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Bioorg Med Chem Lett ; 18(3): 1146-50, 2008 Feb 01.
Article in English | MEDLINE | ID: mdl-18160282

ABSTRACT

We have derived a novel series of neuropeptide Y (NPY) Y5 receptor antagonists from the biphenylurea 3. Cyclohexylurea 21c, a member of the series, is a potent NPY Y5 receptor antagonist that exhibits excellent pharmacokinetic parameters in rats and dogs. On chronic oral administration to diet-induced obese rats, 21c displayed an anti-obesity profile, causing a modest reduction in food intake, a significant decrease in body weight gain, a decrease in adipose mass, and an increase in lean tissue mass.


Subject(s)
Anti-Obesity Agents/chemical synthesis , Anti-Obesity Agents/pharmacology , Receptors, Neuropeptide Y/antagonists & inhibitors , Urea , Administration, Oral , Animals , Anti-Obesity Agents/administration & dosage , Anti-Obesity Agents/chemistry , Combinatorial Chemistry Techniques , Dogs , Humans , Mice , Molecular Structure , Obesity/chemically induced , Rats , Structure-Activity Relationship , Urea/administration & dosage , Urea/analogs & derivatives , Urea/chemical synthesis , Urea/chemistry , Urea/pharmacology
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