Nonsteroidal anti inflammatorys, synthesized

4′-(Methylsulfonyl)acetophenone may be used in the synthesis of: . 3-(4-Methylsulfonylphenyl)-4-phenyl-2(5H)-furanone with potent apoptosis-inducing ability. . Bromo-4-methylsulfonylacetophenone, an intermediate for preparing

4′-(Methylsulfonyl)acetophenone may be used in the synthesis of: . 3-(4-Methylsulfonylphenyl)-4-phenyl-2(5H)-furanone with potent apoptosis-inducing ability. . Bromo-4-methylsulfonylacetophenone, an intermediate for preparing

4′-(Methylsulfonyl)acetophenone may be used in the synthesis of: . 3-(4-Methylsulfonylphenyl)-4-phenyl-2(5H)-furanone with potent apoptosis-inducing ability. . Bromo-4-methylsulfonylacetophenone, an intermediate for preparing

4′-(Methylsulfonyl)acetophenone may be used in the synthesis of: . 3-(4-Methylsulfonylphenyl)-4-phenyl-2(5H)-furanone with potent apoptosis-inducing ability. . Bromo-4-methylsulfonylacetophenone, an intermediate for preparing

4′-(Methylsulfonyl)acetophenone may be used in the synthesis of: . 3-(4-Methylsulfonylphenyl)-4-phenyl-2(5H)-furanone with potent apoptosis-inducing ability. . Bromo-4-methylsulfonylacetophenone, an intermediate for preparing

4-Biphenylacetic acid is a potential non-steroidal antiinflammatory agent and forms solid inclusion complex with β-cyclodextrin. 4-Biphenylacetic acid on interaction with quinolone antibacterial agents induces functional blockade of the

Application Reactant involved in studies of biologically active molecules including: Discovery of indole inhibitors of MMP-13 for treatment of arthritic diseases Synthesis of indolyl ethanones as indoleamine 2,3-dioxygenase inhibitors cis

ACOSCHIMPEROSIDE N-

A xanthin derivative that acts as a potent agonist of adenosine A 2A receptors (K i = 27 nM). Exhibits reduced affinity for A 2B receptors (K i = 67 nM), but offers greater selectivity over A 1R (K i = 290 nM) and A 3R (88.

InformationAMG-47a AMG-47a is a potent, nonselective inhibitor of Lck kinase with IC50 of 3.4 uM and it also inhibits T cell proliferation. AMG-47a exhibit anti-inflammatory activity (ED50) of 11 mg/kg in the anti-CD3-induced production of

InformationAMG-47a AMG-47a is a potent, nonselective inhibitor of Lck kinase with IC50 of 3.4 uM and it also inhibits T cell proliferation. AMG-47a exhibit anti-inflammatory activity (ED50) of 11 mg/kg in the anti-CD3-induced production of

InformationAMG-47a AMG-47a is a potent, nonselective inhibitor of Lck kinase with IC50 of 3.4 uM and it also inhibits T cell proliferation. AMG-47a exhibit anti-inflammatory activity (ED50) of 11 mg/kg in the anti-CD3-induced production of