Synthesis of gossypol atropisomers and derivatives and evaluation of their anti-proliferative and anti-oxidant activity

被引:64
|
作者
Dodou, K
Anderson, RJ
Lough, WJ
Small, DAP
Shelley, MD
Groundwater, PW
机构
[1] Univ Sunderland, Sunderland Pharm Sch, Sunderland SR1 3SD, Durham, England
[2] Stiefel Int R&D, Maidenhead SL6 8XY, Berks, England
[3] Velindre NHS Trust, Cardiff CF14 2TL, S Glam, Wales
关键词
gossypol; atropisomers; psoriasis; anti-oxidant; anti-proliferative;
D O I
10.1016/j.bmc.2005.04.026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gossypol 1, gossypolone 2, and a series of bis 3 and half Schiffs bases 4 of gossypol were synthesised and tested for anti-proliferative and anti-oxidant activity. (-)-Gossypol (-)-1 was the most potent inhibitor of the proliferation of the HPV-16 keratinocyte cell line (using an MTT viability assay) with a GI(50) of 4.8 mu M. The bis Schiffs base of (-)-gossypol with L-tyrosine ethyl ester (-)-3b was the most potent inhibitor of iron/ascorbate dependent lipid peroxidation (using the thiobarbituric acid test), with an IC50 of 11.7 mu M, with (-)-gossypol being the next most potent of the series, with an IC50 of 13.1 mu M. The results from these initial assays suggest that gossypol, as either a racemic mixture rac-1, or the individual atropisomers (-)-1 or (+)-1, has potential for the treatment of psoriasis. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4228 / 4237
页数:10
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