P. Kearney

发表

Solid-Phase Synthesis of 2-Aminothiazoles.

J. Flygare, P. Kearney, Mónica Fernández, 1998, The Journal of organic chemistry.

Solid-phase synthesis of disubstituted guanidines

J. Flygare, P. Kearney, Mónica Fernández, 1998 .

Rothemund and Adler-Longo reactions revisited: synthesis of tetraphenylporphyrins under equilibrium conditions

J. Lindsey, P. Kearney, Irwin C. Schreiman, 1987 .

The design, synthesis, and biological evaluation of PIM kinase inhibitors.

Wei Xu, J. Nuss, Wentao Zhang, 2012, Bioorganic & medicinal chemistry letters.

SAR and in vivo evaluation of 4-aryl-2-aminoalkylpyrimidines as potent and selective Janus kinase 2 (JAK2) inhibitors.

J. Martini, J. Nuss, Wentao Zhang, 2012, Bioorganic & medicinal chemistry letters.

Discovery of XL413, a potent and selective CDC7 inhibitor.

Wei Xu, Charles R. Holst, J. Nuss, 2012, Bioorganic & medicinal chemistry letters.

Molecular recognition in aqueous media. New binding studies provide further insights into the cation-π interaction and related phenomena

J. Forman, L. Mizoue, P. Kearney, 1993 .

Design, synthesis and in vitro evaluation of potent, novel, small molecule inhibitors of plasminogen activator inhibitor-1.

P. Charlton, N. Vicker, J. Golec, 2002, Bioorganic & medicinal chemistry letters.

Methods used to track introduced genetically engineered organisms

J. Tiedje, P. Kearney, 1988 .

Molecular recognition: multipoint contacts with new sizes and shapes

J. Rebek, J. Lindsey, R. Duff, 1988 .

A Selective Receptor for Arginine Derivatives in Aqueous Media. Energetic Consequences of Salt Bridges That Are Highly Exposed to Water

P. Kearney, S. Mecozzi, S. Ngola, 1999 .

Discovery of a new class of glucosylceramide synthase inhibitors.

J. Nuss, S. Richards, P. Lamb, 2011, Bioorganic & medicinal chemistry letters.

Discovery and characterization of an inhibitor of glucosylceramide synthase.

K. Ogilvie, J. Nuss, S. Richards, 2012, Journal of medicinal chemistry.

Development and Application of a Recyclable High-Load Magnetic Co/C Hybrid ROMP-Derived Benzenesulfonyl Chloride Reagent and Utility of Corresponding Analogues.

R. Grass, P. Hanson, Qin Zang, 2017, Organic letters.

Nicotinic receptor binding site probed with unnatural amino acid incorporation in intact cells.

N. Davidson, S. Silverman, W. Zhong, 1995, Science.

Experimental and Computational Studies of Cation-π Interactions in Natural and Synthetic Receptors. Benzene as a Pseudoanion

J. Forman, L. Mizoue, P. Kearney, 1994 .

An Engineered Tetrahymena tRNAGln for in Vivo Incorporation of Unnatural Amino Acids into Proteins by Nonsense Suppression*

H. Lester, F. Du, J. Sampson, 1996, The Journal of Biological Chemistry.

Discovery of INT131: a selective PPARγ modulator that enhances insulin sensitivity.

M. Lindstrom, N. Walker, P. Timmermans, 2013, Bioorganic & medicinal chemistry.

Determinants of Nicotinic Receptor Gating in Natural and Unnatural Side Chain Structures at the M2 9′ Position

H. Lester, W. Zhong, P. Kearney, 1996, Neuron.