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Bioorg Med Chem Lett ; 16(8): 2071-5, 2006 Apr 15.
Article in English | MEDLINE | ID: mdl-16464576

ABSTRACT

The bradykinin 1 (B1) receptor is upregulated during times of inflammation and is important for maintaining inflamed and chronic pain states. Blocking this receptor has been shown to reverse and/or ameliorate pain and inflammation in animal models. In this report, we describe a new class of B1 receptor antagonists that contain the piperidine acetic acid tetralin core. A structure-activity relationship for these analogs is described in this paper. The most potent compounds from this class have IC50s<20 nM in a B1 receptor functional assay. One of these compounds, 13g, shows modest oral bioavailability in rats.


Subject(s)
Analgesics/chemical synthesis , Anti-Inflammatory Agents, Non-Steroidal/chemical synthesis , Bradykinin B1 Receptor Antagonists , Tetrahydronaphthalenes/chemistry , Acetic Acid/chemistry , Administration, Oral , Analgesics/pharmacology , Animals , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Biological Availability , Inhibitory Concentration 50 , Piperidines/chemistry , Rats , Structure-Activity Relationship
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