PG106 TFA is a potent and selective human melanocortin 3 (hMC3) receptor antagonist (IC50= 210 nM) and has noactivity at hMC4 receptors (EC50=9900 nM) and hMC5 receptor[1].
Molecular Weight:
1122.20
Purity:
99.61
Formula:
C53H70F3N13O11
Target:
Melanocortin Receptor
Application Notes:
Peptides
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