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
Department of Medicinal Chemistry, Merck & Co. Inc., PO Box 2000, Rahway, NJ 07065, USA.
Bioorg Med Chem Lett. 2005 Jun 15;15(12):3048-52. doi: 10.1016/j.bmcl.2005.04.028.
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.
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。