Abstract
Recently, we proposed inhibition of aldosterone synthase (CYP11B2) as a novel strategy for the treatment of congestive heart failure and myocardial fibrosis and synthesized a large number of inhibitors. In this work, a pharmacophore model for CYP11B2 inhibitors was developed by superimposition of active and non-active compounds. This model was confirmed by the synthesis of two pyridyl substituted acenaphthene derivatives (A,B). This new class of compounds as well as the pharmacophore could be helpful for the discovery of novel inhibitors.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Acenaphthenes / chemistry
-
Catalysis
-
Chemistry, Pharmaceutical / methods*
-
Computer Simulation
-
Cytochrome P-450 CYP11B2 / antagonists & inhibitors*
-
Drug Design*
-
Drug Evaluation, Preclinical / methods
-
Enzyme Inhibitors / pharmacology*
-
Evaluation Studies as Topic
-
Humans
-
Inhibitory Concentration 50
-
Models, Chemical
-
Models, Molecular
-
Naphthalenes / antagonists & inhibitors
-
Protein Binding
-
Receptors, Drug / chemistry
-
Structure-Activity Relationship
-
Substrate Specificity
-
Temperature
Substances
-
Acenaphthenes
-
Enzyme Inhibitors
-
Naphthalenes
-
Receptors, Drug
-
naphthalene
-
Cytochrome P-450 CYP11B2
-
acenaphthene