L. D. Marrufo

Discovery of PH-797804, a highly selective and potent inhibitor of p38 MAP kinase.

Dean M. Messing, G. Anderson, J. Monahan, 2011, Bioorganic & medicinal chemistry letters.

Substituted N-aryl-6-pyrimidinones: a new class of potent, selective, and orally active p38 MAP kinase inhibitors.

Dean M. Messing, G. Anderson, J. Monahan, 2011, Bioorganic & medicinal chemistry letters.

R-isomers of Arg-Gly-Asp (RGD) mimics as potent αvβ3 inhibitors

D. Griggs, J. Malecha, J. Collins, 2007 .

Discovery of N-substituted pyridinones as potent and selective inhibitors of p38 kinase.

R. Kurumbail, J. Monahan, M. Hepperle, 2009, Bioorganic & medicinal chemistry letters.

Substituted N-aryl-6-pyrimidinones: a new class of potent, selective, and orally active p38 MAP kinase inhibitors.

Dean M. Messing, G. Anderson, J. Monahan, 2011, Bioorganic & medicinal chemistry letters.

Design, synthesis and activity of a potent, selective series of N-aryl pyridinone inhibitors of p38 kinase.

R. Kurumbail, Dean M. Messing, J. F. Schindler, 2011, Bioorganic & medicinal chemistry letters.

R-isomers of Arg-Gly-Asp (RGD) mimics as potent alphavbeta3 inhibitors.

D. Griggs, J. Collins, M. B. Finn, 2007, Bioorganic & medicinal chemistry.

Regeneration and Recovery of Hydriodic Acid after Reduction of Polyols to Fuels1

L. D. Marrufo, J. M. Robinson, Paul T. Herndon, 1999 .