Found | b-D-Glcp-(1-3)-+ | b-D-Glcp-(1-6)-+ | | | a-L-Rhap-(1-2)-b-D-Glcp-(1-28)-Subst23Ac 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 | Show graphically |
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Structure type: oligomer
Compound class: triterpenoid glycoside
Compound class: triterpenoid glycoside
| a-L-Rhap-(1-2)-+ | b-D-Xylp-(1-6)-b-D-Glcp-(1-3)-a-L-Arap-(1-3)-Subst Subst = zizyphoiside A aglycon = SMILES C=C(C)C(C)CC6O[C@]15C[C@]4(CO1)C(CCC3[C@@]2(C)CC{3}[C@H](O)[C@](C)(C)C2CC[C@]34C)C5[C@@]6(C)O | Show graphically |
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Structure type: oligomer
Trivial name: zizyphoiside A
Compound class: triterpenoid glycoside
Trivial name: zizyphoiside A
Compound class: triterpenoid glycoside
| a-L-Arap-(1-3)-+ | a-L-Arap-(1-18)-Subst Subst = bacopasaponin aglycon = SMILES C/C(C)=C\[C@H]6C{18}[C@](C)(O)C4C3CCC2[C@@]1(C)CC{3}[C@H](O)CC1CC[C@@]2(C)[C@]35CCC4(OC5)O6 | Show graphically |
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Structure type: oligomer
Trivial name: bacopasaponin A
Compound class: triterpenoid glycoside
Trivial name: bacopasaponin A
Compound class: triterpenoid glycoside
| a-L-Araf-(1-2)-+ | ?%b-D-Glcp-(1-3)-a-L-Arap-(1-3)-Subst Subst = bacopasaponin aglycon = SMILES C/C(C)=C\[C@H]6C{18}[C@](C)(O)C4C3CCC2[C@@]1(C)CC{3}[C@H](O)CC1CC[C@@]2(C)[C@]35CCC4(OC5)O6 | Show graphically |
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Structure type: oligomer
Trivial name: bacopasaponin B, bacopasaponin C
Compound class: triterpenoid glycoside
Trivial name: bacopasaponin B, bacopasaponin C
Compound class: triterpenoid glycoside
| b-D-Xylp-(1-4)-+ | a-L-Rhap-(1-2)-b-D-Glcp-(1-28)-Subst | a-L-Arap-(1-6)-+ Subst = arjunolic acid = 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 | Show graphically |
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Structure type: oligomer
Compound class: triterpenoid glycoside
Compound class: triterpenoid glycoside