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1. (Article ID: 10463)
Pant G, Panwar MS, Negi DS, Rawat MSM
Spermicidal activity of steroidal and triterpenic glycosides
Current Science 57 (1988)
661
The publication contains the following compound(s):
- Compound ID: 25646
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Glc-(1-3)-Glc-(1-2)-Glc-(1-3)-Subst
Subst = hecogenin = SMILES C[C@@H]1CC[C@]2(O[C@@]3([H])C[C@@]([C@@]4(C)[C@@]3([H])[C@@H]2C)([H])[C@]5([H])CC[C@@]6([H])C{3}[C@@H](O)CC[C@]6(C)[C@@]5([H])CC4=O)OC1 |
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Structure type: oligomer
Compound class: saponin glycoside
Reference(s) to other database(s): CCSD:
29901, CBank-STR:8322
- Compound ID: 25647
Structure type: oligomer
Compound class: saponin glycoside
Reference(s) to other database(s): CCSD:
29902, CBank-STR:514
- Compound ID: 25648
Structure type: oligomer
Compound class: saponin glycoside
Reference(s) to other database(s): CCSD:
29902, CBank-STR:514
- Compound ID: 25649
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Rha-(1-4)-+
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Rha-(1-2)-Glc-(1-3)-Subst
Subst = yamogenin = SMILES C[C@H]1[C@H]2[C@H](C[C@@H]3[C@@]2(CC[C@H]4[C@H]3CC=C5[C@@]4(CC{3}[C@@H](C5)O)C)C)O{22}[C@@]1(CC[C@H](C){26}[CH2]O)O |
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Structure type: oligomer
Compound class: saponin glycoside
- Compound ID: 25650
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Rha-(1-2)-Glc-(1-3)-Subst
Subst = yamogenin = SMILES C[C@H]1[C@H]2[C@H](C[C@@H]3[C@@]2(CC[C@H]4[C@H]3CC=C5[C@@]4(CC{3}[C@@H](C5)O)C)C)O{22}[C@@]1(CC[C@H](C){26}[CH2]O)O |
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Structure type: oligomer
Compound class: saponin glycoside
- Compound ID: 25651
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Glc-(1-3)-+
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Glc-(1-23)-Subst
Subst = hongguanggenin = SMILES [H][C@]1(O[C@@]2(OC[C@H](C)C{23}[C@@H]2O)[C@H]3C)C[C@@]4([H])[C@]5([H])C{6}[C@H](O)[C@@]6([H])C{3}[C@@H](O)CC[C@]6(C)[C@@]5([H])CC[C@]4(C)[C@]13[H] |
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Structure type: oligomer
Compound class: saponin glycoside
- Compound ID: 25652
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Xyl-(1-4)-+
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Glc-(1-3)-Glc-(1-2)-Gal-(1-3)-Subst
Subst = hecogenin = SMILES C[C@@H]1CC[C@]2(O[C@@]3([H])C[C@@]([C@@]4(C)[C@@]3([H])[C@@H]2C)([H])[C@]5([H])CC[C@@]6([H])C{3}[C@@H](O)CC[C@]6(C)[C@@]5([H])CC4=O)OC1 |
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Structure type: oligomer
Compound class: saponin glycoside
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2. (Article ID: 12860)
Yokosuka A, Mimaki Y, Kuroda M, Sashida Y
A new steroidal saponin from the leaves of Agave americana
Planta Medica 66(4) (2000)
393-396
A new bisdesmosidic spirostanol saponin, along with three known saponins, were isolated from Agave americana (Agavaceae). The structure of the new saponin was elucidated as (25R)-3β,6α-dihydroxy-5α-spirostan-12-one 3,6-di-O-β-D-glucopyranoside. Among the isolated saponins, hecogenin tetraglycoside showed cytotoxic activity against HL-60 human promyelocytic leukemia cells with an IC50 value of 4.3 μg/mL.
cytotoxic activity, spirostanol saponin, HL-60 leukemia cells, Agave americana
NCBI PubMed ID: 10865469Publication DOI: 10.1055/s-2000-8546Journal NLM ID: 0066751Publisher: George Thieme
Correspondence: mimakiy

ps.toyaku.ac.jp
Institutions: School of Pharmacy, Tokyo University of Pharmacy and Life Science, Tokyo, Japan
Methods: 13C NMR, 1H NMR, NMR-2D, FAB-MS, TLC, ESI-MS, HPLC, extraction, CC
The publication contains the following compound(s):
- Compound ID: 28952
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b-D-Xylp-(1-3)-+
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b-D-Glcp-(1-2)-b-D-Glcp-(1-4)-b-D-Galp-(1-3)-Subst
Subst = hecogenin = SMILES C[C@@H]1CC[C@]2(O[C@@]3([H])C[C@@]([C@@]4(C)[C@@]3([H])[C@@H]2C)([H])[C@]5([H])CC[C@@]6([H])C{3}[C@@H](O)CC[C@]6(C)[C@@]5([H])CC4=O)OC1 |
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Structure type: oligomer
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 33396
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b-D-Glcp-(1-6)-+
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b-D-Glcp-(1-3)-Subst
Subst = hongguanggenin = SMILES [H][C@]1(O[C@@]2(OC[C@H](C)C{23}[C@@H]2O)[C@H]3C)C[C@@]4([H])[C@]5([H])C{6}[C@H](O)[C@@]6([H])C{3}[C@@H](O)CC[C@]6(C)[C@@]5([H])CC[C@]4(C)[C@]13[H] |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 33397
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b-D-Glcp-(1-6)-+
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b-D-Glcp-(1-3)-Subst
Subst = chlorogenin = SMILES [H][C@]1(O[C@@]2(OC[C@H](C)CC2)[C@H]3C)C[C@@]4([H])[C@]5([H])C{6}[C@H](O)[C@@]6([H])C{3}[C@@H](O)CC[C@]6(C)[C@@]5([H])CC[C@]4(C)[C@]13[H] |
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Structure type: oligomer
Compound class: glycoside
- Compound ID: 33398
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b-D-Glcp-(1-6)-+
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b-D-Glcp-(1-3)-Subst
Subst = (25R)-3β,6α-dihydroxy-5α-spirostan-12-one = SMILES C[C@H]1[C@H]2[C@H](C[C@H]3[C@@H]4C{6}[C@H](O)[C@H]5C{3}[C@@H](O)CC[C@]5(C)[C@H]4CC([C@@]32C)=O)O[C@]16CC[C@@H](C)CO6 |
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Structure type: oligomer
Compound class: glycoside
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