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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.

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Showing 26-50 of 81 citing articles:

Design, synthesis, in vitro evaluation, and docking studies on ibuprofen derived 1,3,4-oxadiazole derivatives as dual α-glucosidase and urease inhibitors
Saima Daud, Obaid‐ur‐Rahman Abid, Asma Sardar, et al.
Medicinal Chemistry Research (2022) Vol. 31, Iss. 2, pp. 316-336
Closed Access | Times Cited: 17
Larvicidal activity of plant extracts by inhibition of detoxification enzymes in Culex pipiens
Habeeb M. Al‐Solami
Journal of King Saud University - Science (2021) Vol. 33, Iss. 3, pp. 101371-101371
Open Access | Times Cited: 24
Dual targeting of acetylcholinesterase and tau aggregation: Design, synthesis and evaluation of multifunctional deoxyvasicinone analogues for Alzheimer’s disease
Shoaib Manzoor, Moustafa T. Gabr, Bisma Rasool, et al.
Bioorganic Chemistry (2021) Vol. 116, pp. 105354-105354
Closed Access | Times Cited: 24
Catalytic Antioxidant Activity of Bis-Aniline-Derived Diselenides as GPx Mimics
Giancarlo V. Botteselle, Welman C. Elias, Luana Bettanin, et al.
Molecules (2021) Vol. 26, Iss. 15, pp. 4446-4446
Open Access | Times Cited: 22
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
Pharmacological assessment of disulfide–triazine hybrids: synthesis, enzyme inhibition, and molecular docking study
Fikret Türkan, Adnan Çetin, Przemysław Rozbicki, et al.
Medicinal Chemistry Research (2024) Vol. 33, Iss. 7, pp. 1205-1217
Closed Access | Times Cited: 2
Synthesis and Biological Studies of Acetophenone-Based Novel Chalcone, Semicarbazone, Thiosemicarbazone and Indolone Derivatives: Structure-Activity Relationship, Molecular Docking, Molecular Dynamics, and Kinetic Studies
Aynur Farzaliyeva, Halil Şenol, Parham Taslimi, et al.
Journal of Molecular Structure (2024) Vol. 1321, pp. 140197-140197
Closed Access | Times Cited: 2
Silver N‐heterocyclic carbene complexes bearing fluorinated benzyl group: Synthesis, characterization, crystal structure, computational studies, and inhibitory properties against some metabolic enzymes
Selma Bal, Özlem Demirci, Betül Şen, et al.
Applied Organometallic Chemistry (2021) Vol. 35, Iss. 9
Closed Access | Times Cited: 21
Novel amino acid Schiff base Zn(II) complexes as new therapeutic approaches in diabetes and Alzheimer's disease: Synthesis, characterization, biological evaluation, and molecular docking studies
Ayşegül Şenocak, Nilay Taş, Parham Taslimi, et al.
Journal of Biochemical and Molecular Toxicology (2021) Vol. 36, Iss. 3
Closed Access | Times Cited: 20
Benzimidazolium salts bearing the trifluoromethyl group as organofluorine compounds: Synthesis, characterization, crystal structure, in silico study, and inhibitory profiles against acetylcholinesterase and α‐glycosidase
Burcu Tezcan, Yetkın Gök, Resul Sevinçek, et al.
Journal of Biochemical and Molecular Toxicology (2022) Vol. 36, Iss. 4
Closed Access | Times Cited: 14
Some phenolic natural compounds as carbonic anhydrase inhibitors: An in vitro and in silico study
Ahmet Gökhan Ağgül, Naim Uzun, Müslüm Kuzu, et al.
Archiv der Pharmazie (2022) Vol. 355, Iss. 6
Closed Access | Times Cited: 13
Enzyme Inhibition Properties and Molecular Docking Studies of 4‐Sulfonate Containing Aryl α‐Hydroxyphosphonates Based Hybrid Molecules
İrfan Şahin, Zeynebe Bingöl, Sultan Onur, et al.
Chemistry & Biodiversity (2022) Vol. 19, Iss. 5
Closed Access | Times Cited: 13
Design, Synthesis, Characterization and Biological Activities of Novel S‐(Acyloxy)butyl‐N,N‐Diethyldithiocarbamate Compounds
A.Y. Karimov, Parham Taslimi, Arzu Orujova, et al.
ChemistrySelect (2023) Vol. 8, Iss. 18
Closed Access | Times Cited: 7
Synthesis, characterization, biochemical, and molecular modeling studies of carvacrol‐based new thiosemicarbazide and 1,3,4‐thiadiazole derivatives
Tenzile Alagöz, Fatma Çalışkan, Hayriye Genç Bilgiçli, et al.
Archiv der Pharmazie (2023) Vol. 356, Iss. 12
Open Access | Times Cited: 7
Novel hypervalent iodine catalyzed synthesis of α-sulfonoxy ketones: Biological activity and molecular docking studies
Ufuk Atmaca, Cemalettin Alp, Hülya Akıncıoğlu, et al.
Journal of Molecular Structure (2021) Vol. 1239, pp. 130492-130492
Closed Access | Times Cited: 17
New quinoxalin‐1,3,4‐oxadiazole derivatives: Synthesis, characterization, in vitro biological evaluations, and molecular modeling studies
Roghieh Mirzazadeh, Mohammad Asgari, Ebrahim Barzegari, et al.
Archiv der Pharmazie (2021) Vol. 354, Iss. 9
Closed Access | Times Cited: 17
Improvement of photochemical and enzyme inhibition properties of new BODIPY compound by conjugation with cisplatin
Ceren Can Karanlık, Gürkan Karanlık, Parham Taslimi, et al.
Polyhedron (2022) Vol. 225, pp. 116042-116042
Closed Access | Times Cited: 11
Hamamelitannin’s Antioxidant Effect and Its Inhibition Capability on α-Glycosidase, Carbonic Anhydrase, Acetylcholinesterase, and Butyrylcholinesterase Enzymes
Lokman Durmaz, Hasan Karageçili, Adem Ertürk, et al.
Processes (2024) Vol. 12, Iss. 11, pp. 2341-2341
Open Access | Times Cited: 1
Synthesis, cytotoxicities, and carbonic anhydrase inhibition activities of pyrazoline–benzenesulfonamide derivatives harboring phenol/polyphenol moieties
Sinan Bilginer, Sanaa K. Bardaweel, Yeliz Demir, et al.
Medicinal Chemistry Research (2022) Vol. 31, Iss. 6, pp. 925-935
Closed Access | Times Cited: 10
Design, Docking, Synthesis and Biological Evaluation of Novel Nicotinohydrazone Derivatives as Potential Butyrylcholinesterase Enzyme Inhibitor
Yusuf İslam Esmer, Ercan Çınar, Eyüp Başaran
ChemistrySelect (2022) Vol. 7, Iss. 33
Closed Access | Times Cited: 10
Sulfonamide-phosphonate hybrids as new carbonic anhydrase inhibitors: In vitro enzymatic inhibition, molecular modeling, and ADMET prediction
Samira Zareei, Maryam Mohammadi‐Khanaposhtani, Mehdi Adib, et al.
Journal of Molecular Structure (2022) Vol. 1271, pp. 134114-134114
Closed Access | Times Cited: 9
Novel triazole bridged quinoline-anthracene derivatives: synthesis, characterization, molecular docking, evaluation of electronic and enzyme inhibitory properties
Ayşegül Gümüş, Nastaran Sadeghian, Morteza Sadeghi, et al.
Journal of Biomolecular Structure and Dynamics (2023), pp. 1-16
Closed Access | Times Cited: 5
Sulfonyl thiourea derivatives from 2‐aminodiarylpyrimidines: In vitro and in silico evaluation as potential carbonic anhydrase I, II, IX, and XII inhibitors
Nguyễn Đình Thành, Nguyễn Thị Kim Giang, Do Son Hai, et al.
Chemical Biology & Drug Design (2024) Vol. 103, Iss. 3
Closed Access | Times Cited: 1
Chemistry of heterocycles as carbonic anhydrase inhibitors: A pathway to novel research in medicinal chemistry review
Anjaneyulu Bendi, Taruna, Rajni Rajni, et al.
Archiv der Pharmazie (2024) Vol. 357, Iss. 7
Closed Access | Times Cited: 1
2-Amino-6-ethoxy-4-arylpyridine-3,5-dicarbonitrile Scaffolds as Potential Acetylcholinesterase and Butyrylcholinesterase Inhibitors
Muhammad Ali, Shahbaz Shamim, Uzma Salar, et al.
Journal of Molecular Structure (2024) Vol. 1321, pp. 139863-139863
Closed Access | Times Cited: 1

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