VX-702

VX-702 Chemical Structure

CAS NO. 479543-46-9

VX-702 is an orally bioavailable inhibitor of p38 MAP kinase that inhibits platelet agonist induced p38 activation (IC50= 4 to 20 nM).

库存: 现货

规格 价格 数量
10 mg
¥ 400.00
50 mg
¥ 1,000.00
100 mg
¥ 1,900.00
200 mg
¥ 3,200.00
Warning 产品仅用于科学研究,不针对患者销售,望谅解.

详情

VX-702 is an orally bioavailable inhibitor of p38 MAP kinase that inhibits platelet agonist induced p38 activation (IC50= 4 to 20 nM).
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.

目录号 A10982
MECHANISM OF ACTION Inhibitor
M. Wt 404.3
Formula C19H12F4N4O2
Solubility DMSO
Purity >98%
Storage at -20°C 3 years Powder
CAS No. 479543-46-9
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

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