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JI-101

    
99.80%

JI-101

源叶(MedMol)
S87149 一键复制产品信息
900573-88-8
C22H20BrN5O2
466.33
1-[1-[(2-氨基吡啶-4-基)甲基]-1H-吲哚-4-基]-3-(5-溴-2-甲氧基苯基)脲
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S87149-5mg买3赠1
99.80%

¥430.00

8 - - - -
S87149-10mg促销
99.80%

¥690.00 ¥552.00

5 - - - -
S87149-50mg促销
99.80%

¥2090.00 ¥1670.00

2 - - - -
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: JI-101 is an orally available multi-kinase inhibitor of VEGFR2, PDGFRβ and EphB4 with potent anti-cancer activity.
靶点: VEGFR2;PDGFRβ;VEGFR;PDGFR;EphrinReceptor
体内研究: JI-101excreted through bile along with its mono- and di-hydroxy metabolites. Following oral administration, JI-101 is rapidly absorbed, reaching Cmax within 2 h. The t1/2 of JI-101 with intravenous and oral route is found to be 1.75±0.79 and 2.66±0.13 h, respectively. The Cl and Vd by intravenous route for JI-101 are found to be 13.0±2.62 mL/min/kg and 2.11±1.42 L/kg, respectively. The tissue distribution of JI-101 is extensive with rapid and preferred uptake into lung tissue. Overall, the oral bioavailability of JI-101 is 55% and the primary route of elimination for JI-101 is feces
参考文献: 1. Gurav SD, et al. Pharmacokinetics, tissue distribution and identification of putative metabolites of JI-101 - a novel triple kinase inhibitor in rats. Arzneimittelforschung. 2012 Jan;62(1):27-34.
溶解性: Soluble  in  DMSO
保存条件: -20°C,避光
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.144 ml 10.722 ml 21.444 ml
5 mM 0.429 ml 2.144 ml 4.289 ml
10 mM 0.214 ml 1.072 ml 2.144 ml
50 mM 0.043 ml 0.214 ml 0.429 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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批号:JS298415 货号:S20001-25g
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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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