产品详情
靶点信息
MEK1 (Cell-free assay) | ||||
14 nM |
In vitro (25°C) | DMSO | Warmed: 80 mg/mL (174.79 mM) | |
Water | Insoluble | ||
Ethanol | Insoluble | ||
In vivo | 4% DMSO+30% PEG 300+5% Tween 80+ddH2O | 4 mg/mL | |
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.1 mM | 21.85 mL | 109.24 mL | 218.48 mL |
0.5 mM | 4.37 mL | 21.85 mL | 43.7 mL |
1 mM | 2.18 mL | 10.92 mL | 21.85 mL |
5 mM | 0.44 mL | 2.18 mL | 4.37 mL |
*The above data is based on the productmolecular weight 457.7. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
目录号 | A10257 |
---|---|
作用机制 | Inhibitor (抑制剂) |
M. Wt | 457.7 |
Formula | C17H15BrClFN4O3 |
Purity | >99% |
Storage | Store lyophilized at -20ºC, keep desiccated. |
CAS No. | 606143-52-6 |
Synonyms | ARRY-142886 |
SMILES | CN1C=NC2=C1C=C(C(=C2F)NC3=C(C=C(C=C3)Br)Cl)C(=O)NOCCO |
产品资料
产品标签
Product Questions
Product Questions
GDC-0973 (Cobimetinib)
GDC-0973 (Cobimetinib,RG7420)是一种有效且高度选择性的MEK1抑制剂,IC50为4.2 nM,对MEK1的选择性选择性是对MEK2的10…
GSK1120212 (JTP-74057, Trametinib)
GSK1120212 (JTP-74057,Trametinib)强烈阻止了MEK1和MEK2激酶的活性,而不是其他98种激酶的活性。
Ulixertinib (BVD-523, VRT752271)
Ulixertinib (BVD-523,VRT752271)是ERK蛋白激酶的吡咯抑制剂。
Cobimetinib (R-enantiomer)
Cobimetinib R-enantiomer是Cobimetinib的R对映异构体,Cobimetinib是一种有力的,高选择性的促分裂原活化蛋白激酶(…
U0126-EtOH
U0126-EtOH是MEK1和MEK2的抑制剂,IC50分别为72 nM和58 nM。
Refametinib (RDEA-119, BAY 86-9766)
Refametinib (RDEA-119,BAY 86-9766)是一种口服生物利用型选择性MEK抑制剂,EC50为 2.0-15 nM。具有潜在的抗肿瘤活性…