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Pyridopyrimidine based cannabinoid-1 receptor inverse agonists: Synthesis and biological evaluation
Authors:John S Debenham  Christina B Madsen-Duggan  Junying Wang  Xinchun Tong  Julie Lao  Tung M Fong  Marie-Therese Schaeffer  Jing Chen Xiao  Cathy CR-R Huang  Chun-Pyn Shen  D Sloan Stribling  Lauren P Shearman  Alison M Strack  D Euan MacIntyre  Jeffrey J Hale  Thomas F Walsh
Institution:1. Department of Medicinal Chemistry, Merck Research Laboratories, PO Box 2000, Rahway, NJ 07065, USA;2. Department of Metabolic Disorders, Merck Research Laboratories, PO Box 2000, Rahway, NJ 07065, USA;3. Department of Pharmacology, Merck Research Laboratories, PO Box 2000, Rahway, NJ 07065, USA
Abstract:The synthesis, SAR and binding affinities are described for cannabinoid-1 receptor (CB1R) specific inverse agonists based on pyridopyrimidine and heterotricyclic scaffolds. Food intake and pharmacokinetic evaluation of several of these compounds indicate that they are effective orally active modulators of CB1R.
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