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Plerixafor octahydrochloride
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。
Plerixafor octahydrochloride图片
CAS NO:155148-31-5
包装与价格:
包装价格(元)
10 mM * 1 mL in Water电议
10mg电议
50mg电议
100mg电议
200mg电议
500mg电议

产品名称
盐酸普乐沙福
AMD3100 octahydrochloride
JM3100 octahydrochloride
SID791 octahydrochloride
产品介绍
Plerixafor octahydrochloride (AMD3100 octahydrochloride) 是一种选择性的CXCR4拮抗剂,IC50为 44 nM。
生物活性

Plerixafor octahydrochloride (AMD3100 octahydrochloride) is a selectiveCXCR4antagonist with anIC50of 44 nM.

IC50& Target

125I-CXCL12-CXCR4

44 nM (IC50)

125I-CXCL12-CXCR7

 

HIV-1

1-10 nM (EC50)

HIV-2

1-10 nM (EC50)

体外研究
(In Vitro)

The CXCR4 inhibitor Plerixafor (AMD3100) is a potent inhibitor of CXCL12-mediated chemotaxis (IC50, 5.7 nM) with a potency slightly better than its affinity for CXCR4. Treating the cells with CCX771 or CXCL11 has no effect on CXCL12-mediated MOLT-4 or U937 TEM. In contrast, 10 μM Plerixafor inhibits CXCL12-mediated TEM in both cells lines[1]. Plerixafor (10 μM)-treated cells show a moderate reduction in cell proliferation compared to CXCL12-stimulated cells, which do not reach statistical significance[2].

体内研究
(In Vivo)

Plerixafor (2 mg/kg) administration to UUO mice exacerbates renal interstitial T cell infiltration, resulting in increased production of the pro-inflammatory cytokines IL-6 and IFN-γ and decreased expression of the anti-inflammatory cytokine IL-10[3]. Both perivascular and interstitial fibrosis are significantly reduced by the CXCR4 antagonist, Plerixafor (AMD3100) at 8 weeks[4]. LD50, mouse, SC: 16.3 mg/kg; LD50, rat, SC: >50 mg/kg; LD50, mouse and rat, IV injection: 5.2 mg/kg.

Clinical Trial
分子量

794.47

性状

Solid

Formula

C28H62Cl8N8

CAS 号

155148-31-5

中文名称

盐酸普乐沙福; 普乐沙福盐酸盐

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°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: 

H2O : 100 mg/mL(125.87 mM;Need ultrasonic)

DMSO :< 1 mg/mL(insoluble or slightly soluble)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM1.2587 mL6.2935 mL12.5870 mL
5 mM0.2517 mL1.2587 mL2.5174 mL
10 mM0.1259 mL0.6294 mL1.2587 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。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: PBS

    Solubility: 120 mg/mL (151.04 mM); Clear solution; Need ultrasonic

*以上所有助溶剂都可在本网站选购。