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1. (Article ID: 11387)
Verotta L, Tato M, Toaima SM
Cycloartane triterpene glycosides from Astragalus sieberi
Phytochemistry 48(8) (1998)
1403-1409
Two new cycloartane saponins were isolated from the aerial parts of Astragalus sieberi. The structures were elucidated by 1D- and 2D- gradient-enhanced NMR analyses and enzymatic hydrolysis as 20(S),24(R)-epoxy-9 beta, 19-cyclolanostan-3 beta,6 alpha,16 beta,25-tetrol-3-O-beta-D-glucopyranoside and 20(S),24(R)-epoxy-9 beta,19-cyclolanostan-3 beta,6 alpha,16 beta,25-tetrol-3-O-beta-D-glucopyranosyl-(1-->2)-beta-D-glucopyranoside.
structural elucidation, Leguminosae, Astragalus sieberi, 1D- and 2D-gradient enhanced NMR techniques, 20(S), 24(R)-epoxy-9 beta, 19-cyclolanostan-3 beta, 6 alpha, 16 beta, 25-tetrol glycosides, sieberoside I and II
Publication DOI: 10.1016/S0031-9422(98)00042-9Journal NLM ID: 0151434Publisher: Elsevier
Institutions: Dipartimento di Chimica Organica e Industriale, Università di Milano, Milan, Italy, Pharmacia and Upjohn, Preclinical Research, Biotechnology-Structural Biology, NMR Lab., Nerviano, Italy, Pharmacognosy Department, Faculty of Pharmacy, University of Alexandria, Alexandria, Egypt
Methods: 13C NMR, 1H NMR, FAB-MS, optical rotation measurement, ROESY, TOCSY, CC, DQF-COSY, extraciton, GHSQC, GHMBC, E-COSY
The publication contains the following compound(s):
- Compound ID: 28942
|
b-D-Glcp-(1-3)-Subst
Subst = cyclogalagenin = SMILES C{25}[C@](C)(O)C6CC[C@@](C)(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)O6 |
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Structure type: monomer
; 651 [M-H]-
C36H60O10
Trivial name: sieberoside I
Compound class: triterpenoid glycoside
- Compound ID: 28943
|
b-D-Glcp-(1-2)-b-D-Glcp-(1-3)-Subst
Subst = cyclogalagenin = SMILES C{25}[C@](C)(O)C6CC[C@@](C)(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)O6 |
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Structure type: oligomer
; 837 [M+Na]+
C42H70O15
Trivial name: sieberoside II
Compound class: triterpenoid glycoside
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