Suppr超能文献

强效且选择性口服生物可利用的β-取代苯丙氨酸衍生的二肽基肽酶IV抑制剂的发现。

Discovery of potent and selective orally bioavailable beta-substituted phenylalanine derived dipeptidyl peptidase IV inhibitors.

作者信息

Edmondson Scott D, Mastracchio Anthony, Duffy Joseph L, Eiermann George J, He Huaibing, Ita Ida, Leiting Barbara, Leone Joseph F, Lyons Kathryn A, Makarewicz Amanda M, Patel Reshma A, Petrov Aleksandr, Wu Joseph K, Thornberry Nancy A, Weber Ann E

机构信息

Department of Medicinal Chemistry, Merck & Co. Inc., PO Box 2000, Rahway, NJ 07065, USA.

出版信息

Bioorg Med Chem Lett. 2005 Jun 15;15(12):3048-52. doi: 10.1016/j.bmcl.2005.04.028.

Abstract

anti-Substituted biaryl beta-methylphenylalanine derived amides have been shown to be potent DPP-IV inhibitors that suffer from suboptimal selectivity and pharmacokinetics. This letter describes the substitution of the beta-methyl substituent with beta-polar substituents, culminating in the discovery of a beta-dimethylamide substituted phenylalanine derivative with an excellent potency, selectivity, and pharmacokinetic profile.

摘要

已表明,抗取代的联芳基β-甲基苯丙氨酸衍生酰胺是有效的二肽基肽酶-IV(DPP-IV)抑制剂,但存在选择性和药代动力学不理想的问题。本信函描述了用β-极性取代基取代β-甲基取代基,最终发现了一种具有优异效力、选择性和药代动力学特征的β-二甲基酰胺取代的苯丙氨酸衍生物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验