401843-91-2Relevant academic research and scientific papers
Optimization of a privileged structure leading to potent and selective human melanocortin subtype-4 receptor ligands
Bakshi, Raman K.,Hong, Qingmei,Tang, Rui,Kalyani, Rubana N.,MacNeil, Tanya,Weinberg, David H.,Van Der Ploeg, Lex H. T.,Patchett, Arthur A.,Nargund, Ravi P.
, p. 1130 - 1133 (2007/10/03)
Design and synthesis of potent MC4 selective agonists based on cyclohexylpiperidine derived cyclic urea, oxazolidinones, and sulfonamide based privileged structures are disclosed.
SUBSTITUTED PIPERIDINES AS MELANOCORTIN RECEPTOR AGONISTS
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Page 29, (2008/06/13)
Certain novel 4-substituted piperidine compounds 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.
