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Synthesis and structure-activity relationship of pyripyropene A derivatives as potent and selective acyl-CoA:cholesterol acyltransferase 2 (ACAT2) inhibitors: part 1.
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2013 Mar 01; Vol. 23 (5), pp. 1285-7. Date of Electronic Publication: 2013 Jan 09. - Publication Year :
- 2013
-
Abstract
- In an effort to develop potent and selective inhibitors toward ACAT2, structure-activity relationship studies were carried out using derivatives based on pyripyropene A (PPPA, 1). We have successfully developed novel PPPA derivatives with a 7-O-substituted benzoyl substituent that significantly exhibit more potent ACAT2 inhibitory activity and higher ACAT2 isozyme selectivity than 1.<br /> (Copyright © 2013 Elsevier Ltd. All rights reserved.)
- Subjects :
- Animals
Enzyme Inhibitors chemical synthesis
Pyridines chemical synthesis
Sesquiterpenes chemical synthesis
Structure-Activity Relationship
Sterol O-Acyltransferase 2
Enzyme Inhibitors chemistry
Enzyme Inhibitors pharmacology
Pyridines chemistry
Pyridines pharmacology
Sesquiterpenes chemistry
Sesquiterpenes pharmacology
Sterol O-Acyltransferase antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1464-3405
- Volume :
- 23
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 23369538
- Full Text :
- https://doi.org/10.1016/j.bmcl.2012.12.099