K. Nguyen

发表

Design and synthesis of potent, selective, and orally bioavailable tetrasubstituted imidazole inhibitors of p38 mitogen-activated protein kinase.

E. A. O'neill, J. Vacca, B. Frantz, 1999, Journal of Medicinal Chemistry.

Isoproterenol Acts as a Biased Agonist of the Alpha-1A-Adrenoceptor that Selectively Activates the MAPK/ERK Pathway

Paul J. Dietrich, A. Ford, M. Milla, 2015, PloS one.

Interaction of the Heparin-Binding Consensus Sequence of β-Amyloid Peptides with Heparin and Heparin-Derived Oligosaccharides.

D. Rabenstein, K. Nguyen, 2016, The journal of physical chemistry. B.

Design and synthesis of potent, selective, and orally bioavailable tetrasubstituted imidazole inhibitors of p38 mitogen-activated protein kinase.

E. A. O'neill, J. Vacca, B. Frantz, 1999, Journal of medicinal chemistry.

Design and Structural Characterization of Potent and Selective Inhibitors of Phosphatidylinositol 4 Kinase IIIβ.

K. Shokat, J. Glenn, J. Burke, 2016, Journal of medicinal chemistry.

Design, synthesis, and biological evaluation of pyrazolopyrimidine-sulfonamides as potent multiple-mitotic kinase (MMK) inhibitors (part I).

L. Silvian, D. Aivazian, Lin Zhang, 2011, Bioorganic & medicinal chemistry letters.

Domain structure of vitronectin. Alignment of active sites.

E. Ruoslahti, M. Pierschbacher, S. Suzuki, 1984, The Journal of biological chemistry.

Discovery and optimization of a series of 3-(3-phenyl-3H-imidazo[4,5-b]pyridin-2-yl)pyridin-2-amines: orally bioavailable, selective, and potent ATP-independent Akt inhibitors.

K. Nguyen, M. Ashwell, R. Nicewonger, 2012, Journal of medicinal chemistry.

Structure-based design of 2,6,7-trisubstituted-7H-pyrrolo[2,3-d]pyrimidines as Aurora kinases inhibitors.

L. Silvian, N. Pathan, Lin Zhang, 2012, Bioorganic & medicinal chemistry letters.

Discovery and Optimization of Potent GPR40 Full Agonists Containing Tricyclic Spirocycles.

Sean P. Brown, J. Medina, M. Bartberger, 2013, ACS medicinal chemistry letters.

Oligo(N-aryl glycines): a new twist on structured peptoids.

Richard Bonneau, Khanh Nguyen, Glenn L. Butterfoss, 2008, Journal of the American Chemical Society.

Synthesis, SAR and biological evaluation of 1,6-disubstituted-1H-pyrazolo[3,4-d]pyrimidines as dual inhibitors of Aurora kinases and CDK1.

L. Silvian, N. Pathan, Lin Zhang, 2012, Bioorganic & medicinal chemistry letters.

Determination of the primary structure and carboxyl pKAs of heparin-derived oligosaccharides by band-selective homonuclear-decoupled two-dimensional 1H NMR

D. Rabenstein, K. Nguyen, 2010, Analytical and bioanalytical chemistry.

The Location and Nature of General Anesthetic Binding Sites on the Active Conformation of Firefly Luciferase; A Time Resolved Photolabeling Study

S. Husain, K. Miller, K. Nguyen, 2012, PloS one.

Interaction of the Heparin-Binding Consensus Sequence of β-Amyloid Peptides with Heparin and Heparin-Derived Oligosaccharides.

D. Rabenstein, K. Nguyen, 2016, Journal of Physical Chemistry B.