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Bioorg Med Chem ; 11(2): 185-92, 2003 Jan 17.
Article in English | MEDLINE | ID: mdl-12470712

ABSTRACT

The melanocortin-4 receptor (MC4) modulates physiological functions such as feeding behavior, nerve regeneration, and drug addiction. Using a high throughput screen based on (125)I-NDP-MSH binding to the human MC4 receptor, we discovered 2,3-diaryl-5-anilino[1,2,4]thiadiazoles 3 as potent and selective MC4 receptor agonists. Through SAR development on the three attached aryl rings, we improved the binding affinity from 174 nM to 4.4 nM IC(50). When delivered intraperitoneally, compounds 3a, 3b, and 3c induced significant inhibition of food intake in a fasting-induced feeding model in rats. When delivered orally, these compounds lost activity, mainly due to rapid metabolism to inactive imidoylthiourea reduction products.


Subject(s)
Feeding Behavior/drug effects , Receptors, Corticotropin/agonists , Thiadiazoles/chemical synthesis , Thiadiazoles/pharmacology , alpha-MSH/analogs & derivatives , Animals , Disease Models, Animal , Fasting/physiology , Feeding Behavior/physiology , Humans , Infusions, Parenteral , Inhibitory Concentration 50 , Iodine Radioisotopes , Male , Melanoma/metabolism , Rats , Rats, Long-Evans , Receptor, Melanocortin, Type 4 , Receptors, Corticotropin/metabolism , Structure-Activity Relationship , Tumor Cells, Cultured , alpha-MSH/metabolism
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