HSP27 inhibitor J2 (Synonyms: J2)
目录号: PL02693 纯度: ≥99%
CAS No. :2133499-85-9
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中文名称
HSP27 inhibitor J2
英文名称
HSP27 inhibitor J2
英文别名
HSP27 inhibitor J2;5-Hydroxy-2-methyl-7-(thiiran-2-ylmethoxy)-4H-chromen-4-one;J2
Cas No.
2133499-85-9
分子式
C13H12O4S
分子量
264.30
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
HSP27 inhibitor J2 (J2) 是一种 HSP27 抑制剂,其显著诱导异常 HSP27 二聚体形成并抑制 HSP27 巨聚合物的产生,从而具有抑制 HSP27 的伴侣功能和降低其细胞保护功能的作用。HSP27 inhibitor J2 (J2) 显著增强 17-AAG 的抗增殖活性,并对顺铂诱导的肺癌细胞生长抑制具有敏感性。
生物活性
HSP27 inhibitor J2 (J2) is a HSP27 inhibitor, which significantly induces abnormal HSP27 dimer formation and inhibits a production of HSP27 giant polymers, thereby having an effect of inhibiting a chaperone function of the HSP27 and reducing a cell protection function thereof. HSP27 inhibitor J2 (J2) remarkably enhances the antiproliferative activity of 17-AAG and sensitizes cisplatin-induced lung cancer cell growth inhibition.
性状
Solid
IC50 & Target[1][2]
HSP27
体外研究(In Vitro)
HSP27 inhibitor J2 (10 μM; 12 h) induces significant abnormal HSP27 dimer formation in NCI-H460.
HSP27 inhibitor J2 (10 μM; 24 h) increases 17-AAG-induced apoptosis in shCTRL cells. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Hwang SY, et al. Synthesis and biological effect of chrom-4-one derivatives as functional inhibitors of heat shockprotein 27. Eur J Med Chem. 2017 Oct 20;139:892-900.
[2]. Younghwa Na, et al. Methods for treating pulmonary fibrosis using chromenone derivatives.
溶解度数据
In Vitro: DMSO : 20 mg/mL (75.67 mM; Need ultrasonic)配制储备液
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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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