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139290-65-6

中文名称 139290-65-6
英文名称 (R)-(+)-ALPHA-(2,3-DIMETHOXYPHENYL)-1-[2-(4-FLUORO-PHENYL)ETHYL]-4-PIPERIDINE METHANOL
CAS 139290-65-6
分子式 C22H28FNO3
分子量 373.46
MOL 文件 139290-65-6.mol
更新日期 2024/05/07 11:50:05
139290-65-6 结构式 139290-65-6 结构式

基本信息

中文别名
氟利色林
诺和灵 M100907
VOLINANSERIN MDL 100907 (R构型)
Volinanserin MDL 100907 (R构型)
英文别名
M 100907
MDL100907
R-MDL 100907
VOLINANSERIN
MDL 100907 NEW
MDL100907-L-tartrate
MDL100907 tartrate salt
MDL 100907 (MDL-100907
MDL-100907(Volinanserin)
Volinanserin (MDL100907)

物理化学性质

熔点89-91°C
储存条件-20°C冷冻
储存条件2-8°C
溶解度二甲基亚砜:≥20mg/mL
形态粉末
颜色灰白色至浅棕色

安全数据

危险性符号(GHS)
GHS09
警示词警告
危险性描述H400
防范说明P273
危险品标志N
危险类别码50
安全说明61
危险品运输编号UN 3077 9 / PGIII
WGK Germany3
139290-65-6价格(试剂级)
报价日期产品编号产品名称CAS号包装价格
2024/04/30HY-14940139290-65-6
Volinanserin
139290-65-65mg1100元
2024/04/30HY-14940139290-65-6
Volinanserin
139290-65-610mM * 1mLin DMSO1210元
2024/04/30HY-14940139290-65-6
Volinanserin
139290-65-610mg1760元

常见问题列表

生物活性
Volinanserin (Volinanserin Hydrochloride Salt, MDL100907, M 100907, MDL-100,907)是一种高度选择性的、有效的 5-HT2 receptor 的拮抗剂,其Ki值为0.36 nM。Volananserin 具有治疗精神紊乱的药物活性。
靶点
TargetValue
5-HT2 receptor
(Cell-free assay)
0.36 nM(Ki)
体外研究

Volinanserin (MDL 100907) is a potent antagonist at the 5-HT 2 receptor, with a K i of 0.36 nM, and shows 300-fold selectivity for 5-HT 2 receptor over 5-HT 1c receptor, alpha-1 and DA D 2 receptors. Volinanserin has antipsychotic activity.

体内研究

Volinanserin (MDL 100907; 0.008-2.0 mg/kg, i.p.) significantly decreases d-amphetamine-stimulated locomotor activity in mice, with an ED 50 of 0.3 mg/kg, but shows no obvious reduction in the base-line locomotor activity in mice. Volinanserin produces atalepsy with an ED 50 of 10-50 mg/kg in rats. Volinanserin does not reduces apomorphine-induced stereotypies or produces catalepsy in rats. 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.

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