CE-245677
目录号: PL12407 纯度: ≥98%
CAS No. :717899-97-3
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中文名称
CE-245677
中文别名
1-(5-(4-氨基-7-异丙基-7H-吡咯并[2,3-d]嘧啶-5-羰基)-2-甲氧基苯基)-3-(2,4-二氯苯基)脲
英文名称
CE-245677
英文别名
GMH17J9LHL;VFCRSIORGUNNGT-UHFFFAOYSA-N;CE 245677 [WHO-DD];1-[5-(4-Amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-2-methoxy-phenyl]-3-(2,4-dichloro-phenyl)-urea;1-(5-(4-Amino-7-isopropyl-pyrrolo(2,3-d)pyrimidine-5-carbonyl)-2-methoxy-phenyl)-3-(2,4-dichlorophenyl)urea;Urea, N-(5-((4-amino-7-(1-methylethyl)-7H-pyrrolo(2,3-d)pyrimidin-5-yl)carbonyl)-2-methoxyphenyl)-N'-(2,4-dichlorophenyl)-;1-[5-(4-Amino-7-propan-2-ylpyrrolo[2,3-d]pyrimidine-5-carbonyl)-2-methoxyphenyl]-3-(2,4-dichlorophen;CE-245677
Cas No.
717899-97-3
分子式
C24H22Cl2N6O3
分子量
513.38
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
CE-245677 是一种有效的,可逆的 Tie2 和 TrkA/B 抑制剂,在细胞体系下,IC50 值分别为 4.7 和 1 nM。
生物活性
CE-245677 is a potent reversible inhibitor of Tie2 and TrkA/B kinases with a cellular IC 50 s of 4.7 and 1 nM.
性状
Solid
体外研究(In Vitro)
CE-245677 is a potent reversible inhibitor of Tie2 and TrkA/B kinases with a cellular IC50 of 4.7 and 1 nM, and displays >100x selectivity against a number of other angiogenic receptor tyrosine kinases, such as KDR, PDGFR, FGFR. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
CE-245677 shows good oral absorption in in vivo rat PK studies (F=80%). has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Susan LaGreca, et al. Identification of selective, orally active Tie2 kinase inhibitors and discovery of CE-245,677 and PF-371,989. Cancer Research. AACR Annual Meeting-Apr 14-18, 2007.
溶解度数据
In Vitro: DMSO : 125 mg/mL (243.48 mM; Need ultrasonic)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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