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PV1162是一种高选择性的Chk2抑制剂,具有0.29 nM的IC50值。该化合物能够通过特异性靶向Chk2 ATP结合位点后方的门控依赖性疏水口袋,阻断ATP与Chk2的结合,从而有效抑制Chk2的磷酸化活性。由于这种机制,PV1162在抗癌治疗中展示了明显的应用前景。
PV1162是一种高选择性的Chk2抑制剂,具有0.29 nM的IC50值。该化合物能够通过特异性靶向Chk2 ATP结合位点后方的门控依赖性疏水口袋,阻断ATP与Chk2的结合,从而有效抑制Chk2的磷酸化活性。由于这种机制,PV1162在抗癌治疗中展示了明显的应用前景。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 询价 | 10-14周 | |
50 mg | 询价 | 10-14周 |
产品描述 | PV1162 is a Chk2-specific inhibitor characterized by a potency with an IC 50 value of 0.29 nM. It operates by specifically targeting the gatekeeper-dependent hydrophobic pocket behind the ATP-binding site (adenine-binding region) to inhibit ATP binding to Chk2, effectively suppressing the phosphorylation activity of Chk2. This compound has demonstrated potential for application in cancer therapy. |
靶点活性 | Chk2:0.29 nM, Chk1:59000 nM |
分子量 | 392.45 |
分子式 | C21H24N6O2 |
CAS No. | 1093793-11-3 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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