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2-Arylpyrimidines: Novel CRF-1 receptor antagonists
- Source :
- Bioorganic & Medicinal Chemistry Letters. 18:4486-4490
- Publication Year :
- 2008
- Publisher :
- Elsevier BV, 2008.
-
Abstract
- The design, synthesis and structure-activity relationship studies of a novel series of CRF-1 receptor antagonists, the 2-arylpyrimidines, are described. The effects of substitution on the aromatic ring and the pyrimidine core on CRF-1 receptor binding were investigated. A number of compounds with K(i) values below 10 nM and lipophilicity in a minimally acceptable range for a CNS drug (cLogP5) were discovered.
- Subjects :
- Pyrimidine
Stereochemistry
Chemistry, Pharmaceutical
Clinical Biochemistry
Molecular Conformation
Pharmaceutical Science
Ether
Receptors, Corticotropin-Releasing Hormone
Biochemistry
Chemical synthesis
Rats, Sprague-Dawley
Structure-Activity Relationship
chemistry.chemical_compound
In vivo
Drug Discovery
Animals
Humans
Receptor
Molecular Biology
Binding Sites
Molecular Structure
Organic Chemistry
Antagonist
In vitro
Rats
Kinetics
Pyrimidines
Models, Chemical
Solubility
chemistry
Drug Design
Lipophilicity
Molecular Medicine
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 18
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry Letters
- Accession number :
- edsair.doi.dedup.....0e03715e3452d8f911694815b9df50eb
- Full Text :
- https://doi.org/10.1016/j.bmcl.2008.07.063