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Plerixafor 8HCl (AMD3100 8HCl). (Synonyms: 盐酸普乐沙福; AMD3100 octahydrochloride; JM3100 octahydrochloride; SID791 octahydrochloride)
目录号: PC10732 纯度: ≥98%
CAS No. :155148-31-5
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中文名称
Plerixafor 8HCl (AMD3100 8HCl).
中文别名
1,1'-[1,4-亚苯基双(亚甲基)]双[1,4,8,11-四氮杂环十四烷];1,1''-[1,4-亚苯基双(亚甲基)]双[1,4,8,11-四氮杂环十四烷];(R)-2,3-二甲基丁酸;AMD 3100辛基盐酸盐;普乐沙福;普乐沙福盐酸盐;普乐沙福盐酸盐标准品;盐酸普乐沙福;普乐沙福HCL;盐酸普瑞克沙因;普乐沙福八盐酸盐
英文名称
Plerixafor 8HCl (AMD3100 8HCl)
英文别名
1,1'-[1,4-Phenylenebis(methylene)]bis[1,4,8,11-tetraazacyclotetradecane];AMD 3100;AMD 3100 octahydrochloride;AMD3100 octahydrochloride hydrate;Plerixafor;Plerixafor (hydrochloride hydrate);Plerixafor 8HCl;Plerixafor 8HCl (AMD3100 8HCl);Plerixafor Hydrochlo;Plerixafor octahydrochloride (AMD 3100 octahydrochloride, JM 3100 , SID-791,Mozobil® );1,4,8,11-Tetraazacyclotetradecane (1,1'-[1,4-phenylenebis(methylene)]bis;AMD 3100 octahydrochloride,1,1'-[1,4-Phenylenebis-(methylene)]-bis-(1,4,8,11-tetraazacyclotetradecane)octahydrochloride;JM3100 octahydrochloride;SID791 octahydrochloride;SID791;JM3100;Bicyclam;BISCYCLAM;AMD3100 HCl;JM 3100 8HCl;AMD3100 8HCl;Plerixafor hcl;Plerixafor octahydrochloride
Cas No.
155148-31-5
分子式
C28H54N8.8[HCl].2[H2O]
分子量
830.50
包装储存

4°C, sealed storage, away from moisture

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

生物活性

Plerixafor octahydrochloride (AMD3100 octahydrochloride) is a selective CXCR4 antagonist with an IC50 of 44 nM.

性状

Solid

IC50 & Target[1][2]

I-CXCL12-CXCR4

44 nM (IC50)

I-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. Plerixafor (10 μM)-treated cells show a moderate reduction in cell proliferation compared to CXCL12-stimulated cells, which do not reach statistical significance.

Medlife has not independently confirmed the accuracy of these methods. They are for reference only.

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. Both perivascular and interstitial fibrosis are significantly reduced by the CXCR4 antagonist, Plerixafor (AMD3100) at 8 weeks. LD50, mouse, SC: 16.3 mg/kg; LD50, rat, SC: >50 mg/kg; LD50, mouse and rat, IV injection: 5.2 mg/kg.

Medlife has not independently confirmed the accuracy of these methods. They are for reference only.

运输条件

Room temperature or refrigerated transportation.

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)

ClinicalTrial
参考文献
溶解度数据
体外研究: 

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

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

配制储备溶液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 1.2587 mL 6.2935 mL 12.5870 mL
5 mM 0.2517 mL 1.2587 mL 2.5174 mL
10 mM 0.1259 mL 0.6294 mL 1.2587 mL
*

产品不同,其溶解度不同。建议根据产品选择合适的溶剂配制储备溶液;配成溶液后,建议分装保存,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°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)。-80°C 储存时,建议在 6 个月内使用,-20°C 储存时,建议在 1 个月内使用。

体内研究:

建议根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都建议先按照 体外研究 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.

    建议依照次序添加每种溶剂: PBS

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

*
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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