CAS NO: | 179248-59-0 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
2mg | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | Src Inhibitor1 is a potent, ATP-competitive and selective dual siteSrctyrosine kinase inhibitor withIC50values of 44 nM forSrcand 88nM for Lck. | ||||||||||||||||
IC50& Target | IC50: 44 nM (Src), 88 nM (Lck)[1] | ||||||||||||||||
体外研究 (In Vitro) | Src-I1 is competitive with both ATP and peptide binding sites of the kinase. The IC50values 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]. | ||||||||||||||||
分子量 | 373.40 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C22H19N3O3 | ||||||||||||||||
CAS 号 | 179248-59-0 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 9.09 mg/mL(24.34 mM;Need ultrasonic) 配制储备液
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