Src Inhibitor 1

Src Inhibitor 1 (Src Kinase Inhibitor 1) 是一种选择性的、高效的、ATP-竞争性的双位点 Src 酪氨酸激酶抑制剂,能够抑制 Src (IC50:44 nM) 和 Lck (IC50:88 nM)。

CAS号

179248-59-0

分子式

C22H19N3O3

主要靶点

Src

仅限科研使用

Cat No : CM06527

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Synonyms

Src Kinase Inhibitor 1|Src-l1



产品信息

Src Inhibitor 1 is a potent and selective dual site Src tyrosine kinase inhibitor.

CAS号 179248-59-0
分子式 C22H19N3O3
主要靶点 Src
主要通路 蛋白酪氨酸激酶|血管生成
分子量 373.4
纯度 100.00%, 此纯度可做参考,具体纯度与批次有关系,可咨询客服
储存条件 Powder: -20°C for 3 years | In solvent: -80°C for 1 year
别名 Src Kinase Inhibitor 1|Src-l1

靶点活性

Lck:88nM|Src:44 nM

体外活性

Src-I1 is competitive with both ATP and peptide binding sites of the kinase. The IC50 values are 44 and 88 nM for Src and Lck, respectively[1]. Src-I1, is found to be a potent inhibitor of Src (IC50=0.18 μM), but also inhibited other Src family members, such as Lck, Csk and Yes with similar potency to Src, and RIP2 (IC50=0.026 μM) with even greater potency. In addition, it inhibited CHK2 with similar potency to Src, and Aurora B with slightly lower potency[2].

溶解度

DMSO:6.2 mg/mL

参考文献

1.Tian G, et al. Structural determinants for potent, selective dual site inhibition of human pp60c-src by 4-anilinoquinazolines. Biochemistry. 2001 Jun 19;40(24):7084-91.
2.Bain J, et al. The selectivity of protein kinase inhibitors: a further update. Biochem J. 2007 Dec 15;408(3):297-315.

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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
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