| Literature DB >> 9182126 |
S Kirmizigül1, N Gören, S W Yang, G A Cordell, C Bozok-Johansson.
Abstract
The roots of Ononis spinosa subsp. leiosperma (Leguminosae) afforded a new glycoside, spinonin (1), possessing a novel skeleton, in addition to the known isoflavonoid glycoside, ononin [7beta-(glucosyloxy)formononetin] (2) and the known pterocarpan, 7-demethoxy-7-D-(glucosyloxy)homopterocarpin (3). The structure of the new isolate was elucidated by spectral methods including 1H and 13C NMR, COSY, APT, HETCOR, HMBC, NOESY, CD, FABMS, HRMS, EIMS, CIMS, and some chemical reactions. Spinonin was inactive against a number of human cancer cell lines and HIV-1 reverse transcriptase. The compounds 1 and 3 showed weak activity against Pseudomonas aeruginosa, whereas 2 was active against beta-hemolytic Streptococcus.Entities:
Mesh:
Substances:
Year: 1997 PMID: 9182126 DOI: 10.1021/np9605652
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050