中文名称: SCH23390 HCL 促销
英文名称: SCH23390 HCL
CAS No: 125941-87-9
分子式: C17H18ClNO.HCl
分子量: 324.24
S10501 SCH23390 HCL ≥98% (psaitong)
包装规格:
5mg 10mg 25mg 100mg in glass bottle
溶解性:
溶于DMS0(≥30mg/mL)
产品描述:

基本信息

产品编号:

S10501

产品名称:

SCH23390 HCL

CAS:

125941-87-9

 

储存条件

粉末

-20℃

四年

 

 

分子式:

C17H18ClNO.HCl

溶于液体

-80℃

6个月

分子量:

324.24

-20℃

1个月

化学名: 

(R)-8-氯-2,3,4,5-四氢-3-甲基-5-苯基-1H-3-苯并氮杂卓-7-醇盐酸盐(R)-2,3,4,5-Tetrahydro-8-chloro-3-methyl-5-phenyl-1H-3-benzazepin-7-ol hydrochloride

Solubility (25°C):

 

体外:

 

DMSO

65mg/mL (200.46mM)

Ethanol

25mg/mL (77.1mM)

Water

20mg/mL (61.68mM)

体内(现配现用):

 

1mg/ml表示微溶或不溶。

普西唐提供的所有化合物浓度为内部测试所得,实际溶液度可能与公布值有所偏差,属于正常的批间细微差异现象。

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;⼀旦配成溶液,请分装保存,避免反复冻融造成的产品失效。

 

制备储备液

 

浓度

 

溶液体积

质量

 

1mg

 

5mg

 

10mg

1mM

3.0841mL

15.4207mL

30.8414mL

5mM

0.6168mL

3.0841mL

6.1683mL

10mM

0.3084mL

1.5421mL

3.0841mL

50mM

0.0617mL

0.3084mL

0.6168mL

 

生物活性

产品描述

一种有效的选择性的多巴胺D1样受体拮抗剂。

靶点

Dopamine Receptor

5-HT Receptor

Potassium Channel

 

体外研究

SCH-23390 (1μM) treatment reverses the inhibitory effects of Isosibiricin on NLRP3 expression and the cleavages of caspase1 and IL-1β in the LPS-induced BV-2 cells.SCH-23390 could reverse the Isosibiricin-mediated inhibition of the NLRP3/caspase-1 inflammasome pathway.SCH-23390 can abolish generalized seizures evoked by the chemoconvulsants.SCH-23390 has also been used in studies of other neurological disorders in which the dopamine system has been implicated,such as psychosis and Parkinson's disease.Apart from the study of neurological disorders,SCH-23390 has been extensively used as a tool in the topographical determination of brain D1 receptors in rodents,nonhuman primates,and humans.SCH-23390 is a very short-acting compound with an elimination half-life of around 25 min following administration of 0.3mg/kg i.p.in the rat.SCH-23390 augments dopamine-induced ductus constriction in CD-1 mouse vessels under newborn O2 conditions.

体内研究

SCH-23390 can abolish generalized seizures evoked by the chemoconvulsants.SCH-23390 has also been used in studies of other neurological disorders in which the dopamine system has been implicated,such as psychosis and Parkinson's disease.Apart from the study of neurological disorders,SCH-23390 has been extensively used as a tool in the topographical determination of brain D1 receptors in rodents,nonhuman primates, and humans.SCH-23390 is a very short-acting compound with an elimination half-life of around 25 min following administration of 0.3mg/kg i.p.in the rat.SCH-23390 augments dopamine-induced ductus constriction in CD-1 mouse vessels under newborn O2 conditions.

 

推荐实验方法(仅供参考)

Rats: All rats receive acclimatization saline injections the two afternoons 1 prior to 2 their test day.At the end of the Training phase,rats (n=15 or 16 rats/group) are assigned to one 3 of three conditions (0,1,or 10μg/kg IP injections of SCH 23390).The day following the Training phase,rats are tested in the operant 6 conditioning chambers for saccharin cue-reactivity (saccharin seeking).

保存条件:
-20℃
UN码:
HazardClass:
危害声明:
安全说明:
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参考文献 & 客户发表文献

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质量 (g) = 浓度 (mol/L) x 体积 (L) x 分子量 (g/mol)

摩尔浓度计算公式

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稀释公式

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    C2=C1/X C2: LOG(C2):
    C3=C2/X C3: LOG(C3):
    C4=C3/X C4: LOG(C4):
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    C6=C5/X C6: LOG(C6):
    C7=C6/X C7: LOG(C7):
    C8=C7/X C8: LOG(C8):