Ksander G M, Savage P, Trapani A J, Balwierczak J L, Jeng A Y
Metabolic and Cardiovascular Diseases Research, Novartis Pharmaceuticals Corporation, Summit, New Jersey 07901, USA.
J Cardiovasc Pharmacol. 1998;31 Suppl 1:S71-3. doi: 10.1097/00005344-199800001-00023.
The purpose of this study was to identify endothelin-converting enzyme (ECE) inhibitors that also possess inhibitory activity for neutral endopeptidase 24.11 (NEP) and angiotensin-converting enzyme (ACE). The ortho-substituted benzofused macrocyclic lactams, such as CGS 26670, are generally potent NEP inhibitors but poor ACE inhibitors. CGS 26670 inhibited ECE activity with an IC50 of 600 nM, whereas it inhibited NEP and ACE activities with IC50 values of 0.9 and > 10,000 nM, respectively. This compound also prevented the conversion of big endothelin-1 (big ET-1) to ET-1 by denuded porcine coronary arterial smooth muscle with an IC50 of 200 nM. The ACE inhibitory activity is greatly is greatly improved in metasubstituted benzofused macrocyclic lactams. For example, CGS 26582 inhibited ECE, NEP, and ACE activities with IC50 values of 620, 4, and 175 nM, respectively. When injected at 30 mg/kg i.v. in conscious rats, followed by a challenge with big ET-1 at 1 nmol/kg i.v., this compound suppressed by 44% the increase in mean arterial blood pressure owing to the generation of ET-1 by ECE. Because ECE, NEP, and ACE play regulatory roles in cardiovascular and renal function, triple inhibitors of these enzymes may represent a novel class of agents for treatment of cardiovascular and renal diseases.
本研究的目的是鉴定同时对中性内肽酶24.11(NEP)和血管紧张素转换酶(ACE)具有抑制活性的内皮素转换酶(ECE)抑制剂。邻位取代的苯并稠合大环内酯类化合物,如CGS 26670,通常是强效的NEP抑制剂,但却是较差的ACE抑制剂。CGS 26670抑制ECE活性的IC50为600 nM,而抑制NEP和ACE活性的IC50值分别为0.9和>10,000 nM。该化合物还能抑制去内皮猪冠状动脉平滑肌将大内皮素-1(big ET-1)转化为ET-1,IC50为200 nM。间位取代的苯并稠合大环内酯类化合物的ACE抑制活性有很大提高。例如,CGS 26582抑制ECE、NEP和ACE活性的IC50值分别为620、4和175 nM。在清醒大鼠中静脉注射30 mg/kg该化合物,随后静脉注射1 nmol/kg的big ET-1进行激发试验,该化合物能抑制因ECE生成ET-1而导致的平均动脉血压升高44%。由于ECE、NEP和ACE在心血管和肾功能中发挥调节作用,这些酶的三联抑制剂可能代表一类治疗心血管和肾脏疾病的新型药物。