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首页> 外文期刊>Xenobiotica: the fate of foreign compounds in biological systems >Preclinical pharmacokinetic characterization of 2-(4-(4-(5-(2-phenyl-5-(trifluoromethyl) oxazole-4-carboxamido)-1H-benzo[d]imidazol-2-yl)phenyl) cyclohexyl) acetic acid, a novel DGAT-1 inhibitor
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Preclinical pharmacokinetic characterization of 2-(4-(4-(5-(2-phenyl-5-(trifluoromethyl) oxazole-4-carboxamido)-1H-benzo[d]imidazol-2-yl)phenyl) cyclohexyl) acetic acid, a novel DGAT-1 inhibitor

机译:2-(4-(4-(5-(2-苯基-5-(三氟甲基)恶唑-4-羧酰胺基)-1H-苯并[d]咪唑-2-基)苯基)环己基)乙酸的临床前药代动力学表征,新型DGAT-1抑制剂

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摘要

1. A novel diacylglyceride acyltransferase-1 (DGAT-1) inhibitor, 2-(4-(4-(5-(2- phenyl-5-(trifluoromethyl) oxazole-4-carboxamido)-1H-benzo[ d] imidazol-2-yl) phenyl) cyclohexyl) acetic acid (KR-69232), was synthesized for a potential therapeutic use against several metabolic disorders, such as obesity, insulin resistance, and type II diabetes, characterized by excessive triglycerides (TGs) in the blood.
机译:1.一种新型的二酰基甘油酯酰基转移酶-1(DGAT-1)抑制剂2-(4-(4-(5-(2-苯基-5-(三氟甲基)恶唑-4-甲酰胺基))-1H-苯并[d]咪唑合成了(-2-yl)苯基)环己基)乙酸(KR-69232),用于治疗多种代谢性疾病(例如肥胖症,胰岛素抵抗和II型糖尿病),这些疾病的特征是甘油三酸酯(TGs)过多血液。

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