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CAS No. : 179248-59-0
MCE 站:Src Inhibitor 1
产品活性:Src Inhibitor 1是高效选择性的,ATP-竞争性的双位点Src酪氨酸激酶抑制剂,对Src和Lck的IC50值分别为44 nM和88 nM。
研究领域:Protein Tyrosine Kinase/RTK
作用靶点:Src
In Vitro: 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. 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.
相关产品:Bioactive Compound Library Plus | Kinase Inhibitor Library | Protein Tyrosine Kinase Compound Library | Anti-Cancer Compound Library | Reprogramming Compound Library | Anti-Pancreatic Cancer Compound Library | Bosutinib | PP2 | SU6656 | WH-4-023 | Pelitinib | Scutellarein | PP1 | 1-Naphthyl PP1 | 1-NM-PP1 | Lck Inhibitor | RK-24466 | Tolimidone | A-770041 | PP121 | PP58 | PD173955 | MNS | AZM475271 | 7-Hydroxy-4H-chromen-4-one | β-Hydroxyisovalerylshikonin | PD-161570 | UM-164 | CGP77675 | Ac-Tyr(PO3H2)-Glu-Glu-Ile-Glu-OH | Caffeic acid-pYEEIE TFA | Damnacanthal
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更新时间:2024/1/2 10:17:29
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