M. Oblak

发表

Structural and functional characterization of enantiomeric glutamic acid derivatives as potential transition state analogue inhibitors of MurD ligase.

M. Hervé, C. Contreras-Martel, D. Blanot, 2007, Journal of molecular biology.

Characterization of quercetin binding site on DNA gyrase.

R. Jerala, T. Šolmajer, M. Oblak, 2003, Biochemical and biophysical research communications.

Prediction of selectivity of alpha1-adrenergic antagonists by counterpropagation neural network (CP-ANN).

J. Zupan, D. Agbaba, M. Novič, 2004, Il Farmaco.

In silico fragment-based discovery of indolin-2-one analogues as potent DNA gyrase inhibitors.

Simona Golic Grdadolnik, Roman Jerala, Marko Oblak, 2005, Bioorganic & medicinal chemistry letters.

4-Substituted trinems as broad spectrum beta-lactamase inhibitors: structure-based design, synthesis, and biological activity.

D. Turk, T. Šolmajer, M. Oblak, 2007, Journal of medicinal chemistry.

Synthesis of 8-Hydroxyimidazo[1,2-a]pyridine-2-carboxylic Acid and Its Derivatives

A. Meden, Uroš Grošelj, M. Oblak, 2008 .

In silico discovery of 2-amino-4-(2,4-dihydroxyphenyl)thiazoles as novel inhibitors of DNA gyrase B.

Andrej Perdih, Marko Oblak, T. Šolmajer, 2010, Bioorganic & medicinal chemistry letters.

Biophysical characterization of an indolinone inhibitor in the ATP-binding site of DNA gyrase.

D. Moras, D. Desplancq, S. Grdadolnik, 2006, Biochemical and biophysical research communications.

Discovery and development of ATPase inhibitors of DNA gyrase as antibacterial agents.

T. Šolmajer, M. Kotnik, M. Oblak, 2007, Current medicinal chemistry.

Quantitative structure–activity relationships of α1 adrenergic antagonists

J. Zupan, D. Agbaba, M. Novič, 2004, Journal of Molecular Modeling.

New High-Throughput Fluorimetric Assay for Discovering Inhibitors of UDP-N-Acetylmuramyl-l-Alanine: d-Glutamate (MurD) Ligase

K. Kristan, M. Kotnik, M. Oblak, 2009, Journal of biomolecular screening.

Quantitative Structure-Activity Relationship of Flavonoid Analogues. 3. Inhibition of p56lck Protein Tyrosine Kinase

Milan Randic, Tomaz Solmajer, Marko Oblak, 2000, J. Chem. Inf. Comput. Sci..

Direct thrombin inhibitors built on the azaphenylalanine scaffold provoke degranulation of mast cells

A. Zega, M. Oblak, U. Urleb, 2006, Thrombosis and Haemostasis.

Thiol-reactive Clenbuterol Analogues Conjugated to Bovine Serum Albumin

T. Šolmajer, M. Oblak, S. Pečar, 2004, Zeitschrift für Naturforschung C - A Journal of Biosciences.

Thrombin inhibitors with novel P1 binding pocket functionality: free energy of binding analysis

T. Šolmajer, M. Hodošček, M. Oblak, 2006, Journal of molecular modeling.