Sulfoximine and sulfodiimine transition state analog inhibitors for carboxypeptidase A
- 1 June 1989
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 111 (12), 4467-4472
- https://doi.org/10.1021/ja00194a049
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- .alpha.-Bromo ketone substrate analogs are powerful reversible inhibitors of carboxypeptidase ABiochemistry, 1985
- 3-Phosphonopropionic acids inhibit carboxypeptidase A as multisubstrate analogues or transition-state analoguesBiochemical Journal, 1985
- Inhibition of carboxypeptidase A by aldehyde and ketone substrate analogsBiochemistry, 1984
- The pH dependency of the zinc and cobalt carboxypeptidase catalyzed enolization of (R)-2-benzyl-3-(p-methoxybenzoyl)propionic acidJournal of the American Chemical Society, 1983
- Proton NMR study of cobalt(II)-substituted carboxypeptidase AJournal of the American Chemical Society, 1982
- Hydrolysis of a thiopeptide by cadmium carboxypeptidase ABiochemical and Biophysical Research Communications, 1981
- A phosphonamidate dipeptide analog as an inhibitor of carboxypeptidase AJournal of the American Chemical Society, 1981
- The pH dependence of peptide hydrolysis by nitrocarboxypeptidase AArchives of Biochemistry and Biophysics, 1980
- Inhibition of thermolysin and carboxypeptidase A by phosphoramidatesBiochemistry, 1979
- Design of potent and specific inhibitors of carboxypeptidases A and BBiochemistry, 1979