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1. (Article ID: 11585)
Nohara T, Yahara S, Kinjo J
Bioactive saponins from solanaceous and leguminous plants
Natural Product Sciences 4(4) (1998)
203-214
Because solanaceous and leguminous natural sources are so widely distributed and are used as foodstuffs and folk medicines, we focussed on these plants and are trying to develop natural medicines after proving the effectiveness of these crude drugs and finding the lead compounds among these natural sources.
antineoplastic activity, thalictoside, plant extract, saponin derivative, solanindane derivative
Journal NLM ID: 9714997Publisher: Seoul, Korea: Korean Society of Pharmacognosy
Institutions: Faculty of Pharmaceutical Sciences, Kumamoto University, Kumamoto, Japan
The publication contains the following compound(s):
- Compound ID: 29751
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b-D-Glcp-(1-2)-+
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?%b-D-Xylp-(1-3)-b-D-Glcp-(1-4)-b-D-Galp-(1-3)-Subst
Subst = 23-hydroxy-demissidine = SMILES C[C@H]6C{23}[C@H](O)C5[C@@H](C)C4C(CC3C2CCC1C{3}[C@@H](O)CC[C@]1(C)C2CC[C@@]34C)N5C6 |
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Structure type: oligomer
Compound class: triterpenoid glycoside
- Compound ID: 29755
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iVl-(1-27)-+
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b-D-Xylp-(1-4)-a-L-Rhap-(1-4)-b-D-Glcp-(1-3)-Subst
Subst = abutiloside A aglycon = SMILES CC({27}CN)CCC(=O)[C@@H](C)C4{16}[C@H](O)CC3C2CCC1C{3}[C@@H](O)CC[C@]1(C)C2CC[C@@]34C |
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Structure type: oligomer
Trivial name: abutiloside A
Compound class: triterpenoid glycoside
- Compound ID: 29752
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b-D-Glcp-(1-6)-+
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b-D-Glcp-(1-2)-b-D-Glcp-(1-3)-Subst1Ac
Subst = tubocaposide B aglycon = SMILES C{25}[C@]1(O)C(=O)OC2C[C@@]1(C)CC2C6CCC5C4C/C=C\3C{3}[C@@H](O)C{1}[C@@H](O)[C@]3(C)C4CC[C@@]56C |
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Structure type: oligomer
Trivial name: tubocaposide B
Compound class: triterpenoid glycoside
- Compound ID: 29753
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b-D-Glcp-(1-6)-b-D-Glcp-(1-3)-Subst
Subst = petunioside A aglycon = SMILES CSC(=O){30}C(O)C67O[C@@H]([C@@H](C)C1CCC2C5C(CC[C@]12C)[C@@]3(C)CC{3}[C@H](O)C{5}[C@]3(O)[C@@H]4O[C@H]45)C[C@@](C)(O6)C(C)(C)O7 |
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Structure type: oligomer
Trivial name: petunioside A
Compound class: triterpenoid glycoside
- Compound ID: 29754
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b-D-Glcp-(1-21)-Subst
Subst = petunioside C aglycon = SMILES C[C@H]({21}[C@H](O)C{23}[C@@](C)(O){25}C(C)(C)O)C1CCC2C5/C(=C\C[C@]12C)C(C)C3(CCC(=O)O3)[C@H]4O[C@@H]45 |
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Structure type: monomer
Trivial name: petunioside C
Compound class: triterpenoid glycoside
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