- Compound ID: 29421
|
b-D-Glcp-(1-5)-Subst
Subst = (1R,4R,5S)-5-hydroxyfenchone = SMILES C[C@]1(C)C(=O)C2(C)C{5}[C@H](O)C1C2 |
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Structure type: monomer
; 331.1739 [M+H]+
C16H26O7
Compound class: glycoside
- Compound ID: 29422
|
b-D-Glcp-(1-6)-Subst
Subst = (1R,4S,6R)-6-hydroxyfenchone = SMILES C[C@]1(C)C(=O)C2(C)CC1C{6}[C@H]2O |
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Structure type: monomer
; 331.1733 [M+H]+
C16H26O7
Compound class: glycoside
- Compound ID: 29423
|
b-D-Glcp-(1-6)-Subst
Subst = (1R,3S,4S,6R)-6,9-dihydroxyfenchone = SMILES C[C@]1({9}CO)C(=O)C2(C)CC1C{6}[C@H]2O |
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Structure type: monomer
; 347.1692 [M+H]+
C16H26O8
Compound class: glycoside
- Compound ID: 29424
|
b-D-Glcp-(1-10)-Subst
Subst = (1S,4R)-10-hydroxyfenchone = SMILES C[C@]1(C)C(=O)C2({10}CO)CCC1C2 |
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Structure type: monomer
; 331.1759 [M+H]+
C16H26O7
Compound class: glycoside
- Compound ID: 29425
|
b-D-Glcp-(1-10)-Subst
Subst = (1S,3S,4R)-8,10-dihydroxyfenchone = SMILES C[C@]1({9}CO)C(=O)C2({10}CO)CCC1C2 |
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Structure type: monomer
; 347.1708 [M+H]+
C16H26O8
Compound class: glycoside
- Compound ID: 29426
|
b-D-Glcp-(1-10)-Subst
Subst = (1S,3R,4R)-8,10-dihydroxyfenchone = SMILES C[C@@]1({8}CO)C(=O)C2({10}CO)CCC1C2 |
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Structure type: monomer
; 347.1699 [M+H]+
C16H26O8
Compound class: glycoside
- Compound ID: 29427
|
b-D-Glcp-(1-2)-Subst
Subst = (1R,2R,4S,6R)-2,6-dihydroxyfenchane = SMILES C[C@@]2(C)C1C{6}[C@@H](O)C(C)(C1){2}[C@@H]2O |
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Structure type: monomer
; 333.1923 [M+H]+
C16H28O7
Compound class: glycoside
- Compound ID: 29428
|
b-D-Glcp-(1-2)-Subst
Subst = (1R,2R,4S,6R)-2,6-dihydroxyfenchane = SMILES C[C@]1(C){2}[C@H](O)C2(C)C{5}[C@H](O)C1C2 |
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Structure type: monomer
; 333.1921 [M+H]+
C16H28O7
Compound class: glycoside
- Compound ID: 29429
|
b-D-Glcp-(1-2)-Subst
Subst = (1R,2S,4R,5S)-2,6,7-trihydroxyfenchane = SMILES C[C@]1(C){2}[C@H](O)C2(C){6}[C@H](O)CC1{7}C2O |
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Structure type: monomer
; 349.1883 [M+H]+
C16H28O8
Compound class: glycoside
- Compound ID: 29430
|
b-D-Glcp-(1-2)-Subst
Subst = (1S,2R,4R)-2-hydroxy-1,8-cineole = SMILES CC1(C)OC2(C)CCC1C{2}[C@H]2O |
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Structure type: monomer
; 333.1924 [M+H]+
C16H28O7
Compound class: glycoside
- Compound ID: 29431
|
b-D-Glcp-(1-2)-Subst
Subst = (1R,2S,4S)-2-hydroxy-1,8-cineole = SMILES CC1(C)OC2(C)CCC1C{2}[C@@H]2O |
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Structure type: monomer
; 333.1937 [M+H]+
C16H28O7
Compound class: glycoside
- Compound ID: 29432
|
b-D-Glcp-(1-2)-Subst
Subst = (1S,2S,4R)-2-hydroxy-1,8-cineole = SMILES CC1(C)OC2(C)CCC1C{2}[C@@H]2O |
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Structure type: monomer
; 333.1890 [M+H]+
C16H28O7
Compound class: glycoside
- Compound ID: 29433
|
b-D-Glcp-(1-2)-Subst
Subst = (1R,2R,4S)-2-hydroxy-1,8-cineole = SMILES CC1(C)OC2(C)CCC1C{2}[C@H]2O |
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Structure type: monomer
; 333.1937 [M+H]+
C16H28O7
Compound class: glycoside
- Compound ID: 29434
|
b-D-Glcp-(1-4)-Subst
Subst = 4-hydroxy-1,8-cineole = SMILES CC1(C)OC2(C)CC{4}C1(O)CC2 |
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Structure type: monomer
; 333.1904 [M+H]+
C16H28O7
Compound class: glycoside
- Compound ID: 29435
|
b-D-Glcp-(1-2)-Subst
Subst = (1R,2R,4S)-2,4-dihydroxy-1,8-cineole = SMILES CC1(C)OC2(C)CC{4}C1(O)C{2}[C@H]2O |
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Structure type: monomer
Trivial name: foeniculoside V
Compound class: glycoside
- Compound ID: 29436
|
b-D-Glcp-(1-2)-Subst
Subst = (1R,2R,4R)-2,4-dihydroxy-1,8-cineole = SMILES CC1(C)OC2(C)CCC1(O)C{2}[C@H]2O |
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Structure type: monomer
Trivial name: foeniculoside VI
Compound class: glycoside
- Compound ID: 29437
|
b-D-Glcp-(1-4)-Subst
Subst = (1R,2R,4R)-2,4-dihydroxy-1,8-cineole = SMILES CC1(C)OC2(C)CC{4}C1(O)C{2}[C@H]2O |
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Structure type: monomer
Trivial name: foeniculoside VII
Compound class: glycoside
- Compound ID: 29438
|
b-D-Glcp-(1-2)-Subst
Subst = 2,6-diexohydroxy-1,8-cineole = SMILES CC1(C)OC2(C){6}[C@@H](O)CC1C{2}[C@H]2O |
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Structure type: monomer
Trivial name: foeniculoside VIII
Compound class: glycoside
- Compound ID: 29439
|
b-D-Glcp-(1-2)-Subst
Subst = (1S,2R,4S,5R)-2,5-dihydroxy-1,8-cieole = SMILES CC1(C)OC2(C)C{5}[C@@H](O)C1C{2}[C@H]2O |
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Structure type: monomer
Trivial name: foeniculoside IX
Compound class: glycoside
- Compound ID: 29440
|
b-D-Glcp-(1-2)-Subst
Subst = (1S,2S,4S)-2,6-dihydroxy-1,8-cineole = SMILES CC1(C)OC2(C)CC{4}C1(O)C{2}[C@@H]2O |
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Structure type: monomer
; 349.1852 [M+H]+
C16H28O8
Compound class: glycoside
- Compound ID: 29441
|
b-D-Glcp-(1-2)-Subst
Subst = (1R,2S,4S,6R)-2,6-dihydroxy-1,8-cineole = SMILES CC1(C)OC2(C){2}[C@@H](O)CC1(O)C{6}[C@H]2O |
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Structure type: monomer
; 349.1853 [M+H]+
C16H28O8
Compound class: glycoside
- Compound ID: 29442
|
b-D-Glcp-(1-2)-Subst
Subst = (1S,2S,4S,5R)-2,5-dihydroxy-1,8-cineole = SMILES CC1(C)OC2(C)C{5}[C@@H](O)C1C{2}[C@@H]2O |
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Structure type: monomer
; 349.1856 [M+H]+
C16H28O8
Compound class: glycoside
- Compound ID: 29443
|
b-D-Glcp-(1-2)-Subst
Subst = (1S,2S,4S)-2,7-dihydroxy-1,8-cineole = SMILES CC1(C)OC2({7}CO)CCC1C{2}[C@@H]2O |
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Structure type: monomer
; 349.1871 [M+H]+
C16H28O8
Compound class: glycoside
- Compound ID: 22483
|
b-D-Glcp-(1-4)-Subst
Subst = sinapic alcohol = SMILES COC1={4}C(O)C(OC)=CC(/C=C/{9}CO)=C1 |
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Structure type: monomer
C17H24O9
Trivial name: syringin
Compound class: glycoside, phenolic glycoside, phenylethanoid glycoside, phenylpropanoid glycoside
Reference(s) to other database(s): CCSD:
39892, CBank-STR:1292
- Compound ID: 29535
|
b-D-Glcp-(1-9)-+
|
b-D-Glcp-(1-4)-Subst
Subst = sinapic alcohol = SMILES COC1={4}C(O)C(OC)=CC(/C=C/{9}CO)=C1 |
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Structure type: oligomer
Trivial name: syinapyl alcohol 4,3'-di-O-β-D-glucopyranoside
Compound class: glycoside, phenylpropanoid glycoside
- Compound ID: 29536
|
/Variants 0/-b-D-Glcp-(1-7)-Bn
/Variants 0/ is:
b-D-Apif-(1-6)-
OR (exclusively)
b-D-Glcp-(1-2)- |
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Structure type: monomer
Trivial name: zizybeoside I, icariside F2
Compound class: glycoside
- Compound ID: 26371
Structure type: monomer
Trivial name: germacrolide glucoside, benzyl β-D-glucopyranoside
Compound class: saponin glycoside, glycoside
Reference(s) to other database(s): CCSD:
48821, CBank-STR:910
- Compound ID: 29537
|
b-D-Glcp-(1-7)-Subst
Subst = salicyl alcohol = SMILES O{2}C1=CC=CC=C1{7}CO |
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Structure type: monomer
Trivial name: isosalicin (2-hydroxybenzyl β-D-glucopyranoside)
Compound class: glycoside
- Compound ID: 29538
|
b-D-Glcp-(1-4)-Subst-(9-1)-Me
Subst = sinapic alcohol = SMILES COC1={4}C(O)C(OC)=CC(/C=C/{9}CO)=C1 |
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Structure type: monomer
; 387.1650 [M+H]+
C18H26O4
Trivial name: methylsyringin
Compound class: glycoside
- Compound ID: 29539
|
b-D-Glcp-(1-3)-Subst4Me
Subst = 5-allylbenzene-1,2,3-triol = SMILES C=CCc1c{5}c(O){4}c(O){3}c(O)c1 |
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Structure type: monomer
; 343.1411 [M+H]+
C16H22O8
Compound class: glycoside
- Compound ID: 29540
|
b-D-Glcp-(1-4)-Subst3Me5Me
Subst = 5-(hydroxymethyl)benzene-1,2,3-triol = SMILES O{7}CC1=C{3}C(O)={4}C(O){5}C(O)=C1 |
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Structure type: monomer
; 369 [M+Na]+
C15H22O9
Compound class: glycoside
- Compound ID: 29541
|
b-D-Glcp-(1-4)-Subst-(9-1)-Me
Subst = p-coumaric alchohol = SMILES O{9}C/C=C/c1cc{4}c(O)cc1 |
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Structure type: monomer
; 327.1414 [M+H]+
C16H22O7
Compound class: glycoside
- Compound ID: 29542
|
b-D-Glcp-(1-4)-Subst
Subst = 4-(2-hydroxypropyl)phenol = SMILES CC(O)Cc1cc{4}c(O)cc1 |
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Structure type: monomer
; 315.1432 [M+H]+
C15H22O7
Compound class: glycoside
- Compound ID: 29543
|
b-D-Glcp-(1-7)-Subst
Subst = p-anisyl alcohol = SMILES COc1ccc({7}CO)cc1 |
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Structure type: monomer
; 301.1292 [M+H]+
C14H20O7
Compound class: glycoside
- Compound ID: 29544
|
S-2)-b-D-Glcp-(1-7)-Subst
Subst = p-anisyl alcohol = SMILES COc1ccc({7}CO)cc1 |
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Structure type: monomer
; 403 [M+H]+
C14H19O10SNa
Compound class: glycoside
- Compound ID: 29545
|
S-3)-b-D-Glcp-(1-8)-Subst-(4-1)-Me
Subst = tyrosol = SMILES O{8}CCC1=CC={4}C(O)C=C1 |
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Structure type: monomer
; 431.0998 [M+H]+
C16H23O10SNa
Compound class: glycoside
- Compound ID: 29546
|
b-D-Glcp-(1-3)-Subst
Subst = (1'R)-1'-(3-hydroxy-4-methoxyphenyl)etane-1',2'-diol = SMILES COc1ccc([C@@H](O)CO)c{3}c1O |
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Structure type: monomer
; 369.1143 [M+Na]+
C15H22O9
Compound class: glycoside
- Compound ID: 26457
|
b-D-Glcp-(1-1)-Subst
Subst = phenylethanol = SMILES O{1}CCC1=CC=CC=C1 |
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Structure type: monomer
C14H20O6
Compound class: glycoside, phenylethanoid glycoside, sesquiterpenoid glycoside
Reference(s) to other database(s): CCSD:
50059, CBank-STR:1046
Found 