Design, Synthesis And Sar Of A Series Of 2-Substituted 4-Amino-Quinazoline Neuropeptide Yy5 Receptor Antagonists

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS(2000)

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摘要
The design of a novel series of NPY-Y-5 receptor antagonists is described. Key elements for the design were the identification of weak Y-5 hits from a Y-1 program, results from a combinatorial approach and database mining. This led to the discovery of the quinazoline 4 and the aryl-sulphonamide moiety as major components of the pharmacophore for Y-5 affinity. The synthesis and SAR towards CGP71683A is described. (C) 2000 Elsevier Science Ltd. All rights reserved.
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