Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10596680 | Bioorganic & Medicinal Chemistry Letters | 2010 | 4 Pages |
Abstract
Chemical treatment of diabetes mellitus is widely studied and controlling of blood glucose level is the main course of therapy. In type 2 diabetes mellitus, insulin resistance is the major problem. An isoflavone C-glucoside, puerarin (1), is known to enhance glucose uptake into the insulin sensitive cell and is thought to be a candidate for treatment of diabetes mellitus. We synthesized 1 and several derivatives to apply for the structure-activity relationship study. The result against 3T3-L1 adipocyte indicated that the C-glucoside part of 1 is unconcerned in its activity when tested in vitro and the main structure responsible for its activity was the isoflavone moiety.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Eisuke Kato, Jun Kawabata,