Syntheses of Nα-(β-naphthylsulfonylaminoglycyl)-argininamides as potential selective synthetic thrombin inhibitors
- 1 November 1988
- journal article
- research article
- Published by Elsevier in European Journal of Medicinal Chemistry
- Vol. 23 (6) , 577-585
- https://doi.org/10.1016/0223-5234(88)90102-x
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Kinetics of the inhibition of thrombin by hirudinBiochemistry, 1986
- On the isolation of the thrombin inhibitor hirudinThrombosis Research, 1985
- The Complete Covalent Structure of Hirudin. Localization of the Disulfide BondsBiological Chemistry Hoppe-Seyler, 1985
- Vitamin K–Dependent ProteinsNew England Journal of Medicine, 1984
- Selective inhibition of thrombin by (2R,4R)-4-methyl-1-[N2-[1,2,3,4-tetrahydro-8-quinolinyl)sulfonyl]-L-arginyl]-2-piperidinecarboxylic acidBiochemistry, 1984
- The vitamin K-dependent carboxylation reactionMolecular and Cellular Biochemistry, 1984
- The functional domain of hirudin, a thrombin‐specific inhibitorFEBS Letters, 1983
- Thrombin inhibitors. 3. Carboxyl-containing amide derivatives of N.alpha.-substituted L-arginineJournal of Medicinal Chemistry, 1980
- Thrombin inhibitors. 1. Ester derivatives of N.alpha.-(arylsulfonyl)-L-arginineJournal of Medicinal Chemistry, 1980
- Thrombin inhibitors. 2. Amide derivatives of N.alpha.-substituted L-arginineJournal of Medicinal Chemistry, 1980