VX-702
Catalog No. A10982
VX-702是一种高选择性p38α MAPK抑制剂,可抑制血小板激动剂诱导的p38激活(IC50 = 4至20 nM)。
Catalog Num | A10982 |
---|---|
M. Wt | 404.3 |
Formula | C19H12F4N4O2 |
Purity | >98% |
Storage | at -20°C 3 years Powder |
CAS No. | 479543-46-9, 745833-23-2 |
Synonyms | VX702, VX 702 |
SMILES | C1=CC(=C(C(=C1)F)N(C2=NC(=C(C=C2)C(=O)N)C3=C(C=C(C=C3)F)F)C(=O)N)F |
VX-702是一种高选择性p38α MAPK抑制剂,可抑制血小板激动剂诱导的p38激活(IC50 = 4至20 nM)。
In vitro (25°C) | DMSO | 77 mg/mL (190.45 mM) | |
Water | Insoluble | ||
Ethanol | Insoluble | ||
In vivo | 30% PEG400+0.5% Tween80+5% propylene glycol | 28 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 | 24.73 mL | 123.67 mL | 247.34 mL |
0.5 mM | 4.95 mL | 24.73 mL | 49.47 mL |
1 mM | 2.47 mL | 12.37 mL | 24.73 mL |
5 mM | 0.49 mL | 2.47 mL | 4.95 mL |
*The above data is based on the productmolecular weight 404.3 . 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.