The effect of 1,3-diaryl-[1H]-pyrazole-4-acetamides on glucose utilization in ob/ob mice

被引:143
作者
Bebernitz, GR
Argentieri, G
Battle, B
Brennan, C
Balkan, B
Burkey, BF
Eckhardt, M
Gao, JP
Kapa, P
Strohschein, RJ
Schuster, HF
Wilson, M
Xu, DD
机构
[1] Novartis Pharmaceut Corp, Novartis Inst Biomed Res, Metab & Cardiovasc Dis, Dept Med Chem, Summit, NJ 07901 USA
[2] Novartis Pharmaceut Corp, Novartis Inst Biomed Res, Metab & Cardiovasc Dis, Dept Pharmacol, Summit, NJ 07901 USA
[3] Novartis Pharmaceut Corp, Novartis Inst Biomed Res, Metab & Cardiovasc Dis, Dept Biochem, Summit, NJ 07901 USA
关键词
D O I
10.1021/jm010032c
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This article provides evidence of a new class of compounds, 1,3-diaryl-[1H]-pyrazole-4-acetamides, initially identified from their ability to increase glucose transport in an adipocyte and muscle cell line and ultimately demonstrating dramatic glucose lowering in ob/ob Mice, a diabetic animal model. The lead compound, 1, possessed some behavioral-like effects which were removed by structural variation during the course of this investigation. Specifically, 11 g (RI = meta-CF3, Ar2 = 4 ' biphenyl, R3 = diethylamide) illustrated the potency of this series with ED50 values for glucose lowering in ob/ob mice of 3.0 mg/kg/day. Concomitant with its effect on glucose lowering, 11g also caused a 50% reduction in insulin levels consistent with an agent that increases whole body insulin sensitivity. 11g showed favorable pharmacokinetic data with acceptable absorption, negligible metabolism, and good duration of action. 11g demonstrated no appreciable adipogenic effect through PPAR gamma agonism, a characteristic of the thiazolidinediones (TZD), and so represents a potentially new class of agents for the treatment of diabetes.
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收藏
页码:2601 / 2611
页数:11
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