Found 1 publication.
Displayed publication 1
Expand all publications
Collapse all publications
Show all as text (SweetDB notation)
Show all graphically (SNFG notation)
1. (Article ID: 11942)
Calis I, Yusufoglu H, Zerbe O, Sticher O
Cephalotoside A: A tridesmosidic cycloartane type glycoside from Astragalus cephalotes var. brevicalyx
Phytochemistry 50(5) (1999)
843-847
A new tridesmosidic cycloartane type glycoside, cephalotoside A was isolated from the roots of Astragalus cephalotes var. brevicalyx in addition to the known glycosides cyclocanthosides A, D and E. The structure of the new compound was determined by spectral (IR, 1H- and 13C-NMR, and FABMS) and chemical (acetylation) methods and established as 3β-(β-D-xylopyranosyl)oxy-16β-(β-D-glucopyranosyl)oxy-24-(β-D-xylopyranosyl)oxy-cycloartane-6α,25-diol.
D, Leguminosae, E, cycloartane glycoside, Astragalus cephalotes var. brevicalyx, cephalotoside A, cyclocanthosides A
Publication DOI: 10.1016/S0031-9422(98)00601-3Journal NLM ID: 0151434Publisher: Elsevier
Correspondence: Çalis I
dominet.in.com.tr>
Institutions: Department of Pharmacognosy, Faculty of Pharmacy, Hacettepe University, Ankara, Turkey, Department of Pharmacy, Swiss Federal Institute of Technology (ETH) Zurich, 8057 Zurich, Switzerland
Methods: 13C NMR, 1H NMR, IR, FAB-MS, optical rotation measurement, acetylation, ROESY, TOCSY, HMBC, HMQC, COSY, MPLC, VLC
The publication contains the following compound(s):
- Compound ID: 28878
|
b-D-Glcp-(1-6)-+
|
b-D-Xylp-(1-3)-Subst
Subst = 3β,6α,16β,24(S),25-pentahydroxycycloartane = SMILES C[C@H](CC{24}[C@@H](O){25}C(C)(C)O)C4{16}[C@@H](O)C[C@@]5(C)C2C{6}[C@H](O)C1[C@@](C)(C){3}[C@@H](O)CC[C@@]13C[C@@]23CC[C@]45C |
Show graphically |
Structure type: oligomer
C30H52O5
Trivial name: cyclocanthoside E
Compound class: saponin glycoside, triterpenoid glycoside
- Compound ID: 31023
|
b-D-Glcp-(1-16)-+
|
b-D-Xylp-(1-24)-Subst
|
b-D-Xylp-(1-3)-+
Subst = 3β,6α,16β,24(S),25-pentahydroxycycloartane = SMILES C[C@H](CC{24}[C@@H](O){25}C(C)(C)O)C4{16}[C@@H](O)C[C@@]5(C)C2C{6}[C@H](O)C1[C@@](C)(C){3}[C@@H](O)CC[C@@]13C[C@@]23CC[C@]45C |
Show graphically |
Structure type: oligomer
; 919 [M+H]+
C46H78O18
Trivial name: cephalotoside A
Compound class: saponin glycoside
- Compound ID: 31024
|
b-D-Xylp2Ac3Ac4Ac-(1-24)-+
|
b-D-Glcp2Ac3Ac4Ac6Ac-(1-16)-Subst6Ac
|
b-D-Xylp2Ac3Ac4Ac-(1-3)-+
Subst = 3β,6α,16β,24(S),25-pentahydroxycycloartane = SMILES C[C@H](CC{24}[C@@H](O){25}C(C)(C)O)C4{16}[C@@H](O)C[C@@]5(C)C2C{6}[C@H](O)C1[C@@](C)(C){3}[C@@H](O)CC[C@@]13C[C@@]23CC[C@]45C |
Show graphically |
Structure type: oligomer
; 1403 [M+Na]+
C68H100O29
Compound class: saponin glycoside
- Compound ID: 31025
|
b-D-Xylp-(1-3)-Subst
Subst = 3β,6α,16β,24(S),25-pentahydroxycycloartane = SMILES C[C@H](CC{24}[C@@H](O){25}C(C)(C)O)C4{16}[C@@H](O)C[C@@]5(C)C2C{6}[C@H](O)C1[C@@](C)(C){3}[C@@H](O)CC[C@@]13C[C@@]23CC[C@]45C |
Show graphically |
Structure type: monomer
Trivial name: cyclocanthoside A
Compound class: saponin glycoside
- Compound ID: 31026
|
b-D-Xylp-(1-3)-+
|
b-D-Glcp-(1-16)-Subst
Subst = 3β,6α,16β,24(S),25-pentahydroxycycloartane = SMILES C[C@H](CC{24}[C@@H](O){25}C(C)(C)O)C4{16}[C@@H](O)C[C@@]5(C)C2C{6}[C@H](O)C1[C@@](C)(C){3}[C@@H](O)CC[C@@]13C[C@@]23CC[C@]45C |
Show graphically |
Structure type: oligomer
Trivial name: cyclocanthoside D
Compound class: saponin 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