- Compound ID: 30716
|
b-D-Glcp-(1-9)-+
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b-D-Glcp-(1-3)-Subst
Subst = (1S,4R,5R)-4-[(1E,3R)-3-hydroxy-1-buten-1-yl]-3,3,5-trimethylcyclohexanol = SMILES C{9}[C@@H](O)/C=C/[C@H]1[C@H](C)C{3}[C@H](O)CC1(C)C |
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Structure type: oligomer
; 535.2727 [M-H]-
C25H44O12
Trivial name: platanionoside A
Compound class: sesquiterpenoid glycoside
- Compound ID: 30717
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b-D-Glcp-(1-9)-+
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b-D-Glcp-(1-3)-Subst
Subst = (1R)-4-[(E,3R)-3-hydroxybut-1-enyl]-3,5,5-trimethylcyclohex-3-en-1-ol = SMILES CC1=C(/C=C/{9}[C@@H](C)O)C(C)(C)C{3}[C@H](O)C1 |
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Structure type: oligomer
; 533.2577 [M-H]-
C25H41O12
Trivial name: platanionoside B
Compound class: sesquiterpenoid glycoside
- Compound ID: 30718
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b-D-Xylp-(1-6)-b-D-Glcp-(1-9)-Subst
Subst = 4,5-dihydroblumenol = SMILES C{9}[C@@H](O)/C=C/{6}[C@@]1(O)[C@H](C)CC(=O)CC1(C)C |
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Structure type: oligomer
; 519.2439 [M-H]-
C24H39O12
Trivial name: platanionoside C
Compound class: sesquiterpenoid glycoside
- Compound ID: 26100
Structure type: oligomer
Trivial name: benzyl β-primeveroside
Compound class: saponin glycoside, glycoside
Reference(s) to other database(s): CCSD:
34652, CBank-STR:4010
- Compound ID: 26459
|
b-D-Glcp-(1-1)-Subst
Subst = aoba alcohol = SMILES CC/C=C\C{1}CO |
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Structure type: monomer
Compound class: glycoside
- Compound ID: 33010
|
b-D-Apif-(1-6)-b-D-Glcp-(1-1)-Subst
Subst = catechol = SMILES O{1}C1=CC=CC={2}C1O |
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Structure type: oligomer
Compound class: glycoside, phenolic glycoside
- Compound ID: 33011
|
b-D-Apif-(1-6)-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
Compound class: glycoside, phenolic glycoside
- Compound ID: 33012
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b-D-Glcp-(1-2)-Subst-(7-2)-Subst1
Subst = salicyl alcohol = SMILES O{2}C1=CC=CC=C1{7}CO;
Subst1 = 2,6-dihydroxybenzoic acid = SMILES C1=C{6}C(=C({2}C(=C1)O){7}C(=O)O)O |
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Structure type: monomer
Compound class: glycoside, phenolic glycoside
- Compound ID: 33013
|
b-D-Glcp-(1-1)-Subst
Subst = 4-hydroxyalangifolioside aglycon = SMILES O{4}C1=CC(CC2={52}C(O)C({57}C(O)=O)={56}C(O)C=C2)={1}C(O)C=C1 |
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Structure type: monomer
Compound class: glycoside, phenolic 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: 27945
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b-D-Glcp-(1-6)-+
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b-D-Glcp-(1-2')-Subst
Subst = 2,6-dihydroxybenzoic acid 2'-hydroxybenzyl ester = SMILES O=C(OCC1=CC=CC={52}C1O)C2={2}C(O)C=CC={6}C2O |
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Structure type: oligomer
Trivial name: henryoside
Compound class: saponin glycoside, glycoside, phenolic glycoside
- Compound ID: 33014
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b-D-Glcp-(1-2)-+
|
b-D-Glcp-(1-2')-Subst
|
b-D-Glcp-(1-6)-+
Subst = 2,6-dihydroxybenzoic acid 2'-hydroxybenzyl ester = SMILES O=C(OCC1=CC=CC={52}C1O)C2={2}C(O)C=CC={6}C2O |
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Structure type: oligomer
Compound class: glycoside, phenolic glycoside
- Compound ID: 33015
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b-D-Glcp-(1-3)-b-D-Glcp-(1-3)-Subst
Subst = alangifolioside aglycon |
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Structure type: oligomer
Trivial name: alangifolioside
Compound class: glycoside, phenolic glycoside
- Compound ID: 32127
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b-D-Glcp-(1-2)-Subst
Subst = demethylalangiside aglycon = SMILES O{56}C1={57}C(O)C=C2[C@H]3C[C@H]4[C@@H](C=C){2}[C@H](O)OC=C4C(N3CCC2=C1)=O |
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Structure type: monomer
Trivial name: demethylalangiside
Compound class: glycoside, phenolic glycoside