CAS NO: | 139290-65-6 |
生物活性 | Volinanserin is a potent and selective antagonist of5-HT2receptor, with aKiof 0.36 nM, and shows 300-fold selectivity for5-HT2receptorover 5-HT1c, alpha-1 and DA D2receptors. Volinanserin has antipsychotic activity. | ||||||||||||||||
IC50& Target |
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体外研究 (In Vitro) | Volinanserin (MDL 100907) is a potent antagonist at the 5-HT2receptor, with a Kiof 0.36 nM, and shows 300-fold selectivity for 5-HT2receptor over 5-HT1creceptor, alpha-1 and DA D2receptors. Volinanserin has antipsychotic activity[1]. | ||||||||||||||||
体内研究 (In Vivo) | Volinanserin (MDL 100907; 0.008-2.0 mg/kg, i.p.) significantly decreases d-amphetamine-stimulated locomotor activity in mice, with an ED50of 0.3 mg/kg, but shows no obvious reduction in the base-line locomotor activity in mice. Volinanserin produces atalepsy with an ED50of 10-50 mg/kg in rats. Volinanserin does not reduces apomorphine-induced stereotypies or produces catalepsy in rats[1]. Volinanserin (M100907) combined with MK-801 significantly decreases reinforcers at 1 μg/kg, but dose-dependently (10, 100 μg/kg) antagonizes the disruptive effect of MK-801 in rats via i.p. administration. Volinanserin (6.25 μg/kg) enhances the antidepressant-like action of desipramine in rats performing under a DRL 72-s schedule, and elevates the antidepressant-like effect of tranylcypromine[2]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 373.46 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C22H28FNO3 | ||||||||||||||||
CAS 号 | 139290-65-6 | ||||||||||||||||
中文名称 | 氟利色林 | ||||||||||||||||
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(133.88 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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