Imatinib Impurity E,96.05%
产品编号:Bellancom-131275| CAS NO:1365802-18-1| 分子式:C52H48N12O2| 分子量:873.02
本网站销售的所有产品仅用于工业应用或者科学研究等非医疗目的,不可用于人类或动物的临床诊断或者治疗,非药用,非食用,
Imatinib Impurity E
产品介绍 | Imatinib Impurity E 是 Imatinib 的杂质。Imatinib 是一种口服生物可用的酪氨酸激酶抑制剂,可选择性抑制 BCR/ABL,v-Abl,PDGFR,c-kit 激酶活性。Imatinib (STI571) 靠近 ATP 结合位点结合,将其锁定在封闭或自我抑制的构象中,因此半竞争性抑制蛋白质的酶活性。Imatinib 还抑制 SARS-CoV 和 MERS-CoV。 | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
生物活性 | Imatinib Impurity E is the impurity of Imatinib. Imatinib is an orally bioavailable tyrosine kinases inhibitor that selectively inhibits BCR/ABL, v-Abl, PDGFR and c-kit kinase activity. Imatinib (STI571) works by binding close to the ATP binding site, locking it in a closed or self-inhibited conformation, therefore inhibiting the enzyme activity of the protein semicompetitively[4]. Imatinib also is an inhibitor of SARS-CoV and MERS-CoV[5]. | ||||||||||||
体外研究 | |||||||||||||
体内研究 | |||||||||||||
体内研究 | |||||||||||||
性状 | Solid | ||||||||||||
溶解性数据 | |||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||
储存方式 |
| ||||||||||||
参考文献 |
|