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VX-702

Chemical Structure : VX-702

CAS No.: 745833-23-2

VX-702 (VX702;VX 702)

Catalog No.: PC-42563Not For Human Use, Lab Use Only.

VX-702 is a potent, selective, second generation p38 MAPK inhibitor with IC50 of 4-20 nM for p38α.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

VX-702 is a potent, selective, second generation p38 MAPK inhibitor with IC50 of 4-20 nM for p38α.
VX-702 displays 14-fold higher potency against the p38α versus p38β.
VX-702 inhibits p38 activation induced by platelet agonists including thrombin, SFLLRN, AYPGKF, U46619 and collagen, without effect on collagen-mediated platelet aggregation.

Physicochemical Properties

M.Wt 404.3178
Formula C19H12F4N4O2
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

DMSO: ≥ 42 mg/mL

Chemical Name/SMILES

3-Pyridinecarboxamide, 6-[(aminocarbonyl)(2,6-difluorophenyl)amino]-2-(2,4-difluorophenyl)-

References

1. Kuliopulos A, et al. Thromb Haemost. 2004 Dec;92(6):1387-93.

2. Damjanov N, et al. Arthritis Rheum. 2009 May;60(5):1232-41.

3. Ding C. Curr Opin Investig Drugs. 2006 Nov;7(11):1020-5.

4. Matsushita T, et al. Am J Pathol. 2017 Apr;187(4):841-850.

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