| Literature DB >> 7452681 |
R Kikumoto, Y Tamao, K Ohkubo, T Tezuka, S Tonomura, S Okamoto, A Hijikata.
Abstract
A series of N alpha-(arylsulfonyl)-L-arginine amide derivatives having carboxamide N-substituents with a carboxyl group was prepared and tested as inhibitors of the clotting activity of thrombin. The most inhibitory compounds were obtained when a carboxyl group was introduced into the carbon next to the amide nitrogen of N alpha-(arylsulfonyl)-L-arginine amide derivatives, e.g., N alpha-(arylsulfonyl)-L-arginyl-N-butyl-, N-(methoxyethyl)- or N-(tetrahydrofurfuryl)glycine and 4-alkyl-1-[N alpha-(arylsulfonyl)-L-arginyl]-2-piperidinecarboxylic acid, with an I50 of 1-3 X 10(-7) M.Entities:
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Year: 1980 PMID: 7452681 DOI: 10.1021/jm00186a003
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446