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Optimization of privileged structures for selective and potent melanocortin subtype-4 receptor ligands. | LitMetric

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Article Abstract

Design, syntheses and structure-activity relationships of N-acetylated piperazine privileged structures containing MC4R agonist compounds were described. The most potent derivatives were low nM MC4R selective full agonists. Several compounds from the series had modest pharmacokinetic properties.

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http://dx.doi.org/10.1016/j.bmcl.2010.06.038DOI Listing

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