CAS NO: | 1446817-84-0 |
生物活性 | Elcubragistat (ABX-1431) is a highly potent, selective, and orally available, CNS-penetrant monoacylglycerol lipase (MAGL) inhibitor with anIC50of 14 nM. | ||||||||||||||||
IC50& Target | IC50: 14 nM (human MGLL)[1] | ||||||||||||||||
体外研究 (In Vitro) | Elcubragistat (ABX-1431) is a potent human MGLL inhibitor (IC50=0.014 μM) with >100-fold selectivity against ABHD6 and >200-fold selectivity against PLA2G7. Elcubragistat inhibits human PC3 cells with an IC50of 0.0022 μM. In the cell-based assay, >100-fold selectivity for MGLL over ABHD6 (IC50=0.253 μM) and PLA2G7 (IC50=494 μM) is maintained[1]. | ||||||||||||||||
体内研究 (In Vivo) | Elcubragistat (ABX-1431) inhibits MGLL activity in rodent brain (ED50=0.5-1.4 mg/kg), increases brain 2-AG concentrations, and suppresses pain behavior in the rat formalin pain model[1]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 507.39 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C20H22F9N3O2 | ||||||||||||||||
CAS 号 | 1446817-84-0 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 125 mg/mL(246.36 mM;Need ultrasonic) 配制储备液
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