Mehanna A S, Dowling M
Division of Pharmaceutical Sciences, Massachusetts College of Pharmacy and Allied Health Sciences, Boston 02115, USA.
J Pharm Biomed Anal. 1999 May;19(6):967-73. doi: 10.1016/s0731-7085(98)00122-8.
A rapid, simple and interference-free method is described to evaluate the inhibitory effects of organic compounds on the activity of angiotensin converting enzyme irrespective of their acid-base properties. The assay is based on the high performance liquid chromatographic separation of the synthetic substrate hippuryl-L-histidyl-L-leucine, the hydrolysis product hippuric acid and the test compound. Using the new method, the diuretic drug ethacrynic acid was found to act as an inhibitor for the enzyme in a non competitive mode.
本文描述了一种快速、简单且无干扰的方法,用于评估有机化合物对血管紧张素转换酶活性的抑制作用,而无需考虑其酸碱性质。该测定基于合成底物马尿酰-L-组氨酰-L-亮氨酸、水解产物马尿酸和测试化合物的高效液相色谱分离。使用该新方法,发现利尿药依他尼酸以非竞争性模式作为该酶的抑制剂。