JMS 17-2 hydrochloride

Pricing Availability   Qty
说明: CX3CR1 antagonist
化学名: 5-[3-[4-(4-Chlorophenyl)-1-piperidinyl]propyl]pyrrolo[1,2-a]quinoxalin-4(5H)-one hydrochloride
纯度: ≥98% (HPLC)
说明书
引用文献
评论
文献 (1)

生物活性 for JMS 17-2 hydrochloride

JMS 17-2 hydrochloride is a chemokine CX3CR1 (fractalkine receptor) antagonist. Inhibits fractalkine-induced ERK phosphorylation and decreases migration of breast cancer cells in vitro. Also inhibits circulating tumor cells from seeding into bone and reduces overall tumor burden in a breast cancer metastasis model.

许可信息

Sold under license from Drexel University.

化合物库 for JMS 17-2 hydrochloride

JMS 17-2 hydrochloride is also offered as part of the Tocriscreen Antiviral Library. 了解 Tocris 化合物库的更多信息。

技术数据 for JMS 17-2 hydrochloride

分子量 456.41
公式 C25H26ClN3O.HCl
储存 Desiccate at RT
纯度 ≥98% (HPLC)
CAS Number 2341841-07-2
Smiles ClC1=CC=C(C2CCN(CC2)CCCN3C(C4=CC=CN4C5=CC=CC=C35)=O)C=C1.Cl

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

溶解性数据 for JMS 17-2 hydrochloride

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 45.64 100
ethanol 22.82 50

制备储备液 for JMS 17-2 hydrochloride

以下数据基于产品分子量 456.41。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
1 mM 2.19 mL 10.96 mL 21.91 mL
5 mM 0.44 mL 2.19 mL 4.38 mL
10 mM 0.22 mL 1.1 mL 2.19 mL
50 mM 0.04 mL 0.22 mL 0.44 mL

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产品说明书 for JMS 17-2 hydrochloride

参考文献 for JMS 17-2 hydrochloride

参考文献是支持产品生物活性的出版物。

Shen et al (2016) Novel small-molecule CX3CR1 antagonist impairs metastatic seeding and colonization of breast cancer cells. Mol. Cancer Res. 14 518 PMID: 27001765


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关键词: JMS 17-2 hydrochloride, JMS 17-2 hydrochloride supplier, JMS17-2, hydrochloride, HCl, 1380392-05-1, fractalkine, receptor, antagonists, antagonism, cx3cr1, chemokines, Other, Chemokine, Receptors, 6378, Tocris Bioscience

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