Doç.Dr. CÜNEYT TÜRKEŞ

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Novel metabolic enzyme inhibitors designed through the molecular hybridization of thiazole and pyrazoline scaffolds.

Sever B., Türkeş C., Altıntop M. D., Demir Y., Akalın Çiftçi G., Beydemir Ş.

Archiv der Pharmazie , cilt.354, sa.12, 2021 (SCI-Expanded)

Infection Medications: Assessment In-Vitro Glutathione S-Transferase Inhibition and Molecular Docking Study

TÜRKEŞ C., Demir Y., Beydemir Ş.

ChemistrySelect , cilt.6, sa.43, ss.11915-11924, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

Biological effects of bis-hydrazone compounds bearing isovanillin moiety on the aldose reductase.

Yapar G., Esra Duran H., Lolak N., Akocak S., Türkeş C., Durgun M., et al.

Bioorganic chemistry , cilt.117, ss.105473, 2021 (SCI-Expanded)

Calcium Channel Blockers: The Effect of Glutathione S-Transferase Enzyme Activity and Molecular Docking Studies

TÜRKEŞ C., Kesebir A. Ö., Demir Y., KÜFREVİOĞLU Ö. İ., Beydemir Ş.

ChemistrySelect , cilt.6, sa.40, ss.11137-11143, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

Benzenesulfonamide derivatives as potent acetylcholinesterase, alpha-glycosidase, and glutathione S-transferase inhibitors: biological evaluation and molecular docking studies

Taslimi P., Işık M., Türkan F., Durgun M., Türkeş C., Gülçin İ., et al.

JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS , cilt.39, sa.15, ss.5449-5460, 2021 (SCI-Expanded)

Transition-Metal Complexes of Bidentate Schiff-Base Ligands: In Vitro and In Silico Evaluation as Non-Classical Carbonic Anhydrase and Potential Acetylcholinesterase Inhibitors

Yaşar Ü., Gönül İ., Türkeş C., Demir Y., Beydemir Ş.

ChemistrySelect , cilt.6, sa.29, ss.7278-7284, 2021 (SCI-Expanded)

Design, synthesis, characterization, in vitro and in silico evaluation of novel imidazo[2,1-b][1,3,4]thiadiazoles as highly potent acetylcholinesterase and non-classical carbonic anhydrase inhibitors

Askin S., Tahtaci H., Türkeş C., Demir Y., Ece A., Akalın Çiftçi G., et al.

BIOORGANIC CHEMISTRY , cilt.113, 2021 (SCI-Expanded)

Synthesis, characterization, and inhibition study of novel substituted phenylureido sulfaguanidine derivatives as α-glycosidase and cholinesterase inhibitors.

Akocak S., Taslimi P., Lolak N., Işık M., Durgun M., Budak Y., et al.

Chemistry & biodiversity , cilt.18, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

Novel benzoic acid derivatives: Synthesis and biological evaluation as multitarget acetylcholinesterase and carbonic anhydrase inhibitors.

Kalaycı M., Türkeş C., Arslan M., Demir Y., Beydemir Ş.

Archiv der Pharmazie , cilt.354, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

A new series of 2,4-thiazolidinediones endowed with potent aldose reductase inhibitory activity

Sever B., Altlntop M. D., Demir Y., Türkeş C., Özbaş K., Çiftçi G. A., et al.

Open Chemistry , cilt.19, sa.1, ss.347-357, 2021 (SCI-Expanded)

Gadolinium-based contrast agents: in vitro paraoxonase 1 inhibition, in silico studies

Beydemir Ş., Türkeş C., Yalçın A.

Drug and Chemical Toxicology , cilt.44, sa.5, ss.508-517, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

Calcium channel blockers: molecular docking and inhibition studies on carbonic anhydrase I and II isoenzymes

Türkeş C., Demir Y., Beydemir S.

Journal of Biomolecular Structure and Dynamics , cilt.39, sa.5, ss.1672-1680, 2021 (SCI-Expanded)

Mannich reaction derived novel boron complexes with amine-bis(phenolate) ligands: Synthesis, spectroscopy and in vitro/in silico biological studies

Kilic A., Beyazsakal L., Işık M., Türkeş C., Necip A., Takım K., et al.

Journal of Organometallic Chemistry , cilt.927, 2020 (SCI-Expanded)

Thiazolyl-pyrazoline derivatives: In vitro and in silico evaluation as potential acetylcholinesterase and carbonic anhydrase inhibitors.

Sever B., Türkeş C., Altıntop M., Demir Y., Beydemir Ş.

International journal of biological macromolecules , cilt.163, ss.1970-1988, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma

Synthesis, characterization, biological evaluation, and in silico studies of novel 1,3-diaryltriazene-substituted sulfathiazole derivatives

Isik M., Akocak S., Lolak N., Taslimi P., Türkeş C., Gülçin İ., et al.

ARCHIV DER PHARMAZIE , cilt.353, sa.9, 2020 (SCI-Expanded)

Synthesis, characterization, inhibition effects, and molecular docking studies as acetylcholinesterase, ?-glycosidase, and carbonic anhydrase inhibitors of novel benzenesulfonamides incorporating 1,3,5-triazine structural motifs

Lolak N., Akocak S., Türkeş C., Taslimi P., Isik M., Beydemir S., et al.

BIOORGANIC CHEMISTRY , cilt.100, 2020 (SCI-Expanded)

Sulfonamides incorporating ketene N,S-acetal bioisosteres as potent carbonic anhydrase and acetylcholinesterase inhibitors

Istrefi Q., Türkeş C., Arslan M., Demir Y., Nixha A. R., Beydemir S., et al.

ARCHIV DER PHARMAZIE , cilt.353, sa.6, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma

Molecular docking and investigation of 4-(benzylideneamino)- and 4-(benzylamino)-benzenesulfonamide derivatives as potent AChE inhibitors

Işık M., Demir Y., Durgun M., Türkeş C., Necip A., Beydemir Ş.

CHEMICAL PAPERS , cilt.74, sa.5, ss.1395-1405, 2020 (SCI-Expanded)

Benzenesulfonamide derivatives containing imine and amine groups: Inhibition on human paraoxonase and molecular docking studies

Isik M., Beydemir S., Demir Y., Durgun M., Türkeş C., Nasir A., et al.

INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES , cilt.146, ss.1111-1123, 2020 (SCI-Expanded)

Inhibition of Human Serum Paraoxonase-I with Antimycotic Drugs: In Vitro and In Silico Studies

Türkeş C., Beydemir S.

APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY , cilt.190, sa.1, ss.252-269, 2020 (SCI-Expanded) Sürdürülebilir Kalkınma

Molecular Docking Studies and Inhibition Properties of Some Antineoplastic Agents against Paraoxonase-I.

Demir Y., Türkeş C., Beydemir Ş.

Anti-cancer agents in medicinal chemistry , cilt.20, ss.887-896, 2020 (SCI-Expanded)

Synthesis, characterisation, biological evaluation and in silico studies of sulphonamide Schiff bases

Durgun M., Türkeş C., Isik M., Demir Y., Sakli A., Kuru A., et al.

JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY , cilt.35, sa.1, ss.950-962, 2020 (SCI-Expanded)

New Isoindole-1,3-dione Substituted Sulfonamides as Potent Inhibitors of Carbonic Anhydrase and Acetylcholinesterase: Design, Synthesis, and Biological Evaluation

Gundogdu S., Türkeş C., Arslan M., Demir Y., Beydemir S.

CHEMISTRYSELECT , cilt.4, sa.45, ss.13347-13355, 2019 (SCI-Expanded)

A potential risk factor for paraoxonase 1: in silico and in-vitro analysis of the biological activity of proton-pump inhibitors

Türkeş C.

JOURNAL OF PHARMACY AND PHARMACOLOGY , cilt.71, sa.10, ss.1553-1564, 2019 (SCI-Expanded)

In Vitro and In Silico Studies on the Toxic Effects of Antibacterial Drugs as Human Serum Paraoxonase 1 Inhibitor

Türkeş C., Beydemir Ş., Küfrevioğlu Ö. İ.

CHEMISTRYSELECT , cilt.4, sa.33, ss.9731-9736, 2019 (SCI-Expanded)

Anti-diabetic Properties of Calcium Channel Blockers: Inhibition Effects on Aldose Reductase Enzyme Activity

Türkeş C., Demir Y., Beydemir Ş.

APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY , cilt.189, sa.1, ss.318-329, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma

Synthesis, biological evaluation and in silico studies of novel N-substituted phthalazine sulfonamide compounds as potent carbonic anhydrase and acetylcholinesterase inhibitors

Türkeş C., Arslan M., Demir Y., Cocaj L., Nixha A. R., Beydemir Ş.

BIOORGANIC CHEMISTRY , cilt.89, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma

Investigation of Potential Paraoxonase-I Inhibitors by Kinetic and Molecular Docking Studies: Chemotherapeutic Drugs

Türkeş C.

PROTEIN AND PEPTIDE LETTERS , cilt.26, sa.6, ss.392-402, 2019 (SCI-Expanded) Sürdürülebilir Kalkınma

In vitro inhibitory effects of palonosetron hydrochloride, bevacizumab and cyclophosphamide on purified paraoxonase-I (hPON1) from human serum

Türkeş C., Söyüt H., Beydemir Ş.

ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY , cilt.42, ss.252-257, 2016 (SCI-Expanded)

Human serum paraoxonase-1 (hPON1): in vitro inhibition effects of moxifloxacin hydrochloride, levofloxacin hemihidrate, cefepime hydrochloride, cefotaxime sodium and ceftizoxime sodium

Türkeş C., Söyüt H., Beydemir Ş.

JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY , cilt.30, sa.4, ss.622-628, 2015 (SCI-Expanded)

Effect of calcium channel blockers on paraoxonase-1 (PON1) activity and oxidative stress

Türkeş C., Söyüt H., Beydemir Ş.

PHARMACOLOGICAL REPORTS , cilt.66, sa.1, ss.74-80, 2014 (SCI-Expanded)

Synthesis and paroxonase activities of novel bromophenols

Akbaba Y., Türkeş C., Polat L., Söyüt H., Şahin E., Menzek A., et al.

JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY , cilt.28, sa.5, ss.1073-1079, 2013 (SCI-Expanded)

Diğer Dergilerde Yayınlanan Makaleler

Inhibition Effects of Phenolic Compounds on Human Serum Paraoxonase-1 Enzyme

Türkeş C.

Journal of the Institute of Science and Technology , cilt.9, sa.2, ss.1013-1022, 2019 (Hakemli Dergi)

Inhibition Effects of Gemcitabine Hydrochloride, Acyclovir, and 5-Fluorouracil on Human Serum Paraoxonase-1 (hPON1): In Vitro

Türkeş C., Söyüt H., Beydemir Ş.

Open Journal of Biochemistry , cilt.1, sa.1, ss.10-15, 2013 (Hakemli Dergi)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

New Schiff Base Ligand-Complexes: Synthesis, Characterization, and Biological Evaluation

Tuna Yıldırım S., Türkeş C., Kağan Yeniçeri E. K., Duran H. E., Altay A., Beydemir Ş.

3rd Eurasia Biochemical Approaches & Technologies Congress (EBAT), Antalya, Türkiye, 4 - 07 Kasım 2021, ss.98

Synthesis and Biological Evaluation of Novel Schiff Base Ligand-Complexes as Potential Cholinesterase Inhibitors

Tuna Yıldırım S., Türkeş C., Duran H. E., Beydemir Ş.

3rd Eurasia Biochemical Approaches & Technologies Congress (EBAT), Antalya, Türkiye, 4 - 07 Kasım 2021, ss.1

Novel Schiff Base Ligand-Complexes: Synthesis, Characterization, and Biological Evaluation as Aldose Reductase Inhibitors

Tuna Yıldırım S., Türkeş C., Duran H. E., Beydemir Ş.

3rd Eurasia Biochemical Approaches & Technologies Congress (EBAT), Antalya, Türkiye, 4 - 07 Kasım 2021, ss.1

Inhibition Effect of 7-deazahypoxanthine on Some Metabolic Enzymes

Demir Y., Türkeş C., Ertano B. Y., Aksakal E., Erdoğan O., Beydemir Ş.

3rd Eurasia Biochemical Approaches & Technologies Congress (EBAT), Antalya, Türkiye, 4 - 07 Kasım 2021, ss.1

Synthesis, Characterization, Biological Evaluation and Molecular Docking Studies of Novel Azoimine Compounds with Sulfisoxazole Backbone

Işık M., Lolak N., Akocak S., Duran H. E., Türkeş C., Durgun M., et al.

3rd Eurasia Biochemical Approaches & Technologies Congress (EBAT), Antalya, Türkiye, 4 - 07 Kasım 2021, ss.96

The Influence of Some Antibiotic Drugs on Aldose Reductase and Sorbitol Dehydrogenase Enzymes

Türkeş C., Demir Y., Beydemir Ş.

3rd Eurasia Biochemical Approaches & Technologies Congress (EBAT), Antalya, Türkiye, 4 - 07 Kasım 2021, ss.1

Synthesis and Biological Evaluation of Novel Schiff Base Ligand-Complexes as Potential Cholinesterase Inhibitors

TUNA YILDIRIM S., TÜRKEŞ C., DURAN H. E., BEYDEMİR Ş.

3rd Eurasia Biochemical Approaches & Technologies Congress (EBAT), Antalya, Türkiye, 4 - 07 Kasım 2021

Synthesis of Novel 1-Benzyl-2-Substituted-Benzimidazole-5-Sulfonamide Derivatives and Investigation of Their Effects on Cholinesterases and Carbonic Anhydrase Enzymes

Er A., Eroğlu Y., Bozbey İ., Türkeş C.

13th International Symposium on Pharmaceutical Sciences, Ankara, Türkiye, 22 - 25 Haziran 2021, ss.56

New Schiff Base Ligand-Complexes as Carbonic Anhydrase and Cholinesterase Enzyme Inhibitors: Synthesis, Characterization and in Vitro / in Silico Evaluation

Tuna Yıldırım S., Güğercin R. S., Duran H. E., Türkeş C.

13th International Symposium on Pharmaceutical Sciences, Ankara, Türkiye, 22 - 25 Haziran 2021, ss.107

Inhibitory Properties of Bis-thiomethylcyclohexanone Derivatives on Aldose Reductase Enzyme Activity

TÜRKEŞ C., DEMİR Y., BİÇER A., BEYDEMİR Ş., TURGUT CİN G., GÜLTEKİN M. S.

Eurasia Biochemical Approaches Technologies (EBAT) Congress, Antalya, Türkiye, 26 - 29 Ekim 2019

Influence of Some Phenolic Compounds on Aldose Reductase and Sorbitol Dehydrogenase Enzymes

TÜRKEŞ C., DEMİR Y., BEYDEMİR Ş.

Eurasia Biochemical Approaches Technologies (EBAT) Congress, Antalya, Türkiye, 26 - 29 Ekim 2019