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X-376

    
10mM in DMSO

X-376

源叶(MedMol)
T95744 一键复制产品信息
1365267-27-1
C25H25Cl2FN6O3
547.41
3-​Pyridazinecarboxamid​e,6-​amino-​5-​[(1R)​-​1-​(2,​6-​dichloro-​3-​fluorophenyl)​ethoxy]​-​N-​[4-​[(4-​methyl-​1-​piperazinyl)​carbonyl]​phenyl]​-
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
T95744-1ml促销
10mM in DMSO

¥206.00 ¥185.00

4 - - - -
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: ALK抑制剂;ALK Inhibitors;;InformationX-376 X-376 is an ALK inhibitor and potentially useful in non-small cell lung cancer.TargetsALK
体内研究: The effects of X-376 in vivo against H3122 xenografts are examined. A pharmacokinetic study reveals that X-376 shows substantial bioavailability and moderate half-lives in vivo. Nude mice harboring H3122 xenografts are treated with X-376 at 50 mg/kg bid. X-376 significantly delays the growth of tumors compared to vehicle alone. In the xenograft experiments, X-376 appears well-tolerated in vivo. Mouse weight is unaffected by X-376 treatment. Drug-treated mice appear healthy and do not display any signs of compound related toxicity. To further assess potential side effects of X-376, additional systemic toxicity and toxico-kinetic studies are performed in Sprague Dawley (SD) rats. Following 10 days of repeated oral administration of X-376 at 25, 50, 100 mg/kg in SD rats, all animals survive to study termination. The no significant toxicity (NST) levels are determined to be 50 mg/kg for X-376. At NST levels, X-376 achieves an AUC of 41 μM×hr and a Cmax of 5.04 μM.
参考文献: 1. Lovly CM, et al. Insights into ALK-driven cancers revealed through development of novel ALK tyrosine kinaseinhibitors. Cancer Res. 2011 Jul 15;71(14):4920-31.
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 1.827 ml 9.134 ml 18.268 ml
5 mM 0.365 ml 1.827 ml 3.654 ml
10 mM 0.183 ml 0.913 ml 1.827 ml
50 mM 0.037 ml 0.183 ml 0.365 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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