γ1-MSH is an agonist of the melanocortin MC3 receptor, exhibiting a Ki of 34 nM for the rat MC3 receptor. This compound demonstrates approximately 40-fold selectivity over the MC4 receptor, with a Ki of 1318 nM. γ1-MSH is valuable for research applications exploring the role of melanocortin receptors in metabolic processes and neuroendocrine regulation.
γ1-MSH is an agonist of the melanocortin MC3 receptor, exhibiting a Ki of 34 nM for the rat MC3 receptor. This compound demonstrates approximately 40-fold selectivity over the MC4 receptor, with a Ki of 1318 nM. γ1-MSH is valuable for research applications exploring the role of melanocortin receptors in metabolic processes and neuroendocrine regulation.
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