VX-702 50mg 50mg | Purity Not Available
Adooq Bioscience
VX-702 is an orally bioavailable inhibitor of p38 MAP kinase that inhibits platelet agonist induced p38 activation (IC50= 4 to 20 nM).
More Information Supplier PageVX-702 is an orally bioavailable inhibitor of p38 MAP kinase that inhibits platelet agonist induced p38 activation (IC50= 4 to 20 nM).
More Information Supplier PageVX-702 is an orally bioavailable inhibitor of p38 MAP kinase that inhibits platelet agonist induced p38 activation (IC50= 4 to 20 nM).
More Information Supplier PageVX-702 is an orally bioavailable inhibitor of p38 MAP kinase that inhibits platelet agonist induced p38 activation (IC50= 4 to 20 nM).
More Information Supplier PageVX-765 is a novel Caspase-1 inhibitor,which is an enzyme that controls the generation of two cytokines, IL-1b and IL-18.
More Information Supplier PageVX-765 is a novel Caspase-1 inhibitor,which is an enzyme that controls the generation of two cytokines, IL-1b and IL-18.
More Information Supplier PageVX-809 is the second investigational oral candidate compound for the treatment of cystic fibrosis (CF).
More Information Supplier PageVX-809 is the second investigational oral candidate compound for the treatment of cystic fibrosis (CF).
More Information Supplier PageVX-809 is the second investigational oral candidate compound for the treatment of cystic fibrosis (CF).
More Information Supplier Page