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CGS 34043:一种非肽类、强效且长效的内皮素转化酶-1和中性内肽酶24.11双重抑制剂。

CGS 34043: a non-peptidic, potent and long-acting dual inhibitor of endothelin converting enzyme-1 and neutral endopeptidase 24.11.

作者信息

Trapani A J, De Lombaert S, Beil M E, Bruseo C W, Savage P, Chou M, Jeng A Y

机构信息

Novartis Institute for Biomedical Research, Summit, NJ 07901, USA.

出版信息

Life Sci. 2000;67(9):1025-33. doi: 10.1016/s0024-3205(00)00695-0.

DOI:10.1016/s0024-3205(00)00695-0
PMID:10954036
Abstract

Endothelin-1 (ET- 1) is a potent vasoconstrictor. Its biosynthesis is catalyzed by endothelin converting enzyme (ECE). In contrast, atrial natriuretic peptide (ANP) is a potent vasorelaxant and diuretic, and it is mainly degraded by neutral endopeptidase 24.11 (NEP). Therefore, compounds that can suppress the production of ET-1 by inhibiting ECE while simultaneously potentiating the levels of ANP by inhibiting NEP may be novel agents for the treatment of cardiovascular and renal dysfunction. CGS 34043 is one such compound, which inhibited the activities of ECE-1a and NEP with IC50 values of 5.8 and 110 nM, respectively. In vivo, it inhibited the pressor response induced by big ET-1, the precursor of ET-1, dose-dependently in rats, and the inhibition was sustained for at least 2 hr. In addition, CGS 34043 increased plasma ANP by 150% up to 4 hr after an intravenous dose of 10 mg/kg in conscious rats infused with ANP. However, this compound had no effect on the angiotensin I-induced pressor response. These results demonstrate that CGS 34043 is a potent and long-lasting dual inhibitor of ECE-1 and NEP. Consequently, it may be beneficial for the treatment of diseases in which an overproduction of ET-1 and/or enhanced degradation of ANP plays a pathogenic role. The activity of CGS 34753, an orally active prodrug of CGS 34043, is also described.

摘要

内皮素 -1(ET - 1)是一种强效血管收缩剂。其生物合成由内皮素转换酶(ECE)催化。相比之下,心房利钠肽(ANP)是一种强效血管舒张剂和利尿剂,主要由中性内肽酶24.11(NEP)降解。因此,能够通过抑制ECE来抑制ET - 1的产生,同时通过抑制NEP来提高ANP水平的化合物可能是治疗心血管和肾功能障碍的新型药物。CGS 34043就是这样一种化合物,它对ECE - 1a和NEP活性的抑制IC50值分别为5.8 nM和110 nM。在体内,它能剂量依赖性地抑制ET - 1的前体大ET - 1在大鼠中诱导的升压反应,且这种抑制作用至少持续2小时。此外,在静脉注射10 mg/kg剂量后,CGS 34043能使清醒大鼠体内的血浆ANP在长达4小时内升高150%。然而,该化合物对血管紧张素I诱导的升压反应没有影响。这些结果表明,CGS 34043是一种强效且持久的ECE - 1和NEP双重抑制剂。因此,它可能对治疗ET - 1过度产生和/或ANP降解增强起致病作用的疾病有益。文中还描述了CGS 34043的口服活性前体药物CGS 34753的活性。

相似文献

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CGS 34043: a non-peptidic, potent and long-acting dual inhibitor of endothelin converting enzyme-1 and neutral endopeptidase 24.11.CGS 34043:一种非肽类、强效且长效的内皮素转化酶-1和中性内肽酶24.11双重抑制剂。
Life Sci. 2000;67(9):1025-33. doi: 10.1016/s0024-3205(00)00695-0.
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Inhibition of big ET-1-induced pressor response by an orally active dual inhibitor of endothelin-converting enzyme and neutral endopeptidase 24.11.内皮素转化酶和中性内肽酶24.11的口服活性双重抑制剂对大内皮素-1诱导的升压反应的抑制作用
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Pharmacological profile of a non-peptidic dual inhibitor of neutral endopeptidase 24.11 and endothelin-converting enzyme.中性内肽酶24.11和内皮素转化酶的非肽类双重抑制剂的药理学特性
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CGS 35601 and its orally active prodrug CGS 37808 as triple inhibitors of endothelin-converting enzyme-1, neutral endopeptidase 24.11, and angiotensin-converting enzyme.CGS 35601及其口服活性前药CGS 37808作为内皮素转化酶-1、中性内肽酶24.11和血管紧张素转化酶的三联抑制剂。
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Potent and selective non-peptidic inhibitors of endothelin-converting enzyme-1 with sustained duration of action.具有持久作用时间的强效且选择性的内皮素转化酶-1非肽类抑制剂。
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Combined inhibition of neutral endopeptidase with angiotensin converting enzyme or endothelin converting enzyme in experimental diabetes.在实验性糖尿病中联合抑制中性内肽酶与血管紧张素转换酶或内皮素转换酶
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Triple vasopeptidase inhibition normalizes blood pressure in conscious, unrestrained, and spontaneously hypertensive rats.三重血管肽酶抑制可使清醒、不受限制的自发性高血压大鼠血压恢复正常。
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