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新型正常血糖和降血脂药物。1.

Novel euglycemic and hypolipidemic agents. 1.

作者信息

Lohray B B, Bhushan V, Rao B P, Madhavan G R, Murali N, Rao K N, Reddy A K, Rajesh B M, Reddy P G, Chakrabarti R, Vikramadithyan R K, Rajagopalan R, Mamidi R N, Jajoo H K, Subramaniam S

机构信息

Medicinal and Organic Chemistry, Pharmacology, and Clinical Research, Dr. Reddy's Research Foundation, Bollaram Road, Miyapur Hyderabad 500 050, India.

出版信息

J Med Chem. 1998 May 7;41(10):1619-30. doi: 10.1021/jm970444e.

Abstract

A series of [[(heterocyclyl)ethoxy]benzyl]-2,4-thiazolidinediones have been synthesized by the condensation of corresponding aldehyde 1 and 2,4-thiazolidinedione followed by hydrogenation. Both unsaturated thiazolidinedione 2 and its saturated counterpart 3 have shown antihyperglycemic activity. Many of these compounds have shown superior euglycemic and hypolipidemic activity compared to troglitazone (CS 045). The indole analogue DRF-2189 (3g) was found to be a very potent insulin sensitizer, comparable to BRL-49653 in genetically obese C57BL/6J-ob/ob and 57BL/KsJ-db/db mice. Pharmacokinetic and tissue distribution studies conducted on BRL-49653 and DRF-2189 (3g) indicate that these drugs are well-distributed in target tissues. On the basis of euglycemic activity as well as enhanced selectivity against reduction of triglycerides in plasma, DRF-2189 (3g) has been selected for further evaluation.

摘要

通过相应的醛1与2,4-噻唑烷二酮缩合然后氢化,合成了一系列[[(杂环基)乙氧基]苄基]-2,4-噻唑烷二酮。不饱和噻唑烷二酮2及其饱和类似物3均显示出抗高血糖活性。与曲格列酮(CS 045)相比,这些化合物中的许多已显示出优异的血糖正常化和降血脂活性。发现吲哚类似物DRF-2189(3g)是一种非常有效的胰岛素增敏剂,在遗传性肥胖的C57BL/6J-ob/ob和57BL/KsJ-db/db小鼠中与BRL-49653相当。对BRL-49653和DRF-2189(3g)进行的药代动力学和组织分布研究表明,这些药物在靶组织中分布良好。基于血糖正常化活性以及对血浆中甘油三酯降低的增强选择性,已选择DRF-2189(3g)进行进一步评估。

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