Thrombin inhibitors. 1. Ester derivatives of N.alpha.-(arylsulfonyl)-L-arginine
- 1 August 1980
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Medicinal Chemistry
- Vol. 23 (8) , 827-830
- https://doi.org/10.1021/jm00182a003
Abstract
A series of N.alpha.-(arylsulfonyl)-L-arginine esters was prepared and tested as inhibitors of the clotting activity of animal thrombin. N.alpha.-Dansyl-L-arginine methyl ester was the most inhibitory of the N.alpha.-(arylsulfonyl)-L-arginine methyl esters. The most potent inhibitors were the n-propyl and n-butyl esters of N.alpha.-dansyl-L-arginine with an I50 [median inhibitory concentration] of 2 .times. 10-6 M. Esters of unsaturated straight-chain alcohols with a chain length of 4 C were as inhibitory as the n-butyl ester. The inhibitors were hydrolyzed by thrombin and trypsin more slowly than N.alpha.-tosyl-L-arginine methyl ester.This publication has 1 reference indexed in Scilit: