This MCH analog is a potent hMCH-1R agonist with more than 200-times selectivity with respect to hMCH-2R. Bednarek, MA; et al., J. Biol. Chem., 277, 13821 (2002).
M.W.: 1449.8

This MCH analog is a potent hMCH-1R agonist with more than 200-times selectivity with respect to hMCH-2R. Bednarek, MA; et al., J. Biol. Chem., 277, 13821 (2002).
M.W.: 1449.8