Nebih Lolak

Adıyaman University — Turkey

Biochemistry, Genetics and Molecular Biology · Life Sciences

22h-index1.5kcitations53works2.22yr avg
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Research Topics

Enzyme function and inhibition(40), Cholinesterase and Neurodegenerative Diseases(25), Synthesis and Catalytic Reactions(18), Phenothiazines and Benzothiazines Synthesis and Activities(16), Chemical Reactions and Mechanisms(13)

Publications53 total

Design and Synthesis of 4-Arylazo Pyrazole Carboxamides as Dual AChE/BChE Inhibitors: Kinetic and In Silico Evaluation
Pharmaceuticals·2026Open Access
Isovanillin-derived bis-hydrazones as dual cholinesterase and carbonic anhydrase inhibitors: synthesis, enzymatic profiling, and computational insights from molecular docking and dynamics
Future Medicinal Chemistry·2026· 1 citedOpen Access
Isovanillin-derived bis-hydrazones as dual cholinesterase and carbonic anhydrase inhibitors: synthesis, enzymatic profiling, and computational insights from molecular docking and dynamics
Figshare·2026Open Access
Design and Synthesis of 4-Arylazo Pyrazole Carboxamides as Dual AChE/BChE Inhibitors: Kinetic and In Silico Evaluation
Repository KITopen (Karlsruhe Institute of Technology)·2026Open Access
Isovanillin-derived bis-hydrazones as dual cholinesterase and carbonic anhydrase inhibitors: synthesis, enzymatic profiling, and computational insights from molecular docking and dynamics
Figshare·2026Open Access
Exploring the Carbonic Anhydrase Activation Properties of 4-arylazo-3,5- diamino-1H-pyrazoles against hCA I, II, IV, and VII isoenzymes
Current Topics in Medicinal Chemistry·2025· 2 cited
In silico prediction of some peroxisome proliferator-activated receptor (PPAR) agonists targeted drugs as potential SARS-Cov-2 inhibitors
Bioorganic & Medicinal Chemistry Reports·2025Open Access
Sulfonamide‐Bearing Pyrazolone Derivatives as Multitarget Therapeutic Agents: Design, Synthesis, Characterization, Biological Evaluation, In Silico <scp>ADME</scp>/T Profiling and Molecular Docking Study
Pharmacology Research & Perspectives·2025· 8 citedOpen Access
Investigating the Anti‐Inflammatory Potential of SLC‐0111: A Carbonic Anhydrase Inhibitor Targeting Cyclooxygenase‐Mediated Inflammatory Pathways in a Carrageenan‐Induced Rat Model
Journal of Biochemical and Molecular Toxicology·2025· 2 citedOpen Access
Interactions of novel 1,3-diaryltriazene-sulfamethazines with carbonic anhydrases: Kinetic studies and in silico simulations
Archives of Biochemistry and Biophysics·2024· 7 cited
Bis‐Ureido‐Substituted Benzenesulfonamides: Evaluation of Their Antibacterial, Anticholinesterase, and Cytotoxicity Properties
ChemistrySelect·2024· 3 cited
1,3-Diaryl Triazenes Incorporating Disulfonamides Show Both AntiproliferativeActivity and Effective Inhibition of Tumor-associated Carbonic Anhydrases IX andXII
Anti-Cancer Agents in Medicinal Chemistry·2024
Exploring the potency of diazo‐coumarin containing hybrid molecules: Selective inhibition of tumor‐associated carbonic anhydrase isoforms IX and XII
ChemMedChem·2024· 6 cited
Design and Synthesis of Pyrazole Carboxamide Derivatives as Selective Cholinesterase and Carbonic Anhydrase Inhibitors: Molecular Docking and Biological Evaluation
Chemistry & Biodiversity·2023· 22 citedOpen Access
Investigation of Antimicrobial, Cytotoxic, and Larvicidal Activities of Favipiravir
ChemistrySelect·2023· 1 cited
Potent and selective carbonic anhydrase inhibition activities of pyrazolones bearing benzenesulfonamides
Bioorganic & Medicinal Chemistry Letters·2023· 12 citedOpen Access
Synthesis and Characterization of Novel 1,3‐Diaryltriazene‐Substituted Sulfaguanidine Derivatives as Selective Carbonic Anhydrase Inhibitors: Biological Evaluation, <i>in Silico</i> ADME/T and Molecular Docking Study
Chemistry & Biodiversity·2023· 5 cited
In vitro multitarget activity of sulfadiazine substituted triazenes as antimicrobial, cytotoxic, and larvicidal agents
Journal of Biochemical and Molecular Toxicology·2023· 8 citedOpen Access
Evaluation of cytotoxic, antifungal, and larvicidal activities of different bis‐sulfonamide Schiff base compounds
Journal of Biochemical and Molecular Toxicology·2023· 5 citedOpen Access
Novel 1,3-diaryltriazene-substituted sulfaguanidine derivatives as selective carbonic anhydrase inhibitors: Synthesis, characterization, inhibition effects, and molecular docking studies
Research Square (Research Square)·2023· 2 citedOpen Access
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Frequent Co-authors

Süleyman Akocak(44), Claudiu T. Supuran(16), Cüneyt Türkeş(14), Mustafa Durgun(13), Mesut Işık(11), Şükrü Beydemir(11), Hatice Esra Duran(8), Silvia Bua(7), Mehmet Boğa(6), İlhami Gülçın(5), Nebih Lolak(5), Muhammed Tuneğ(5), Andrea Petreni(5), Parham Taslımı(4), Alessio Nocentini(4), Gulcin Karakoc(4), Yakup Budak(3), Murat Koca(3), Tuba Tekeli(3), Aslınur Doğan(3)