Acylated piperidine derivatives as melanocortin-4 receptor...

C - Chemistry – Metallurgy – 07 – D

Patent

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C07D 413/14 (2006.01) A61K 31/435 (2006.01) A61K 31/445 (2006.01) A61K 31/454 (2006.01) A61K 31/4545 (2006.01) A61K 31/47 (2006.01) A61K 31/495 (2006.01) A61K 31/55 (2006.01) C07D 211/62 (2006.01) C07D 211/64 (2006.01) C07D 211/68 (2006.01) C07D 217/02 (2006.01) C07D 223/16 (2006.01) C07D 401/06 (2006.01) C07D 401/12 (2006.01) C07D 401/14 (2006.01) C07D 403/06 (2006.01) C07D 413/06 (2006.01) C07D 491/08 (2006.01)

Patent

CA 2439149

Certain novel 4-substituted N-acylated piperidine derivatives are agonists of the human melanocortin receptor(s) and, in particular, are selective agonists of the human melanocortin-4 receptor (MC-4R). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the activation of MC-4R, such as obesity, diabetes, sexual dysfunction, including erectile dysfunction and female sexual dysfunction.

L'invention concerne certains nouveaux dérivés de pipéridine N-acétylée substitués en 4 utilisés comme agonistes du ou des récepteur(s) humain(s) de mélanocortine, et en particulier des agonistes sélectifs du récepteur humain de mélanocortine-4 (MC-4R). Ces dérivés sont utilisés pour traiter, lutter contre, ou prévenir des maladies et des troubles sensibles à l'activation de MC-4R, tels que l'obésité, les diabètes, un dysfonctionnement sexuel, notamment une dysfonction érectile et une dysfonction sexuelle chez la femme.

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