogenin = SMILES COc2cc(O)c1c(=O)oc({9}CO)cc1c2 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23000
|
b-D-Glcp-(1-15)-Subst
Subst = aspergillusene A = SMILES C/C(C1={1}C(O)C=C({15}CO)C=C1)=C\CCC(C)C |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 21657
|
a-D-Manp-(1-16)-Subst
Subst = 16-hydroxynorisopimar-7-en-4-ol = SMILES C[C@@]12[C@](CC=C3[C@]2([H])CC[C@](C)(C{16}CO)C3)([H]){4}[C@](C)(O)CCC1 |
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Structure type: monomer
Trivial name: elaeicolaside B
Compound class: glycoside, isopimarane diterpene glycoside
- Compound ID: 22402
|
a-D-Manp-(1-16)-Subst
Subst = hymatoxin K aglycon = SMILES O=C1[C@@]2(C)CCC[C@@]3(C)[C@@]2([H])C(O1)C=C4{9}[C@]3(O)CC[C@@](C{16}CO)(C)C4[H] |
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Structure type: monomer
Trivial name: hymatoxin K
Compound class: glycoside, diterpene glycoside
- Compound ID: 22403
|
a-D-Manp-(1-16)-Subst
Subst = hymatoxin L aglycon = SMILES O=C1[C@@]2(C)CCC[C@@]3(C)[C@@]2([H])C(O1)C=C4[C@]3([H])CC[C@@](C{16}CO)(C){14}[C@@H]4O |
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Structure type: monomer
Trivial name: hymatoxin L
Compound class: glycoside, diterpene glycoside
- Compound ID: 22871
|
a-D-Manp-(1-16)-Subst
Subst = 16-hydroxyisopimar-6,8(14)-dien-19-oic acid = SMILES C[C@@]12[C@](C=CC3=C[C@@](C)(C{16}CO)CC[C@@]32[H])([H])[C@]({19}C(O)=O)(C)CCC1 |
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Structure type: monomer
Trivial name: elaeicolaside C
Compound class: glycoside, isopimarane diterpene glycoside
- Compound ID: 22962
|
a-D-Manp-(1-16)-Subst
Subst = elaeicolaside A aglycon = SMILES C[C@@]12[C@](C{7}[C@H](O)C3=C[C@@](C)(C{16}CO)CC[C@@]32[H])([H])[C@](C)(OO)CCC1 |
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Structure type: monomer
Trivial name: elaeicolaside A
Compound class: glycoside
- Compound ID: 18783
|
b-D-Glcp4Me-(1-6)-Subst
Subst = indigotide B aglycon = SMILES C[C@@H]1OC2=CC3=C({5}C(O)=C2C([C@H]1C)=O){6}C(O)=C{8}C(O)=C3 |
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Structure type: monomer
C22H25O10
Trivial name: indigotide B
Compound class: glycoside, polyketide glycoside
- Compound ID: 22917
|
b-D-Glcp4Me6Ac-(1-6)-Subst7Me
Subst = (S,E)-6,7,8-trihydroxy-3-(pent-3-en-1-yl)isochroman-1-one = SMILES C/C=C/CC[C@H]1CC2=C(C(O1)=O){8}C(O)={7}C(O){6}C(O)=C2 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22918
|
b-D-Glcp4Me-(1-6)-Subst7Me
Subst = (S,E)-6,7,8-trihydroxy-3-(pent-3-en-1-yl)isochroman-1-one = SMILES C/C=C/CC[C@H]1CC2=C(C(O1)=O){8}C(O)={7}C(O){6}C(O)=C2 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22919
|
b-D-Glcp4Me-(1-6)-Subst
Subst = (S,E)-6,8-dihydroxy-3-(pent-3-en-1-yl)isochroman-1-one = SMILES C/C=C/CC[C@H]1CC2=C(C(O1)=O){8}C(O)=C{6}C(O)=C2 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22920
|
b-D-Glcp4Me-(1-6)-Subst
Subst = (S,E)-5,6,8-trihydroxy-3-(pent-3-en-1-yl)isochroman-1-one = SMILES C/C=C/CC[C@H]1CC2=C(C(O1)=O){8}C(O)=C{6}C(O)={5}C2O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22921
|
b-D-Glcp4Me-(1-7)-Subst
Subst = (S,E)-6,7,8-trihydroxy-3-(pent-3-en-1-yl)isochroman-1-one = SMILES C/C=C/CC[C@H]1CC2=C(C(O1)=O){8}C(O)={7}C(O){6}C(O)=C2 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22922
|
b-D-Glcp4Me-(1-6)-Subst7Me
Subst = (E)-6,7,8-trihydroxy-3-(pent-3-en-1-yl)-1H-isochromen-1-one = SMILES C/C=C/CCC1=CC2=C(C(O1)=O){8}C(O)={7}C(O){6}C(O)=C2 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22936
|
b-D-Glcp4Me-(1-6)-Subst
Subst = indigotide G, H aglycon = SMILES C[C@H]1OC2=CC3=C({5}C(O)=C2C([C@@H]1C)=O){6}C(O)=C{8}C(O)=C3 |
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Structure type: monomer
Trivial name: indigotide G
Compound class: glycoside
- Compound ID: 22937
|
b-D-Glcp4Me-(1-8)-Subst
Subst = indigotide G, H aglycon = SMILES C[C@H]1OC2=CC3=C({5}C(O)=C2C([C@@H]1C)=O){6}C(O)=C{8}C(O)=C3 |
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Structure type: monomer
Trivial name: indigotide H
Compound class: glycoside
- Compound ID: 19554
|
b-D-Manp4Me-(1-13)-Subst
Subst = rogerson aglycon = SMILES CC[C@H](C)C[C@H](C)/C=C(C)/{13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(=O)O |
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Structure type: monomer
Trivial name: rogerson B
Compound class: glycoside
- Compound ID: 22884
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b-D-Manp4Me-(1-13)-Subst1Me
Subst = rogerson aglycon = SMILES CC[C@H](C)C[C@H](C)/C=C(C)/{13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(=O)O |
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Structure type: monomer
Trivial name: rogerson A
Compound class: glycoside
- Compound ID: 22886
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a-L-Rhap-(1-5)-+
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b-D-Manp-(1-13)-Subst
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a-L-Rhap-(1-9)-+
Subst = phialotide A, B, C, D aglycon = SMILES O{17}C(C(CC)C)C(C)/C=C(C)/{13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(O)=O |
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Structure type: oligomer
Trivial name: phialotide A
Compound class: glycoside
- Compound ID: 22887
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b-D-Manp-(1-9)-+
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a-L-Rhap-(1-5)-Subst
Subst = phialotide A, B, C, D aglycon = SMILES O{17}C(C(CC)C)C(C)/C=C(C)/{13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(O)=O |
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Structure type: oligomer
Trivial name: phialotide B
Compound class: glycoside
- Compound ID: 22888
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a-L-Rhap-(1-9)-+
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a-L-Rhap-(1-5)-Subst
Subst = phialotide A, B, C, D aglycon = SMILES O{17}C(C(CC)C)C(C)/C=C(C)/{13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(O)=O |
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Structure type: oligomer
Trivial name: phialotide C
Compound class: glycoside
- Compound ID: 22889
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a-L-Rhap-(1-5)-Subst
Subst = phialotide A, B, C, D aglycon = SMILES O{17}C(C(CC)C)C(C)/C=C(C)/{13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(O)=O |
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Structure type: monomer
Trivial name: phialotide D
Compound class: glycoside
- Compound ID: 22890
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a-L-Rhap-(1-7)-+
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b-D-Manp-(1-11)-Subst
Subst = phialotide E aglycon = SMILES O{19}C(C(CC)C)C(C)/C=C(C)/{15}[C@@H](O)[C@@H](C)/C=C(C)/{11}[C@@H](O)[C@@H](C)/C=C(C)/{7}[C@@H](O)[C@@H](C)/C=C(C)/{3}C(O)C({1}C(O)=O)C |
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Structure type: oligomer
Trivial name: phialotide E
Compound class: glycoside
- Compound ID: 22891
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b-D-Manp-(1-9)-+
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a-L-Rhap-(1-5)-Subst
Subst = phialotide F, G, H aglycon = SMILES O{17}C(/C(C)=C/C({21}C(O)C(CC)C)C)C(C)/C=C(C)/{13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(O)=O |
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Structure type: oligomer
Trivial name: phialotide F
Compound class: glycoside
- Compound ID: 22892
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a-L-Rhap-(1-5)-+
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b-D-Manp-(1-13)-Subst
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a-L-Rhap-(1-9)-+
Subst = phialotide F, G, H aglycon = SMILES O{17}C(/C(C)=C/C({21}C(O)C(CC)C)C)C(C)/C=C(C)/{13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(O)=O |
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Structure type: oligomer
Trivial name: phialotide G
Compound class: glycoside
- Compound ID: 22893
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a-L-Rhap-(1-9)-+
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a-L-Rhap-(1-5)-Subst
Subst = phialotide F, G, H aglycon = SMILES O{17}C(/C(C)=C/C({21}C(O)C(CC)C)C)C(C)/C=C(C)/{13}[C@@H](O)[C@@H](C)/C=C(C)/{9}[C@@H](O)[C@@H](C)/C=C(C)/{5}[C@@H](O)[C@@H](C)/C=C(C)/{1}C(O)=O |
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Structure type: oligomer
Trivial name: phialotide H
Compound class: glycoside
- Compound ID: 22895
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D-1,4dxylHexp-(1C-3)-Subst
Subst = YM-202204 aglycon = SMILES CC(C/C=C/C(C)=C/C(CC(C)CC)C){14}C(C(/C=C(C)/C=C/{8}C(O)C(C)c1oc(=O){3}c{4}c(O)c1)C)O |
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Structure type: monomer
Trivial name: YM-202204
Compound class: glycoside
- Compound ID: 22896
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D-1,4dxylHexp-(1C-3)-Subst
Subst = S39163/F–I aglycon = SMILES CC(C/C=C/C(C)=C/C(CC(C)CC)C){14}C(C(/C=C(C)/C=C/{8}C(O)C(C)(C)c1oc(=O){3}c{4}c(O)c1)C)O |
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Structure type: monomer
Trivial name: S39163/F–I
Compound class: glycoside
- Compound ID: 22897
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D-1,4dxylHexp-(1C-3)-Subst
Subst = dactylfungin A aglycon = SMILES CC(CC({31}CO)/C=C(/C=C/{8}C(C(c(c{4}c(O){3}c1)oc1=O)(C)C)O)C)CC(C)C/C(C)=C/C=C/C(C)=C/C(CC)C |
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Structure type: monomer
Trivial name: dactylfungin A
Compound class: glycoside
- Compound ID: 22898
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D-1,4dxylHexp-(1C-3)-Subst
Subst = dactylfungin B aglycon = SMILES CC(CC({31}CO)/C=C(/C=C/{8}C(C(c(c1)o{2}c(O){3}cc1=O)(C)C)O)C)CC(C)C/C(C)=C/C=C/C(C)=C/C(CC)C |
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Structure type: monomer
Trivial name: dactylfungin B
Compound class: glycoside
- Compound ID: 20886
Structure type: monomer
Trivial name: vitexin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 22902
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b-D-Glcp4Me-(1-8)-Subst
Subst = akanthopyrone A aglycon = SMILES O=c1c({7}CO)c(OC)cc({8}[C@@H](O)CCCCCCCCC)o1 |
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Structure type: monomer
Trivial name: akanthopyrone A
Compound class: glycoside
- Compound ID: 22903
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b-D-Glcp4Me-(1-8)-Subst
Subst = akanthopyrone B aglycon = SMILES O=c1c({7}CO)c(OC)cc({8}[C@@H](O)CCCCCCCC{17}CO)o1 |
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Structure type: monomer
Trivial name: akanthopyrone B
Compound class: glycoside
- Compound ID: 22904
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b-D-Glcp4Me-(1-8)-Subst
Subst = akanthopyrone C aglycon = SMILES O=c1c(C)c(OC)cc({8}[C@@H](O)CCCCCCCC{17}CO)o1 |
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Structure type: monomer
Trivial name: akanthopyrone C
Compound class: glycoside
- Compound ID: 22905
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b-D-Glcp4Me-(1-8)-Subst
Subst = akanthopyrone D aglycon = SMILES CCCCCCC{8}[C@H](O)c(o1)cc(OC)c({7}CO)c1=O |
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Structure type: monomer
Trivial name: akanthopyrone D
Compound class: glycoside
- Compound ID: 22930
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b-D-Glcp4Me-(1-1)-Subst
Subst = naphtalene-1,6-diol = SMILES Oc2ccc1{1}c(O)cccc1c2 |
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Structure type: monomer
Trivial name: akanthol
Compound class: glycoside
- Compound ID: 23123
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b-D-Glcp4Me-(1-2)-Subst
Subst = 3,6-diisopropylpyrazine-2,5-diol = SMILES CC(C)c1n{2}c(O)c(C(C)C)nc1O |
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Structure type: monomer
Trivial name: akanthozine
Compound class: glycoside
- Compound ID: 22906
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b-D-Manp4Me-(1-7)-Subst4Me
Subst = (S)-4-hydroxy-6-((S)-1-hydroxypentyl)-5,6-dihydro-2H-pyran-2-one = SMILES CCCC{7}[C@H](O)[C@@H]1C/{4}C(O)=C\C(=O)O1 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22913
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b-D-Glcp-(1-6)-Subst
Subst = nigrosphaerin A aglycon = SMILES O{6}C1=CC({4}C(O)=C2C3=C{53}C(O)={54}C(O)C=C3)=C(C(O2)=O){8}C(O)=C1 |
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Structure type: monomer
Trivial name: nigrosphaerin A
Compound class: glycoside
- Compound ID: 20233
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a-D-Ribf-(1-6)-Subst
Subst = isotorachrysone = SMILES COC1=C{6}C(O)=CC2=C1{1}C(O)=C(C(C)=O)C(C)=C2 |
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Structure type: monomer
Compound class: glycoside
Reference(s) to other database(s): GenDB:JQ743649
- Compound ID: 22933
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a-D-Ribf-(1-6)-Subst
Subst = 3-methylnaphthalene-1,6,8-triol = SMILES O{1}C1=CC(C)=CC2=C1{8}C(O)=C{6}C(O)=C2 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22934
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a-D-Ribf-(1-6)-Subst
Subst = 8-methoxynaphthalene-1,6-diol = SMILES O{1}C1=CC=CC2=C1C(OC)=C{6}C(O)=C2 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22938
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b-D-Glcp4Me-(1-9)-Subst
Subst = rubrofusarin = SMILES COc3c{9}c(O)c2{10}c(O)c1c(=O)cc(C)oc1cc2c3 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23024
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b-D-Glcp4Me-(1-6)-Subst
Subst = norlichexanthone = SMILES CC1=C{6}C(O)=CC(OC2=C3{1}C(O)=C{3}C(O)=C2)=C1C3=O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22939
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b-D-Glcp4Me-(1-7)-Subst
Subst = 5,7-dihydroxy-2,6-dimethyl-4H-chromen-4-one = SMILES O=C(C=C(C)O1)C2=C1C={7}C(O)C(C)={5}C2O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22940
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b-D-Glcp4Me-(1-7)-Subst
Subst = 5,7-dihydroxy-2,8-dimethyl-4H-chromen-4-one = SMILES O=C(C=C(C)O1)C2=C1C(C)={7}C(O)C={5}C2O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22953
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a-D-Glcp-(1-19)-Subst
Subst = isopimara-7,15-diene-3β,19-diol = SMILES C[C@](C1)(C=C)CCC2C1=CCC3[C@]2(C)CC{3}C(O)[C@]3(C){19}CO |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22954
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a-D-Glcp-(1-19)-Subst
Subst = 19-hydroxyisopimara-7,15-dien-3-one = SMILES C=C[C@@]3(C)CC[C@H]1/C(=C\CC2[C@@](C)({19}CO)C(=O)CC[C@]12C)C3 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22955
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a-D-GlcpNAc-(1-19)-Subst
Subst = isopimara-7,15-diene-3β,19-diol = SMILES C[C@](C1)(C=C)CCC2C1=CCC3[C@]2(C)CC{3}C(O)[C@]3(C){19}CO |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22956
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a-D-GlcpNAc-(1-19)-Subst
Subst = 19-hydroxyisopimara-7,15-dien-3-one = SMILES C=C[C@@]3(C)CC[C@H]1/C(=C\CC2[C@@](C)({19}CO)C(=O)CC[C@]12C)C3 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22957
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a-D-Glcp-(1-19)-Subst
Subst = 7-oxoisopimara-8(9),15-diene-3β,19β-diol = SMILES C[C@](C1)(C=C)CCC([C@@](C2C3)(C)CC{3}C(O)[C@]2(C){19}CO)=C1C3=O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22958
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a-D-GlcpNAc-(1-19)-Subst
Subst = 7-oxoisopimara-8(9),15-diene-3β,19β-diol = SMILES C[C@](C1)(C=C)CCC([C@@](C2C3)(C)CC{3}C(O)[C@]2(C){19}CO)=C1C3=O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22960
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a-D-Glcp-(1-16)-Subst
Subst = 16-hydroxynorisopimar-7-en-4-ol = SMILES C[C@@]12[C@](CC=C3[C@]2([H])CC[C@](C)(C{16}CO)C3)([H]){4}[C@](C)(O)CCC1 |
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Structure type: monomer
Trivial name: xylapapuside A
Compound class: glycoside
- Compound ID: 22961
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a-D-Manp-(1-16)-Subst
Subst = xylapapuside B aglycon = SMILES [H][C@]/12CC[C@](C)(C{16}CO)CC1=C\C[C@@]3(C){4}[C@@](C)(O)CCC[C@]23C |
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Structure type: monomer
Trivial name: xylapapuside B
Compound class: glycoside
- Compound ID: 20875
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Subst1-(1-3)-b-D-6dAltp4Me-(1-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4;
Subst1 = hexa-2E,4Z-dienoic acid = SMILES C/C=C\C=C\{1}C(=O)O |
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Structure type: monomer
Trivial name: isozofimarin
Compound class: glycoside
Reference(s) to other database(s): GenDB:FJ175177
- Compound ID: 20876
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Subst-(1-3:2-3)-b-D-Sugp4Me-(1-17)-Subst1
Subst = 2S-hydroxysebacic acid, 2S-hydroxydecanedioic acid = SMILES O=C(O)CCCCCCC{2}[C@H](O){1}C(=O)O;
Sug = 6-deoxy-3-hydroxy-arabino-hexose = SMILES C[C@H]1O{1}[C@@H](O)[C@@H](O){3}C(O)(O){4}[C@@H]1O;
Subst1 = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4 |
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Structure type: monomer
Trivial name: moriniafungin
Compound class: glycoside
- Compound ID: 20872
|
b-D-6dAltp3Ac4Me-(1-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4 |
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Structure type: monomer
Trivial name: GR135402-6
Compound class: glycoside
- Compound ID: 20873
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Subst1-(1-3)-b-D-6dAltp4Me-(1-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4;
Subst1 = 2-methylhexa-2Z,4E-dienoic acid = SMILES C/C=C/C=C(/C)\{1}C(=O)O |
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Structure type: monomer
Trivial name: GR135402-7, GR135402
Compound class: glycoside
- Compound ID: 22981
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Subst1-(1-3)-b-D-6dAltp4Me-(1-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4;
Subst1 = 2-methylhexa-2Z,4Z-dienoic acid = SMILES C\C=C/C=C(/C)\{1}C(=O)O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22982
|
Subst1-(1-3)-b-D-6dAltp4Me-(1-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4;
Subst1 = 2-methylhexa-2E,4Z-dienoic acid = SMILES C/C=C/C=C(\C)\{1}C(=O)O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22983
|
Subst1-(1-3)-b-D-6dAltp4Me-(1-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4;
Subst1 = 2-methylhexa-2E,4E-dienoic acid = SMILES C\C=C/C=C(/C)/{1}C(=O)O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22984
|
Subst1-(1-3)-b-D-Altp4Me-(1-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4;
Subst1 = 2-methylhexa-2Z,4E-dienoic acid = SMILES C/C=C/C=C(/C)\{1}C(=O)O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22985
|
b-D-6dAltp-(1-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4;
Subst1 = 2-methylhexa-2Z,4Z-dienoic acid = SMILES C\C=C/C=C(/C)\{1}C(=O)O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 22987
|
b-D-Sugf2Ac-(6-17)-Subst
Subst = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4;
Subst1 = 2-methylhexa-2Z,4Z-dienoic acid = SMILES C\C=C/C=C(/C)\{1}C(=O)O;
Sug = tricyclic uronic acid = SMILES O{6}[C@]1([C@@H]([C@H]2O[C@H]3O1)C)O[C@@H]3{2}[C@H]2O |
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Structure type: monomer
Trivial name: BE-31405
Compound class: glycoside
- Compound ID: 22988
|
Subst-(1-3:2-3)-b-D-Sugp4Me-(1-17)-Subst1
Subst = 2S-hydroxysuberic acid, 2S-hydroxyoctanedioic acid = SMILES O=C(O)CCCCC{2}[C@H](O){1}C(=O)O;
Sug = 6-deoxy-3-hydroxy-arabino-hexose = SMILES C[C@H]1O{1}[C@@H](O)[C@@H](O){3}C(O)(O){4}[C@@H]1O;
Subst1 = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4 |
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Structure type: monomer
Trivial name: moriniafungin B
Compound class: glycoside
- Compound ID: 22989
|
Subst-(1-3:2-3)-b-D-Sugp4Me-(1-17)-Subst1
Subst = 2S-hydroxyadipic acid, 2S-hydroxyhexanedioic acid = SMILES O=C(O)CCC{2}[C@H](O){1}C(=O)O;
Sug = 6-deoxy-3-hydroxy-arabino-hexose = SMILES C[C@H]1O{1}[C@@H](O)[C@@H](O){3}C(O)(O){4}[C@@H]1O;
Subst1 = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4 |
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Structure type: monomer
Trivial name: moriniafungin C
Compound class: glycoside
- Compound ID: 22990
|
Subst6Me-(1-3:2-3)-b-D-Sugp4Me-(1-17)-Subst1
Subst = 2S-hydroxyadipic acid, 2S-hydroxyhexanedioic acid = SMILES O={6}C(O)CCC{2}[C@H](O){1}C(=O)O;
Sug = 6-deoxy-3-hydroxy-arabino-hexose = SMILES C[C@H]1O{1}[C@@H](O)[C@@H](O){3}C(O)(O){4}[C@@H]1O;
Subst1 = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4 |
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Structure type: monomer
Trivial name: moriniafungin D
Compound class: glycoside
- Compound ID: 22991
|
Subst10Me-(1-3:2-3)-b-D-Sugp4Me-(1-17)-Subst1
Subst = 2S-hydroxysebasic acid, 2S-hydroxydecanedioic acid = SMILES O={10}C(O)CCCCCCC{2}[C@H](O){1}C(=O)O;
Sug = 6-deoxy-3-hydroxy-arabino-hexose = SMILES C[C@H]1O{1}[C@@H](O)[C@@H](O){3}C(O)(O){4}[C@@H]1O;
Subst1 = sordaricin = SMILES C[C@@H]1CC[C@@H]2[C@@H]1C[C@]3({17}CO)[C@@H]4C[C@@]2(C=O)[C@@]3({13}C(O)=O)C(C(C)C)=C4 |
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Structure type: monomer
Trivial name: moriniafungin E
Compound class: glycoside
- Compound ID: 22992
|
Subst-(1-3:2-3)-b-D-Sugp4Me-(1-17)-Subst1
Subst = 2S-hydroxysebasic acid, 2S-hydroxydecanedioic acid = SMILES O=C(O)CCCCCCC{2}[C@H](O){1}C(=O)O;
Sug = 6-deoxy-3-hydroxy-arabino-hexose = SMILES C[C@H]1O{1}[C@@H](O)[C@@H](O){3}C(O)(O){4}[C@@H]1O;
Subst1 = sordaricin B = SMILES CC(C)/C3=C/[C@@H]2C[C@]4({15}C(=O)O)[C@@H]1CC[C@@H](C)[C@H]1C[C@@]2({17}CO)[C@]34{13}C(=O)O |
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Structure type: monomer
Trivial name: moriniafungin F
Compound class: glycoside
- Compound ID: 22993
|
Subst10Me-(1-3:2-3)-b-D-Sugp4Me-(1-17)-Subst1
Subst = 2S-hydroxysebasic acid, 2S-hydroxydecanedioic acid = SMILES O={10}C(O)CCCCCCC{2}[C@H](O){1}C(=O)O;
Sug = 6-deoxy-3-hydroxy-arabino-hexose = SMILES C[C@H]1O{1}[C@@H](O)[C@@H](O){3}C(O)(O){4}[C@@H]1O;
Subst1 = sordaricin B = SMILES CC(C)/C3=C/[C@@H]2C[C@]4({15}C(=O)O)[C@@H]1CC[C@@H](C)[C@H]1C[C@@]2({17}CO)[C@]34{13}C(=O)O |
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Structure type: monomer
Trivial name: moriniafungin G
Compound class: glycoside
- Compound ID: 22999
|
a-D-Glcp-(1-13)-Subst
Subst = sporuloside aglycon = SMILES CC1=C(C)C(C)=C(CCC[C@@]2({13}CO)C)C2=C1 |
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Structure type: monomer
Trivial name: sporuloside
Compound class: glycoside
- Compound ID: 23001
|
b-D-Glcp-(1-12)-Subst
Subst = (2S,5S,10R)-2-((S)-1,2-dihydroxypropan-2-yl)-6,10-dimethylspiro[4.5]dec-6-en-8-one = SMILES O=C1C[C@@H](C)[C@@]2(CC[C@H]({11}[C@](C)(O){12}CO)C2)C(C)=C1 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23003
|
b-D-Glcp4Me-(1-6)-Subst
Subst = versicolorin B = SMILES C1CO[C@H]2[C@@H]1C3=C(O2)C=C4C(={4}C3O)C(=O)C5=C(C4=O)C={6}C(C={8}C5O)O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23004
|
b-D-Glcp4Me-(1-6)-Subst
Subst = 1-hydroxyversicolorin B = SMILES O{4}C1=C(C(C2=C(C={6}C(O)C={8}C2O)C3=O)=O)C3=CC(O4)=C1[C@H]5[C@@H]4OC{1}[C@H]5O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23005
|
b-D-Glcp4Me-(1-6)-Subst
Subst = nidurufin = SMILES C[C@]12CC{1}[C@@H]([C@H](O1)C3=C(O2)C=C4C(={4}C3O)C(=O)C5=C(C4=O)C={6}C(C={8}C5O)O)O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23022
|
b-L-Arap4Me-(1-11)-Subst
Subst = 6-demethylsterigmatocystin = SMILES O=C1C2=C(C([C@H](C=CO3)[C@H]3O4)=C4C={11}C2O)OC5=C1{15}C(O)=CC=C5 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23006
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-8)-Subst
Subst = torosachrysone = SMILES COc1c{8}c(O)c2c(O)c3c(cc2c1)C{3}[C@](C)(O)CC3=O |
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Structure type: oligomer
Compound class: glycoside, anthraquinone glycoside
- Compound ID: 23007
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-8)-Subst
Subst = (S)-torosachrysone = SMILES COc1c{8}c(O)c2{9}c(O)c3c(cc2c1)C{3}[C@@](C)(O)CC3=O |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 21950
|
b-D-Glcp-(1-1)-Subst
Subst = emodin = SMILES O{1}C(C=C(C=C1C(C2=C3{8}C(O)=C{6}C(O)=C2)=O)C)=C1C3=O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23008
|
b-D-Glcp-(1-1)-Subst
Subst = dermocybin = SMILES CC1=CC2=C(C(C3=C({5}C(O)=C(OC){7}C(O)={8}C3O)C2=O)=O){1}C(O)=C1 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23009
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-8)-Subst
Subst = (1S,3S)-1,3,5,8-tetrahydroxy-6-methoxy-3-methyl-1,2,3,4,4a,9a-hexahydroanthracene-9,10-dione = SMILES O{1}[C@@H]1C(C(C2=C({5}C(O)=C(OC)C={8}C2O)C3=O)=O)C3C{3}[C@](C)(O)C1 |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 23010
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-4)-Subst
Subst = 1,4-dihydroxy-2-methoxyanthracene-9,10-dione = SMILES O=C1C2=C({1}C(O)=C(OC)C={4}C2O)C(C3=C1C=CC=C3)=O |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 23011
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-4)-Subst
Subst = 1,4,5-trihydroxy-2-methoxyanthracene-9,10-dione = SMILES O=C1C2=C({1}C(O)=C(OC)C={4}C2O)C(C3=C1{5}C(O)=CC=C3)=O |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 23012
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-1)-Subst
Subst = 1-hydroxy-3-methoxyanthracene-9,10-dione = SMILES O=C1C2=C(C=C(OC)C={1}C2O)C(C3=C1C=CC=C3)=O |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 23013
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-8)-Subst
Subst = (1S,3S)-1,3,8-trihydroxy-6-methoxy-3-methyl-1,2,3,4,4a,9a-hexahydroanthracene-9,10-dione = SMILES O{1}[C@@H]1C(C(C2=C(C=C(OC)C={8}C2O)C3=O)=O)C3C{3}[C@](C)(O)C1 |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 23018
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-8)-Subst
Subst = dermochrysone = SMILES O=C1C2={9}C(O)C3=C(C=C(OC)C={8}C3O)C=C2C{3}[C@@](C1)(O)CC(C)=O |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 23015
|
a-D-Glcp6Ac-(1-7)-Subst
Subst = macrosporin = SMILES CC1=CC2=C(C={7}C1O)C(=O)C3=C(C2=O)C=C(C={1}C3O)OC |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23016
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-8)-Subst
Subst = ω-hydroxyxanthorin = SMILES OC1=CC({11}CO)=CC2=C1C(C3=C({6}C(O)=C(OC)C={8}C3O)C2=O)=O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23017
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-8)-Subst
Subst = xanthorin = SMILES CC1=CC2=C(C(C3=C({6}C(O)=C(OC)C={8}C3O)C2=O)=O)C(O)=C1 |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 23023
|
b-D-Glcp-(1-9)-Subst
Subst = sporormielloside aglycon = SMILES COC1={9}C(O)C2=C(C(C3=C(O2)C=C(C)C={14}C3O)=O){6}C(O)=C1 |
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Structure type: monomer
Trivial name: sporormielloside
Compound class: glycoside
- Compound ID: 23026
|
a-L-Rhap-(1-7)-Subst
Subst = 7-hydroxy-5-methoxy-4,6-dimethylphthalide = SMILES COc2c(C){7}c(O)c1C(=O)OCc1c2C |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23027
|
b-D-Glcp-(1-7)-Subst
Subst = 7-hydroxy-5-methoxy-4,6-dimethylphthalide = SMILES COc2c(C){7}c(O)c1C(=O)OCc1c2C |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 18697
Structure type: monomer
Trivial name: cerebroside B
Compound class: glycolipid, glycosphingolipid, glycoside, cerebroside
- Compound ID: 23057
|
R-2HOC15-(1-2)-+
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b-D-Glcp-(1-1)-Subst
Subst = (2S,3R,4E,8E)-9-methyl-4,8-sphingadienine-C21 = SMILES C/C(CCCCCCCCCCCC)=C\CC/C=C/{3}[C@H]({2}[C@H]({1}CO)N)O |
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Structure type: monomer
Trivial name: allantoside
Compound class: glycoside
- Compound ID: 23058
|
b-D-Glcp-(1-1)-+
|
R-2HOC16={t3}-(1-2)-Subst
Subst = (2S,3R,4E,8E,10E)-9-methyl-4,8,10-sphingatrienine-C22 = SMILES O{1}C{2}[C@@H]({3}[C@@H](/C=C/CC/C=C(/C=C/CCCCCCCCCCC)C)O)N |
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Structure type: monomer
Trivial name: allantoside
Compound class: glycoside
- Compound ID: 23059
|
R-2HOMar-(1-2)-+
|
b-D-Glcp-(1-1)-Subst
Subst = (2S,3R,4E,8E)-2-amino-9-methylheptadeca-4,8-diene-1,3-diol = SMILES CCCCCCCC/C(C)=C/CC/C=C/{3}[C@@H](O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: ophiocordylongiiside A
Compound class: glycoside
- Compound ID: 23066
|
Subst-(1-2)-+
|
b-D-Glcp-(1-1)-Subst1
Subst = 2R-hydroxy-icos-3E-enoic acid = SMILES CCCCCCCCCCCCCCCC/C=C/{2}[C@@H](O){1}C(O)=O;
Subst1 = (2S,4E,8E)-9-methyl-4,8-sphingadienine-C18 = SMILES CCCCCCCCC/C(C)=C/CC/C=C/{3}C(O){2}[C@@H](N){1}CO |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23069
|
2HOPam-(1-2)-+
|
b-D-Glcp-(1-1)-Subst
Subst = (2S,4E,8E)-4,8-sphingadienine-C18 = SMILES CCCCCCCCC/C=C/CC/C=C/{3}C(O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: cerebroside A1
Compound class: glycoside
- Compound ID: 23070
|
2HOPam-(1-2)-+
|
b-D-Glcp-(1-1)-Subst
Subst = (2S,4E,8Z)-4,8-sphingadienine-C18 = SMILES CCCCCCCCC/C=C\CC/C=C/{3}C(O){2}[C@@H](N){1}CO |
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Structure type: monomer
Trivial name: cerebroside A2
Compound class: glycoside
- Compound ID: 23071
|
Subst-(1-6)-b-D-Galp-(1-4)-a-D-Sugp-(3-1)-Subst1
Subst = 8-hydroxydeca-2E,4Z-dienoic acid = SMILES CCC(O)CC/C=C\C=C\{1}C(=O)O;
Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O;
Subst1 = 7-hydroxy-8,14-dimethylhexadeca-2E,4E,8E,10E-tetraenoic acid = SMILES CCC(C)CC/C=C/C=C(C)/{7}C(O)C/C=C/C=C/{1}C(=O)O |
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Structure type: oligomer
Trivial name: L-687,781
Compound class: glycoside
- Compound ID: 23072
|
Subst-(1-6)-b-D-Galp-(1-4)-a-D-Sugp-(3-1)-Subst1
Subst = octa-2E,4E,6E-trienoic acid = SMILES C/C=C/C=C/C=C/{1}C(=O)O;
Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O;
Subst1 = 7-hydroxy-8,14-dimethylhexadeca-2E,4E,8E,10E-tetraenoic acid = SMILES CCC(C)CC/C=C/C=C(C)/{7}C(O)C/C=C/C=C/{1}C(=O)O |
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Structure type: oligomer
Trivial name: Mer-WF3010
Compound class: glycoside
- Compound ID: 23073
|
b-D-Galp-(1-4)-a-D-Sugp-(3-1)-Subst
Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O;
Subst = (2E,4E,12E)-7-hydroxy-8,14-dimethylhexadeca-2,4,12-trienoic acid = SMILES CCC(C)/C=C/CCCC(C){7}C(O)C/C=C/C=C/{1}C(=O)O |
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Structure type: oligomer
Trivial name: F-10748 A1
Compound class: glycoside
- Compound ID: 23074
|
But-(1-6)-b-D-Galp-(1-4)-a-D-Sugp-(3-1)-Subst
Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O;
Subst = (2E,4E,12E)-7-hydroxy-8,14-dimethylhexadeca-2,4,12-trienoic acid = SMILES CCC(C)/C=C/CCCC(C){7}C(O)C/C=C/C=C/{1}C(=O)O |
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Structure type: oligomer
Trivial name: F-10748 B1
Compound class: glycoside
- Compound ID: 23075
|
Vl-(1-6)-b-D-Galp-(1-4)-a-D-Sugp-(3-1)-Subst
Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O;
Subst = (2E,4E,12E)-7-hydroxy-8,14-dimethylhexadeca-2,4,12-trienoic acid = SMILES CCC(C)/C=C/CCCC(C){7}C(O)C/C=C/C=C/{1}C(=O)O |
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Structure type: oligomer
Trivial name: F-10748 C1
Compound class: glycoside
- Compound ID: 23076
|
Hxo-(1-6)-b-D-Galp-(1-4)-a-D-Sugp-(3-1)-Subst
Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O;
Subst = (2E,4E,12E)-7-hydroxy-8,14-dimethylhexadeca-2,4,12-trienoic acid = SMILES CCC(C)/C=C/CCCC(C){7}C(O)C/C=C/C=C/{1}C(=O)O |
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Structure type: oligomer
Trivial name: F-10748 D1
Compound class: glycoside
- Compound ID: 23080
|
Subst-(1-3)-+
|
b-D-Galp-(1-4)-b-D-1dGlcp-(1C-6)-Subst1
Subst = (2E,4E,12E)-7-hydroxy-8,14-dimethylhexadeca-2,4,12-trienoic acid = SMILES CCC(C)/C=C/CCCC(C){7}C(O)C/C=C/C=C/{1}C(=O)O;
Subst1 = 5-(hydroxymethyl)benzene-1,3-diol = SMILES O{1}C1=C{3}C(O)=CC({7}CO)={6}C1 |
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Structure type: oligomer
Trivial name: F-10748 A2
Compound class: glycoside
- Compound ID: 23081
|
Subst-(1-3)-+
|
But-(1-6)-b-D-Galp-(1-4)-b-D-1dGlcp-(1C-6)-Subst1
Subst = (2E,4E,12E)-7-hydroxy-8,14-dimethylhexadeca-2,4,12-trienoic acid = SMILES CCC(C)/C=C/CCCC(C){7}C(O)C/C=C/C=C/{1}C(=O)O;
Subst1 = 5-(hydroxymethyl)benzene-1,3-diol = SMILES O{1}C1=C{3}C(O)=CC({7}CO)={6}C1 |
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Structure type: oligomer
Trivial name: F-10748 B2
Compound class: glycoside
- Compound ID: 23082
|
Subst-(1-3)-+
|
Vl-(1-6)-b-D-Galp-(1-4)-b-D-1dGlcp-(1C-6)-Subst1
Subst = (2E,4E,12E)-7-hydroxy-8,14-dimethylhexadeca-2,4,12-trienoic acid = SMILES CCC(C)/C=C/CCCC(C){7}C(O)C/C=C/C=C/{1}C(=O)O;
Subst1 = 5-(hydroxymethyl)benzene-1,3-diol = SMILES O{1}C1=C{3}C(O)=CC({7}CO)={6}C1 |
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Structure type: oligomer
Trivial name: F-10748 C2
Compound class: glycoside
- Compound ID: 23083
|
Subst-(1-3)-+
|
Hxo-(1-6)-b-D-Galp-(1-4)-b-D-1dGlcp-(1C-6)-Subst1
Subst = (2E,4E,12E)-7-hydroxy-8,14-dimethylhexadeca-2,4,12-trienoic acid = SMILES CCC(C)/C=C/CCCC(C){7}C(O)C/C=C/C=C/{1}C(=O)O;
Subst1 = 5-(hydroxymethyl)benzene-1,3-diol = SMILES O{1}C1=C{3}C(O)=CC({7}CO)={6}C1 |
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Structure type: oligomer
Trivial name: F-10748 D2
Compound class: glycoside
- Compound ID: 23077
|
Subst-(1-6)-b-D-Galp-(1-4)-a-D-Sugp-(3-1)-Subst1
Sug = Glc 1O,1C-derivative with 3,5-dihydroxybenzyl alcohol 1O,2C = SMILES OC[C@H]3O[C@]2(OCc1cc(O)cc(O)c12)[C@H](O){3}[C@@H](O){4}[C@@H]3O;
Subst1 = (2E,4E,12E)-7-hydroxy-8,14-dimethylhexadeca-2,4,12-trienoic acid = SMILES CCC(C)/C=C/CCCC(C){7}C(O)C/C=C/C=C/{1}C(=O)O;
Subst = deca-2E,4E,6E-trienoic acid = SMILES CCC/C=C/C=C/C=C/{1}C(=O)O |
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Structure type: oligomer
Trivial name: BU-4794F
Compound class: glycoside
- Compound ID: 23085
|
Subst1-(1-3)-+
|
Subst-(1-6)-b-D-Galp-(1-4)-b-D-1dGlcp-(1C-6)-Subst2
Subst = stillingic acid = SMILES CCCCC/C=C\C=C\{1}C(=O)O;
Subst1 = (2E,4E)-7-hydroxydeca-2,4-dienoic acid = SMILES CCC{7}C(O)C/C=C/C=C/{1}C(=O)O;
Subst2 = 5-(hydroxymethyl)benzene-1,3-diol = SMILES O{1}C1=C{3}C(O)=CC({7}CO)={6}C1 |
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Structure type: oligomer
Trivial name: corynecandin
Compound class: glycoside
- Compound ID: 23093
|
b-D-GlcpA-(1-4)-Subst-(7-4)-Ors
Subst = 2,4-dihydroxy-6-pentadecanoylbenzoic acid = SMILES CCCCCCCCCCCCCCCC1=C({7}C(O)=O){2}C(O)=C{4}C(O)=C1 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23094
|
b-D-GlcpA6Me-(1-4)-Subst-(7-4)-Ors
Subst = 2,4-dihydroxy-6-pentadecanoylbenzoic acid = SMILES CCCCCCCCCCCCCCCC1=C({7}C(O)=O){2}C(O)=C{4}C(O)=C1 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23095
|
b-D-Galp-(1-4)-Subst-(7-4)-Ors
Subst = 2,4-dihydroxy-6-pentadecanoylbenzoic acid = SMILES CCCCCCCCCCCCCCCC1=C({7}C(O)=O){2}C(O)=C{4}C(O)=C1 |
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Structure type: monomer
Trivial name: aquastatin A
Compound class: glycoside
- Compound ID: 23096
|
b-D-Glcp-(1-6)-Subst-(7-4)-Subst
Subst = 2-nonyl-4,6-dihydroxybenzoic acid = SMILES O{6}C1={5}C{4}C(O)=CC(CCCCCCCCC)=C1{7}C(O)=O |
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Structure type: monomer
Trivial name: exophillic acid
Compound class: glycoside
- Compound ID: 23097
|
b-D-Glcp-(1-6)-Subst-(7-4)-Subst
Subst = 2-heptyl-4,6-dihydroxybenzoic acid = SMILES O{6}C1={5}C{4}C(O)=CC(CCCCCCC)=C1{7}C(O)=O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23100
|
b-D-GlcpA-(1-2)-Subst-(7-1)-Subst1
Subst = 2,4-dihydroxy-6-propylbenzoic acid = SMILES O={7}C(O)C1={2}C(O)C={4}C(O)C=C1CCC;
Subst1 = 5-pentylbenzene-1,3-diol = SMILES O{1}C1=CC(CCCCC)=C{3}C(O)=C1 |
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Structure type: monomer
Trivial name: ascotricin A
Compound class: glycoside
- Compound ID: 23101
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b-D-GlcpA-(1-2)-Subst-(7-1)-Subst1
Subst = 2,4-dihydroxy-6-pentylbenzoic acid = SMILES O={7}C(O)C1={2}C(O)C={4}C(O)C=C1CCCCC;
Subst1 = 5-pentylbenzene-1,3-diol = SMILES O{1}C1=CC(CCCCC)=C{3}C(O)=C1 |
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Structure type: monomer
Trivial name: ascotricin B
Compound class: glycoside
- Compound ID: 23102
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b-D-Manp2Ac-(1-5)-D-Man2Ac-onic-(1-23)-Subst
Subst = caloporoside aglycon = SMILES C{23}[C@H](CCCCCCCCCCCCCCCC1=C({1}C(O)=O){3}C(O)=CC=C1)O |
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Structure type: oligomer
Trivial name: deacetyl-caloporoside
Compound class: glycoside
- Compound ID: 23103
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b-D-Manp-(1-23)-Subst
Subst = caloporoside aglycon = SMILES C{23}[C@H](CCCCCCCCCCCCCCCC1=C({1}C(O)=O){3}C(O)=CC=C1)O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23116
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Subst1-(1-6)-b-D-Glcp-(1-7)-Subst
Subst = genistein = SMILES O=C1C(C2=CC={54}C(O)C=C2)=COC3=C1{5}C(O)={6}C{7}C(O)={8}C3;
Subst1 = crotonic acid = SMILES C/C=C/{1}C(O)=O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23117
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a-D-Ribf-(1-7)-Subst
Subst = genistein = SMILES O=C1C(C2=CC={54}C(O)C=C2)=COC3=C1{5}C(O)={6}C{7}C(O)={8}C3 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23118
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b-D-Glcp6Ac-(1-7)-Subst
Subst = daidzein = SMILES O=C1C(C2=CC={54}C(O)C=C2)=COC3=C1C=C{7}C(O)={8}C3 |
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Structure type: monomer
Trivial name: daidzin
Compound class: glycoside, flavonoid glycoside, flavone glycoside
- Compound ID: 23119
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b-D-Glcp6Ac-(1-7)-Subst
Subst = genistein = SMILES O=C1C(C2=CC={54}C(O)C=C2)=COC3=C1{5}C(O)={6}C{7}C(O)={8}C3 |
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Structure type: monomer
Trivial name: genistin
Compound class: glycoside, flavonoid glycoside, flavone glycoside
- Compound ID: 23120
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b-D-Glcp-(1-10)-Subst
Subst = ophioglonin = SMILES C1C2=C(C=C{3}C(={4}C2O)O)C3=C(O1)C(=O)C4={8}C(C={10}C(C=C4O3)O)O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23122
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b-D-Glcp-(1-5)-Subst
Subst = chartarlactam D aglycon = SMILES O{5}C1=C(CC2([C@](CC{18}[C@@H](O)C3(C)C)(C)[C@H]3CC[C@H]2C)O4)C4=C(CNC5=O)C5=C1 |
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Structure type: monomer
Trivial name: chartarlactam D
Compound class: glycoside
- Compound ID: 23124
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b-D-Glcp4Me-(1-4')-Subst
Subst = orbiocrellin A aglycon = SMILES O{54}C1=CC=C(C2=C{1}N(O)C(C(C3C(C)CCC(C)O3)={4}C2O)=O)C=C1 |
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Structure type: monomer
Trivial name: orbiocrellin A
Compound class: glycoside
- Compound ID: 19783
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b-D-Glcp-(1-2)-Subst3Ac
Subst = enfumafungin aglycon = SMILES CC(C)[C@@H](C)[C@@]5(C)CC[C@]4(C)[C@H]/3CC[C@H]1[C@@]2(C)COC(O)[C@@]1(C{3}[C@@H](O){2}[C@@H]2O)C3=C\C[C@@]4(C)[C@@H]5{16}C(=O)O |
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Structure type: monomer
Trivial name: enfumafungin
Compound class: glycoside, triterpene glycoside
- Compound ID: 23136
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b-D-Glcp-(1-1)-Subst2Me
Subst = 3,6-diphenylbenzene-1,2,4-triol = SMILES O{2}C1=C(C2=CC=CC=C2){4}C(O)=CC(C3=CC=CC=C3)={1}C1O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 23146
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b-D-Glcp-(1-1)-Subst-(4-1)-Me
Subst = 2,4-dihydroxy-5-chloro-6-propylphenol = SMILES CCCc1{1}c(O)c(O)c{4}c(O)c1Cl |
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Structure type: monomer
Trivial name: globosumoside A
Compound class: glycoside
- Compound ID: 23147
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b-D-Glcp6Ac-(1-1)-Subst-(4-1)-Me
Subst = 2,4-dihydroxy-5-chloro-6-propyl-phenol = SMILES CCCc1{1}c(O)c(O)c{4}c(O)c1Cl |
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Structure type: monomer
Trivial name: globosumoside B
Compound class: glycoside
- Compound ID: 23160
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a-L-Rhap-(1-1)-Subst
Subst = 2,5,6-trimethylresorcinol = SMILES Cc1cc(O)c(C){1}c(O)c1C |
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Structure type: monomer
Trivial name: pestarhamnose A
Compound class: glycoside
- Compound ID: 23161
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a-L-Rhap-(1-1)-Subst
Subst = 2,4,5-trimethylresorcinol = SMILES Cc1c{1}c(O)c(C)c(O)c1C |
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Structure type: monomer
Trivial name: pestarhamnose B
Compound class: glycoside
- Compound ID: 23162
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a-L-Rhap-(1-1)-Subst
Subst = 2,5-dimethylresorcinol = SMILES Cc1c{1}c(O)c(C)c(O)c1 |
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Structure type: monomer
Trivial name: pestarhamnose C
Compound class: glycoside
Oligosaccharide elicitors from pathogens have been shown to play major roles in host plant defense responses involving plant-pathogen chemoperception and interaction. In the present study, chitosan and oligochitosan were prepared from pathogen Fusarium sambucinum, and their effects on infection of Zanthoxylum bungeanum stems were investigated. Results showed that oligochitosan inhibited the infection of the pathogen, and that the oligochitosan fraction with a degree of polymerization (DP) between 5 and 6 showed the optimal effect. Oligochitosan DP5 was purified from fraction DP5-6 and was structurally characterized using electrospray ionization mass spectrometry, Fourier transform infrared spectroscopy, and nuclear magnetic resonance spectroscopy. Oligochitosan DP5 showed significant inhibition against the infection of the pathogenic fungi on host plant stems. An investigation of the mechanism underlying this effect showed that oligochitosan DP5 increased the activities of defensive enzymes and accumulation of phenolics in host Z. bungeanum. These results suggest that oligochitosan from pathogenic fungi can mediate the infection of host plants with a pathogen by acting as an elicitor that triggers the defense system of a plant. This information will be valuable for further exploration of the interactions between the pathogen F. sambucinum and host plant Z. bungeanum.