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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:

Fluorinated thiazole–thiosemicarbazones hybrids as potential PPAR-γ agonist and α-amylase, α-glucosidase antagonists: Design, synthesis, in silico ADMET and docking studies and hypoglycemic evaluation
Eman A. Fayed, A. Ben Thabet, Shimaa M. Abd El‐Gilil, et al.
Journal of Molecular Structure (2023) Vol. 1301, pp. 137374-137374
Closed Access | Times Cited: 11

Showing 11 citing articles:

Innovation of 6-sulfonamide-2H-chromene derivatives as antidiabetic agents targeting α-amylase, α-glycosidase, and PPAR-γ inhibitors with in silico molecular docking simulation
Hamdy Khamees Thabet, Ahmed Ragab, Mohd Imran, et al.
RSC Advances (2024) Vol. 14, Iss. 22, pp. 15691-15705
Open Access | Times Cited: 9
Fluorinated indeno-quinoxaline bearing thiazole moieties as hypoglycaemic agents targeting α -amylase, and α -glucosidase: synthesis, molecular docking, and ADMET studies
Nirvana A. Gohar, Eman A. Fayed, Yousry A. Ammar, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2024) Vol. 39, Iss. 1
Open Access | Times Cited: 8
Key molecular scaffolds in the development of clinically viable α-amylase inhibitors
Rahul Pratap Singh, Jayant Sindhu, Devender Singh, et al.
Future Medicinal Chemistry (2025) Vol. 17, Iss. 3, pp. 347-362
Closed Access
Novel Pyrrolidine-bearing quinoxaline inhibitors of DNA Gyrase, RNA polymerase and spike glycoprotein
Maha A. Ebrahim, Triveena M. Ramsis, Nirvana A. Gohar, et al.
Bioorganic Chemistry (2025) Vol. 156, pp. 108218-108218
Closed Access
Discovery of Hydrazine Clubbed Thiazoles as Potential Antidiabetic Agents: Synthesis, Biological Evaluation, and Molecular Docking Studies
Betül Kaya, Hakan Tahtacı, Bilge Çi̇ftci̇, et al.
Drug Development Research (2025) Vol. 86, Iss. 1
Open Access
Insights into antimicrobial potential of functionalized thiazoles: In vitro and in silico analysis
Hamid Aziz
Journal of Molecular Liquids (2025), pp. 127064-127064
Closed Access
Synthesis of 4-Diazocyclohexane-Based Sulfonamide Drug scaffolds: Investigating Enzyme Inhibition, Antioxidant, and ADMET properties
Adnan Çetin, Ercan Oğuz, Elif Akın Kazancıoğlu, et al.
Journal of Molecular Structure (2025), pp. 141708-141708
Closed Access
Exploring a novel thiazole derivatives hybrid with fluorinated-indenoquinoxaline as dual inhibitors targeting VEGFR2/AKT and apoptosis inducers against hepatocellular carcinoma with docking simulation
Moustafa S. Abusaif, Ahmed Ragab, Eman A. Fayed, et al.
Bioorganic Chemistry (2024) Vol. 154, pp. 108023-108023
Closed Access | Times Cited: 3
Synthesis, Antimicrobial Evaluation, DFT, in Silico‐Docking, and ADMET Investigations of Novel Chromene‐based 2,4‐Thiazolidinediones
Mohamed S. Mohamed Ahmed, Redhab A. J. Alfraiji, Fawzy A. Attaby, et al.
Chemistry & Biodiversity (2024)
Closed Access | Times Cited: 1
Expression of PPAR-γ TF by newly synthesized thiazolidine-2,4-diones to manage glycemic control: Insights from in silico, in vitro and experimental pharmacology in wistar rats
Shankar Gharge, Shankar G. Alegaon, Shriram D. Ranade, et al.
Bioorganic Chemistry (2024) Vol. 153, pp. 107966-107966
Closed Access | Times Cited: 1
Discovery of Novel Bicyclic and Tricyclic Cyclohepta[b]thiophene Derivatives as Multipotent AChE and BChE Inhibitors, In-Vivo and In-Vitro Assays, ADMET and Molecular Docking Simulation
Eman A. Fayed, Samiha A. El‐Sebaey, Maha A. Ebrahim, et al.
European Journal of Medicinal Chemistry (2024) Vol. 284, pp. 117201-117201
Closed Access | Times Cited: 1
Design, Synthesis of 3‐(Aryl)‐1‐(2‐p‐tolylthiazol‐4‐yl)prop‐2‐en‐1‐ones as Alpha(α)‐Amylase Inhibitors
Hafsa Iqbal, Muhammad Haroon, Tashfeen Akhtar, et al.
Chemistry & Biodiversity (2024) Vol. 21, Iss. 9
Closed Access
Synthesis, biologic properties, and molecular modeling studies of bis-indole based thiosemicarbazones
Sadık M. Ceyhan, Murat Bingul, Hasan Şahin, et al.
Monatshefte für Chemie - Chemical Monthly (2024) Vol. 155, Iss. 10, pp. 977-988
Closed Access
Novel rhodanine-thiazole hybrids as potential antidiabetic agents: A structure-based drug design approach
Shankar Gharge, Shankar G. Alegaon, Shriram D. Ranade, et al.
RSC Medicinal Chemistry (2024)
Closed Access
Novel thiazole derivatives: Design, synthesis, antibacterial evaluation, DFT, molecular docking and in-silico ADMET investigations
Mohamed S. Mohamed Ahmed, Fawzy A. Attaby, Redhab A. J. Alfraiji, et al.
Synthetic Communications (2024), pp. 1-21
Closed Access
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