J. Kowalski

发表

Increasing protein stability using a rational approach combining sequence homology and structural alignment: Stabilizing the WW domain

J. Kelly, J W Kelly, X. Jiang, 2001, Protein science : a publication of the Protein Society.

Reversal of H3K9me2 by a small-molecule inhibitor for the G9a histone methyltransferase.

Karl Mechtler, Carol Ann Homon, Stephen Rea, 2007, Molecular cell.

N-Arylsulfonyl-α-amino carboxamides are potent and selective inhibitors of the chemokine receptor CCR10 that show efficacy in the murine DNFB model of contact hypersensitivity.

D. Jeanfavre, N. Moss, Jiang-Ping Wu, 2016, Bioorganic & medicinal chemistry letters.

5-Aminomethylbenzimidazoles as potent ITK antagonists.

J. Woska, D. Jeanfavre, M. Kashem, 2009, Bioorganic & medicinal chemistry letters.

A new reagent for solid and solution phase synthesis of protected guanidines from amines

M. Lipton, J. Kowalski, Y. F. Yong, 1999 .

Hit-to-lead studies on benzimidazole inhibitors of ITK: discovery of a novel class of kinase inhibitors.

Noel S. Wilson, C. Cywin, G. Roth, 2007, Bioorganic & medicinal chemistry letters.

Diverse 2-carboxamide-3-amino-substituted quinoxalines: synthesis and reactivity investigation for library generation.

George E. Lee, J. Kowalski, S. Leonard, 2006, Journal of combinatorial chemistry.

Rapid synthesis of an array of trisubstituted urea-based soluble epoxide hydrolase inhibitors facilitated by a novel solid-phase method.

I. Muegge, C. Cywin, A. Swinamer, 2010, Bioorganic & medicinal chemistry letters.

Solid-phase total synthesis and structure proof of callipeltin B.

M. Lipton, Alan G. Benson, J. Kowalski, 2006, Journal of the American Chemical Society.

Solid phase synthesis of a diketopiperazine catalyst containing the unnatural amino acid (S)-norarginine

M. Lipton, J. Kowalski, 1996 .

NMR solution structure of the isolated Apo Pin1 WW domain: comparison to the x-ray crystal structures of Pin1.

J. Kelly, Jeffery W Kelly, Kai Liu, 2002, Biopolymers.

On-resin cyclization of the cyclic depsipeptide callipeltin B

M. Lipton, Alan G. Benson, J. Kowalski, 2002 .

Facile incorporation of urea pseudopeptides into protease substrate analogue inhibitors.

M. Lipton, J. Kowalski, A. Myers, 2004, Bioorganic & medicinal chemistry letters.