The design of a new group of angiotensin-converting enzyme inhibitors
- 18 October 1982
- journal article
- Published by Wiley in FEBS Letters
- Vol. 147 (2), 175-179
- https://doi.org/10.1016/0014-5793(82)81036-3
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Angiotensin-converting enzyme inhibitors: importance of the amide carbonyl of mercaptoacyl amino acids for hydrogen bonding to the enzymeJournal of Medicinal Chemistry, 1982
- Inhibition and affinity chromatography of human serum angiotensin converting enzyme with cysteinyl-proline derivativesArchives of Biochemistry and Biophysics, 1981
- SQ 14,225: 1-(D-3-mercapto-2-methylpropionyl)-L-prolineActa Crystallographica Section B: Structural Science, Crystal Engineering and Materials, 1980
- A new class of angiotensin-converting enzyme inhibitorsNature, 1980
- HYDROGEN BONDS IN CRYSTAL STRUCTURES OF AMINO ACIDS, PEPTIDES AND RELATED MOLECULESInternational Journal of Peptide and Protein Research, 1979
- The morse curve as a non-bonded potential functionChemical Physics Letters, 1978
- Design of potent competitive inhibitors of angiotensin-converting enzyme. Carboxyalkanoyl and mercaptoalkanoyl amino acidsBiochemistry, 1977
- Design of Specific Inhibitors of Angiotensin-Converting Enzyme: New Class of Orally Active Antihypertensive AgentsScience, 1977
- Intermolecular potentials from crystal data. III. Determination of empirical potentials and application to the packing configurations and lattice energies in crystals of hydrocarbons, carboxylic acids, amines, and amidesThe Journal of Physical Chemistry, 1974
- Conformational Analysis of Macromolecules. III. Helical Structures of Polyglycine and Poly-L-AlanineThe Journal of Chemical Physics, 1966