Found 2 publications.
Displayed publications from 1 to 2
Expand all publications
Collapse all publications
Show all as text (SweetDB notation)
Show all graphically (SNFG notation)
1. (Article ID: 11631)
Rashid A, Firdous S, Ahmad VU, Khan KM, Usmani SB, Ahmed M
A new glycoside from Polianthes tuberosa Linn
Pakistan Journal of Scientific and Industrial Research 42(1) (1999)
46
steroidal glycoside, Liliaceae, higher alcohol, Polianthes tuberosa linn
The publication contains the following compound(s):
Expand this publication
Collapse this publication
2. (Article ID: 12485)
Mimaki Y, Yokosuka A, Sashida Y
Steroidal glycosides from the aerial parts of Polianthes tuberosa
Journal of Natural Products 63(11) (2000)
1519-1523
A chemical investigation of the aerial parts of Polianthes tuberosa resulted in the isolation of a new bisdesmosidic cholestane glycoside (1) and three new spirostanol saponins (2-4), along with a known cholestane glycoside. The structures of new glycosides were determined by spectroscopic analysis, including 2D NMR spectroscopic data, and the results of hydrolytic cleavage. The isolated compounds were evaluated for their cytotoxic activity on HL-60 human promyelocytic leukemia cells.
cytotoxicity, steroidal glycosides, Polianthes tuberosa, HL-60 leukemia cells
NCBI PubMed ID: 11087596Publication DOI: 10.1021/np000230rJournal NLM ID: 7906882Publisher: American Society of Pharmacognosy
Correspondence: mimakiy
ps.toyaku.ac.jp
Institutions: School of Pharmacy, Tokyo University of Pharmacy and Life Science, Hachioji, Japan
Methods: 13C NMR, 1H NMR, EI-MS, NMR-2D, TLC, HPLC, extraction, evaporation, centrifugation, HR-EI-MS
The publication contains the following compound(s):
- Compound ID: 32389
|
b-D-Glcp-(1-1)-+
|
b-D-Apif-(1-16)-Subst
Subst = cholest-5-ene-1β,3β,16β,22S-tetrol = SMILES CC(C)CC{22}[C@H](O)[C@@H](C)[C@H]1{16}[C@@H](O)C[C@@]2([H])[C@]3([H])CC=C4C{3}[C@@H](O)C{1}[C@@H](O)[C@]4(C)[C@@]3([H])CC[C@]12C |
Show graphically |
Structure type: oligomer
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 32390
|
b-D-Xylp-(1-3)-+
|
b-D-Xylp-(1-3)-b-D-Glcp-(1-2)-b-D-Glcp-(1-4)-b-D-Galp-(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] |
Show graphically |
Structure type: oligomer
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 32391
|
b-D-Xylp-(1-3)-+
|
b-D-Xylp-(1-3)-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 |
Show graphically |
Structure type: oligomer
Compound class: glycoside, triterpenoid glycoside
- Compound ID: 32392
|
b-D-Xylp-(1-3)-+
|
b-D-Xylp-(1-3)-b-D-Glcp-(1-2)-b-D-Glcp-(1-4)-b-D-Galp-(1-3)-Subst
Subst = 9-dehydrohecogenin = SMILES C[C@H]1[C@H]2[C@H](C[C@H]3[C@@H]4CC[C@H]5C{3}[C@@H](O)CC[C@]5(C)C4=CC([C@@]32C)=O)O[C@]16CC[C@@H](C)CO6 |
Show graphically |
Structure type: oligomer
Compound class: glycoside, triterpenoid glycoside
Expand this publication
Collapse this publication
Total list of publication IDs on all result pages of the current query:
Total list of corresponding CSDB IDs (permanent record IDs):
Execution: <1 sec