VX-702 100mg
VX-702 is an orally bioavailable inhibitor of p38 MAP kinase that inhibits platelet agonist induced p38 activation (IC50= 4 to 20 nM).
| Trivial name | VX-702 100mg |
| Catalog Number | A10982-100 |
| Alternative Name(s) | 6-[(Aminocarbonyl)(2,6-difluorophenyl)amino]-2-(2,4-difluorophenyl)-3-pyridinecarboxamide |
| Molecular Formula | C19H12F4N4O2 |
| CAS# | 479543-46-9 |
| 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 |
| Size | 100mg |
| Supplier Page | http://www.adooq.com/vx-702.html |