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BMS-470539 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。
BMS-470539 dihydrochloride图片
CAS NO:2341796-82-3
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
200mg电议

产品介绍
BMS-470539 dihydrochloride 是一种高效的选择性黑皮质素 1 受体 (MC-1 R) 激动剂,IC50为 120 nM,EC50为 28 nM。BMS-470539 dihydrochloride 不激活 MC-3R,并且对 MC-4R 和 MC-5R 的激活活性非常弱。BMS-470539 dihydrochloride 具有强效的抗炎特性。
生物活性

BMS-470539 dihydrochloride is a highly potent and selectivemelanocortin-1 receptor (MC-1R)agonist with anIC50of 120 nM, anEC50of 28 nM. BMS-470539 dihydrochloride does not activate MC-3R and is a very weak partial agonist at MC-4R and MC-5R. BMS-470539 dihydrochloride has potently anti-inflammatory properties[1][2][3].

IC50& Target

IC50: 120 nM (Melanocortin-1 receptor); EC50: 28 nM (Melanocortin-1 receptor)[1]

体外研究
(In Vitro)

An HBL melanoma cell line is established that stably expresses a NF-κB luciferase reporter. In these cells, 0.5 ng/mL TNF-α induces a dose-dependent increase in NF-κB luciferase activity. Treatment of HBL-NF-κB cells with BMS-470539 elicits a dose-dependent, statistically significant reduction in TNF-α-stimulated NF-κB luciferase activity. BMS-470539 has no effect on luciferase reporter activity in the absence of TNF-α stimulation. In nontransfected HBL cells, treatment with BMS-470539 results in a dose-dependent inhibition of NF-B nuclear translocation[2].

体内研究
(In Vivo)

BMS-470539 (2.05-18.47 mg/kg; intravenous injection; for 125 minutes; WT and MC1 receptor recessive e/e mice) treatment inhibits cell adhesion and emigration with no effect on cell rolling. And also inhibits the tissue expression of both CXCL1 and CCL2[3].

Animal Model:Wild-type (WT) and MC1 receptor recessive e/e mice induced with ischaemia-reperfusion[3]
Dosage:2.05 mg/kg, 6.16 mg/kg and 18.47 mg/kg
Administration:Intravenous injection; for 125 minutes
Result:Inhibited cell adhesion and emigration with no effect on cell rolling. Inhibited tissue expression of both CXCL1 and CCL2.
分子量

632.62

性状

Solid

Formula

C32H43Cl2N5O4

CAS 号

2341796-82-3

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

溶解性数据
In Vitro: 

DMSO : ≥ 125 mg/mL(197.59 mM)

H2O : ≥ 100 mg/mL(158.07 mM)

*"≥" means soluble, but saturation unknown.

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM1.5807 mL7.9036 mL15.8073 mL
5 mM0.3161 mL1.5807 mL3.1615 mL
10 mM0.1581 mL0.7904 mL1.5807 mL
*

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
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month (sealed storage, away from moisture)。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。