H2L 5765834 is an antagonist of lysophosphatidic acid receptors LPA1, LPA3, and LPA5, with IC50s of 94, 752, and 463 nM respectively.
性状
Solid
IC50 & Target[1][2]
LPA3 Receptor
752 nM (IC50)
LPA5 Receptor
463 nM (IC50)
LPA1 Receptor
94 nM (IC50)
体外研究(In Vitro)
H2L 5765834 displays no effect on LPA2 or LPA4 receptors.
H2L 5765834 inhibits LPA-induced platelet shape change with an IC50 of 13.73±2.52 μM.
Medlife has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
H2L 5765834 (20 mg/kg; i.p.) could not affect the LPA-induced decrease of alanine transaminase (ALT) in the acetaminophen (APAP) overdose-induced acute liver injury model.
Medlife has not independently confirmed the accuracy of these methods. They are for reference only.