Marder M, Viola H, Bacigaluppo J A, Colombo M I, Wasowski C, Wolfman C, Medina J H, Rúveda E A, Paladini A C
Facultad de Farmacia y Bioquímica, Instituto de Química y Fisicoquímica Biológicas, Junín 956, Buenos Aires, 1113, Argentina.
Biochem Biophys Res Commun. 1998 Aug 19;249(2):481-5. doi: 10.1006/bbrc.1998.9146.
Solution phase combinatorial synthesis of flavone derivatives and evaluation of their affinity for the central benzodiazepine receptors is described. The libraries preparation is simple and provides a convenient method for rapid compound generation and screening. Thirty one new compounds were obtained of which the most promising, as high affinity benzodiazepine receptor ligands, were 6-bromo-3'-fluoroflavone; 6,3'-dichloroflavone; 6-bromo-3'-chloroflavone and 6-chloro-3'-bromoflavone.
本文描述了黄酮衍生物的溶液相组合合成及其对中枢苯二氮䓬受体亲和力的评估。文库制备简单,为快速生成和筛选化合物提供了一种便捷方法。获得了31种新化合物,其中作为高亲和力苯二氮䓬受体配体最有前景的是6-溴-3'-氟黄酮、6,3'-二氯黄酮、6-溴-3'-氯黄酮和6-氯-3'-溴黄酮。