SCH900776 (S-isomer) is the S-isomer form of SCH900776(HY-15532), which is a potent, selective and orally bioavailable inhibitor of checkpoint kinase Chk1 (IC50 = 3 nM), highly selective against Chk2 (IC50 = 1500 nM) and cyclin-dependent kinase CDK2 (IC50 = 160 nM).
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化学信息
| 名称 | SCH900776 S-isomer |
| Iupac 化学名称 | 6-bromo-3-(1-methylpyrazol-4-yl)-5-[(3S)-piperidin-3-yl]pyrazolo[1,5-a]pyrimidin-7-amine |
| 同义词 | SCH 900776 S-isomer; SCH-900776 S-isomer |
| 英文同义词 | SCH 900776 S-isomer; SCH-900776 S-isomer |
| 分子式 | C15H18BrN7 |
| 分子量 | 376.254 |
| Smile | CN1C=C(C=N1)C2=C3N=C(C(=C(N3N=C2)N)Br)C4CCCNC4 |
| InChiKey | GMIZZEXBPRLVIV-UHFFFAOYSA-N |
| InChi | InChI=1S/C15H18BrN7/c1-22-8-10(6-19-22)11-7-20-23-14(17)12(16)13(21-15(11)23)9-3-2-4-18-5-9/h6-9,18H,2-5,17H2,1H3 |
| Cas号 | 891494-64-7 |
| 相关CAS号 | |
| 外观性状 | Solid powder |
| 纯度 | 98% |
| 存储 | -20 ºC for 3 years |
| 可溶性 | Soluble in DMSO |
| 处理方式 | |
| 运输条件 | Shipped under ambient temperature |
| 海关编码 | |
| Targets | |
| Mechanism | |
| Cell study | |
| Animal study | |
| Clinical study | |