货号:A869154 同义名: MK-8776 S-isomer
SCH-900776 is the S-isomer form of SCH900776, 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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产品名称 | Chk1 ↓ ↑ | Chk2 ↓ ↑ | 其他靶点 | 纯度 | |||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Rabusertib |
++
Chk1, IC50: 7 nM |
99%+ | |||||||||||||||||
PF-477736 |
++++
Chk1, Ki: 0.49 nM |
98%+ | |||||||||||||||||
Prexasertib 2HCl |
++++
Chk1, Ki: 0.9 nM |
++
Chk2, IC50: 8 nM |
RSK | 98% | |||||||||||||||
AZD-7762 |
+++
Chk1, IC50: 5 nM |
++
Chk2, IC50: <10 nM |
99%+ | ||||||||||||||||
CHIR-124 |
++++
Chk1, IC50: 0.3 nM |
GSK-3,PDGFR,FLT3 | 98% | ||||||||||||||||
SCH900776 |
+++
Chk1, IC50: 3 nM |
99%+ | |||||||||||||||||
SAR-020106 |
+
Chk1, IC50: 13.3 nM |
98% | |||||||||||||||||
CCT245737 |
+++
Chk1, IC50: 1.4 nM |
97+% | |||||||||||||||||
BML-277 |
+
Chk2, IC50: 15 nM |
99%+ | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
描述 | SCH-900776 is the S-isomer form of SCH900776, 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). |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.66mL 0.53mL 0.27mL |
13.29mL 2.66mL 1.33mL |
26.58mL 5.32mL 2.66mL |
CAS号 | 891494-64-7 |
分子式 | C15H18BrN7 |
分子量 | 376.254 |
别名 | MK-8776 S-isomer |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Keep in dark place,Inert atmosphere,2-8°C |
溶解度 |
DMSO: 105 mg/mL(279.07 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
动物实验配方 |