T-10418 is a potent and highly selective G2A/GPR132 agonist. T-10418 has an EC50 of 0.82 µM for human G2A activation. T-10418 has good water solubility, metabolic stability, and pharmacokinetic properties. T-10418 can be used for the research of various diseases such as neuropathic pain, acute myeloid leukemia, and inflammation[1].
Molekulargewicht:
376.41
Reinheit:
99.78
CAS Nummer:
[1608784-68-4]
Formel:
C22H20N2O4
Target-Kategorie:
G2A (GPR132)
Anwendungsbeschreibung:
Reference compound
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