| Literature DB >> 29578343 |
Mark D Ericson, Anamika Singh1, Srinivasa R Tala1, Erica M Haslach1, Marvin L S Dirain1, Jay W Schaub1, Viktor Flores1, Natalie Eick1, Cody J Lensing, Katie T Freeman, Branden A Smeester, Danielle N Adank, Stacey L Wilber, Robert Speth2,3, Carrie Haskell-Luevano1.
Abstract
β-Defensin 3 (BD3) was identified as a ligand for the melanocortin receptors (MCRs) in 2007, although the pharmacology activity of BD3 has not been clearly elucidated. Herein, it is demonstrated that human BD3 and mouse BD3 are full micromolar agonists at the MCRs. Furthermore, mouse β-defensin 1 (BD1) and human BD1 are also MCR micromolar agonists. This work identifies BD1 as an endogenous MCR ligand and clarifies the controversial role of BD3 as a micromolar agonist.Entities:
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Year: 2018 PMID: 29578343 PMCID: PMC6007841 DOI: 10.1021/acs.jmedchem.8b00251
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446