M. Bogusky

发表

Comparison of the dynamics of the membrane‐bound form of fd coat protein in micelles and in bilayers by solution and solid‐state nitrogen‐15 nuclear magnetic resonance spectroscopy

S. Opella, M. Bogusky, G. Leo, 1988, Proteins.

Nitrogen-15 NMR spectroscopy of proteins in solution

P. Lu, S. Opella, M. Bogusky, 1990 .

One- and two- dimensional 15N/1H NMR of filamentous phage coat proteins in solution.

S. Opella, M. Bogusky, P. Tsang, 1985, Biochemical and biophysical research communications.

HIV-1 vaccine development: constrained peptide immunogens show improved binding to the anti-HIV-1 gp41 MAb.

G. McGaughey, R. Freidinger, J. Shiver, 2003, Biochemistry.

Protein backbone dynamics by solid-state and solution 15N NMR spectroscopy

S. Opella, M. Bogusky, G. Leo, 1987 .

Discovery of [(2R,5R)‐5‐{[(5‐Fluoropyridin‐2‐yl)oxy]methyl}‐2‐methylpiperidin‐1‐yl][5‐methyl‐2‐(pyrimidin‐2‐yl)phenyl]methanone (MK‐6096): A Dual Orexin Receptor Antagonist with Potent Sleep‐Promoting Properties

Steven V. Fox, John D. Schreier, S. Doran, 2012, ChemMedChem.

Cyclopsychotride A, a biologically active, 31-residue cyclic peptide isolated from Psychotria longipes.

P. Anderson, M. Sardana, M. Bogusky, 1994, Journal of natural products.

Discovery of a Potent, CNS‐Penetrant Orexin Receptor Antagonist Based on an N,N‐Disubstituted‐1,4‐diazepane Scaffold that Promotes Sleep in Rats

John D. Schreier, S. Doran, J. Renger, 2009, ChemMedChem.

Dynamics of the multidomain fibrinolytic protein urokinase from two-dimensional NMR

C. Dobson, R. Oswald, R. Smith, 1989, Nature.

Reversible independent unfolding of the domains of urokinase monitored by 1H NMR.

C. Dobson, R. Smith, M. Bogusky, 1989, Biochemistry.

Amide and α-keto carbonyl inhibitors of thrombin based on arginine and lysine: Synthesis, stability and biological characterization

D. Veber, R. Nutt, S. Brady, 1995 .

NMR and molecular modeling characterization of RGD containing peptides.

D. Veber, P. Anderson, R. Nutt, 2009, International journal of peptide and protein research.

Discovery of the dual orexin receptor antagonist [(7R)-4-(5-chloro-1,3-benzoxazol-2-yl)-7-methyl-1,4-diazepan-1-yl][5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl]methanone (MK-4305) for the treatment of insomnia.

John D. Schreier, S. Doran, G. McGaughey, 2010, Journal of medicinal chemistry.

Synthesis and biological evaluation of unnatural canthine alkaloids

C. Lindsley, M. Bogusky, G. Hartman, 2005 .

Structure of synthetic peptide analogues of an eggshell protein of Schistosoma mansoni

J. S. Cordingley, M. Bogusky, H. Mach, 1993, Protein science : a publication of the Protein Society.

Two tarantula peptides inhibit activation of multiple sodium channels.

V. Garsky, M. Bogusky, V. Warren, 2002, Biochemistry.

Fourier Transform Mass Spectrometry and Nuclear Magnetic Resonance Analysis for the Rapid and Accurate Characterization of Hexacosanoylceramide

M. Bogusky, W. J. Simonsick, C. W. Ross, 2016, International journal of molecular sciences.

Conformational analysis of N,N-disubstituted-1,4-diazepane orexin receptor antagonists and implications for receptor binding.

G. McGaughey, J. Renger, P. Coleman, 2009, Bioorganic & medicinal chemistry letters.

3-Aminopyrrolidinone farnesyltransferase inhibitors: design of macrocyclic compounds with improved pharmacokinetics and excellent cell potency.

A. D. Rodrigues, J Christopher Culberson, Ronald Robinson, 2002, Journal of medicinal chemistry.

3,8-Diazabicyclo[3.2.1]octan-2-one peptide mimetics: synthesis of a conformationally restricted inhibitor of farnesyltransferase.

M. Bogusky, J. Culberson, C. Dinsmore, 2001, Organic letters.

N-arylpiperazinone inhibitors of farnesyltransferase: discovery and biological activity.

J. Huff, J. Davide, N. Kohl, 1999, Journal of medicinal chemistry.

Structure-Function Relationships in the Neuropeptide S Receptor

Christopher M. Tan, D. Slipetz, M. Crackower, 2006, Journal of Biological Chemistry.

Conformation of a novel tetrapeptide inhibitor NH2-D-Trp-D-Met-Phe(pCl)-Gla-NH2 bound to farnesyl-protein transferase.

V. Garsky, A. Pessi, M. Bogusky, 1999, The journal of peptide research : official journal of the American Peptide Society.

NMR studies of novel inhibitors bound to farnesyl‐protein transferase

M. Bogusky, S. Pitzenberger, K. Koblan, 1995, Protein science : a publication of the Protein Society.

Progress towards the development of a HIV-1 gp41-directed vaccine.

G. McGaughey, R. Freidinger, J. Shiver, 2004, Current HIV research.

Structure and dynamics of the Pf1 filamentous bacteriophage coat protein in micelles.

S. Opella, M. Bogusky, R. Schiksnis, 1987, Biochemistry.

Rational design and synthesis of selective BACE-1 inhibitors.

D. Hazuda, S. Singh, V. Garsky, 2004, Bioorganic & medicinal chemistry letters.

Potent antagonists of the Kv1.5 potassium channel: synthesis and evaluation of analogous N,N-diisopropyl-2-(pyridine-3-yl)acetamides.

K. K. Nanda, C. Lindsley, R. Spencer, 2006, Bioorganic & medicinal chemistry letters.

Secondary structure of filamentous bacteriophage coat protein is preserved in lipid environments.

S. Opella, M. Bogusky, R. Schiksnis, 1988, Journal of molecular biology.

Conformational restriction of flexible ligands guided by the transferred noe experiment: potent macrocyclic inhibitors of farnesyltransferase.

J. Huff, M. Bogusky, S. Graham, 2001, Journal of the American Chemical Society.

Characterization of a Solid State Reaction Product from a Lyophilized Formulation of a Cyclic Heptapeptide. A Novel Example of an Excipient-Induced Oxidation

M. Kaufman, M. Bogusky, J. A. Zimmerman, 1996, Pharmaceutical Research.

Enhancement of α-Helicity in the HIV-1 Inhibitory Peptide DP178 Leads to an Increased Affinity for Human Monoclonal Antibody 2F5 but Does Not Elicit Neutralizing Responses in Vitro

J. Shiver, V. Garsky, M. Citron, 2002, The Journal of Biological Chemistry.

Synthesis and solution conformation of c(D-Trp-D-Cys(SO3-Na+)-Pro-D-Val-Leu), a potent endothelin-A receptor antagonist.

R. Nutt, S. Brady, M. Bogusky, 2009, International journal of peptide and protein research.

The solution conformation Ac‐Pen‐Arg‐Gly‐Asp‐Cys‐OH, a potent fibrinogen receptor antagonist

D. Veber, R. Nutt, S. Brady, 1993, Biopolymers.