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cis-(Z)-Flupentixol dihydrochloride
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
cis-(Z)-Flupentixol dihydrochloride图片
CAS NO:51529-01-2

盐酸氟哌噻吨
cis-(Z)-Flupenthixol dihydrochloride
cis-(Z)-Flupentixol dihydrochloride 是有效、选择性的多巴胺DA D1/D2受体的拮抗剂,其对D2 受体和5-HT2AKi值分别为 0.38 nM 和 7 nM。
生物活性

cis-(Z)-Flupentixol dihydrochloride is a potent and selectiveDA D1/D2 receptorantagonist, withKivalues of 0.38 nM and 7 nM for D2 receptor and5-HT2A, respectively[1][2].

IC50& Target[2]

D2Receptor

 

D2Receptor

0.38 nM (Ki)

5-HT2AReceptor

7 nM (Ki)

体内研究
(In Vivo)

cis-(Z)-Flupentixol (0.25, or 0.5 mg/kg, i.p.) pretreatment dose-dependently reduces cocaine-induced activity[1].

Animal Model:Rats[1].
Dosage:0.125, 0.25, or 0.5 mg/kg.
Administration:IP.
Result:Reduced cocaine-induced activity.
分子量

507.44

Formula

C23H27Cl2F3N2OS

CAS 号

51529-01-2

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

溶解性数据
In Vitro: 

DMSO : 62.5 mg/mL(123.17 mM;Need ultrasonic)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM1.9707 mL9.8534 mL19.7068 mL
5 mM0.3941 mL1.9707 mL3.9414 mL
10 mM0.1971 mL0.9853 mL1.9707 mL
 
 
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