B. Brus

Boris Brus, Maja Bjelošević, Pegi Ahlin Grabnar, 2018, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Novel toll-like receptor 4 (TLR4) antagonists identified by structure- and ligand-based virtual screening.

S. Turk, V. Hodnik, G. Anderluh, 2013, European journal of medicinal chemistry.

LiSiCA: A Software for Ligand-Based Virtual Screening and Its Application for the Discovery of Butyrylcholinesterase Inhibitors

Dusanka Janezic, Janez Konc, Damijan Knez, 2015, J. Chem. Inf. Model..

Nonpeptidic Selective Inhibitors of the Chymotrypsin-Like (β5 i) Subunit of the Immunoproteasome.

Janez Konc, D. Janežič, I. Mlinarič-Raščan, 2016, Angewandte Chemie.

Multiple Ligands Targeting Cholinesterases and β‐Amyloid: Synthesis, Biological Evaluation of Heterodimeric Compounds with Benzylamine Pharmacophore

M. Bajda, B. Malawska, S. Gobec, 2015, Archiv der Pharmazie.

Identification and characterization of the novel reversible and selective cathepsin X inhibitors

J. Kos, S. Gobec, D. Knez, 2017, Scientific Reports.

Expression of human aldo-keto reductase 1C2 in cell lines of peritoneal endometriosis: Potential implications in metabolism of progesterone and dydrogesterone and inhibition by progestins

S. Gobec, Izidor Sosič, T. Rižner, 2012, The Journal of Steroid Biochemistry and Molecular Biology.

Development of multifunctional, heterodimeric isoindoline-1,3-dione derivatives as cholinesterase and β-amyloid aggregation inhibitors with neuroprotective properties.

J. Kos, M. Bajda, N. Guzior, 2015, European journal of medicinal chemistry.

New enzymatic assay for the AKR1C enzymes.

S. Gobec, T. Rižner, B. Štefane, 2013, Chemico-biological interactions.

N-Propargylpiperidines with naphthalene-2-carboxamide or naphthalene-2-sulfonamide moieties: Potential multifunctional anti-Alzheimer's agents.

J. Kos, N. Coquelle, J. Colletier, 2017, Bioorganic & medicinal chemistry.

Structure-based development of nitroxoline derivatives as potential multifunctional anti-Alzheimer agents.

N. Coquelle, J. Colletier, Janez Mravljak, 2015, Bioorganic & medicinal chemistry.

Discovery of highly potent, nonsteroidal 17β-hydroxysteroid dehydrogenase type 1 inhibitors by virtual high-throughput screening

S. Turk, S. Gobec, J. Cesar, 2011, The Journal of Steroid Biochemistry and Molecular Biology.

Discovery of new MurA inhibitors using induced-fit simulation and docking.

Dušanka Janežič, Janez Konc, Stanislav Gobec, 2017, Bioorganic & medicinal chemistry letters.

Development of multifunctional, heterodimeric isoindoline-1,3-dione derivatives as cholinesterase and β-amyloid aggregation inhibitors with neuroprotective properties.

J. Kos, M. Bajda, B. Malawska, 2015, European journal of medicinal chemistry.

Nonpeptidic Selective Inhibitors of the Chymotrypsin-Like (β5 i) Subunit of the Immunoproteasome.

Janez Konc, D. Janežič, I. Mlinarič-Raščan, 2016, Angewandte Chemie.

Selective Cytotoxicity of Amidinopiperidine Based Compounds Towards Burkitt’s Lymphoma Cells Involves Proteasome Inhibition

I. Mlinarič-Raščan, S. Gobec, Aleš Obreza, 2012, PloS one.

Expression of human aldo-keto reductase 1C2 in cell lines of peritoneal endometriosis: Potential implications in metabolism of progesterone and dydrogesterone and inhibition by progestins

S. Gobec, Izidor Sosič, T. Rižner, 2012, The Journal of Steroid Biochemistry and Molecular Biology.

Isoindoline-1,3-dione derivatives targeting cholinesterases: design, synthesis and biological evaluation of potential anti-Alzheimer's agents.

M. Bajda, B. Malawska, S. Gobec, 2015, Bioorganic & medicinal chemistry.