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Hesperadin,抑制剂

    
≥98%

Hesperadin

源叶(MedMol)
S81474 一键复制产品信息
422513-13-1
C29H32N4O3S
516.67
(Z)-N-(2-oxo-3-(phenyl(4-(piperidin-1-ylmethyl)phenylamino)methylene)indolin-5-yl)ethanesulfonamide;Hesperadin
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S81474-5mg促销
≥98%

¥690.00 ¥620.00

10 - 2 - -
S81474-25mg促销
≥98%

¥2730.00 ¥2460.00

8 - - - -
S81474-100mg促销
≥98%

¥8240.00 ¥7410.00

货期:3-5天 - - - -
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: Hesperadin is an ATP competitive indolinone inhibitor of Aurora A and B. Hesperadin inhibits Aurora B with an IC50 of 250 nM. Hesperadin inhibits the growth of Trypanosoma brucei by blocking nuclear division and cytokinesis. Hesperadin also is a broad-spectrum influenza antiviral
靶点: Trypanosoma;Aurora B:250 nM (IC50);InfluenzaVirus; Parasite; AuroraKinase; Autophagy
体内研究: Hesperadin (20 mg/kg/d; i.v.) prolongs the survival of xenograft mice via synergistic effect with temozolomide (TMZ)
参考文献: 1. Neal J, et, al. The cell cycle as a therapeutic target against Trypanosoma brucei: Hesperadin inhibits Aurora kinase-1 and blocks mitotic progression in bloodstream forms. Mol Microbiol. 2009 Apr; 72(2): 442-58. 2. Wahafu A, et, al. Targeting Aurora kinase B attenuates chemoresistance in glioblastoma via a synergistic manner with temozolomide. Pathol Res Pract. 2019 Nov; 215(11): 152617. 3. Hu Y, et, al. Chemical Genomics Approach Leads to the Identification of Hesperadin, an Aurora B Kinase Inhibitor, as a Broad-Spectrum Influenza Antiviral. Int J Mol Sci. 2017 Sep 8;18(9):1929.
溶解性: Soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.935 ml 9.677 ml 19.355 ml
5 mM 0.387 ml 1.935 ml 3.871 ml
10 mM 0.194 ml 0.968 ml 1.935 ml
50 mM 0.039 ml 0.194 ml 0.387 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

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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