- Compound ID: 27564
Structure type: oligomer
Trivial name: MG(p)DG
Compound class: galactolipid
- Compound ID: 27565
|
b-D-Galp-(1-3)-+
|
C16={c7,c10,c13}-(1-1)-D-Gro
|
Subst-(1-2)-+
Subst = oxophytodienoic acid = SMILES CCC/C=C\CC1C(C=CC1=O)CCCCCCC{1}C(O)=O |
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Structure type: oligomer
Trivial name: MGDG-O
Compound class: galactolipid
- Compound ID: 27566
|
LIP-(1-1)-+
|
a-D-Gal-(1-6)-a-D-Gal-(1-6)-b-D-Galp-(1-3)-D-Gro
|
LIP-(1-2)-+ |
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Structure type: oligomer
Trivial name: TriGDG
Compound class: galactolipid
- Compound ID: 27567
|
LIP-(1-1)-+
|
a-D-Gal-(1-6)-a-D-Gal-(1-6)-a-D-Gal-(1-6)-b-D-Galp-(1-3)-D-Gro
|
LIP-(1-2)-+ |
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Structure type: oligomer
Trivial name: TetraGDG
Compound class: galactolipid
- Compound ID: 28462
Structure type: structural motif or average structure
Compound class: polysaccharide, xyloglucan
Reference(s) to other database(s): GTC:G04846ZN
- Compound ID: 24580
|
b-D-Galp-(1-2)-a-D-Xylp-(1-6)-+
|
b-D-Galp-(1-2)-a-D-Xylp-(1-6)-+ |
| |
a-D-Xylp-(1-6)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp |
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Structure type: oligomer
Trivial name: XLLG
Compound class: xyloglucan
Reference(s) to other database(s): GTC:G06184LI, CCSD:
17579, CBank-STR:17935
- Compound ID: 24578
|
a-D-Xylp-(1-6)-+
|
b-D-Galp-(1-2)-a-D-Xylp-(1-6)-+ |
| |
a-D-Xylp-(1-6)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp |
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Structure type: oligomer
Trivial name: XLXG
Compound class: N-glycan, xyloglucan
Reference(s) to other database(s): GTC:G74494LI, CCSD:
17223, CBank-STR:16704
- Compound ID: 28463
|
b-D-Galp-(1-2)-a-D-Xylp-(1-6)-+
|
b-D-Galp-(1-2)-a-D-Xylp-(1-6)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp |
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Structure type: oligomer
Compound class: xyloglucan
Reference(s) to other database(s): GTC:G80477OI
- Compound ID: 28464
Structure type: oligomer
Compound class: xyloglucan
Reference(s) to other database(s): GTC:G09284NG
- Compound ID: 28524
|
a-D-GalpA-(1-4)-a-D-GalpA-(1-4)-{{{-a-D-GalpA-(1-4)-}}}/n=4-8/-a-D-GalpA |
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Structure type: fragment of a bigger structure
Compound class: galacturonan
Reference(s) to other database(s): GTC:G77590YF
- Compound ID: 28525
Structure type: fragment of a bigger structure
Reference(s) to other database(s): GTC:G73238WA
- Compound ID: 28526
Structure type: fragment of a bigger structure
Reference(s) to other database(s): GTC:G13809LQ
- Compound ID: 28527
|
a-L-Fucp2Me-(1-2)-+
|
a-L-Rhap-(1-2)-a-L-Arap-(1-4)-a-D-Galp-(1-2)-b-AcefA-(1-3)-b-L-Rhap-(1-3)-b-D-Apif |
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Structure type: fragment of a bigger structure
- Compound ID: 28528
|
a-D-GalpA-(1-2)-+
|
a-D-Xylp2Me-(1-3)-+ |
| |
a-D-Galp-(1-2)-b-D-GlcpA-(1-4)-a-L-Fucp-(1-4)-b-L-Rhap-(1-3)-b-D-Apif
|
b-D-GalpA-(1-3)-+ |
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Structure type: fragment of a bigger structure
- Compound ID: 6650
Structure type: homopolymer
Trivial name: cellulose, β-(1,4)-glucan, cellulose, β-(1,4)-glucan
Compound class: EPS, O-polysaccharide, cell wall polysaccharide, glucan, polysaccharide
Reference(s) to other database(s): GTC:G75830OM, GlycomeDB:
27885, CCSD:
50051, CBank-STR:4229
- Compound ID: 19993
|
a-D-Manp-(1-6)-+
|
a-D-Manp-(1-3)-b-D-Manp-(1-4)-b-D-GlcpNAc-(1-4)-b-D-GlcpNAc-(1--/(->4) Asn-X-Ser/Thr (protein)/ |
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Structure type: oligomer
Aglycon: (->4) Asn-X-Ser/Thr (protein)
Compound class: N-glycan
Reference(s) to other database(s): GTC:G22768VO
- Compound ID: 28538
|
b-D-GlcpNAc-(1-2)-a-D-Manp-(1-6)-+ a-Fuc-(1-3)-+
| |
b-D-GlcpNAc-(1-2)-a-D-Manp-(1-3)-b-D-Manp-(1-4)-b-D-GlcpNAc-(1-4)-b-D-GlcpNAc-(1--/(->4) Asn-X-Ser/Thr (protein)/
|
a-Xylp-(1-2)-+ |
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Structure type: oligomer
Aglycon: (->4) Asn-X-Ser/Thr (protein)
Compound class: N-glycan
Reference(s) to other database(s): GTC:G28383QP
- Compound ID: 28539
|
a-Fucp-(1-4)-+
|
b-Galp-(1-3)-b-D-GlcpNAc-(1-2)-a-D-Manp-(1-6)-+
|
b-Fucp-(1-4)-+ | a-Fuc-(1-3)-+
| | |
b-Galp-(1-3)-b-D-GlcpNAc-(1-2)-a-D-Manp-(1-3)-b-D-Manp-(1-4)-b-D-GlcpNAc-(1-4)-b-D-GlcpNAc-(1--/(->4) Asn-X-Ser/Thr (protein)/
|
a-Xylp-(1-2)-+ |
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Structure type: oligomer
Aglycon: (->4) Asn-X-Ser/Thr (protein)
Compound class: N-glycan
Reference(s) to other database(s): GTC:G53915LK
- Compound ID: 28543
|
b-D-GlcpNAc-(1-2)-a-D-Manp-(1-3)-+
|
a-D-Manp-(1-6)-+ | ?%a-Fuc-(1-3)-+
| | |
a-D-Manp-(1-3)-a-D-Manp-(1-6)-b-D-Manp-(1-4)-b-D-GlcpNAc-(1-4)-b-D-GlcpNAc-(1--/(->4) Asn-X-Ser/Thr (protein)/
|
?%a-Xylp-(1-2)-+ |
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Structure type: oligomer
Aglycon: (->4) Asn-X-Ser/Thr (protein)
Compound class: N-glycan
Reference(s) to other database(s): GTC:G57677LM
- Compound ID: 24800
Structure type: polymer chemical repeating unit
Trivial name: rhamnogalactouronan
Compound class: rhamnogalacturonan
Reference(s) to other database(s): GTC:G28839TI, CCSD:
50038, CBank-STR:3824
- Compound ID: 19962
|
a-D-Manp-(1-2)-a-D-Manp-(1-6)-+
|
a-D-Manp-(1-2)-a-D-Manp-(1-3)-a-D-Manp-(1-6)-+
|
a-Glcp-(1-2)-a-Glcp-(1-3)-a-Glcp-(1-3)-a-D-Manp-(1-2)-a-D-Manp-(1-2)-a-D-Man-(1-3)-a-D-Man-(1-4)-b-D-GlcpNAc-(1-4)-b-D-GlcpNAc-(1--/(->4) Asn-X-Ser/Thr (protein)/ |
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Structure type: oligomer
Aglycon: (->4) Asn-X-Ser/Thr (protein)
Compound class: N-glycan
Reference(s) to other database(s): GTC:G57862SA
- Compound ID: 23730
Structure type: oligomer
Trivial name: chacotrioside, chacotriose dioscin, dioscin, trigonelloside C, dioscin prosapogenin A
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
29844, CBank-STR:6359
- Compound ID: 29103
|
Gallic-(7-6)-+
|
Gallic-(7-3)-+ |
| |
Gallic-(7-2)-b-D-Glcp-(1-7)-Gallic
|
Gallic-(7-4)-+ |
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Structure type: monomer
Trivial name: pentagalloylglucose
Compound class: glycoside, phenolic glycoside
- Compound ID: 29111
|
Gallic-(7-2)-+ Gallic-(7-2)-+
| |
Subst1-(7-6:7'-4)-b-D-Glcp-(1-7)-Subst2-(2-3)-Gallic-(7-1)-b-D-Glcp-(4-7':6-7)-Subst1
| |
Gallic-(7-3)-+ Gallic-(7-3)-+
Subst1 = hexahydroxydiphenic acid = SMILES O{3}C1={4}C(O){5}C(O)=C(C2={55}C(O){54}C(O)={53}C(O)C=C2{57}C(O)=O)C({7}C(O)=O)=C1;
Subst2 = 3,4,5-trihydroxysalicylic acid = SMILES O{5}C1={4}C(O){3}C(O)={2}C(O)C({7}C(O)=O)=C1 |
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Structure type: oligomer
Trivial name: coriariin A
Compound class: glycoside
- Compound ID: 29112
|
Subst1-(7-6:7'-4)-+ Subst1-(7-2:7'-3)-+
| |
Subst1-(7-2:7'-3)-a-D-Glcp-(1-7)-Subst2-(2-3)-Gallic-(7-1)-a-D-Glcp-(4-7':6-7)-Subst1
Subst1 = hexahydroxydiphenic acid = SMILES O{3}C1={4}C(O){5}C(O)=C(C2={55}C(O){54}C(O)={53}C(O)C=C2{57}C(O)=O)C({7}C(O)=O)=C1;
Subst2 = 3,4,5-trihydroxysalicylic acid = SMILES O{5}C1={4}C(O){3}C(O)={2}C(O)C({7}C(O)=O)=C1 |
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Structure type: oligomer
Trivial name: agrimoniin
Compound class: glycoside
- Compound ID: 21233
Structure type: structural motif or average structure
Trivial name: glycogen, starch, amylopectin, amylopectin, phytoglycogen, amylopectin, amylose, amylose, amylopectin
Compound class: glucan
Reference(s) to other database(s): GTC:G68717OT
- Compound ID: 31211
|
Caf-(9-4)-+
|
a-L-Rhap-(1-3)-b-D-Glcp-(1-8)-Subst
Subst = 4-(1,2-dihydroxyethyl)benzene-1,2-diol = SMILES O{7}C({8}CO)C1=C{3}C(O)={4}C(O)C=C1 |
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Structure type: oligomer
Trivial name: hydroxyacteoside
Compound class: glycoside
- Compound ID: 31212
|
Caf-(9-4)-+
|
a-L-Rhap-(1-6)-b-D-Glcp-(1-8)-Subst
Subst = 4-(1,2-dihydroxyethyl)benzene-1,2-diol = SMILES O{7}C({8}CO)C1=C{3}C(O)={4}C(O)C=C1 |
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Structure type: oligomer
Trivial name: suspensaside
Compound class: glycoside
- Compound ID: 22429
Structure type: oligomer
Trivial name: acteoside, verbascoside, acteoside, verbascoside, trans-verbascoside, verbascoside, acteoside
Compound class: saponin glycoside, glycoside, phenolic glycoside, phenylethanoid glycoside, phenylpropanoid glycoside, iridoid glycoside, lignan glycoside
- Compound ID: 28029
Structure type: oligomer
Trivial name: forsythiaside
Compound class: saponin glycoside, glycoside, phenolic glycoside, lignan glycoside
- Compound ID: 31213
|
a-L-Rhap-(1-3)-+
|
a-L-Arap-(1-2)-b-D-Glcp-(1-8)-3,4,8HOPhet
|
Caf-(9-4)-+ |
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Structure type: oligomer
Trivial name: ehrenoside
Compound class: glycoside
- Compound ID: 31348
|
b-D-Glcp1S-(1-2)-Subst
Subst = (E)-N-(sulfooxy)but-3-enimidothioic acid = SMILES C=CC/{2}C(S)=N\OS(=O)(O)=O |
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Structure type: monomer
Trivial name: sinigrin
Compound class: glycoside, glucosinolate
- Compound ID: 26875
|
b-D-Glcp-(1-2)-Subst
Subst = 2-hydroxy-methyl-propiononitrile = SMILES C{2}C(O)(C#N)C |
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Structure type: monomer
Trivial name: linamarin
Compound class: glycoside, cyanogenic glycoside
Reference(s) to other database(s): CCSD:
43659, CBank-STR:1199
- Compound ID: 27278
|
b-D-Glcp-(1-1)-Subst
Subst = hydroquinone = SMILES O{1}C1=CC={4}C(O)C=C1 |
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Structure type: monomer
Trivial name: arbutin
Compound class: glycoside, flavonol glycoside
- Compound ID: 29194
|
b-D-Glcp-(1-2)-Subst
Subst = salicyl alcohol = SMILES O{2}C1=CC=CC=C1{7}CO |
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Structure type: monomer
Trivial name: salicin
Compound class: glycoside, phenolic glycoside
- Compound ID: 5326
Structure type: homopolymer
Trivial name: β-(1,4)-xylan
Compound class: EPS, polysaccharide, xylan
Reference(s) to other database(s): GTC:G75244KS, GlycomeDB:
6153, CCSD:
50044, CBank-STR:1702
- Compound ID: 31395
|
b-D-Galp-(1-?)-b-D-Xylp-(1-6)-+
|
b-D-Galp-(1-?)-b-D-Xylp-(1-6)-+ |
| |
a-L-Araf-(1-2)-+ | |
| | |
b-D-Xylp-(1-6)-+ | | |
| | | |
b-D-Xylp-(1-6)-+ | | b-D-Xylp-(1-6)-+ | |
| | | | | |
-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-
| |
b-D-Xylp-(1-6)-+ b-D-Xylp-(1-3)-+ |
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Structure type: structural motif or average structure
Compound class: polysaccharide
- Compound ID: 31396
|
b-D-Xylp-(1-3)-+
|
b-D-Galp-(1-?)-b-D-Xylp-(1-6)-+ |
| |
a-L-Araf-(1-2)-+ | |
| | |
b-D-Xylp-(1-6)-+ | b-D-Xylp-(1-6)-+ | |
| | | | |
-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-
| |
b-D-Xylp-(1-6)-+ b-D-Xylp-(1-6)-+ |
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Structure type: structural motif or average structure
Compound class: polysaccharide
- Compound ID: 31397
|
b-D-Galp-(1-?)-b-D-Xylp-(1-6)-+
|
b-D-Galp-(1-?)-b-D-Xylp-(1-6)-+ |
| |
b-D-Xylp-(1-6)-+ b-D-Xylp-(1-6)-+ b-D-Xylp-(1-6)-+ | |
| | | | |
-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-
|
b-D-Xylp-(1-3)-+ |
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Structure type: structural motif or average structure
Compound class: polysaccharide
- Compound ID: 31398
|
a-L-Araf-(1-2)-+
|
b-D-Xylp-(1-6)-+ |
| |
b-D-Xylp-(1-6)-+ | | b-D-Xylp-(1-6)-+ b-D-Xylp-(1-3)-+
| | | | |
-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-
|
b-D-Xylp-(1-6)-+ |
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Structure type: structural motif or average structure
Compound class: polysaccharide
- Compound ID: 31399
|
b-D-Galp-(1-?)-b-D-Xylp-(1-6)-+
|
b-D-Galp-(1-?)-b-D-Xylp-(1-6)-+ |
| |
b-D-Glcp-(1-3)-b-D-Xylp-(1-6)-+ | |
| | |
b-D-Xylp-(1-6)-+ | | |
| | | |
b-D-Xylp-(1-6)-+ | | b-D-Xylp-(1-6)-+ | |
| | | | | |
-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-
| |
a-L-Araf-(1-2)-+ b-D-Xylp-(1-3)-+ |
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Structure type: structural motif or average structure
Compound class: polysaccharide
- Compound ID: 31380
|
b-D-Glcp-(1-6)-b-D-Glcp-(1-7)-Subst
Subst = D-mandelonitrile = SMILES O{7}[C@H](C1=CC=CC=C1)C#N |
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Structure type: oligomer
Trivial name: amygdalin
Compound class: glycoside, cyanogenic glycoside
- Compound ID: 30867
|
b-D-Glcp-(1-7)-Subst
Subst = (S)-4-hydroxymandelonitrile = SMILES c1cc(ccc1{7}[C@@H](C#N)O)O |
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Structure type: monomer
Trivial name: (S)-dhurrin, dhurrin
Compound class: glycoside, cyanogenic glycoside
- Compound ID: 28894
Structure type: oligomer
Trivial name: glycyrrhizin
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 29528
|
b-D-Glcp-(1-7)-Subst
Subst = ptaquilosin = SMILES C/C2=C/{7}[C@]1(O)C[C@@H](C)C(=O)[C@@H]1{4}[C@](C)(O)C23CC3 |
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Structure type: monomer
C20H30O8
Trivial name: ptaquiloside
Compound class: glycoside, sesquiterpenoid glycoside
- Compound ID: 23941
Structure type: oligomer
Trivial name: solatriose, α-solanine, solatriose α-solanine, solanine solatriose, solanine
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
49712, CBank-STR:8737
- Compound ID: 23940
Structure type: oligomer
Trivial name: solamargine, chacotriose, α-chaconine, solamargine α-chaconine, chaconine, chacotriose solanidine α-chaconine, chacotriose α-chaconine
Compound class: saponin glycoside, glycoside
Reference(s) to other database(s): CCSD:
49713, CBank-STR:6366
- Compound ID: 20822
Structure type: oligomer
C27H30O16
Trivial name: rutin, rutoside, rutin, quercetin rutinoside, rutoside, quercetin 3-O-rutinose, quercetin-3-O-rutinoside, quercetin 3-O-rutinoside
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside
Reference(s) to other database(s): CCSD:
50720, CBank-STR:3399
- Compound ID: 31482
Structure type: structural motif or average structure
Compound class: galactomannan
- Compound ID: 31484
|
b-D-Glcp-(1-19)-Subst23Me
Subst = strictosidinic acid aglycon = SMILES C=C[C@@H]1[C@H](C[C@H]2C3=C(C4=CC=CC=C4N3)CCN2)C({23}C(O)=O)=CO{19}[C@H]1O |
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Structure type: monomer
Trivial name: strictosidine
Compound class: glycoside
Reference(s) to other database(s): GenDB:AF112888
- Compound ID: 31507
Structure type: structural motif or average structure
Compound class: polysaccharide, dextran
- Compound ID: 18531
Structure type: monomer
Compound class: glycolipid, glycosphingolipid, glycosylceramide, ceramide
- Compound ID: 31564
Structure type: oligomer
Compound class: glycolipid, glycosylceramide
- Compound ID: 31565
Structure type: oligomer
Compound class: glycolipid, glycosylceramide
- Compound ID: 31571
Structure type: oligomer
Compound class: glycoside
- Compound ID: 31572
|
{{{-a-L-Araf-(1-5)-}}}a-L-Araf-(1-4)-{{{-b-D-Galp-(1-4)-}}}b-D-Galp-(1-4)-+
|
{{{-a-L-Araf-(1-5)-}}}a-L-Araf-(1-4)-+ |
| |
{{{-a-L-Araf-(1-5)-}}}a-L-Araf-(1-4)-{{{-b-D-Galp-(1-4)-}}}b-D-Galp-(1-4)-+ {{{-b-D-Galp-(1-4)-}}}b-D-Galp-(1-4)-+ | |
| | | |
-4)-a-D-GalpA-(1-2)-a-L-Rhap-(1-4)-a-D-GalpA-(1-2)-a-L-Rhap-(1-4)-a-D-GalpA-(1-2)-a-L-Rhap-(1-4)-a-D-GalpA-(1-2)-a-L-Rhap-(1-4)-a-D-GalpA-(1-2)-a-L-Rhap-(1-4)-a-D-GalpA-(1-2)-a-L-Rhap-(1-4)-a-D-GalpA-(1-2)-a-L-Rhap-(1- |
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Structure type: structural motif or average structure
Compound class: polysaccharide
- Compound ID: 26897
|
b-D-Glcp-(1-3)-Subst
Subst = delphinidin = SMILES O{3}C1=C(C2=C{53}C(O)={54}C(O){55}C(O)=C2)[O+]=C3C={7}C(O)C={5}C(O)C3=C1 |
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Structure type: monomer
Trivial name: delphin
Compound class: glycoside, flavonoid glycoside, anthocyanin glycoside, anthocyanin glucoside
Reference(s) to other database(s): CCSD:
43648, CBank-STR:982
- Compound ID: 26794
Structure type: monomer
Compound class: glycoside, flavonoid glycoside, anthocyanin glycoside, anthocyanin glucoside
Reference(s) to other database(s): CCSD:
43647, CBank-STR:930
- Compound ID: 31341
|
b-D-Glcp-(1-3)-Subst
Subst = pelargonidin = SMILES O{3}C1=C(C2=CC={54}C(O)C=C2)[O+]=C3C={7}C(O)C={5}C(O)C3=C1 |
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Structure type: monomer
Compound class: glycoside, flavonoid glycoside, anthocyanin glucoside
- Compound ID: 22408
|
b-D-Glcp-(1-3)-Subst
Subst = malvidin = SMILES O{3}C1=C(C2=CC(OC)={54}C(O)C(OC)=C2)[O+]=C3C={7}C(O)C={5}C(O)C3=C1 |
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Structure type: monomer
Trivial name: malvin
Compound class: glycoside, flavonoid glycoside, anthocyanin glucoside
- Compound ID: 31612
Structure type: monomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31609
|
b-D-Glcp-(1-5)-+
|
b-D-Glcp-(1-3)-Subst
Subst = delphinidin = SMILES O{3}C1=C(C2=C{53}C(O)={54}C(O){55}C(O)=C2)[O+]=C3C={7}C(O)C={5}C(O)C3=C1 |
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Structure type: oligomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 26896
Structure type: oligomer
Compound class: glycoside, flavonoid glycoside, anthocyanin glycoside
Reference(s) to other database(s): CCSD:
43646, CBank-STR:2936
- Compound ID: 31637
|
b-D-Glcp-(1-5)-+
|
b-D-Glcp-(1-3)-Subst
Subst = pelargonidin = SMILES O{3}C1=C(C2=CC={54}C(O)C=C2)[O+]=C3C={7}C(O)C={5}C(O)C3=C1 |
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Structure type: oligomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 26895
|
b-D-Glcp-(1-5)-+
|
b-D-Glcp-(1-3)-Subst
Subst = malvidin = SMILES O{3}C1=C(C2=CC(OC)={54}C(O)C(OC)=C2)[O+]=C3C={7}C(O)C={5}C(O)C3=C1 |
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Structure type: oligomer
Compound class: glycoside, flavonoid glycoside, anthocyanin glycoside
Reference(s) to other database(s): CCSD:
43645, CBank-STR:2937
- Compound ID: 31611
Structure type: oligomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 21438
Structure type: monomer
Trivial name: isoquercitrin
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside
Reference(s) to other database(s): CCSD:
49965, CBank-STR:953
- Compound ID: 31657
Structure type: monomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 20724
Structure type: oligomer
Trivial name: maltose, maltobiose, maltodextrin
Compound class: glucan
Reference(s) to other database(s): GTC:G07411ON, CCSD:
5782, CBank-STR:2712
- Compound ID: 20726
Structure type: oligomer
Trivial name: maltotriose, maltodextrin
Compound class: glucan
Reference(s) to other database(s): GTC:G96370VA, CCSD:
5782, CBank-STR:2712
- Compound ID: 27423
Structure type: oligomer
Trivial name: maltotetraose, maltodextrin
Compound class: glucan, maltosaccharide
Reference(s) to other database(s): GTC:G87171PZ, CCSD:
5782, CBank-STR:2712
- Compound ID: 27424
|
a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp |
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Structure type: oligomer
Trivial name: maltodextrin
Compound class: glucan, maltosaccharide
Reference(s) to other database(s): GTC:G50146AM, CCSD:
5782, CBank-STR:2712
- Compound ID: 31680
|
a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp |
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Structure type: oligomer
Trivial name: maltodextrin
Compound class: glucan
- Compound ID: 31681
|
a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp |
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Structure type: oligomer
Trivial name: maltodextrin
Compound class: glucan
- Compound ID: 31682
|
a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp |
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Structure type: oligomer
Trivial name: maltodextrin
Compound class: glucan
- Compound ID: 31683
|
a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp |
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Structure type: oligomer
Trivial name: maltodextrin
Compound class: glucan
- Compound ID: 31684
|
a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp |
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Structure type: oligomer
Trivial name: maltodextrin
Compound class: glucan
- Compound ID: 31685
|
a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp |
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Structure type: oligomer
Trivial name: maltodextrin
Compound class: glucan
- Compound ID: 31686
|
a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp-(1-4)-a-D-Glcp |
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Structure type: oligomer
Trivial name: maltodextrin
Compound class: glucan
- Compound ID: 347
Structure type: oligomer
Trivial name: 1-kestose, inulin
Compound class: fructan, fructo-oligosaccharide
Reference(s) to other database(s): GTC:G11260CN, GlycomeDB:
396, CCSD:
26122, CBank-STR:5624, GenDB:MH445969, US-PT:US2017298332A1
- Compound ID: 547
Structure type: oligomer
Trivial name: nystose, inulin, 1,1-kestotetraose
Compound class: fructan
Reference(s) to other database(s): GTC:G60726JL, GlycomeDB:
63, CCSD:
23519, CBank-STR:9595, GenDB:MH445969, US-PT:US2017298332A1
- Compound ID: 19077
|
b-D-Fruf-(2-1)-b-D-Fruf-(2-1)-b-D-Fruf-(2-1)-b-D-Fruf-(2-1)-a-D-Glcp |
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Structure type: oligomer
Trivial name: inulin, fructosylnystose
Compound class: fructan
Reference(s) to other database(s): GTC:G14615XY
- Compound ID: 22453
Structure type: monomer
C21H20O11
Trivial name: quercitrin, baohuoside-II, quercetin 3-rhamnoside, quercetin 3-O-rhamnoside
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside
Reference(s) to other database(s): CCSD:
49971, CBank-STR:599
- Compound ID: 27277
Structure type: monomer
C21H20O12
Trivial name: myricitrin
Compound class: glycoside, flavonoid glycoside, flavonol glycoside
Reference(s) to other database(s): CCSD:
49968, CBank-STR:384
- Compound ID: 31892
|
b-D-Glcp-(1-7)-Subst
Subst = cichorigenin = SMILES O{7}C(C=C(OC1=O)C(C=C1)=C2)={6}C2O |
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Structure type: monomer
Trivial name: esculin, cichoriin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 23677
Structure type: oligomer
Trivial name: soyasaponin I, astrachrysoside A soyasaponin I, soyasaponin 1, saponin Bb soyasaponin I, soyasaponin Bb
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
48360, CBank-STR:9568, PubChem:122097
- Compound ID: 23676
Structure type: oligomer
Trivial name: soyasaponin II, soyasaponin 2, saponin Bc soyasaponin II, soyasaponin Bc
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
48361, CBank-STR:6049, PubChem:443614
- Compound ID: 23817
Structure type: oligomer
Trivial name: azukisaponin V, dehydrosoyasaponin I, azukisaponin, kaikasaponin
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
9282, CBank-STR:22158
- Compound ID: 24075
Structure type: oligomer
Trivial name: Wisteriasaponin C, astragaloside VIII
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
20147, CBank-STR:7566
- Compound ID: 24441
|
a-L-Rhap-(1-2)-b-D-Galp-(1-2)-b-D-GlcpA-(1-3)-Subst
Subst = sophoradiol = SMILES C[C@]12CC{3}[C@H](O)C(C)(C)[C@@H]1CC[C@]3(C)[C@@H]2CC=C4[C@@]3(C)CC[C@]5(C)[C@H]4CC(C)(C)C{22}[C@H]5O |
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Structure type: oligomer
Trivial name: kaikosaponin III, kaikasaponin III
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
28655, CBank-STR:9561
- Compound ID: 24440
|
a-L-Rhap-(1-2)-a-L-Arap-(1-2)-b-D-GlcpA-(1-3)-Subst
Subst = sophoradiol = SMILES C[C@]12CC{3}[C@H](O)C(C)(C)[C@@H]1CC[C@]3(C)[C@@H]2CC=C4[C@@]3(C)CC[C@]5(C)[C@H]4CC(C)(C)C{22}[C@H]5O |
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Structure type: oligomer
Trivial name: kaikasaponin I
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
15478, CBank-STR:6048
- Compound ID: 23678
Structure type: oligomer
Trivial name: soyasaponin III, saponin Bb' soyasaponin III, soyasaponin Bb'
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
48362, CBank-STR:5471
- Compound ID: 24724
|
b-D-Galp-(1-2)-b-D-GlcpA-(1-3)-Subst
Subst = sophoradiol = SMILES C[C@]12CC{3}[C@H](O)C(C)(C)[C@@H]1CC[C@]3(C)[C@@H]2CC=C4[C@@]3(C)CC[C@]5(C)[C@H]4CC(C)(C)C{22}[C@H]5O |
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Structure type: oligomer
Trivial name: kaikasaponin I
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
17887, CBank-STR:7644
- Compound ID: 24279
Structure type: oligomer
Trivial name: Azukisaponin II, azukisaponin II
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
9280, CBank-STR:22157
- Compound ID: 27515
Structure type: monomer
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
9281, CBank-STR:1434
- Compound ID: 23985
|
a-L-Rhap-(1-2)-b-D-Galp-(1-2)-b-D-GlcpA-(1-3)-Subst
Subst = soyasapogenol E = SMILES C[C@@]({24}CO)([C@](CC[C@@]([C@](CC[C@@]12C)3C)4C)5[H]){3}[C@@H](O)CC[C@]5(C)[C@@]4([H])CC=C3[C@]2([H])CC(C)(C)CC1=O |
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Structure type: oligomer
Trivial name: dehydrosoyasaponin I, saponin Be, soyasaponin Be
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
38957, CBank-STR:9569
- Compound ID: 31802
|
a-L-Rhap-(1-2)-b-D-Xylp-(1-2)-b-D-GlcpA-(1-3)-Subst
Subst = soyasapogenol E = SMILES C[C@@]({24}CO)([C@](CC[C@@]([C@](CC[C@@]12C)3C)4C)5[H]){3}[C@@H](O)CC[C@]5(C)[C@@]4([H])CC=C3[C@]2([H])CC(C)(C)CC1=O |
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Structure type: oligomer
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 30372
Structure type: monomer
Trivial name: isoorientin, homoorientin, isoorientin
Compound class: glycoside, flavonoid glycoside, flavone glycoside
- Compound ID: 31989
| Cyclic
-6)-b-D-Glcp-(1-2)-b-D-Glcp-(1-3)-Subst-(28-1)-a-L-Arap-(2-1)-a-L-Rhap-(4-1)-3HO3MeGlt-(5-
Subst = bayogenin = SMILES O{2}[C@@H]1{3}[C@H](O)[C@@](C)({23}CO)[C@@](CC[C@]2(C)[C@]3([H])CC=C4[C@@]2(C)CC[C@]5({28}C(O)=O)[C@@]4([H])CC(C)(C)CC5)([H])[C@]3(C)C1;
3HO3MeGlt = 3-hydroxy-3-methylglutaric acid |
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Structure type: cyclic polymer repeating unit
Trivial name: lobatoside B
Compound class: glycoside
- Compound ID: 31990
| Cyclic
-4)-a-L-Arap-(1-2)-b-D-Glcp-(1-3)-Subst-(28-1)-a-L-Arap-(2-1)-a-L-Rhap-(4-1)-3HO3MeGlt-(5-
Subst = bayogenin = SMILES O{2}[C@@H]1{3}[C@H](O)[C@@](C)({23}CO)[C@@](CC[C@]2(C)[C@]3([H])CC=C4[C@@]2(C)CC[C@]5({28}C(O)=O)[C@@]4([H])CC(C)(C)CC5)([H])[C@]3(C)C1;
3HO3MeGlt = 3-hydroxy-3-methylglutaric acid |
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Structure type: cyclic polymer repeating unit
Trivial name: lobatoside C
Compound class: glycoside
- Compound ID: 31991
| Cyclic
b-D-Glcp-(1-3)-+
|
-4)-a-L-Arap-(1-2)-b-D-Glcp-(1-3)-Subst-(28-1)-a-L-Arap-(2-1)-a-L-Rhap-(4-1)-3HO3MeGlt-(5-
Subst = bayogenin = SMILES O{2}[C@@H]1{3}[C@H](O)[C@@](C)({23}CO)[C@@](CC[C@]2(C)[C@]3([H])CC=C4[C@@]2(C)CC[C@]5({28}C(O)=O)[C@@]4([H])CC(C)(C)CC5)([H])[C@]3(C)C1;
3HO3MeGlt = 3-hydroxy-3-methylglutaric acid |
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Structure type: cyclic polymer repeating unit
Trivial name: lobatoside D
Compound class: glycoside
- Compound ID: 31992
| Cyclic
b-D-Glcp-(1-3)-+
|
-6)-b-D-Galp-(1-2)-b-D-Glcp-(1-3)-Subst-(28-1)-a-L-Arap-(2-1)-a-L-Rhap-(4-1)-3HO3MeGlt-(5-
Subst = bayogenin = SMILES O{2}[C@@H]1{3}[C@H](O)[C@@](C)({23}CO)[C@@](CC[C@]2(C)[C@]3([H])CC=C4[C@@]2(C)CC[C@]5({28}C(O)=O)[C@@]4([H])CC(C)(C)CC5)([H])[C@]3(C)C1;
3HO3MeGlt = 3-hydroxy-3-methylglutaric acid |
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Structure type: cyclic polymer repeating unit
Trivial name: lobatoside E
Compound class: glycoside
- Compound ID: 31993
| Cyclic
b-D-Xylp-(1-3)-+
|
-4)-a-L-Arap-(1-2)-b-D-Glcp-(1-3)-Subst-(28-1)-a-L-Arap-(2-1)-a-L-Rhap-(4-1)-3HO3MeGlt-(5-
Subst = bayogenin = SMILES O{2}[C@@H]1{3}[C@H](O)[C@@](C)({23}CO)[C@@](CC[C@]2(C)[C@]3([H])CC=C4[C@@]2(C)CC[C@]5({28}C(O)=O)[C@@]4([H])CC(C)(C)CC5)([H])[C@]3(C)C1 |
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Structure type: cyclic polymer repeating unit
Trivial name: tubeimoside I, tubeimoside 1
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 31994
|
b-D-Glcp-(1-3)-+
|
3HOBut-(1-3)-3HOBut-(1-3)-3HOBut-(1-3)-+ |
| |
a-L-Rhap-(1-3)-b-D-Xylp-(1-4)-a-L-Rhap-(1-2)-a-L-Fucp-(1-28)-Polygalacic |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 31995
|
b-D-Glcp-(1-3)-+
|
3HOBut-(1-3)-3HOBut-(1-3)-+ |
| |
a-L-Rhap-(1-3)-b-D-Xylp-(1-4)-a-L-Rhap-(1-2)-a-L-Fucp-(1-28)-Polygalacic |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 31996
|
b-D-Glcp-(1-3)-b-D-Glcp-(1-3)-+
|
3HOBut-(1-3)-3HOBut-(1-3)-3HOBut-(1-3)-+ |
| |
a-L-Rhap-(1-3)-b-D-Xylp-(1-4)-a-L-Rhap-(1-2)-a-L-Fucp-(1-28)-Polygalacic |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 31997
|
b-D-Glcp-(1-3)-b-D-Glcp-(1-3)-+
|
3HOBut-(1-3)-3HOBut-(1-3)-+ |
| |
a-L-Rhap-(1-3)-b-D-Xylp-(1-4)-a-L-Rhap-(1-2)-a-L-Fucp-(1-28)-Polygalacic |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 31998
|
b-D-Xylp-(1-4)-+ b-D-Glcp-(1-3)-+
| |
b-D-Apif-(1-3)-a-L-Rhap-(1-2)-a-L-Arap-(1-28)-Polygalacic |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 31999
|
b-D-Glcp-(1-3)-b-D-Glcp-(1-3)-+
|
b-D-Xylp-(1-4)-+ |
| |
b-D-Apif-(1-3)-a-L-Rhap-(1-2)-a-L-Arap-(1-28)-Polygalacic |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 32000
|
a-L-Rhap-(1-2)-+
|
a-D-Arap-(1-4)-+ |
| |
b-D-Xylp-(1-3)-b-D-Fucp-(1-28)-Polygalacic |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 32001
|
b-D-Xylp-(1-4)-+
|
a-L-Rhap-(1-3)-b-D-Glcp-(1-3)-+
|
b-D-Glcp-(1-4)-a-L-Rhap-(1-2)-a-L-Arap-(1-28)-Echinocystic |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 26724
Structure type: monomer
Trivial name: afzelin
Compound class: glycoside, flavonoid glycoside, triterpenoid glycoside, flavonol glycoside
Reference(s) to other database(s): CCSD:
41324, CBank-STR:605
- Compound ID: 20490
|
b-D-Glcp-(1-3)-Subst
Subst = β-sitosterol = SMILES O{3}[C@H](C1)CC[C@@]2(C)C1=CC[C@]3([H])[C@@]2([H])CC[C@@]4(C)[C@]3([H])CC[C@]4([C@@H](C)CC[C@@H](CC)C(C)C)[H] |
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Structure type: monomer
Trivial name: daucosterol, β-daucosterol, β-sitosterol, β-sitosterol-β-D-glucoside, androsine, saxifragifolin B, β-sitosterol 3-O-β-D-glucopyranoside
Compound class: saponin glycoside, glycoside, steroid glycoside, triterpenoid glycoside
Reference(s) to other database(s): GenDB:MK026953.1
- Compound ID: 32004
|
b-D-Glcp-(1-3)-+
|
Subst1-3Me4Me-(9-4)-+ |
| |
b-D-Galp-(1-4)-b-D-Xylp-(1-4)-a-L-Rhap-(1-2)-b-D-Fucp-(1-28)-Subst
Subst = presenegenin = SMILES C[C@@]12CC[C@@H]3[C@@](C{2}[C@H](O){3}[C@H](O)[C@]3({23}C(O)=O)C)(C)[C@H]1CC=C4[C@@]2({27}CO)CC[C@]5({28}C(O)=O)[C@H]4CC(C)(C)CC5;
Subst1 = 3,4-dihydroxy-cis-cinnamic acid = SMILES O={9}C(O)/C=C\C1=CC={4}C(O){3}C(O)=C1 |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 32005
|
b-D-Glcp-(1-3)-+
|
Fer4Me-(9-4)-+ |
| |
b-D-Galp-(1-4)-b-D-Xylp-(1-4)-a-L-Rhap-(1-2)-b-D-Fucp-(1-28)-Subst
Subst = presenegenin = SMILES C[C@@]12CC[C@@H]3[C@@](C{2}[C@H](O){3}[C@H](O)[C@]3({23}C(O)=O)C)(C)[C@H]1CC=C4[C@@]2({27}CO)CC[C@]5({28}C(O)=O)[C@H]4CC(C)(C)CC5 |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 32006
|
b-D-Glcp-(1-3)-+
|
Subst1-4Me-(9-4)-+ |
| |
b-D-Galp-(1-4)-b-D-Xylp-(1-4)-a-L-Rhap-(1-2)-b-D-Fucp-(1-28)-Subst
Subst = presenegenin = SMILES C[C@@]12CC[C@@H]3[C@@](C{2}[C@H](O){3}[C@H](O)[C@]3({23}C(O)=O)C)(C)[C@H]1CC=C4[C@@]2({27}CO)CC[C@]5({28}C(O)=O)[C@H]4CC(C)(C)CC5;
Subst1 = cis-p-coumaric acid = SMILES O={9}C(O)/C=C\c1cc{4}c(O)cc1 |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 32007
|
b-D-Glcp-(1-3)-+
|
pCoum4Me-(9-4)-+ |
| |
b-D-Galp-(1-4)-b-D-Xylp-(1-4)-a-L-Rhap-(1-2)-b-D-Fucp-(1-28)-Subst
Subst = presenegenin = SMILES C[C@@]12CC[C@@H]3[C@@](C{2}[C@H](O){3}[C@H](O)[C@]3({23}C(O)=O)C)(C)[C@H]1CC=C4[C@@]2({27}CO)CC[C@]5({28}C(O)=O)[C@H]4CC(C)(C)CC5 |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 32008
|
b-D-Glcp-(1-3)-+
|
b-D-Galp-(1-4)-b-D-Xylp-(1-4)-a-L-Rhap-(1-2)-b-D-Fucp-(1-28)-Subst
Subst = presenegenin = SMILES C[C@@]12CC[C@@H]3[C@@](C{2}[C@H](O){3}[C@H](O)[C@]3({23}C(O)=O)C)(C)[C@H]1CC=C4[C@@]2({27}CO)CC[C@]5({28}C(O)=O)[C@H]4CC(C)(C)CC5;
Subst1 = cis-p-coumaric acid = SMILES O={9}C(O)/C=C\c1cc{4}c(O)cc1 |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 32009
|
b-D-Glcp-(1-3)-+
|
Subst1-4Me-(9-4)-+ |
| |
b-D-Galp-(1-4)-b-D-Xylp-(1-4)-a-L-Rhap-(1-2)-b-D-Fucp-(1-28)-Subst
|
a-L-Rhap-(1-3)-+
Subst = presenegenin = SMILES C[C@@]12CC[C@@H]3[C@@](C{2}[C@H](O){3}[C@H](O)[C@]3({23}C(O)=O)C)(C)[C@H]1CC=C4[C@@]2({27}CO)CC[C@]5({28}C(O)=O)[C@H]4CC(C)(C)CC5;
Subst1 = cis-p-coumaric acid = SMILES O={9}C(O)/C=C\c1cc{4}c(O)cc1 |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 32010
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b-D-Glcp-(1-3)-+
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a-L-Rhap-(1-3)-+ |
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b-D-Galp-(1-4)-b-D-Xylp-(1-4)-a-L-Rhap-(1-2)-b-D-Fucp-(1-28)-Subst
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pCoum4Me-(9-4)-+
Subst = presenegenin = SMILES C[C@@]12CC[C@@H]3[C@@](C{2}[C@H](O){3}[C@H](O)[C@]3({23}C(O)=O)C)(C)[C@H]1CC=C4[C@@]2({27}CO)CC[C@]5({28}C(O)=O)[C@H]4CC(C)(C)CC5 |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 32011
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b-D-Glcp-(1-3)-+
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a-L-Rhap-(1-3)-+ |
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b-D-Galp-(1-4)-b-D-Xylp-(1-4)-a-L-Rhap-(1-2)-b-D-Fucp-(1-28)-Subst
Subst = presenegenin = SMILES C[C@@]12CC[C@@H]3[C@@](C{2}[C@H](O){3}[C@H](O)[C@]3({23}C(O)=O)C)(C)[C@H]1CC=C4[C@@]2({27}CO)CC[C@]5({28}C(O)=O)[C@H]4CC(C)(C)CC5 |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 32012
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b-D-Glcp-(1-3)-+
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b-D-Glcp6Ac-(1-3)-+ |
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b-D-Galp-(1-4)-b-D-Xylp-(1-4)-a-L-Rhap-(1-2)-b-D-Fucp-(1-28)-Subst
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Subst1-(9-4)-+
Subst = presenegenin = SMILES C[C@@]12CC[C@@H]3[C@@](C{2}[C@H](O){3}[C@H](O)[C@]3({23}C(O)=O)C)(C)[C@H]1CC=C4[C@@]2({27}CO)CC[C@]5({28}C(O)=O)[C@H]4CC(C)(C)CC5;
Subst1 = cis-p-coumaric acid = SMILES O={9}C(O)/C=C\c1cc{4}c(O)cc1 |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 32013
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b-D-Glcp-(1-3)-+
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b-D-Glcp6Ac-(1-3)-+ |
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b-D-Galp-(1-4)-b-D-Xylp-(1-4)-a-L-Rhap-(1-2)-b-D-Fucp-(1-28)-Subst
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pCoum-(9-4)-+
Subst = presenegenin = SMILES C[C@@]12CC[C@@H]3[C@@](C{2}[C@H](O){3}[C@H](O)[C@]3({23}C(O)=O)C)(C)[C@H]1CC=C4[C@@]2({27}CO)CC[C@]5({28}C(O)=O)[C@H]4CC(C)(C)CC5 |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 32014
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b-D-Glcp-(1-3)-+
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b-D-Glcp-(1-3)-+ |
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b-D-Galp-(1-4)-b-D-Xylp-(1-4)-a-L-Rhap-(1-2)-b-D-Fucp-(1-28)-Subst
Subst = presenegenin = SMILES C[C@@]12CC[C@@H]3[C@@](C{2}[C@H](O){3}[C@H](O)[C@]3({23}C(O)=O)C)(C)[C@H]1CC=C4[C@@]2({27}CO)CC[C@]5({28}C(O)=O)[C@H]4CC(C)(C)CC5 |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 32015
Structure type: oligomer
Compound class: glycoside
- Compound ID: 32016
Structure type: oligomer
Compound class: glycoside
- Compound ID: 1267
Structure type: homopolymer
Trivial name: methyl glucose lipopolysaccharide, glucan, maltosaccharide, α-1,4-D-glucan, amylose, α-glucan, glycogen backbone, α-(1,4)-glucan, starch, α-(1-4)-glucan, starch, glycogen
Compound class: CPS, EPS, O-polysaccharide, cell wall polysaccharide, glucan, polysaccharide, methyl glucose lipopolysaccharide
Reference(s) to other database(s): GTC:G05740LL, GlycomeDB:
12100, CCSD:
4943, CBank-STR:819
- Compound ID: 32173
Structure type: structural motif or average structure
Compound class: polysaccharide, galacturonan
- Compound ID: 26869
Structure type: oligomer
Trivial name: naringin, rhoifolin
Compound class: glycoside, flavonoid glycoside, flavonol glycoside
Reference(s) to other database(s): CCSD:
43146, CBank-STR:3414
- Compound ID: 26870
Structure type: oligomer
Trivial name: narirutin, isorhoifolin
Compound class: glycoside, flavonoid glycoside
Reference(s) to other database(s): CCSD:
43147, CBank-STR:3418
- Compound ID: 32245
Structure type: oligomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 22375
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a-L-Rhap-(1-2)-b-D-Glcp-(1-7)-Subst
Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13 |
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Structure type: oligomer
Trivial name: naringin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31207
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a-L-Rhap-(1-6)-b-D-Glcp-(1-7)-Subst
Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13 |
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Structure type: oligomer
Trivial name: naringin, narirutin, narurutin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 26007
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a-L-Rhap-(1-6)-b-D-Glcp-(1-7)-Subst
Subst = hesperetin = SMILES O=C(C1=C(O/2)C={7}C(O)C={5}C1O)CC2=C3C={54}C(C(OC)=CC/3)O |
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Structure type: oligomer
Trivial name: hesperidin
Compound class: glycoside, flavonoid glycoside, flavonol glycoside
Reference(s) to other database(s): CCSD:
49861, CBank-STR:3421
- Compound ID: 25908
Structure type: oligomer
C27H30O15
Trivial name: nicotiflorin
Compound class: glycoside, flavonoid glycoside, flavonol glycoside
Reference(s) to other database(s): CCSD:
41325, CBank-STR:3415
- Compound ID: 31185
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b-D-Glcp-(1-28)-Subst
Subst = arjungenin = SMILES C[C@@]12CC[C@@H]3[C@@](C{2}[C@@H](O){3}[C@H](O)[C@]3({24}CO)C)(C)[C@H]1CC=C4[C@@]2(C)CC[C@]5({28}C(O)=O)[C@H]4{22}[C@H](O)C(C)(C)CC5 |
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Structure type: monomer
Trivial name: arjunglucoside I, arjunglucoside
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 32277
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a-L-Araf-(1-3)-a-L-Araf-(1-3)-b-D-Galp-(1-6)-b-D-Galp-(1-6)-+
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a-L-Rhap-(1-4)-b-D-GalpA-(1-6)-b-D-Galp-(1-6)-+ |
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a-L-Araf-(1-3)-+ | |
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b-D-GalpA4Me-(1-6)-b-D-Galp-(1-6)-b-D-Galp-(1-6)-b-D-Galp-(1-6)-b-D-Galp-(1-6)-+ | |
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-3)-b-D-Galp-(1-3)-b-D-Galp-(1-3)-b-D-Galp-(1-3)-b-D-Galp-(1-3)-b-D-Galp-(1-3)-b-D-Galp-(1-3)-b-D-Galp-(1- |
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Structure type: structural motif or average structure
Compound class: arabinogalactan, polysaccharide
- Compound ID: 28317
Structure type: monomer
Trivial name: MGDG
Compound class: glycolipid, glycoside
- Compound ID: 32374
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a-L-Rhap-(1-6)-b-D-Glcp-(1-7)-Subst4'Me
Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13 |
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Structure type: oligomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31393
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a-L-Rhap-(1-6)-b-D-Glcp-(1-7)-Subst
Subst = eriodictyol = SMILES O=C1C[C@H](OC2=C1{5}C(O)=C{7}C(O)=C2)C3=C{53}C(O)={54}C(O)C=C3 |
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Structure type: oligomer
Trivial name: eriocitrin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31394
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a-L-Rhap-(1-2)-b-D-Glcp-(1-7)-Subst
Subst = eriodictyol = SMILES O=C1C[C@H](OC2=C1{5}C(O)=C{7}C(O)=C2)C3=C{53}C(O)={54}C(O)C=C3 |
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Structure type: oligomer
Trivial name: neoeriocitrin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 26871
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a-L-Rhap-(1-2)-b-D-Glcp-(1-7)-Subst
Subst = hesperetin = SMILES O=C(C1=C(O/2)C={7}C(O)C={5}C1O)CC2=C3C={54}C(C(OC)=CC/3)O |
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Structure type: oligomer
Trivial name: neohesperidin
Compound class: glycoside, flavonoid glycoside
Reference(s) to other database(s): CCSD:
43148, CBank-STR:3419
- Compound ID: 32375
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a-L-Rhap-(1-2)-b-D-Glcp-(1-7)-Subst4'Me
Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13 |
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Structure type: oligomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 21410
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b-D-Glcp-(1-7)-Subst
Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13 |
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Structure type: monomer
Trivial name: prunin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32057
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b-D-Glcp1S-(1-2)-Subst
Subst = (E)-3-hydroxy-N-(sulfooxy)pent-4-enimidothioic acid = SMILES C=CC(O)C/{2}C(S)=N\OS(=O)(O)=O |
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Structure type: monomer
Trivial name: epi-progoitrin, epiprogoitrin, progoitrin
Compound class: glycoside, glucosinolate
- Compound ID: 32061
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b-D-Glcp1S-(1-2)-Subst
Subst = (1E,4E)-5-(methylsulfinyl)-N-(sulfooxy)pent-4-enimidothioic acid = SMILES S/{2}C(CC/C=C/S(C)=O)=N/OS(=O)(O)=O |
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Structure type: monomer
Trivial name: glucoraphenin, glucoraphanin
Compound class: glycoside, glucosinolate
- Compound ID: 32062
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b-D-Glcp1S-(1-2)-Subst
Subst = (E)-4-(methylsulfonyl)-N-(sulfooxy)butanimidothioic acid = SMILES S/{2}C(CCCS(C)(=O)=O)=N/OS(=O)(O)=O |
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Structure type: monomer
Trivial name: glucocheirolin
Compound class: glycoside, glucosinolate
- Compound ID: 32058
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b-D-Glcp1S-(1-2)-Subst
Subst = (E)-2-phenyl-N-(sulfooxy)ethanimidothioic acid = SMILES S/{2}C(CC1=CC=CC=C1)=N/OS(=O)(O)=O |
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Structure type: monomer
Trivial name: glucotropaeolin
Compound class: glycoside, glucosinolate
- Compound ID: 32059
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b-D-Glcp1S-(1-2)-Subst
Subst = (E)-2-(4-hydroxyphenyl)-N-(sulfooxy)ethanimidothioic acid = SMILES S/{2}C(CC1=CC(O)=CC=C1)=N/OS(=O)(O)=O |
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Structure type: monomer
Trivial name: sinalbin
Compound class: glycoside, glucosinolate
- Compound ID: 30214
Structure type: monomer
Trivial name: galactinol
Compound class: glycoside
- Compound ID: 32544
Structure type: monomer
Compound class: glycolipid
- Compound ID: 32545
Structure type: oligomer
Compound class: glycolipid
- Compound ID: 32546
Structure type: monomer
Compound class: glycolipid
- Compound ID: 32549
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Subst-(7-2:7'-4)-+
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Subst1-(7-3:7'-6)-b-D-Glcp-(1-7)-Gallic
Subst = hexahydroxydiphenic acid = SMILES O{3}C1={4}C(O){5}C(O)=C(C2={55}C(O){54}C(O)={53}C(O)C=C2{57}C(O)=O)C({7}C(O)=O)=C1;
Subst1 = euphorbin A aglycon 1 = SMILES O=C1C=C([C@@](C(O)([C@@]1(O)O2)O)([H])C3=C2C(O)=C(C=C3{7}C(O)=O)O){57}C(O)=O |
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Structure type: monomer
Trivial name: geraniin
Compound class: glycoside, phenolic glycoside
- Compound ID: 32550
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Subst-(7-4:7'-6)-+
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Subst-(7-2:7'-3)-b-D-Glcp
Subst = hexahydroxydiphenic acid = SMILES O{3}C1={4}C(O){5}C(O)=C(C2={55}C(O){54}C(O)={53}C(O)C=C2{57}C(O)=O)C({7}C(O)=O)=C1 |
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Structure type: monomer
Trivial name: pedunculagin
Compound class: glycoside, phenolic glycoside
- Compound ID: 32551
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Subst-(7-6:7'-3)-+
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Subst1-(9-2:12-4)-b-D-Glcp-(1-7)-Gallic
Subst = hexahydroxydiphenic acid = SMILES O{3}C1={4}C(O){5}C(O)=C(C2={55}C(O){54}C(O)={53}C(O)C=C2{57}C(O)=O)C({7}C(O)=O)=C1;
Subst1 = 2-(3S-5-carboxy-3,7,8-trihydroxy-2-oxochroman-4-yl)malonic acid = SMILES O={9}C(C(C={7}C({8}C(O)=C1O2)O)=C1C(C({11}C(O)=O){12}C(O)=O){3}[C@H](O)C2=O)O |
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Structure type: monomer
Trivial name: chebulagic acid
Compound class: glycoside, phenolic glycoside
- Compound ID: 28034
Structure type: oligomer
Trivial name: decaffeoylacteoside
Compound class: saponin glycoside, glycoside, phenolic glycoside
- Compound ID: 22430
Structure type: oligomer
Trivial name: acteoside isomer, isoacteoside, isoverbascoside
Compound class: saponin glycoside, glycoside, phenolic glycoside, phenylethanoid glycoside
- Compound ID: 30497
Structure type: oligomer
Trivial name: leucosceptoside A
Compound class: glycoside, phenolic glycoside, phenylpropanoid glycoside
- Compound ID: 32618
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Fer-(9-4)-+
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a-L-Arap-(1-2)-a-L-Rhap-(1-3)-b-D-Glcp-(1-8)-3,4,8HOPhet |
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Structure type: oligomer
Compound class: glycoside, phenolic glycoside
- Compound ID: 30321
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Caf-(9-4)-+
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a-L-Arap-(1-2)-a-L-Rhap-(1-3)-b-D-Glcp-(1-8)-3,4,8HOPhet |
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Structure type: oligomer
Trivial name: lavandulifolioside
Compound class: glycoside, phenolic glycoside, phenylethanoid glycoside, phenylpropanoid glycoside
- Compound ID: 31652
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Caf-(9-4)-+
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b-D-Glcp-(1-2)-a-L-Rhap-(1-3)-b-D-Glcp-(1-8)-3,4,8HOPhet |
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Structure type: oligomer
Trivial name: incanoside C
Compound class: glycoside, phenolic glycoside
- Compound ID: 32619
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Caf-(9-4)-+
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b-D-Xylp-(1-2)-a-L-Rhap-(1-3)-b-D-Glcp-(1-8)-3,4,8HOPhet |
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Structure type: oligomer
Compound class: glycoside, phenolic glycoside
- Compound ID: 31769
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Caf-(9-4)-+
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a-L-Rhap-(1-2)-a-L-Rhap-(1-3)-b-D-Glcp-(1-8)-3,4,8HOPhet |
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Structure type: oligomer
Compound class: glycoside, phenolic glycoside
- Compound ID: 32620
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Subst-(1-6)-+
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a-L-Rhap-(1-3)-b-D-Glcp-(1-8)-3,4,8HOPhet
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Caf-(9-4)-+
Subst = unknown iridoid |
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Structure type: oligomer
Compound class: glycoside, phenolic glycoside
- Compound ID: 32621
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Caf-(9-4)-+
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a-L-Lyxp-(1-2)-a-L-Rhap-(1-3)-b-D-Glcp-(1-8)-3,4,8HOPhet |
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Structure type: oligomer
Compound class: glycoside, phenolic glycoside
- Compound ID: 32506
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Caf-(9-4)-+
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a-L-Rhap-(1-3)-b-D-Glcp-(1-8)-Subst
Subst = phenylethane-3,4,7,8-tetrol = SMILES O{8}CC(O)C1=CC(O)=C(O)C=C1 |
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Structure type: oligomer
Trivial name: plantamajoside, β-hydroxyacteoside
Compound class: glycoside, phenolic glycoside
- Compound ID: 32631
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b-D-Glcp-(1-7)-Subst6Me4'Me
Subst = 6-hydroxydaidzein = SMILES O=c1c(-c2cc{54}c(O)cc2)coc2c{7}c(O){6}c(O)cc12 |
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Structure type: oligomer
Trivial name: afromosin
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 32632
Structure type: monomer
Trivial name: gleditsiasaponin C
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 32633
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b-D-GlcpA-(1-2)-b-D-GlcpA-(1-3)-Subst
Subst = gymnocladussaponin G aglycon |
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Structure type: oligomer
Trivial name: gymnocladussaponin G
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 23964
Structure type: oligomer
C41H66O12
Trivial name: Kalopanax-saponin A, α-hederin, kalopanaxsaponin A
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
39886, CBank-STR:2464
- Compound ID: 23791
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b-D-Glcp-(1-3)-b-D-Fucp-(1-3)-Subst
Subst = saikogenin F = SMILES C[C@@]1({23}CO){3}[C@@H](O)CC[C@]2(C)[C@@]3([H])C=C[C@]45[C@]6([H])CC(C)(C)CC[C@@](CO5)6{16}[C@@H](O)C[C@](C)4[C@@](C)3CC[C@@]12[H] |
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Structure type: oligomer
Trivial name: saikosaponin a, saikosaponin-a
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
27760, CBank-STR:3093
- Compound ID: 32636
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a-L-Arap-(1-22)-+
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a-L-Rhap-(1-2)-b-D-Galp-(1-2)-b-D-GlcpA-(1-3)-SoyasapogenolA |
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Structure type: oligomer
Trivial name: kudzusaponin SA3
Compound class: glycoside
- Compound ID: 32637
Structure type: monomer
Trivial name: sapindoside B
Compound class: glycoside
- Compound ID: 30448
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Tig-(1-21)-+
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b-D-Glcp-(1-4)-+ |
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b-D-Glcp-(1-2)-b-D-GlcpA-(1-3)-Subst22Ac
Subst = protoaescigenin = SMILES C[C@]12CC{3}[C@H](O)[C@](C)({24}CO)C1CC[C@]3(C)C2CC=C4[C@@]3(C)C{16}[C@@H](O)[C@]5({28}CO)[C@H]4CC(C)(C){21}[C@@H](O){22}[C@@H]5O |
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Structure type: oligomer
Trivial name: escin Ia
Compound class: saponin glycoside, glycoside
- Compound ID: 30449
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Ang-(1-21)-+
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b-D-Glcp-(1-4)-+ |
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b-D-Glcp-(1-2)-b-D-GlcpA-(1-3)-Subst22Ac
Subst = protoaescigenin = SMILES C[C@]12CC{3}[C@H](O)[C@](C)({24}CO)C1CC[C@]3(C)C2CC=C4[C@@]3(C)C{16}[C@@H](O)[C@]5({28}CO)[C@H]4CC(C)(C){21}[C@@H](O){22}[C@@H]5O |
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Structure type: oligomer
Trivial name: escin Ib
Compound class: saponin glycoside, glycoside
- Compound ID: 30450
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Tig-(1-21)-+
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b-D-Glcp-(1-4)-+ |
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b-D-Xylp-(1-2)-b-D-GlcpA-(1-3)-Subst22Ac
Subst = protoaescigenin = SMILES C[C@]12CC{3}[C@H](O)[C@](C)({24}CO)C1CC[C@]3(C)C2CC=C4[C@@]3(C)C{16}[C@@H](O)[C@]5({28}CO)[C@H]4CC(C)(C){21}[C@@H](O){22}[C@@H]5O |
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Structure type: oligomer
Trivial name: escin IIa
Compound class: saponin glycoside, glycoside
- Compound ID: 30451
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Ang-(1-21)-+
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b-D-Glcp-(1-4)-+ |
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b-D-Xylp-(1-2)-b-D-GlcpA-(1-3)-Subst22Ac
Subst = protoaescigenin = SMILES C[C@]12CC{3}[C@H](O)[C@](C)({24}CO)C1CC[C@]3(C)C2CC=C4[C@@]3(C)C{16}[C@@H](O)[C@]5({28}CO)[C@H]4CC(C)(C){21}[C@@H](O){22}[C@@H]5O |
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Structure type: oligomer
Trivial name: escin IIb
Compound class: saponin glycoside, glycoside
- Compound ID: 24397
Structure type: oligomer
Trivial name: chikusetsusaponin Ia, chikusetsusaponin 1a
Compound class: saponin glycoside, glycoside
Reference(s) to other database(s): CCSD:
27054, CBank-STR:4028
- Compound ID: 32641
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b-D-Glcp-(1-2)-b-D-Galp-(1-3)-Subst
Subst = timosaponin E1 aglycon = SMILES O{3}[C@H]1CC[C@@]2(C)[C@H](CCC3C2CC[C@@]4(C)C3{15}[C@@H](O)C5C4[C@H](C){19}C(O)(CCC({23}CO)C)O5)C1 |
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Structure type: oligomer
Trivial name: timosaponin E1
Compound class: glycoside
- Compound ID: 32642
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b-D-Glcp-(1-2)-b-D-Galp-(1-3)-Subst
Subst = timosaponin E2 aglycon |
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Structure type: oligomer
Trivial name: timosaponin E2
Compound class: glycoside
- Compound ID: 32653
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a-D-Xylp-(1-6)-+
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a-D-Xylp-(1-6)-+ |
| |
a-L-Fucp-(1-2)-b-D-Galp-(1-2)-a-D-Xylp-(1-6)-+ | |
| | |
a-D-Xylp-(1-6)-+ | | |
| | | |
a-L-Fucp-(1-2)-b-D-Galp-(1-2)-a-D-Xylp-(1-6)-+ | | | |
| | | | |
a-D-Xylp-(1-6)-+ | | | | |
| | | | | |
a-D-Xylp-(1-6)-+ | | a-D-Xylp-(1-6)-+ | | a-D-Xylp-(1-6)-+ | |
| | | | | | | | |
-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1-4)-b-D-Glcp-(1- |
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Structure type: structural motif or average structure
Compound class: polysaccharide
- Compound ID: 32654
|
a-D-GlcpA4Me-(1-2)-+ a-L-Ara-(1-?)-+ a-D-GlcpA4Me-(1-2)-+
| | |
-4)-a-D-Xylp-(1-4)-a-D-Xylp-(1-4)-a-D-Xylp-(1-4)-a-D-Xylp-(1-4)-a-D-Xylp-(1-4)-a-D-Xylp-(1-4)-a-D-Xylp-(1-4)-a-D-Xylp-(1-4)-a-D-Xylp-(1-4)-a-D-Xylp-(1-4)-a-D-Xylp-(1-4)-a-D-Xylp-(1- |
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Structure type: structural motif or average structure
Compound class: polysaccharide
- Compound ID: 32655
|
a-D-Galp-(1-6)-+
|
a-D-Galp-(1-6)-+ |
| |
a-D-Galp-(1-6)-+ | |
| | |
a-D-Galp-(1-6)-+ | a-D-Galp-(1-6)-+ | a-D-Galp-(1-6)-+ |
| | | | | |
-4)-b-D-Manp-(1-4)-b-D-Manp-(1-4)-b-D-Manp-(1-4)-b-D-Manp-(1-4)-b-D-Manp-(1-4)-b-D-Manp-(1-4)-b-D-Manp-(1-4)-b-D-Manp-(1-4)-b-D-Manp-(1-4)-b-D-Manp-(1- |
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Structure type: structural motif or average structure
Compound class: polysaccharide
- Compound ID: 32656
|
-4)-a-D-GalpA6Me-(1-4)-a-D-GalpA6Me-(1-4)-a-D-GalpA6Me-(1-4)-a-D-GalpA6Me-(1-4)-a-D-GalpA-(1-4)-a-D-GalpA-(1-4)-a-D-GalpA-(1- |
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Structure type: structural motif or average structure
Compound class: polysaccharide
- Compound ID: 32657
|
Subst-(1-4)-+
|
-4)-a-D-GalpA-(1-2)-a-L-Rhap-(1-
Subst = oligo or polysaccharide side-branch |
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Structure type: structural motif or average structure
Compound class: polysaccharide
- Compound ID: 32697
Structure type: oligomer
Trivial name: sophorose
- Compound ID: 24241
Structure type: oligomer
Trivial name: cellobiose
Compound class: glucomannan
Reference(s) to other database(s): GTC:G84824ZO
- Compound ID: 16765
Structure type: oligomer
Trivial name: isomaltose
Reference(s) to other database(s): GTC:G69864PN
- Compound ID: 19050
Structure type: oligomer
Trivial name: gentiobiose, bruceacanthinoside
Compound class: glycoside, Apotirucallane triterpe glycoside
Reference(s) to other database(s): GTC:G09183JD, CCSD:
37198, CBank-STR:4177
- Compound ID: 32722
Structure type: monomer
; 432
Trivial name: cosmosiin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32723
Structure type: monomer
; 446
Trivial name: tilianin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32724
Structure type: monomer
; 448
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32725
Structure type: monomer
; 448
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32726
Structure type: monomer
; 448
Trivial name: astragalin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32727
Structure type: monomer
; 464
Trivial name: isoquercitrin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32728
Structure type: monomer
; 464
Trivial name: hyperoside
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32729
Structure type: monomer
; 448
Trivial name: quercitrin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 30504
Structure type: monomer
; 464
C21H20O12
Trivial name: myricitrin
Compound class: glycoside, flavonoid glycoside, flavone glycoside
- Compound ID: 32730
Structure type: monomer
; 546
Trivial name: eudiposide
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32731
|
b-D-Glcp-(1-7)-Subst
Subst = hesperetin = SMILES O=C(C1=C(O/2)C={7}C(O)C={5}C1O)CC2=C3C={54}C(C(OC)=CC/3)O |
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Structure type: monomer
; 466
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32732
Structure type: oligomer
; 578
Trivial name: rhoifolin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32733
Structure type: oligomer
; 594
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32734
Structure type: oligomer
; 610
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32735
Structure type: oligomer
; 594
Trivial name: nicotiflorin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32736
Structure type: oligomer
; 610
Trivial name: rutin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32737
Structure type: oligomer
; 610
Trivial name: antoside
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32738
Structure type: oligomer
; 564
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32739
|
b-D-Glcp-(1-7)-+
|
a-L-Rhap-(1-3)-Subst
Subst = anhydroicaritin = SMILES C/C(C)=C\CC1=C2C(C({3}C(O)=C(C3=CC=C(OC)C=C3)O2)=O)={5}C(O)C={7}C1O |
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Structure type: oligomer
; 676
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32740
Structure type: oligomer
; 740
Trivial name: clitorin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32741
Structure type: oligomer
; 740
Trivial name: robinin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32742
Structure type: oligomer
; 756
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32748
Structure type: monomer
; 448
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32749
|
b-D-Glcp-(1-7)-Subst
Subst = hesperetin = SMILES O=C(C1=C(O/2)C={7}C(O)C={5}C1O)CC2=C3C={54}C(C(OC)=CC/3)O |
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Structure type: monomer
; 464
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32750
|
a-L-Rhap-(1-2)-b-D-Glcp-(1-7)-Subst
Subst = naringenin = SMILES O=C1CC(C2=CC={54}C(O)C=C2)OC3=C{7}C(O)={6}C{5}C(O)=C13 |
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Structure type: oligomer
; 580
Trivial name: naringin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32751
Structure type: oligomer
; 594
Trivial name: poncirin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32752
|
a-L-Rhap-(1-2)-b-D-Glcp-(1-7)-Subst
Subst = hesperetin = SMILES O=C(C1=C(O/2)C={7}C(O)C={5}C1O)CC2=C3C={54}C(C(OC)=CC/3)O |
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Structure type: oligomer
; 610
Trivial name: neohesperidin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 30505
|
a-L-Rhap-(1-6)-b-D-Glcp-(1-7)-Subst
Subst = hesperetin = SMILES O=C(C1=C(O/2)C={7}C(O)C={5}C1O)CC2=C3C={54}C(C(OC)=CC/3)O |
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Structure type: oligomer
; 610
C28H34O15
Trivial name: hesperidin
Compound class: glycoside, flavonoid glycoside, flavone glycoside
- Compound ID: 27808
Structure type: monomer
Trivial name: vitexin, vicenin-2
Compound class: glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside
- Compound ID: 28144
Structure type: monomer
Trivial name: vitexin, isovitexin, isoorientin, isovitexin (apigenin C-6 glucoside), isovitextin
Compound class: glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside
- Compound ID: 29906
Structure type: monomer
Trivial name: swertisin
Compound class: glycoside, flavonoid glycoside, flavonol glycoside
- Compound ID: 27748
Structure type: oligomer
Trivial name: vicenin-2, vicenin II
Compound class: saponin glycoside, glycoside, C-glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside
- Compound ID: 32846
|
Subst-(7'-6:7-4)-+
|
Subst-(7'-3:7-2)-b-D-Glcp-(1-7)-Gallic
Subst = hexahydroxydiphenic acid = SMILES O{3}C1={4}C(O){5}C(O)=C(C2={55}C(O){54}C(O)={53}C(O)C=C2{57}C(O)=O)C({7}C(O)=O)=C1 |
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Structure type: monomer
Trivial name: casuarictin, ellagitannin
Compound class: glycoside, phenolic glycoside
- Compound ID: 32824
Structure type: oligomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 32428
Structure type: oligomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 21445
|
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 |
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Structure type: monomer
Trivial name: genistin, genistein glucoside
Compound class: glycoside, flavonoid glycoside
Reference(s) to other database(s): CCSD:
48436, CBank-STR:1217
- Compound ID: 27627
|
b-D-Glcp-(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
C21H20O9
Trivial name: daidzin
Compound class: glycoside, flavonoid glycoside
- Compound ID: 23949
|
a-L-Rhap-(1-2)-a-L-Arap-(1-3)-+
|
a-L-Rhap-(1-4)-b-D-Glcp-(1-6)-b-D-Glcp-(1-28)-Hederagenin |
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Structure type: oligomer
C59H96O26
Trivial name: Kizutasaponin, Kalopanax-saponin B, kalopanax-saponin B, kalopanaxsaponin B, Kizutasaponin K12, hederasaponin C
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
5523, CBank-STR:11737
- Compound ID: 26872
Structure type: monomer
Trivial name: glucoluteolin, luteolin 7-glucoside
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside, flavone glucoside
Reference(s) to other database(s): CCSD:
50066, CBank-STR:939
- Compound ID: 31219
Structure type: oligomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 21989
Structure type: monomer
Trivial name: hyperoside, hyperin, hyperoside, hyperin, baohuoside-II, quercetin 3-galactoside, vulgarsaponin B
Compound class: saponin glycoside, glycoside, flavonoid glycoside, flavonol glycoside, flavone glycoside, flavanone glycoside
Reference(s) to other database(s): CCSD:
49969, CBank-STR:1983
- Compound ID: 26382
Structure type: monomer
Trivial name: catalpol
Compound class: glycoside, iridoid glycoside
Reference(s) to other database(s): CCSD:
39192, CBank-STR:1056
- Compound ID: 33071
Structure type: monomer
Trivial name: lotaustralin
Compound class: glycoside
- Compound ID: 26372
|
b-D-Glcp-(1-7)-Subst
Subst = D-mandelonitrile = SMILES O{7}[C@H](C1=CC=CC=C1)C#N |
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Structure type: monomer
Trivial name: prunasin
Compound class: glycoside, cyanogenic glycoside, nitrile glycoside
Reference(s) to other database(s): CCSD:
39172, CBank-STR:1147
- Compound ID: 33072
|
S-4)-Subst-(1-1)-b-D-Glcp
Subst = tetraphyllin B aglycon = SMILES N#C{1}[C@@]1(O)/C=C\{4}[C@@H](O)C1 |
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Structure type: monomer
Trivial name: tetraphyllin B sulfate
Compound class: glycoside
- Compound ID: 33073
|
Subst-(1-1)-b-D-Glcp
Subst = volkenin aglycon = SMILES N#C{1}[C@]1(O)/C=C\{4}[C@H](O)C1 |
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Structure type: monomer
Trivial name: epivolkenin
Compound class: glycoside
- Compound ID: 33074
Structure type: monomer
Trivial name: sarauricilarin
Compound class: glycoside
- Compound ID: 26751
|
b-D-Glcp-(1-1)-Subst
Subst = methylazoxymethanol = SMILES O{1}C/[N+]([O-])=N/C |
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Structure type: monomer
Trivial name: cycasin
Compound class: glycoside
Reference(s) to other database(s): CCSD:
8453, CBank-STR:11813
- Compound ID: 32386
Structure type: monomer
Compound class: glycoside, phenolic glycoside
Reference(s) to other database(s): GenDB:AF287143
- Compound ID: 31374
|
b-D-Glcp-(1-2)-Subst7Me
Subst = 2,4,7-trihydroxy-1,4-benzoxazine-3(4H)-one = SMILES O{7}C1=CC2=C(C=C1)N(C(=O){2}C(O2)O){4}O |
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Structure type: monomer
Trivial name: DIMBOA glucoside
Compound class: glycoside
- Compound ID: 33157
|
b-D-Glcp-(1-5)-Subst
Subst = betanidin = SMILES O{4}C(C=C1/2)={5}C(O)C=C1C[C@@H](C([O-])=O)[N+]2=C/C=C3C[C@@H]({58}C(O)=O)NC({56}C(O)=O)=C/3 |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 27310
|
b-D-Glcp-(1-3)-Subst
Subst = digitoxigenin = SMILES O{3}[C@H]1CC[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@H](C(CO5)=CC5=O)CC{14}[C@]4(O)[C@]3([H])CC[C@@]([H])2C1 |
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Structure type: monomer
Compound class: saponin glycoside, glycoside
Reference(s) to other database(s): CCSD:
50107, CBank-STR:1014
- Compound ID: 26850
Structure type: monomer
Trivial name: γ-chaconine
Compound class: saponin glycoside, glycoside
Reference(s) to other database(s): CCSD:
43170, CBank-STR:965
- Compound ID: 33158
|
b-D-Glcp-(1-4)-Subst
Subst = picrocrocin aglycon = SMILES O=CC1=C(C)C{4}C(O)CC1(C)C |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 30766
|
b-D-Glcp-(1-17)-Subst
Subst = limonin = SMILES CC1(C)O[C@H]2CC(=O)OC[C@@]23[C@H]1CC(=O)[C@]1(C)[C@@H]3CC[C@@](C)({17}[C@@H](O)c2ccoc2)[C@@]12O[C@@H]2{16}C(=O)O |
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Structure type: monomer
Compound class: glycoside, sesquiterpenoid glycoside, limonoid glycoside
- Compound ID: 33159
|
b-D-Glcp-(1-4)-Subst
Subst = vanillin = SMILES COC1={4}C(C=CC(=C1)C=O)O |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 15325
Structure type: homopolymer
Trivial name: chitin
Compound class: O-polysaccharide, cell wall polysaccharide, glucan, polysaccharide, chitin
Reference(s) to other database(s): GTC:G97099AY, CCSD:
46067, CBank-STR:5851, GenDB:KF905651
- Compound ID: 30398
Structure type: monomer
Trivial name: calenduloside E
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
- Compound ID: 33444
Structure type: monomer
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 30414
Structure type: monomer
Compound class: glycoside, triterpenoid glycoside, flavonol glycoside
- Compound ID: 33445
Structure type: oligomer
Trivial name: momordin Ic
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 33446
Structure type: oligomer
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 33447
Structure type: oligomer
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 30806
Structure type: oligomer
Trivial name: momordin I
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
- Compound ID: 31534
Structure type: oligomer
Trivial name: chikusetsusaponin IVa, chikusetsusaponin-IVa
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 29661
Structure type: oligomer
Trivial name: momordin IIc
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
- Compound ID: 33448
Structure type: oligomer
Trivial name: chikusetsusaponin IV
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 30531
Structure type: oligomer
Trivial name: chikusetsusaponin V, ginsenoside Ro, ginsenoside Ro, chikusetsusaponin V, chikusetsusaponin-V
Compound class: saponin glycoside, glycoside, triterpenoid glycoside
- Compound ID: 31263
|
b-D-Glcp-(1-2)-Subst
Subst = phloretin = SMILES O=C(C1={6}C(C={4}C(C={2}C1O)O)O)CCC2=CC={54}C(O)C=C2 |
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Structure type: monomer
Trivial name: phloridzin, phloridzosid
Compound class: glycoside, flavonoid glycoside
Found 