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AZD7507

    
≥99%

4-(2-fluoro-4-methylanilino)-6-[4-(2-hydroxyethyl)piperazin-1-yl]-7-methoxycinnoline-3-carboxamide

源叶(MedMol)
Y65384 一键复制产品信息
1041852-85-0
C23H27FN6O3
454.5
AZD-7507; AZD 7507.
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
Y65384-5mg
≥99%

¥990.00

货期:3-5天 - - - -
Y65384-10mg
≥99%

¥1590.00

货期:3-5天 - - - -
Y65384-25mg
≥99%

¥2940.00

货期:3-5天 - - - -
Y65384-100mg
≥99%

¥5560.00

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: AZD7507 is a potent and orally active CSF-1R inhibitor, with antitumor activity.
靶点: CSF-1R;CSF-1R; HER; SodiumChannel
体外研究: AZD7507 (Compound 31) inhibits the proliferation of 3T3 cells engineered to express CSF-1R and stimulated with CSF-1 (IC50, 32 nM), shows inhibitory activity against hERG and NaV1.5, with IC50s of >30 and 26 μM
体内研究: AZD7507 has good rat oral PK, with in vivo clearance of 7 mL/min/kg and 42% bioavailability. In the canine L-type Ca channel assay, the IC50 is >20 μM[1]. AZD7507 significantly decreases the number of CD68+ macrophages in mice, and also reduces the volume and mass in mice bearing CC-LP-1 and SNU-1079 cells, but not WITT-1 cells
参考文献: 1. Scott DA, et al. Mitigation of cardiovascular toxicity in a series of CSF-1R inhibitors, and the identification of AZD7507. Bioorg Med Chem Lett. 2013 Aug 15;23(16):4591-6.
2. Boulter L, et al. WNT signaling drives cholangiocarcinoma growth and can be pharmacologically inhibited. Send to J Clin Invest. 2015 Mar 2;125(3):1269-85.
溶解性: Soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.2 ml 11.001 ml 22.002 ml
5 mM 0.44 ml 2.2 ml 4.4 ml
10 mM 0.22 ml 1.1 ml 2.2 ml
50 mM 0.044 ml 0.22 ml 0.44 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

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