Structure−Activity Relationships of Novel Cyclic α-MSH/β-MSH Hybrid Analogues That Lead to Potent and Selective Ligands for the Human MC3R and Human MC5R
Author:
Affiliation:
1. Department of Chemistry, University of Arizona, Tucson, Arizona 85721 and Department of Pharmaceutical Chemistry, University of Napoli “Federico II”, Via D. Montesano, 49, 80131 Napoli, Italy
Publisher
American Chemical Society (ACS)
Subject
Drug Discovery,Molecular Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/jm030111j
Reference38 articles.
1. Regulation of the Synthesis of Steroidogenic Enzymes in Adrenal Cortical Cells by ACTH
2. Molecular cloning and expression of the human melanocyte stimulating hormone receptor cDNA
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