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J Med Chem ; 48(24): 7517-9, 2005 Dec 01.
Article in English | MEDLINE | ID: mdl-16302793

ABSTRACT

4'-Octyl-4-biphenylcarboxylic acid (1g, AC-55649) was identified as a highly isoform-selective agonist at the human RARbeta2 receptor in a functional intact cell-based screening assay. The subsequent hit to lead optimization transformed the lipophilic, poorly soluble hit into a more potent and orally available compound (2, AC-261066) with retained beta2 selectivity and greatly improved physiochemical properties. Being an isoform-selective RARbeta2 receptor agonist that discriminates between nuclear receptor isoforms having identical ligand binding domains, 2 will be useful as a pharmacological research tool but also a valuable starting point for drug development.


Subject(s)
Benzoates/chemical synthesis , Biphenyl Compounds/chemical synthesis , Receptors, Retinoic Acid/agonists , Thiazoles/chemical synthesis , Administration, Oral , Animals , Benzoates/chemistry , Benzoates/pharmacology , Binding Sites , Biological Availability , Biphenyl Compounds/chemistry , Biphenyl Compounds/pharmacology , Cells, Cultured , Humans , Models, Molecular , Protein Isoforms/agonists , Protein Structure, Tertiary , Rats , Solubility , Structure-Activity Relationship , Thiazoles/chemistry , Thiazoles/pharmacology , Transcription, Genetic
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