CAS NO: | 192703-06-3 |
生物活性 | SR144528 is a potent and selectiveCB2receptorantagonist with aKiof 0.6 nM. | ||||||||||||||||
IC50& Target | Ki: 0.6 nM (CB2 receptor)[1] | ||||||||||||||||
体外研究 (In Vitro) | SR144528 is a potent and selective CB2 receptor antagonist with a Kiof 0.6 nM. SR144528 alone is able to stimulate in a concentration-dependent manner (EC50=26±6 nM, two experiments) the forskolin-sensitive adenylyl cyclase activity in CHO-CB2 cells with a maximum effect at 1 μM (4-fold stimulation) whereas at this concentration it has no significant effect on CHO-CB1 cells (15% inhibition)[1]. Raw 264.7 macrophages supplemented with SR144528 display reduced caspase-3 activity. SR144528 inhibits microsomal acyl-coenzymeA:cholesterol acyltransferase (ACAT) activity in a concentration-dependent manner with an IC50value of 3.6±1.1 μM. At 10 μM, SR144528 inhibits ACAT activities ~68%[2]. | ||||||||||||||||
体内研究 (In Vivo) | No effect on the binding of [3H]-CP 55,940 to its specific sites in the brain is observed after either oral (up to 10 mg/kg) or i.c.v. (10 μg/animal) administration of SR144528 in mice. The occupancy by SR144528 of the spleen cannabinoid receptor is time-dependent and significant for at least 18 hours after oral administration at 3 mg/kg[1]. SR144528 does not induce any significant effect on gastrointestinal (GI) motility when given alone. SR144528 does not block but enhances delayedgastric emptying[3]. | ||||||||||||||||
分子量 | 476.05 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C29H34ClN3O | ||||||||||||||||
CAS 号 | 192703-06-3 | ||||||||||||||||
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 : 50 mg/mL(105.03 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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