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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Molecular docking and inhibition studies of vulpinic, carnosic and usnic acids on polyol pathway enzymes
Yeliz Demir, Hamid Ceylan, Cüneyt Türkeş, et al.
Journal of Biomolecular Structure and Dynamics (2021) Vol. 40, Iss. 22, pp. 12008-12021
Closed Access | Times Cited: 77

Showing 1-25 of 77 citing articles:

Cytotoxic effect, enzyme inhibition, and in silico studies of some novel N-substituted sulfonyl amides incorporating 1,3,4-oxadiazol structural motif
Özcan Güleç, Cüneyt Türkeş, Mustafa Arslan, et al.
Molecular Diversity (2022) Vol. 26, Iss. 5, pp. 2825-2845
Open Access | Times Cited: 79
Design, synthesis, biological evaluation and molecular docking studies of novel 1H-1,2,3-Triazole derivatives as potent inhibitors of carbonic anhydrase, acetylcholinesterase and aldose reductase
Derya Aktaş Anıl, Busra Ozturk Aydin, Yeliz Demir, et al.
Journal of Molecular Structure (2022) Vol. 1257, pp. 132613-132613
Closed Access | Times Cited: 72
Discovery of novel benzenesulfonamides incorporating 1,2,3-triazole scaffold as carbonic anhydrase I, II, IX, and XII inhibitors
Aida Buza, Cüneyt Türkeş, Mustafa Arslan, et al.
International Journal of Biological Macromolecules (2023) Vol. 239, pp. 124232-124232
Closed Access | Times Cited: 60
Novel spiroindoline derivatives targeting aldose reductase against diabetic complications: Bioactivity, cytotoxicity, and molecular modeling studies
Özcan Güleç, Cüneyt Türkeş, Mustafa Arslan, et al.
Bioorganic Chemistry (2024) Vol. 145, pp. 107221-107221
Closed Access | Times Cited: 38
Using deep learning and molecular dynamics simulations to unravel the regulation mechanism of peptides as noncompetitive inhibitor of xanthine oxidase
Yi He, Kaifeng Liu, Fuyan Cao, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 12
Novel metabolic enzyme inhibitors designed through the molecular hybridization of thiazole and pyrazoline scaffolds
Belgin Sever, Cüneyt Türkeş, Mehlika Dilek Altıntop, et al.
Archiv der Pharmazie (2021) Vol. 354, Iss. 12
Closed Access | Times Cited: 70
Biological effects of bis-hydrazone compounds bearing isovanillin moiety on the aldose reductase
Gönül Yapar, Hatice Esra Duran, Nebih Lolak, et al.
Bioorganic Chemistry (2021) Vol. 117, pp. 105473-105473
Closed Access | Times Cited: 59
Antispasmodic activity of carnosic acid extracted from rosmarinus officinalis: Isolation, spectroscopic characterization, DFT studies, and in silico molecular docking investigations
Kun Wei, Hitler Louis, Wilfred Emori, et al.
Journal of Molecular Structure (2022) Vol. 1260, pp. 132795-132795
Closed Access | Times Cited: 49
Novel bis-ureido-substituted sulfaguanidines and sulfisoxazoles as carbonic anhydrase and acetylcholinesterase inhibitors
Nebih Lolak, Süleyman Akocak, Mustafa Durgun, et al.
Molecular Diversity (2022) Vol. 27, Iss. 4, pp. 1735-1749
Closed Access | Times Cited: 47
Synthesis and characterization of novel acyl hydrazones derived from vanillin as potential aldose reductase inhibitors
Yeliz Demir, Feyzi Sinan Tokalı, Erbay Kalay, et al.
Molecular Diversity (2022) Vol. 27, Iss. 4, pp. 1713-1733
Closed Access | Times Cited: 46
Isolation of Some Phenolic Compounds from Plantago subulata L. and Determination of Their Antidiabetic, Anticholinesterase, Antiepileptic and Antioxidant Activity
Muhammet Serhat Özaslan, Rüya Sağlamtaş, Yeliz Demir, et al.
Chemistry & Biodiversity (2022) Vol. 19, Iss. 8
Closed Access | Times Cited: 45
Enzyme inhibition, molecular docking, and density functional theory studies of new thiosemicarbazones incorporating the 4‐hydroxy‐3,5‐dimethoxy benzaldehyde motif
Yeliz Demir, Cüneyt Türkeş, M. Serdar Çavuş, et al.
Archiv der Pharmazie (2022) Vol. 356, Iss. 4
Closed Access | Times Cited: 36
Novel acetic acid derivatives containing quinazolin‐4(3H)‐one ring: Synthesis, in vitro, and in silico evaluation of potent aldose reductase inhibitors
Feyzi Sinan Tokalı, Yeliz Demir, Cüneyt Türkeş, et al.
Drug Development Research (2023) Vol. 84, Iss. 2, pp. 275-295
Closed Access | Times Cited: 34
A novel series of thiosemicarbazone hybrid scaffolds: Design, synthesis, DFT studies, metabolic enzyme inhibition properties, and molecular docking calculations
Hasan Yakan, Halit Muğlu, Cüneyt Türkeş, et al.
Journal of Molecular Structure (2023) Vol. 1280, pp. 135077-135077
Closed Access | Times Cited: 27
Exploration of Some Bis‐Sulfide and Bis‐Sulfone Derivatives as Non‐Classical Aldose Reductase İnhibitors
Cüneyt Türkeş, Yeliz Demir, Abdullah Biçer, et al.
ChemistrySelect (2023) Vol. 8, Iss. 5
Closed Access | Times Cited: 19
Astragalus Polysaccharide Ameliorates Renal Inflammatory Responses in a Diabetic Nephropathy by Suppressing the TLR4/NF-κB Pathway
Mingfei Guo, Jiarong Gao, Lei Jiang, et al.
Drug Design Development and Therapy (2023) Vol. Volume 17, pp. 2107-2118
Open Access | Times Cited: 19
Autophagy, Pyroptosis and Ferroptosis are Rising Stars in the Pathogenesis of Diabetic Nephropathy
Xiudan Li, Lifeng Gao, Xuyang Li, et al.
Diabetes Metabolic Syndrome and Obesity (2024) Vol. Volume 17, pp. 1289-1299
Open Access | Times Cited: 8
Discovery of new 2,4-diaminopyrimidines derivatives as EGFRT790M kinase inhibitors: a structure-based approach with DFT calculation, drug-likeness, ADME-toxicity properties evaluation and MD simulation
Muhammad Tukur Ibrahim, Kamal Tabti, Safiya Abdulsalam, et al.
Journal of Umm Al-Qura University for Applied Sciences (2024) Vol. 10, Iss. 2, pp. 257-273
Open Access | Times Cited: 6
Renal protection by acacetin in streptozotocin-induced diabetic nephropathy via TLR4/NF-κB pathway modulation in rats
H.M. Yu, Min Guo
Advances in Clinical and Experimental Medicine (2025) Vol. 34, Iss. 9
Open Access
Comparative analysis of biodesulfurization of dibenzothiophene (DBT) and 4,6-dimethyl dibenzothiophene (4,6-DMDBT) by 4S pathway using molecular simulations
Pushpita Das, Umesh, Lepakshi Barbora, et al.
Preparative Biochemistry & Biotechnology (2025), pp. 1-17
Closed Access
Synthesis, biological evaluation, and in silico study of novel library sulfonates containing quinazolin‐4(3H)‐one derivatives as potential aldose reductase inhibitors
Feyzi Sinan Tokalı, Yeliz Demir, İbrahim Hakkı Demircioğlu, et al.
Drug Development Research (2021)
Closed Access | Times Cited: 48
N‐substituted phthalazine sulfonamide derivatives as non‐classical aldose reductase inhibitors
Cüneyt Türkeş, Mustafa Arslan, Yeliz Demir, et al.
Journal of Molecular Recognition (2022) Vol. 35, Iss. 12
Closed Access | Times Cited: 30
Carvacrol protects against λ‐Cyhalothrin‐induced hepatotoxicity and nephrotoxicity by modulating oxidative stress, inflammation, apoptosis, endoplasmic reticulum stress, and autophagy
Mustafa İleritürk, Fatih Mehmet Kandemir
Environmental Toxicology (2023) Vol. 38, Iss. 7, pp. 1535-1547
Closed Access | Times Cited: 14
The Role of Immune Cells in DKD: Mechanisms and Targeted Therapies
Qiu-Yue Peng, Ying An, Zongzhe Jiang, et al.
Journal of Inflammation Research (2024) Vol. Volume 17, pp. 2103-2118
Open Access | Times Cited: 4
Effects of Carnosic and Usnic Acid on Pentose Phosphate Pathway Enzymes: An Experimental and Molecular Docking Study
Yeliz Demir, Neslihan Öztürk, Murat Isıyel, et al.
ChemistrySelect (2024) Vol. 9, Iss. 27
Closed Access | Times Cited: 4
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