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.