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CHR-6494

    
99.60%

CHR-6494

源叶(MedMol)
S82876 一键复制产品信息
1333377-65-3
C16H16N6
292.34
3-(1H-Indazol-5-yl)-N-propylimidazo[1,2-b]pyridazin-6-amine
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S82876-5mg买3赠1
99.60%

¥352.00

5 - - - -
S82876-10mg买3赠1
99.60%

¥664.00

6 - - - -
S82876-50mg买3赠1
99.60%

¥2310.00

2 - - - -
S82876-100mg
≥98%

¥3420.00

货期:2-3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: CHR-6494 is a potent inhibitor of haspin, with an IC50 of 2 nM. CHR-6494 inhibits histone H3T3 phosphorylation. CHR-6494 can be used in the research of cancer
靶点: haspin:2 nM (IC50);Others
体内研究: CHR-6494 (50 mg/kg; i.p. in two cycles of five consecutive days for 15 days) inhibits the growth of tumor and cuases no obvious body weight change in nude mice bearing HCT-116 human colorectal cancer cells. CHR-6494 (20 mg/kg; intraperitoneal injection for 15 consecutive days) inhibits the tumor volume and weight compared with the control group in nude mice bearing MDA-MB-231 xenograft tumors. CHR-6494 (20 mg/kg; intraperitoneal injection for 15 consecutive days) enhances the tumor volume and weight inhibition of MLN8237 (20 mg/kg; p.o.) in vivo
参考文献: 1. Huertas D, et al. Antitumor activity of a small-molecule inhibitor of the histone kinase Haspin. Oncogene. 2012 Mar 15;31(11):1408-18. 2. Han L, et al. Anti-Melanoma Activities of Haspin Inhibitor CHR-6494 Deployed as a Single Agent or in a Synergistic Combination with MEK Inhibitor. J Cancer. 2017 Aug 25;8(15):2933-2943. 3. Chen A, et al. CRISPR/Cas9 screening identifies a kinetochore-microtubule dependent mechanism for Aurora-A inhibitor resistance in breast cancer. Cancer Commun (Lond). 2021 Feb;41(2):121-139.
溶解性: DMSO  :  50  mg/mL  (171.03  mM;  Need  ultrasonic)
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 3.421 ml 17.103 ml 34.207 ml
5 mM 0.684 ml 3.421 ml 6.841 ml
10 mM 0.342 ml 1.71 ml 3.421 ml
50 mM 0.068 ml 0.342 ml 0.684 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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