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KR-62436,即6-{2-[2-(5-氰基-4,5-二氢吡唑-1-基)-2-氧代乙基氨基]乙基氨基}烟腈,是一种具有抗高血糖活性的新型二肽基肽酶-IV(DPP-IV)抑制剂。

KR-62436, 6-{2-[2-(5-cyano-4,5-dihydropyrazol-1-yl)-2-oxoethylamino]ethylamino}nicotinonitrile, is a novel dipeptidyl peptidase-IV (DPP-IV) inhibitor with anti-hyperglycemic activity.

作者信息

Kim Kwang-Rok, Rhee Sang-Dal, Kim Hee Youn, Jung Won Hoon, Yang Sung-Don, Kim Sung Soo, Ahn Jin Hee, Cheon Hyae Gyeong

机构信息

Medicinal Science Division, Korea Research Institute of Chemical Technology, Jang-Dong 100, Yusung Gu, TaeJon, 305-343, South Korea.

出版信息

Eur J Pharmacol. 2005 Jul 25;518(1):63-70. doi: 10.1016/j.ejphar.2005.05.030.

Abstract

Dipeptidyl peptidase-IV (DPP-IV) is involved in the inactivation of glucagon-like peptide-1 (GLP-1), a potent insulinotropic peptide. Thus, DPP-IV inhibition can be an effective approach to treat type 2 diabetes mellitus by potentiating insulin secretion. This study describes the biological effects of a new DPP-IV inhibitor, KR-62436 (6-{2-[2-(5-cyano-4,5-dihydropyrazol-1-yl)-2-oxoethylamino]ethylamino}nicotinonitrile) in vitro and in vivo. KR-62436 inhibited rat plasma DPP-IV, porcine kidney DPP-IV as well as human DPP-IV (Caco-2) with IC50 values of 0.78, 0.49, 0.14 microM, respectively. In addition, the compound (10 microM) almost completely inhibited DPP-IV-mediated degradation of GLP-1 in vitro. KR-62436 inhibited the enzyme in a competitive manner, and exhibited selectivity against several proteases including proline-specific proteases. In vivo efficacy of the compound was examined by using normal C57BL/6J mice and ob/ob mice, a type 2 diabetes animal model. Administration of KR-62436 to C57BL/6J mice either orally or subcutaneously resulted in the suppression of plasma DPP-IV activity, increase in intact GLP-1 and insulin levels in plasma. Furthermore, the plasma glucose concentrations during oral glucose tolerance test (OGTT) were reduced upon oral administration of KR-62436. This study demonstrates that KR-62436 could be a good lead compound for further development as a new anti-diabetic agent.

摘要

二肽基肽酶-IV(DPP-IV)参与胰高血糖素样肽-1(GLP-1,一种强效促胰岛素肽)的失活。因此,抑制DPP-IV可通过增强胰岛素分泌成为治疗2型糖尿病的有效方法。本研究描述了一种新型DPP-IV抑制剂KR-62436(6-{2-[2-(5-氰基-4,5-二氢吡唑-1-基)-2-氧代乙基氨基]乙基氨基}烟腈)在体外和体内的生物学效应。KR-62436抑制大鼠血浆DPP-IV、猪肾DPP-IV以及人DPP-IV(Caco-2),其IC50值分别为0.78、0.49、0.14微摩尔。此外,该化合物(10微摩尔)在体外几乎完全抑制DPP-IV介导的GLP-1降解。KR-62436以竞争性方式抑制该酶,并对包括脯氨酸特异性蛋白酶在内的几种蛋白酶表现出选择性。通过使用正常C57BL/6J小鼠和2型糖尿病动物模型ob/ob小鼠来检测该化合物的体内疗效。对C57BL/6J小鼠口服或皮下给予KR-62436会导致血浆DPP-IV活性受到抑制,血浆中完整GLP-1和胰岛素水平升高。此外,口服KR-62436后,口服葡萄糖耐量试验(OGTT)期间的血浆葡萄糖浓度降低。本研究表明,KR-62436可能是一种有潜力的先导化合物,可进一步开发成为新型抗糖尿病药物。

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