Optimization of a privileged structure leading to potent and selective human melanocortin subtype-4 receptor ligands
- Bioorg Med Chem Lett. 2006 Mar 1;16(5):1130-3. doi: 10.1016/j.bmcl.2005.11.095.
Affiliations
- 1. Department of Medicinal Chemistry, Merck Research Laboratories, Rahway, NJ 07065-0900, USA. [email protected]
PMID: 16364639
DOI: 10.1016/j.bmcl.2005.11.095
Abstract
Design and synthesis of potent MC4 selective agonists based on cyclohexylpiperidine derived cyclic urea, oxazolidinones, and sulfonamide based privileged structures are disclosed.