MSG606 TP2002
Specifications
| 1mg/5mg/10mg/25mg/50mg/100mg |
Bioactivity:
Potent human MC1 receptor antagonist (IC50 = 17 nM). Also partial agonist at human MC3 and MC5 receptors (EC50 values are 59 and 1300 nM, respectively). Exhibits binding affinity for A375 melanoma cells in vitro. Reverses morphine-induced hyperalgesia in
CAS nr:
1416983-77-1
Purity:
98%
Molecular Weight:
1347,51
SMILES:
Formula:
C62H82N20O13S
Pathway:
Target:
