Abstract:
:Pharmacologically motivated natural product investigations have yielded a large variety of structurally unique lead compounds with interesting biomedical properties, but the natural roles of these molecules often remain unknown. In the present investigation, a series of benzyl substituted-flavone derivatives have been synthesized from the lead compounds and were screened against 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical scavenging and α-glucosidase inhibitory properties. The resulting activity profiles of these flavone derivatives were compared for degree of similarity to the profile of 1-3. Most of the synthesized derivatives displayed potent activities when compared to the parent compounds. Maximum potencies for DPPH free radical scavenging activity were observed only in compounds containing the 4-hydroxyl substitution and 3-methoxyl group on the phenyl ring. While the 2- and 4-hydroxyl group substitutions on the phenyl ring seem to be crucial for the intestinal α-glucosidase inhibitory activity.
journal_name
J Asian Nat Prod Resjournal_title
Journal of Asian natural products researchauthors
Kumar GS,Tiwari AK,Rao VR,Prasad KR,Ali AZ,Babu KSdoi
10.1080/10286020.2010.511190subject
Has Abstractpub_date
2010-11-01 00:00:00pages
978-84issue
11eissn
1028-6020issn
1477-2213pii
929278769journal_volume
12pub_type
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