| Literature DB >> 19252319 |
Afsar Khan1, Viqar Uddin Ahmad, Umar Farooq, Sadia Bader, Saima Arshad.
Abstract
A BuOH-soluble part of the methanolic extract from the roots of Otostegia limbata yielded two new flavonol glycosides; kaempferol 3-O-[beta-D-glucopyranosyl-(1-->2)-[beta-D-glucopyranosyl-(1-->3)]-[beta-D-glucopyranosyl-(1-->4)]-alpha-L-rhamnopyranoside]-7-O-[alpha-L-rhamnopyranoside] (1) and kaempferol 3-O-[beta-D-glucopyranosyl-(1-->4)-beta-D-6'''''[4-hydroxy (E)-cinnamoyl]glucopyranosyl-(1-->3)-[beta-D-glucopyranosyl-(1-->2)]-alpha-L-rhamnopyranoside]-7-O-[alpha-L-rhamnopyranoside] (2). The structures of these compounds were elucidated by spectroscopic and chemical means. To the best of our knowledge, these are the largest flavonoids derivatives described so far from the genus Otostegia.Entities:
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Year: 2009 PMID: 19252319 DOI: 10.1248/cpb.57.276
Source DB: PubMed Journal: Chem Pharm Bull (Tokyo) ISSN: 0009-2363 Impact factor: 1.645