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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:

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
Sercan Askin, Hakan Tahtacı, Cüneyt Türkeş, et al.
Bioorganic Chemistry (2021) Vol. 113, pp. 105009-105009
Closed Access | Times Cited: 92

Showing 26-50 of 92 citing articles:

Design, synthesis, and aldose reductase inhibitory effect of some novel carboxylic acid derivatives bearing 2-substituted-6-aryloxo-pyridazinone moiety
Mevlüt Akdağ, Azime Berna Özçelik, Yeliz Demir, et al.
Journal of Molecular Structure (2022) Vol. 1258, pp. 132675-132675
Closed Access | Times Cited: 30
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
New N -(1,3,4-thiadiazole-2-yl)acetamide derivatives as human carbonic anhydrase I and II and acetylcholinesterase inhibitors
Sam Dawbaa, Cüneyt Türkeş, Demokrat Nuha, et al.
Journal of Biomolecular Structure and Dynamics (2024), pp. 1-19
Closed Access | Times Cited: 4
Structure-based inhibition of acetylcholinesterase and butyrylcholinesterase with 2-Aryl-6-carboxamide benzoxazole derivatives: synthesis, enzymatic assay, and in silico studies
Burak Kuzu, Mehmet Abdullah Alagöz, Yeliz Demir, et al.
Molecular Diversity (2024)
Open Access | Times Cited: 4
Biological evaluation and in silico study of benzohydrazide derivatives as paraoxonase 1 inhibitors
Işıl Nihan Korkmaz, Cüneyt Türkeş, Yeliz Demir, et al.
Journal of Biochemical and Molecular Toxicology (2022) Vol. 36, Iss. 11
Closed Access | Times Cited: 25
In Vitro Inhibitory Activity and Molecular Docking Study of Selected Natural Phenolic Compounds as AR and SDH Inhibitors**
Cüneyt Türkeş, Yeliz Demir, Şükrü Beydemir
ChemistrySelect (2022) Vol. 7, Iss. 48
Open Access | Times Cited: 23
Solvent-Free Synthesis, In Vitro and In Silico Studies of Novel Potential 1,3,4-Thiadiazole-Based Molecules against Microbial Pathogens
Ihsan A. Shehadi, Mohamad T. Abdelrahman, Mohamed Abdelraof, et al.
Molecules (2022) Vol. 27, Iss. 2, pp. 342-342
Open Access | Times Cited: 22
Methyl benzoate derivatives: in vitro Paraoxonase 1 inhibition and in silico studies
Işıl Nihan Korkmaz, Cüneyt Türkeş, Yeliz Demir, et al.
Journal of Biochemical and Molecular Toxicology (2022) Vol. 36, Iss. 10
Closed Access | Times Cited: 21
Thiadiazole – A promising structure in design and development of anti-Alzheimer agents
Maryam Hatami, Zahra Basri, Batool Khani Sakhvidi, et al.
International Immunopharmacology (2023) Vol. 118, pp. 110027-110027
Closed Access | Times Cited: 12
1,3,4-Thiadiazole: A Versatile Pharmacophore of Medicinal Significance
Madhu Bala, Poonam Piplani, Amar Deep Ankalgi, et al.
Medicinal Chemistry (2023) Vol. 19, Iss. 8, pp. 730-756
Closed Access | Times Cited: 11
Molecular Docking Studies and the Effect of Fluorophenylthiourea Derivatives on Glutathione‐Dependent Enzymes
Yeliz Demir, Cüneyt Türkeş, Ömer İrfan Küfrevioğlu, et al.
Chemistry & Biodiversity (2022) Vol. 20, Iss. 1
Closed Access | Times Cited: 20
Boosting the antimicrobial performance based on new fused spirothiazolidine framework analogs
Walaa I. El-Sofany, Eman M. Flefel, Osama M. Darwesh, et al.
Journal of the Iranian Chemical Society (2022) Vol. 19, Iss. 10, pp. 4223-4236
Open Access | Times Cited: 19
Towards Covid-19 TMPRSS2 enzyme inhibitors and antimicrobial agents: Synthesis, antimicrobial potency, molecular docking, and drug-likeness prediction of thiadiazole-triazole hybrids
Huda R. M. Rashdan, Aboubakr H. Abdelmonsef
Journal of Molecular Structure (2022) Vol. 1268, pp. 133659-133659
Open Access | Times Cited: 18
Targeting Neuroinflammation as Disease Modifying Approach to Alzheimer’s Disease: Potential and Challenges
Smita Jain, Ritu Singh, Sarvesh Paliwal, et al.
Mini-Reviews in Medicinal Chemistry (2023) Vol. 23, Iss. 22, pp. 2097-2116
Closed Access | Times Cited: 10
Ophthalmic drugs: in vitro paraoxonase 1 inhibition and molecular docking studies
Büşra Çalışkan, Yeliz Demir, Cüneyt Türkeş
Biotechnology and Applied Biochemistry (2021) Vol. 69, Iss. 6, pp. 2273-2283
Closed Access | Times Cited: 24
The synthesis, biological evaluation and in silico studies of asymmetric 3,5-diaryl-rhodanines as novel inhibitors of human carbonic anhydrase isoenzymes
Kemal Yararli, Ebru Bilen Ozer, Sinan Bayındır, et al.
Journal of Molecular Structure (2022) Vol. 1276, pp. 134783-134783
Closed Access | Times Cited: 16
Identification, crystallization, and first X-ray structure analyses of phenyl boronic acid-based inhibitors of human carbonic anhydrase-II
Saima Rasheed, Noor ul Huda, S. Zoë Fisher, et al.
International Journal of Biological Macromolecules (2024) Vol. 267, pp. 131268-131268
Closed Access | Times Cited: 2
The untold story of starch as a catalyst for organic reactions
Masoud Sadeghi
RSC Advances (2024) Vol. 14, Iss. 18, pp. 12676-12702
Open Access | Times Cited: 2
Synthesis of Bilaterally Thiadiazole Substituted vic-Dioxime Ligands and Investigation of Their Polymeric Metal Complexes
Omar Khalid, M. Salah, Ahmed Hamdi Mirghani, et al.
Journal of Molecular Structure (2024) Vol. 1318, pp. 139234-139234
Closed Access | Times Cited: 2
Phthalimide‐tethered imidazolium salts: Synthesis, characterization, enzyme inhibitory properties, and in silico studies
Murat Yiğit, Yeliz Demir, Duygu Barut Celepci, et al.
Archiv der Pharmazie (2022) Vol. 355, Iss. 12
Open Access | Times Cited: 13
Bis-pharmacophore of cinnamaldehyde-clubbed thiosemicarbazones as potent carbonic anhydrase-II inhibitors
Asif Rasool, Zahra Batool, Majid Khan, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 13
Anticholinesterase Compounds from Endemic Prangos uechtritzii
Gökay Albayrak, Serdar Demir, Halil Koyu, et al.
Chemistry & Biodiversity (2022) Vol. 19, Iss. 11
Closed Access | Times Cited: 12
Design, synthesis, biological evaluation and docking analysis of pyrrolidine-benzenesulfonamides as carbonic anhydrase or acetylcholinesterase inhibitors and antimicrobial agents
Samet Poyraz, H. Ali Döndaş, Cem Yamalı, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 42, Iss. 7, pp. 3441-3458
Closed Access | Times Cited: 6
Synthesis, Theoretical, in Silico and in Vitro Biological Evaluation Studies of New Thiosemicarbazones as Enzyme Inhibitors
Musa Erdoğan, M. Serdar Çavuş, Halit Muğlu, et al.
Chemistry & Biodiversity (2023) Vol. 20, Iss. 11
Closed Access | Times Cited: 6
Design, synthesis, and biological evaluation of novel tryptanthrin derivatives as selective acetylcholinesterase inhibitors for the treatment of Alzheimer's disease
Jucheng Xia, Shuanghong Dong, Lili Yang, et al.
Bioorganic Chemistry (2023) Vol. 143, pp. 106980-106980
Closed Access | Times Cited: 6

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