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:

Synthesis, in vitro biological analysis and molecular docking studies of new thiadiazole-based thiourea derivatives as dual inhibitors of a-amylase and a-glucosidase
Imran Khan, Wajid Rehman, Fazal Rahim, et al.
Arabian Journal of Chemistry (2023) Vol. 16, Iss. 9, pp. 105078-105078
Open Access | Times Cited: 10

Showing 10 citing articles:

Investigation on Diabetes and Mechanism of Thiadiazole–Schiff Base as Therapeutic Hybrid: Enzyme Activity and Molecular Docking Studies
Tayyiaba Iqbal, Shoaib Khan, Rafaqat Hussain, et al.
ChemistrySelect (2025) Vol. 10, Iss. 5
Closed Access

Advancing drug discovery: Thiadiazole derivatives as multifaceted agents in medicinal chemistry and pharmacology
Benjamin Ayodipupo Babalola, Lekhnath Sharma, Olanike G. Olowokere, et al.
Bioorganic & Medicinal Chemistry (2024) Vol. 112, pp. 117876-117876
Closed Access | Times Cited: 2

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

Synthesis, biological evaluation, and molecular modelling of substituted thiazolyl thiourea derivatives: A new class of prolyl oligopeptidase inhibitors
Saira Naseem, Angelo Oneto, Saeed Ullah, et al.
International Journal of Biological Macromolecules (2024) Vol. 275, pp. 133571-133571
Closed Access | Times Cited: 1

Insights into the role of potent thiadiazole based Schiff base derivatives in targeting type-II diabetes: A combine in-vitro and in-silico approaches
Tayyiaba Iqbal, Shoaib Khan, Fakher Rahim, et al.
Journal of Molecular Structure (2024) Vol. 1321, pp. 140000-140000
Closed Access | Times Cited: 1

Carbonylbis(hydrazine‐1‐carbothioamide) derivatives as a new class of α‐glucosidase inhibitors and their mechanistic insights via molecular docking and dynamic simulations
Saira Naseem, Shamool Fatima, Saeed Ullah, et al.
Archiv der Pharmazie (2023) Vol. 357, Iss. 3
Closed Access | Times Cited: 2

Synthesis, Computational Study, and In Vitro α-Glucosidase Inhibitory Action of Thiourea Derivatives Based on 3-Aminopyridin-2(1H)-Ones
Zarina Shulgau, Ирина В. Паламарчук, Shynggys Sergazy, et al.
Molecules (2024) Vol. 29, Iss. 15, pp. 3627-3627
Open Access

Design, synthesis docking and molecular dynamics studies of 2-amino-4-phenylthiazole-indole hybrids as α-glucosidase inhibitors
Fateme Gholami, Mohammad Halimi, Mohammad Hosein Sayahi, et al.
Journal of Molecular Structure (2023) Vol. 1299, pp. 137061-137061
Closed Access | Times Cited: 1

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