- Compound ID: 24025
Structure type: oligomer
Compound class: saponin glycoside
Reference(s) to other database(s): CCSD:
12539, CBank-STR:7547
- Compound ID: 31306
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b-D-Glcp-(1-22)-Subst
Subst = macrophyllosaponins aglycon = SMILES O{3}[C@H]1C{1}[C@H](O)[C@]23C[C@]24CC[C@]5(C)C([C@@H](CC{21}[C@H](O){22}C(C)(O)C)C)CC[C@@]5(C)C4{7}[C@@H](O)CC3C1(C)C |
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Structure type: monomer
Trivial name: macrophyllosaponin C
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 31307
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b-D-Xylp-(1-2)-b-D-Xylp-(1-3)-Subst
Subst = macrophyllosaponins aglycon = SMILES O{3}[C@H]1C{1}[C@H](O)[C@]23C[C@]24CC[C@]5(C)C([C@@H](CC{21}[C@H](O){22}C(C)(O)C)C)CC[C@@]5(C)C4{7}[C@@H](O)CC3C1(C)C |
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Structure type: oligomer
Trivial name: macrophyllosaponin D
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 27627
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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: 21445
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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: 31752
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b-D-Glcp-(1-7)-Subst4'Me
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
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31753
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b-D-Glcp-(1-7)-Subst4'Me
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, flavonoid glycoside
- Compound ID: 31754
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b-D-Glcp-(1-4')-Subst7Me
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: trifoside
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: 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: 31755
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a-L-Rhap-(1-6)-b-D-Glcp-(1-7)-Subst
Subst = (R)-naringenin = SMILES O=C1C[C@H](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: 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: 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: 31756
Structure type: oligomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31757
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b-D-Glcp-(1-4')-+
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b-D-1dGlcp-(1C-8)-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: oligomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31758
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b-D-1dGlcp-(1C-8)-Subst
Subst = 7,3',4'-trihydroxy-isoflavone = SMILES O=C1C(C2=C{53}C(O)={54}C(O)C=C2)=COC3=C1C=C{7}C(O)={8}C3 |
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Structure type: monomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 27630
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b-D-1dGlcp-(1C-8)-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: puerarin
Compound class: glycoside, C-glycoside, flavonoid glycoside
- Compound ID: 31759
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b-D-1dGlcp-(1C-8)-Subst3'Me
Subst = 7,3',4'-trihydroxy-isoflavone = SMILES O=C1C(C2=C{53}C(O)={54}C(O)C=C2)=COC3=C1C=C{7}C(O)={8}C3 |
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Structure type: monomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31760
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b-D-Xylp-(1-6)-b-D-1dGlcp-(1C-8)-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: oligomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31761
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b-D-Xylp-(1-6)-b-D-1dGlcp-(1C-8)-Subst3'Me
Subst = 7,3',4'-trihydroxy-isoflavone = SMILES O=C1C(C2=C{53}C(O)={54}C(O)C=C2)=COC3=C1C=C{7}C(O)={8}C3 |
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Structure type: oligomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31762
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b-D-Glcp-(1-7)-Subst4'Et
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
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31763
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b-D-Glcp-(1-7)-Subst
Subst = 7,3',4'-trihydroxy-isoflavone = SMILES O=C1C(C2=C{53}C(O)={54}C(O)C=C2)=COC3=C1C=C{7}C(O)={8}C3 |
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Structure type: monomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31764
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b-D-Glcp-(1-7)-Subst3'Me
Subst = 7,3',4'-trihydroxy-isoflavone = SMILES O=C1C(C2=C{53}C(O)={54}C(O)C=C2)=COC3=C1C=C{7}C(O)={8}C3 |
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Structure type: monomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31765
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Mal-(1-6)-b-D-Glcp-(1-7)-Subst3'Me
Subst = 7,3',4'-trihydroxy-isoflavone = SMILES O=C1C(C2=C{53}C(O)={54}C(O)C=C2)=COC3=C1C=C{7}C(O)={8}C3 |
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Structure type: monomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31766
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b-D-Glcp-(1-3)-Subst
Subst = astrapterocarpan = SMILES COC1=C(OC)C2=C([C@@H]3COC4=C(C=C{3}C(O)=C4)[C@@H]3O2)C=C1 |
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Structure type: monomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 31767
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Mal-(1-6)-b-D-Glcp-(1-3)-Subst
Subst = astrapterocarpan = SMILES COC1=C(OC)C2=C([C@@H]3COC4=C(C=C{3}C(O)=C4)[C@@H]3O2)C=C1 |
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Structure type: monomer
Compound class: glycoside, flavonoid glycoside
- Compound ID: 23837
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b-D-Glcp-(1-2)-b-D-Glcp-(1-3)-+
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b-D-Glcp-(1-6)-b-D-Glcp-(1-20)-Protopanaxadiol20s |
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Structure type: oligomer
Trivial name: ginsenoside-Rb1, ginsenoside Rb1, ginsenoside Re, ginsenoside Rc, ginsenoside
Compound class: saponin glycoside, glycoside, flavonoid glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
45438, CBank-STR:11119
- Compound ID: 23838
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b-D-Glcp-(1-2)-b-D-Glcp-(1-3)-+
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a-L-Arap-(1-6)-b-D-Glcp-(1-20)-Protopanaxadiol20s |
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Structure type: oligomer
Trivial name: ginsenoside-Rb2, ginsenoside Rb2, ginsenoside Rd, ginsenoside Rg1, ginsenoside
Compound class: saponin glycoside, glycoside, flavonoid glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
45433, CBank-STR:10762
- Compound ID: 23840
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b-D-Glcp-(1-2)-b-D-Glcp-(1-3)-+
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a-L-Araf-(1-6)-b-D-Glcp-(1-20)-Protopanaxadiol20s |
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Structure type: oligomer
Trivial name: ginsenoside-Rc, ginsenoside Rf, ginsenoside Rc, ginsenoside
Compound class: saponin glycoside, glycoside, flavonoid glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
45437, CBank-STR:10761
- Compound ID: 23841
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b-D-Glcp-(1-20)-+
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b-D-Glcp-(1-2)-b-D-Glcp-(1-3)-Protopanaxadiol20s |
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Structure type: oligomer
Trivial name: ginsenoside-Rd, ginsenoside Rb1, ginsenoside Rd, ginsenoside Re, ginsenoside
Compound class: saponin glycoside, glycoside, flavonoid glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
45434, CBank-STR:187
- Compound ID: 23845
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b-D-Glcp-(1-20)-+
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a-L-Rhap-(1-2)-b-D-Glcp-(1-6)-Protopanaxatriol20s |
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Structure type: oligomer
Trivial name: ginsenoside-Re, ginsenoside Rb2, ginsenoside Re, ginsenoside Rc, ginsenoside
Compound class: saponin glycoside, glycoside, flavonoid glycoside, triterpenoid glycoside
Reference(s) to other database(s): CCSD:
45436, CBank-STR:6753
- Compound ID: 32610
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b-D-Glcp-(1-1)-Subst
Subst = 3-nitropropanol = SMILES O=[N+]([O-])CC{1}CO |
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Structure type: monomer
Trivial name: miserotoxin
Compound class: glycoside
Found 