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Tuğçe Gür Maz
Tuğçe Gür Maz
在 gazi.edu.tr 的电子邮件经过验证
标题
引用次数
引用次数
年份
Drug discovery approaches targeting 5-lipoxygenase-activating protein (FLAP) for inhibition of cellular leukotriene biosynthesis
ZT Gür, B Çalışkan, E Banoglu
European Journal of Medicinal Chemistry 153, 34-48, 2018
642018
Identification of multi-target inhibitors of leukotriene and prostaglandin E2 biosynthesis by structural tuning of the FLAP inhibitor BRP-7
ZT Gür, B Çalışkan, UI Garscha, A Olgaç, US Schubert, J Gerstmeier, ...
European Journal of Medicinal Chemistry, 876-899, 2018
292018
Shifting the biosynthesis of leukotrienes toward specialized pro-resolving mediators by the 5-lipoxygenase-activating protein (FLAP) antagonist BRP-201
C Kretzer, PM Jordan, R Bilancia, A Rossi, T Gür Maz, E Banoglu, ...
Journal of inflammation research, 911-925, 2022
212022
Benzimidazole derivatives as potent and isoform selective tumor-associated carbonic anhydrase IX/XII inhibitors
AG Uslu, TG Maz, A Nocentini, E Banoglu, CT Supuran, B Çalışkan
Bioorganic Chemistry 95, 103544, 2020
172020
Novel potent benzimidazole-based microsomal prostaglandin E2 synthase-1 (mPGES-1) inhibitors derived from BRP-201 that also inhibit leukotriene C4 synthase
AG Ergül, TG Maz, C Kretzer, A Olğaç, PM Jordan, B Çalışkan, O Werz, ...
European Journal of Medicinal Chemistry 231, 114167, 2022
132022
Novel Piperazine Amides of Cinnamic Acid Derivatives as Tyrosinase Inhibitors
ZT Gur, FS Senol, S Shekfeh, IE Orhan, E Banoglu, B Caliskan
Letters in Drug Design & Discovery, 2019
112019
Optimisation by Design of Experiment of Benzimidazol-2-One Synthesis under Flow Conditions
S Mostarda, T Gür Maz, A Piccinno, B Cerra, E Banoglu
Molecules 24 (13), 2447, 2019
92019
Simple heteroaryl modifications in the 4, 5-diarylisoxazol-3-carboxylic acid scaffold favorably modulates the activity as dual mPGES-1/5-LO inhibitors with in vivo efficacy
T Gürses, A Olğaç, U Garscha, TG Maz, NB Bal, O Uludağ, B Çalışkan, ...
Bioorganic Chemistry 112, 104861, 2021
82021
A Series of Thiadiazolyl‐Benzenesulfonamides Incorporating an Aromatic Tail as Isoform‐Selective, Potent Carbonic Anhydrase II/XII Inhibitors
E Banoglu, T Ercanlı, T Gür Maz, D Vullo, A Bonardi, P Gratteri, ...
ChemMedChem 17 (10), e202200056, 2022
62022
Exploration of anti-tyrosinase effect of Geranium glaberrimum Boiss. & Heldr. with in silico approach and survey of 21 Geranium species
OC Ozer, IE Orhan, B Çalışkan, FSS Deniz, A Gokbulut, TG Maz, A Aysal, ...
Journal of Herbal Medicine 27, 100431, 2021
52021
Benzoxazolone-5-urea derivatives as human soluble epoxide hydrolase (sEH) inhibitors
T Gur Maz, B Koc, PM Jordan, K Ibis, B Çalışkan, O Werz, E Banoglu
ACS omega 8 (2), 2445-2454, 2023
32023
Design, Synthesis and Evaluation of Aryl‐Tailored Oxadiazole‐thiones as New Urease Inhibitors
TG Maz, HB Caliskan, I Capan, B Caliskan, B Özçelik, E Banoglu
ChemistrySelect 8 (8), e202204449, 2023
22023
Design and Synthesis of Some Arylhydrazone Derivatives as Potential FAAH Inhibitors
ZTG Maz, S TURANLI, HB CALISKAN
Journal of Faculty of Pharmacy of Ankara University 47 (1), 111-119, 2023
22023
Crystal structure and Hirshfeld surface analysis of methyl 1-(2, 4-dichlorobenzyl)-5-methyl-1H-pyrazole-3-carboxylate
A Aydin, M Akkurt, ZT Gur, E Banoglu
European Journal of Chemistry 9 (4), 347-352, 2018
22018
Crystal structure and Hirshfeld surface analysis of 1-(2, 4-dichlorobenzyl)-5-methyl-N-(thiophene-2-sulfonyl)-1H-pyrazole-3-carboxamide
A Aydin, M Akkurt, ZT Gur, E Banoğlu
Acta Crystallographica Section E: Crystallographic Communications 74 (5 …, 2018
22018
Development and molecular modeling studies of new thiadiazole piperazine urea derivatives as potential fatty acid amide hydrolase inhibitors
T Gur Maz, S Turanlı, HB Caliskan, B Çalışkan, E Banoglu
Archiv der Pharmazie 355 (8), 2200082, 2022
12022
Novel 1, 3, 4-oxadiazole derivatives as highly potent microsomal prostaglandin E2 synthase-1 (mPGES-1) inhibitors
TG Maz, P Dahlke, AG Ergül, A Olğaç, PM Jordan, B Çalışkan, O Werz, ...
Bioorganic Chemistry 147, 107383, 2024
2024
Synthesis of some piperazine/piperidine amides of chromone-2-carboxylic acid as potential soluble epoxide hydrolase (sEH) inhibitors
TG Maz, HB Caliskan
Organic Communications 16 (1), 34, 2023
2023
Novel potent benzimidazole-based microsomal prostaglandin E2 synthase-1 (mPGES-1) inhibitors derived from BRP-201 that also inhibit leukotriene C4 synthase
AG Ergul, TG Maz, C Kretzer, A Olgac, PM Jordan, B Caliskan, O Werz, ...
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY 231, 2022
2022
Synthesis and evaluation of antibacterial and antimycobacterial activities of some new pyrazole derivatives
T Gur Maz, N Karaca, S Levent, B Çalışkan, F Demirci, E Banoğlu
Journal of Research in Pharmacy 25 (5), 531-539, 2021
2021
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