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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:

Design and synthesis of phenoxymethybenzoimidazole incorporating different aryl thiazole-triazole acetamide derivatives as α-glycosidase inhibitors
Anita Nasli Esfahani, Aida Iraji, Amir Alamir, et al.
Molecular Diversity (2021) Vol. 26, Iss. 4, pp. 1995-2009
Open Access | Times Cited: 16

Showing 16 citing articles:

Benzimidazole-Triazole Hybrids as Antimicrobial and Antiviral Agents: A Systematic Review
Maria Marinescu
Antibiotics (2023) Vol. 12, Iss. 7, pp. 1220-1220
Open Access | Times Cited: 28
Substituted piperazine conjugated to quinoline-thiosemicarbazide as potent α-glucosidase inhibitors to target hyperglycemia
Mehran Ghasemi, Mohammad Mahdavi, Maryam Dehghan, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Rational design, synthesis, in vitro, and in-silico studies of pyrazole‑phthalazine hybrids as new α‑glucosidase inhibitors
M. N. A. Md. Roshan, Roghieh Mirzazadeh, Azadeh Tajmir-Riahi, et al.
Scientific Reports (2025) Vol. 15, Iss. 1
Open Access
Cyanoacetohydrazide linked to 1,2,3-triazole derivatives: a new class of α-glucosidase inhibitors
Aida Iraji, Diba Shareghi-Brojeni, Somayeh Mojtabavi, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 33
Design, synthesis, and in silico studies of quinoline-based-benzo[d]imidazole bearing different acetamide derivatives as potent α-glucosidase inhibitors
Milad Noori, Ali Davoodi, Aida Iraji, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 31
Precision single-atom editing: new frontiers in nitrogen insertion and substitution for the generation of N-heterocycles
Xue Li, Jia Xu, Zhigang Xu
Organic Chemistry Frontiers (2024) Vol. 11, Iss. 14, pp. 4041-4053
Closed Access | Times Cited: 4
Development of thiazole-appended novel hydrazones as a new class of α-amylase inhibitors with anticancer assets: an in silico and in vitro approach
Sandhya Chahal, Jyoti Punia, Payal Rani, et al.
RSC Medicinal Chemistry (2023) Vol. 14, Iss. 4, pp. 757-781
Open Access | Times Cited: 8
Coumarin linked to 2-phenylbenzimidazole derivatives as potent α-glucosidase inhibitors
Mina Sadeghi Ganjeh, Ali Mazlomifar, Ashraf Sadat Shahvelayti, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 2
Quinazolinone-1,2,3-triazole-acetamide conjugates as potent α-glucosidase inhibitors: synthesis, enzyme inhibition, kinetic analysis, and molecular docking study
Sara Moghadam Farid, Aida Iraji, Somayeh Mojtabavi, et al.
RSC Medicinal Chemistry (2023) Vol. 14, Iss. 3, pp. 520-533
Open Access | Times Cited: 7
Synthesis, in vitro α-glucosidase inhibitory activities, and molecular dynamic simulations of novel 4-hydroxyquinolinone-hydrazones as potential antidiabetic agents
Nahal Shayegan, Sirous Haghipour, Nader Tanideh, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 7
Synthesis of novel coumarin-based thiosemicarbazones and their implications in diabetic management via in-vitro and in-silico approaches
Syeda Bakhtawar Zahra, Saeed Ullah, Sobia Ahsan Halim, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 6
Synthesis and bioactivities evaluation of quinazolin-4(3H)-one derivatives as α-glucosidase inhibitors
Mahshid Moheb, Aida Iraji, Navid Dastyafteh, et al.
BMC Chemistry (2022) Vol. 16, Iss. 1
Open Access | Times Cited: 10
Triazolo‐linked benzimidazoles as tubulin polymerization inhibitors and DNA intercalators: Design, synthesis, cytotoxicity, and docking studies
Kritika Laxmikeshav, Sayali Mone, Geetanjali Devabattula, et al.
Archiv der Pharmazie (2023) Vol. 356, Iss. 5
Closed Access | Times Cited: 5
Discovery of novel flavonoid derivatives as potential dual inhibitors against α-glucosidase and α-amylase: virtual screening, synthesis, and biological evaluation
Tan Thanh, Minh-Hoang Phan, Thao Thi Thai, et al.
Molecular Diversity (2023) Vol. 28, Iss. 3, pp. 1629-1650
Closed Access | Times Cited: 5
Non-small cell lung cancer sensitisation to platinum chemotherapy via new thiazole-triazole hybrids acting as dual T-type CCB/MMP-9 inhibitors
Hassan El Gamal, Khadiga Ahmed Ismail, A-Mohsen M. E. Omar, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2024) Vol. 39, Iss. 1
Open Access | Times Cited: 1
New solid phase methodology for the synthesis of biscoumarin derivatives: experimental and in silico approaches
Elham Zarenezhad, Mohammad Nazari Montazer, Masoumeh Tabatabaee, et al.
BMC Chemistry (2022) Vol. 16, Iss. 1
Open Access | Times Cited: 8
Synthesis and biological assessment of benzimidazole-acrylonitrile-1,2,3-triazole derivatives as α-glucosidase inhibitors
Mahdi Hatamfayazi, Mohammad Mahdavi, Shahram Moradi Dehaghi, et al.
Bioorganic Chemistry (2024) Vol. 154, pp. 108060-108060
Closed Access
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