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Boris Brus
Observed names:
B. Brus,
Brus, Boris
Observed institution:
University of Ljubljana
OpenAlex ID:
A5023896672
Discovery, Biological Evaluation, and Crystal Structure of a Novel Nanomolar Selective Butyrylcholinesterase Inhibitor
2014
·
Boris Brus
, Urban Košak
, et al.
·
Journal of Medicinal Chemistry
·
287
Development of an in-vivo active reversible butyrylcholinesterase inhibitor
2016
·
Urban Košak
, Boris Brus
, et al.
·
Scientific Reports
·
178
PDF
The Magic of Crystal Structure-Based Inhibitor Optimization: Development of a Butyrylcholinesterase Inhibitor with Picomolar Affinity and in Vivo Activity
2017
·
Urban Košak
, Boris Brus
, et al.
·
Journal of Medicinal Chemistry
·
168
LiSiCA: A Software for Ligand-Based Virtual Screening and Its Application for the Discovery of Butyrylcholinesterase Inhibitors
2015
·
Samo Lešnik
, Tanja Štular
, et al.
·
Journal of Chemical Information and Modeling
·
91
Development of multifunctional, heterodimeric isoindoline-1,3-dione derivatives as cholinesterase and β-amyloid aggregation inhibitors with neuroprotective properties
2015
·
Natalia Guzior
, Marek Bajda
, et al.
·
European Journal of Medicinal Chemistry
·
69
N-Propargylpiperidines with naphthalene-2-carboxamide or naphthalene-2-sulfonamide moieties: Potential multifunctional anti-Alzheimer’s agents
2016
·
Urban Košak
, Damijan Knez
, et al.
·
Bioorganic & Medicinal Chemistry
·
68
Structure-based development of nitroxoline derivatives as potential multifunctional anti-Alzheimer agents
2015
·
Damijan Knez
, Boris Brus
, et al.
·
Bioorganic & Medicinal Chemistry
·
60
Aggressive conditions during primary drying as a contemporary approach to optimise freeze-drying cycles of biopharmaceuticals
2018
·
Maja Bjelošević
, Katarina Bolko Seljak
, et al.
·
European Journal of Pharmaceutical Sciences
·
55
Isoindoline-1,3-dione derivatives targeting cholinesterases: Design, synthesis and biological evaluation of potential anti-Alzheimer’s agents
2015
·
Natalia Guzior
, Marek Bajda
, et al.
·
Bioorganic & Medicinal Chemistry
·
55
Synthesis of new N-benzylpiperidine derivatives as cholinesterase inhibitors with β-amyloid anti-aggregation properties and beneficial effects on memory in vivo
2015
·
Anna Więckowska
, Krzysztof Więckowski
, et al.
·
Bioorganic & Medicinal Chemistry
·
50
Nonpeptidic Selective Inhibitors of the Chymotrypsin‐Like (β5 i) Subunit of the Immunoproteasome
2016
·
Izidor Sosič
, Martina Gobec
, et al.
·
Angewandte Chemie International Edition
·
47
Novel toll-like receptor 4 (TLR4) antagonists identified by structure- and ligand-based virtual screening
2013
·
Urban Švajger
, Boris Brus
, et al.
·
European Journal of Medicinal Chemistry
·
46
Discovery of new MurA inhibitors using induced-fit simulation and docking
2017
·
Kaja Rožman
, Samo Lešnik
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
32
The formation and effect of mannitol hemihydrate on the stability of monoclonal antibody in the lyophilized state
2019
·
Maja Anko
, Maja Bjelošević
, et al.
·
International Journal of Pharmaceutics
·
31
Nep1-like proteins as a target for plant pathogen control
2021
·
Katja Pirc
, Vesna Hodnik
, et al.
·
PLoS Pathogens
·
29
PDF
Identification and characterization of the novel reversible and selective cathepsin X inhibitors
2017
·
Urša Pečar Fonović
, Ana Mitrović
, et al.
·
Scientific Reports
·
22
PDF
Straightforward synthesis of orthogonally protected piperidin-3-ylmethanamine and piperidin-4-ylmethanamine derivatives
2014
·
Urban Košak
, Boris Brus
, et al.
·
Tetrahedron Letters
·
17
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
2012
·
Nataša Beranič
, Petra Brožič
, et al.
·
The Journal of Steroid Biochemistry and Molecular Biology
·
16
Novel Inhibitors of Trihydroxynaphthalene Reductase with Antifungal Activity Identified by Ligand-Based and Structure-Based Virtual Screening
2011
·
Mojca Brunskole Švegelj
, Samo Turk
, et al.
·
Journal of Chemical Information and Modeling
·
14
Multiple Ligands Targeting Cholinesterases and β‐Amyloid: Synthesis, Biological Evaluation of Heterodimeric Compounds with Benzylamine Pharmacophore
2015
·
Natalia Szałaj
, Marek Bajda
, et al.
·
Archiv der Pharmazie
·
12
Discovery of highly potent, nonsteroidal 17β-hydroxysteroid dehydrogenase type 1 inhibitors by virtual high-throughput screening
2011
·
Štefan Starčević
, Samo Turk
, et al.
·
The Journal of Steroid Biochemistry and Molecular Biology
·
12
Synthetic tripeptides as alternate substrates of murein peptide ligase (Mpl)
2012
·
Mireille Hervé
, Andreja Kovač
, et al.
·
Biochimie
·
11
New enzymatic assay for the AKR1C enzymes
2012
·
Nataša Beranič
, Bogdan Štefane
, et al.
·
Chemico-Biological Interactions
·
11
Selective Cytotoxicity of Amidinopiperidine Based Compounds Towards Burkitt’s Lymphoma Cells Involves Proteasome Inhibition
2012
·
Martina Gobec
, Ales Obreza
, et al.
·
PLoS ONE
·
8
PDF
Nonpeptidic Selective Inhibitors of the Chymotrypsin‐Like (β5 i) Subunit of the Immunoproteasome
2016
·
Izidor Sosič
, Martina Gobec
, et al.
·
Angewandte Chemie
·
3
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Works count:
35
Citation count:
1,393
H-index:
17
I10-index:
23
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