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VER-50589

    
10mM in DMSO

VER-50589

源叶(MedMol)
T94376 一键复制产品信息
747413-08-7
C19H17ClN2O5
388.8
5-(5-chloro-2,4-dihydroxyphenyl)-N-ethyl-4-(4-methoxyphenyl)-3-isoxazolecarboxamide
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
T94376-1ml促销
10mM in DMSO

¥720.00 ¥648.00

9 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: 一种抑制Hsp90的异恶唑化合物,Hsp90是一种热激蛋白,在分子折叠中起分子伴侣,细胞信号的作用;an isoxazole compound that inhibits Hsp90, a heat shock protein that acts as a molecular chaperone with roles in protein folding, cell signa;VER-50589是一种抑制Hsp90的异恶唑化合物,Hsp90是一种热休克蛋白,在分子折叠,细胞信号转导和癌症中起着分子伴侣的作用。| VER-50589是一种异恶唑化合物,已显示通过抑制Hsp90抑制Hsp90。 IC50值为21 nM。当针对人类癌细胞系进行测试时,它产生的平均细胞抗增殖GI50值为78 nM。与抑制Hsp90一致,VER-50589还显示出诱导HSP27和Hsp72的表达,同时减少了客体蛋白C-RAF,B-RAF,survivin和PRMT5,从而导致细胞周期停滞和凋亡。VER-5;VER-50589 is an isoxazole compound that inhibits Hsp90, a heat shock protein that acts as a molecular chaperone with roles in protein folding, cell signaling, and cancer.|VER-50589 is an isoxazole compound that has been shown to inhibit Hsp90 with an IC50 value of 21 nM. It produces a mean cellular antiproliferative GI50 value of 78 nM when tested against a human cancer cell line panel. Consistent with inhibition of Hsp90, VER-50589 has also been shown to induce the expression of HSP27 and Hsp72 while reducing the client proteins C-RAF, B-RAF, survivin, and PRMT5, causing cell cycle arrest and apoptosis. VER-50589 shows favorable pharmacokinetics and impairs tumor growth in animals. Importantly, glioblastoma cells do not acquire resistance to VER-50589 and resistance to other Hsp90 inhibitors does not produce cross-resistance to VER-50589.
保存条件: -80℃(运输条件:冰袋低温运输)
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.572 ml 12.86 ml 25.72 ml
5 mM 0.514 ml 2.572 ml 5.144 ml
10 mM 0.257 ml 1.286 ml 2.572 ml
50 mM 0.051 ml 0.257 ml 0.514 ml
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参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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