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Matic Proj
Matic Proj
Medicinal Chemistry, Analytical Development
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Targeting the deubiquitinase USP7 for degradation with PROTACs
A Murgai, I Sosič, M Gobec, P Lemnitzer, M Proj, S Wittenburg, R Voget, ...
Chemical Communications 58 (63), 8858-8861, 2022
322022
Redox active or thiol reactive? Optimization of rapid screens to identify less evident nuisance compounds
M Proj, D Knez, I Sosič, S Gobec
Drug discovery today 27 (6), 1733-1742, 2022
182022
Discovery of immunoproteasome inhibitors using large-scale covalent virtual screening
A Scarpino, D Bajusz, M Proj, M Gobec, I Sosič, S Gobec, GG Ferenczy, ...
Molecules 24 (14), 2590, 2019
162019
Covalent inhibitors of bacterial peptidoglycan biosynthesis enzyme MurA with chloroacetamide warhead
K Grabrijan, M Hrast, M Proj, A Dolšak, I Zdovc, T Imre, L Petri, ...
European journal of medicinal chemistry 243, 114752, 2022
132022
Andrographolide derivatives target the KEAP1/NRF2 axis and possess potent anti‐SARS‐CoV‐2 activity
B Schulte, M König, BI Escher, S Wittenburg, M Proj, V Wolf, C Lemke, ...
ChemMedChem 17 (5), e202100732, 2022
132022
Discovery of selective fragment-sized immunoproteasome inhibitors
L Kollár, M Gobec, B Szilágyi, M Proj, D Knez, P Ábrányi-Balogh, L Petri, ...
European Journal of Medicinal Chemistry 219, 113455, 2021
122021
Discovery of compounds with viscosity-reducing effects on biopharmaceutical formulations with monoclonal antibodies
M Proj, M Zidar, B Lebar, N Strašek, G Miličić, A Žula, S Gobec
Computational and structural biotechnology journal 20, 5420-5429, 2022
112022
Leveraging ligand affinity and properties: discovery of novel benzamide-type cereblon binders for the design of PROTACs
C Steinebach, A Bricelj, A Murgai, I Sosic, L Bischof, YLD Ng, C Heim, ...
Journal of medicinal chemistry 66 (21), 14513-14543, 2023
92023
Structure-activity relationships of triazole-benzodioxine inhibitors of cathepsin X
UP Fonović, D Knez, M Hrast, N Zidar, M Proj, S Gobec, J Kos
European Journal of Medicinal Chemistry 193, 112218, 2020
92020
Tunable Heteroaromatic Nitriles for Selective Bioorthogonal Click Reaction with Cysteine
M Proj, N Strašek, S Pajk, D Knez, I Sosič
Bioconjugate chemistry 34 (7), 1271-1281, 2023
82023
ProBiS-Dock: A hybrid multitemplate homology flexible docking algorithm enabled by protein binding site comparison
J Konc, S Lesnik, B Skrlj, M Sova, M Proj, D Knez, S Gobec, D Janezic
Journal of chemical information and modeling 62 (6), 1573-1584, 2022
82022
Fragment-sized thiazoles in fragment-based drug discovery campaigns: friend or foe?
M Proj, M Hrast, D Knez, K Bozovičar, K Grabrijan, A Meden, S Gobec, ...
ACS medicinal chemistry letters 13 (12), 1905-1910, 2022
62022
New inhibitors of cathepsin V impair tumor cell proliferation and elastin degradation and increase immune cell cytotoxicity
A Mitrović, E Senjor, M Jukić, L Bolčina, M Prunk, M Proj, MP Nanut, ...
Computational and structural biotechnology journal 20, 4667-4687, 2022
62022
Synthesis and biochemical evaluation of warhead-decorated psoralens as (Immuno) Proteasome inhibitors
ES Schiffrer, M Proj, M Gobec, L Rejc, A Šterman, J Mravljak, S Gobec, ...
Molecules 26 (2), 356, 2021
62021
Synthesis and NMR spectroscopic assignment of chlorinated benzimidazole-2-thione derivatives
M Proj, I Sosič, S Gobec
Tetrahedron Letters 60 (39), 151078, 2019
62019
Encoding BRAF inhibitor functions in protein degraders
DSJ Miller, SA Voell, I Sosič, M Proj, OW Rossanese, G Schnakenburg, ...
RSC medicinal chemistry 13 (6), 731-736, 2022
52022
Fragment-sized and bidentate (Immuno) proteasome inhibitors derived from cysteine and threonine targeting warheads
L Kollár, M Gobec, M Proj, L Smrdel, D Knez, T Imre, Á Gömöry, L Petri, ...
Cells 10 (12), 3431, 2021
52021
The search for novel proline analogs for viscosity reduction and stabilization of highly concentrated monoclonal antibody solutions
M Prašnikar, M Proj, MB Žiberna, B Lebar, B Knez, N Kržišnik, R Roškar, ...
International journal of pharmaceutics 655, 124055, 2024
42024
Optimization of triazolo [4, 5-d] pyrimidines towards human CC chemokine receptor 7 (CCR7) antagonists
M Van Hoof, S Claes, M Proj, T Van Loy, D Schols, S Gobec, W Dehaen, ...
European journal of medicinal chemistry 251, 115240, 2023
42023
A set of experimentally validated decoys for the human CC chemokine receptor 7 (CCR7) obtained by virtual screening
M Proj, S De Jonghe, T Van Loy, M Jukič, A Meden, L Ciber, Č Podlipnik, ...
Frontiers in pharmacology 13, 855653, 2022
42022
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