Ondetti M A, Rubin B, Cushman D W
Science. 1977 Apr 22;196(4288):441-4. doi: 10.1126/science.191908.
A hypothetical model of the active site of angiotensin-converting enzyme, based on known chemical and kinetic properties of the enzyme, has enabled us to design a new class of potent and specific inhibitors. These compounds, carboxyalkanoyl and mercaptoalkanoyl derivatives of proline, inhibit the contractile response of guinea pig ileal strip to angiotensin I and augment its response to bradykinin. When administered orally to rats, these agents inhibit the pressor effect of angiotensin I, augment the vasodepressor effect of bradykinin, and lower blood pressure in a model of renovascular hypertension.
基于血管紧张素转换酶已知的化学和动力学特性,构建了一个该酶活性位点的假设模型,这使我们能够设计出一类新型的强效且特异性的抑制剂。这些化合物,即脯氨酸的羧基烷酰基和巯基烷酰基衍生物,可抑制豚鼠回肠肌条对血管紧张素I的收缩反应,并增强其对缓激肽的反应。当给大鼠口服这些药物时,它们可抑制血管紧张素I的升压作用,增强缓激肽的血管降压作用,并降低肾血管性高血压模型中的血压。