AT7867(857531-00-1)(≥98%)
特别提示:包括AT7867在内,本公司的所有产品仅可用于科研实验,严禁用于临床医疗及其他非科研用途!
| CAS号 | 857531-00-1 |
| 分子式 | C20H20ClN3 |
| 分子量 | 337.86 |
| 沸点 | 530.2℃/760 mmHg |
| 溶解性 | DMSO ≥66mg/mL Water<1.2mg/mL Ethanol ≥4.6mg/mL |
| 存贮条件 | 储存温度-20℃ |
| 密度 | 1.2000 |
| 应用 | A potent ATP-competitive inhibitor of Akt1,Akt2 and Akt3 |
| 产品介绍 | AT7867是ATP竞争性Akt1/2/3和p70S6K/PKA抑制剂,IC50分别为32 nM/17 nM/47 nM和85 nM/20 nM,对AGC激酶家族以外的蛋白几乎无活性。 |
| 备注 | AT7867 is a potent ATP-competitive inhibitor ofAkt1/2/3andp70S6K/PKAwithIC50of 32 nM/17 nM/47 nM and 85 nM/20 nM,respectively;little activity outside the AGC kinase family. |
| 生化机理 |
AT7867 is a potent and oral AKT and p70 S6 kinase inhibitor with an IC50 of 17 nM. |
| 别名 | 4-(4-氯苯基)-4-[4-(1H-吡唑-4-基)苯基]哌啶;pyrazole-based inhibitor 9;4-(4-Chlorophenyl)-4-[4-(1H-pyrazol-4-yl)phenyl]piperidine |
| 货号 | 名称 | 规格 |
| YT342 | PP2A和PP1抑制剂(冈田酸钾盐) | 10μg |
| M00177 | c-Kit/Bcr-Abl/PDGFR酪氨酸激酶抑制剂 | 1mL(10mM)|100mg|200mg|500mg|1g|5g |
| M01069 | 蛋白酶体糜蛋白酶样活性抑制剂(Delanzomib) | 1mL(10mM)|5mg|10mg|50mg|100mg |
| M01218 | MET抑制剂(LY2801653 dihydrochloride) | 1mL(10mM)|2mg|5mg|10mg|50mg|100mg |
| M01625 | VEGFR2抑制剂(Cediranib maleate) | 1mL(10mM)|5mg|10mg|50mg|100mg |
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