Back to Search
Start Over
Inhibition of human leukocyte elastase. 1. Inhibition by C-7-substituted cephalosporin tert-butyl esters
- Source :
- Journal of medicinal chemistry. 33(9)
- Publication Year :
- 1990
-
Abstract
- Time-dependent inhibitors of the enzyme human leukocyte elastase have been developed based on the cephem nucleus. A series of cephalosporin tert-butyl esters has been examined, and the activity of these compounds has been found to be very sensitive to C-7 substituents, with small, alpha-oriented, electron-withdrawing groups showing greatest activity. Additionally, the oxidation state of the sulfur atom has been found to play a role in potency, with sulfones showing considerably greater activity than the corresponding sulfides or beta-sulfoxides. The alpha-sulfoxides were inactive.
- Subjects :
- Chemical Phenomena
medicine.drug_class
Stereochemistry
Cephalosporin
Carboxylic Acids
chemistry.chemical_element
Human Leukocyte Elastase
Structure-Activity Relationship
Oxidation state
Drug Discovery
medicine
Potency
Humans
chemistry.chemical_classification
Cephem
Pancreatic Elastase
Esters
Sulfur
Cephalosporins
Chemistry
medicine.anatomical_structure
Enzyme
chemistry
Molecular Medicine
Leukocyte Elastase
Nucleus
Subjects
Details
- ISSN :
- 00222623
- Volume :
- 33
- Issue :
- 9
- Database :
- OpenAIRE
- Journal :
- Journal of medicinal chemistry
- Accession number :
- edsair.doi.dedup.....229b2b1691997125c8b04ceb65397224