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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:

1,3,4-Thiadiazole Scaffold: As Anti-Epileptic Agents
Tulika Anthwal, Sumitra Nain
Frontiers in Chemistry (2022) Vol. 9
Open Access | Times Cited: 31

Showing 1-25 of 31 citing articles:

Design, synthesis, and in-Silco ADME prediction of some novel bis(1,3,4-thiadiazoles) encapsulated lipid chitosan nano capsule decorative with magnetic nanoparticles and their potential anti-helicobacter pylori activity
Mostafa E. Salem, Ahmed H. M. Elwahy, Hamdi M. Hassaneen, et al.
International Journal of Biological Macromolecules (2025), pp. 139746-139746
Closed Access | Times Cited: 1
Diverse Biological Activities of 1,3,4-Thiadiazole Scaffold
Tulika Anthwal, Sarvesh Paliwal, Sumitra Nain
Chemistry (2022) Vol. 4, Iss. 4, pp. 1654-1671
Open Access | Times Cited: 35
An efficient eco-friendly, simple, and green synthesis of some new spiro-N-(4-sulfamoyl-phenyl)-1,3,4-thiadiazole-2-carboxamide derivatives as potential inhibitors of SARS-CoV-2 proteases: drug-likeness, pharmacophore, molecular docking, and DFT exploration
Ahmed M. M. El‐Saghier, Souhaila S. Enaili, Aly Abdou, et al.
Molecular Diversity (2023) Vol. 28, Iss. 1, pp. 249-270
Open Access | Times Cited: 26
Design, Synthesis, and Mode of Action of Thioacetamide Derivatives as the Algicide Candidate Based on Active Substructure Splicing Strategy
Shi Huang, Lingzi Zuo, Liexiong Zhang, et al.
Journal of Agricultural and Food Chemistry (2024) Vol. 72, Iss. 13, pp. 7021-7032
Closed Access | Times Cited: 6
Synthesis, in-vitro α-glucosidase inhibition and molecular docking studies of 1,3,4-thiadiazole-5,6-diphenyl-1,2,4-triazine hybrids: Potential leads in the search of new antidiabetic drugs
Hariom Kumar, Manoj Dhameja, Sirisha Kurella, et al.
Journal of Molecular Structure (2022) Vol. 1273, pp. 134339-134339
Closed Access | Times Cited: 29
An Understanding of Mechanism-Based Approaches for 1,3,4-Oxadiazole Scaffolds as Cytotoxic Agents and Enzyme Inhibitors
Davinder Kumar, Navidha Aggarwal, Aakash Deep, et al.
Pharmaceuticals (2023) Vol. 16, Iss. 2, pp. 254-254
Open Access | Times Cited: 19
Mechanism-based approaches of 1,3,4 thiadiazole scaffolds as potent enzyme inhibitors for cytotoxicity and antiviral activity
Davinder Kumar, Harsh Kumar, Virender Kumar, et al.
Medicine in Drug Discovery (2022) Vol. 17, pp. 100150-100150
Open Access | Times Cited: 24
Synthesis and photodynamic activity of novel thieno[3,2–b]thiophene fused BODIPYs with good bio-solubility and anti-aggregation effect
N. Cao, Ying Jiang, Zhi-Bing Song, et al.
Bioorganic Chemistry (2024) Vol. 143, pp. 107097-107097
Closed Access | Times Cited: 3
Emerging synthetic Strategies and Pharmacological Insights of 1,3,4-Thiadiazole Derivatives: A Comprehensive Review
Davinder Kumar, Navidha Aggarwal, Virender Kumar, et al.
Future Medicinal Chemistry (2024) Vol. 16, Iss. 6, pp. 563-581
Closed Access | Times Cited: 3
Unveiling the chemistry of 1,3,4‐oxadiazoles and thiadiazols: A comprehensive review
Vivek Kumar Gour, Shaikh Yahya, Mohammad Shahar Yar
Archiv der Pharmazie (2023) Vol. 357, Iss. 1
Open Access | Times Cited: 9
Synthesis and Anti‐Bacterial Evaluation of Novel Scaffolds Based on Bis‐Thiazole or bis‐1,3,4‐Thiadiazole Linked to Thieno[2,3‐b]Thiophene as New Hybrid Molecules
Yara N. Laboud, Doaa Zahran, Hamdi M. Hassaneen, et al.
ChemistrySelect (2024) Vol. 9, Iss. 14
Closed Access | Times Cited: 2
Design, synthesis, antimicrobial activity, and mechanism of novel 3‐(2,4‐dichlorophenyl)‐[1,2,4]triazolo[3,4‐b][1,3,4]thiadiazole derivatives
Yu‐Guo Zheng, Mei Chen, Renfeng Zhang, et al.
Pest Management Science (2024) Vol. 80, Iss. 10, pp. 5388-5399
Closed Access | Times Cited: 2
2-Substituted-3-(5-Substituted-1,3,4-oxadiazol/thiadiazol-2-yl) Thiazolidin-4-one Derivatives: Synthesis, Anticancer, Antimicrobial, and Antioxidant Potential
Davinder Kumar, Navidha Aggarwal, Harsh Kumar, et al.
Pharmaceuticals (2023) Vol. 16, Iss. 6, pp. 805-805
Open Access | Times Cited: 6
1,3,4-Thiadiazole: A Versatile Scaffold for Drug Discovery
Ravi K. Mittal, Raghav Mishra, Vikram Sharma, et al.
Letters in Organic Chemistry (2023) Vol. 21, Iss. 5, pp. 400-413
Closed Access | Times Cited: 6
A method for the synthesis of spiro-1,3,4-thiadiazolines
A. V. Komkov, Leonid G. Menchikov, Andrey S. Dmitrenok, et al.
Chemistry of Heterocyclic Compounds (2024) Vol. 60, Iss. 3-4, pp. 183-189
Closed Access | Times Cited: 1
Development of new chiral 1,2,4-triazole-3-thiones and 1,3,4-thiadiazoles with promising in vivo anticonvulsant activity targeting GABAergic system and voltage-gated sodium channels (VGSCs)
Ayşegül Karaküçük‐İyidoğan, Eyüp Başaran, Gizem Tatar-Yılmaz, et al.
Bioorganic Chemistry (2024) Vol. 151, pp. 107662-107662
Closed Access | Times Cited: 1
Interaction of 2-Amino-1,3,4-thiadiazoles with 1,2,4-Triazine-5-carbonitriles
Alexey P. Krinochkin, Ya. K. Shtaitz, E. A. Kudryashova, et al.
Doklady Chemistry (2022) Vol. 504, Iss. 1, pp. 79-82
Closed Access | Times Cited: 5
Alternative and one-pot synthesis of new conjugated 5-aryl-1,3,4-thiadiazole azo dyes
Monika Olesiejuk, Agnieszka Kudelko, Marcin Świątkowski
Dyes and Pigments (2023) Vol. 220, pp. 111721-111721
Closed Access | Times Cited: 2
Functionalization of 2-Mercapto-5-methyl-1,3,4-thiadiazole: 2-(ω-Haloalkylthio) Thiadiazoles vs. Symmetrical Bis-Thiadiazoles
Zhanina S. Petkova, Rusi I. Rusew, Boris Shivachev, et al.
Molecules (2024) Vol. 29, Iss. 9, pp. 1938-1938
Open Access
Light-assisted Green and Efficient Construction of Thiadiazole/ Selenadiazole Derivatives
Changting Wen, Guojin Sun, Lang Liu, et al.
Green Chemistry (2024) Vol. 26, Iss. 13, pp. 7944-7950
Closed Access
3-Spiroandrostene-substituted 1,3,4-thiadiazolines
A. V. Komkov, Leonid G. Menchikov, Andrey S. Dmitrenok, et al.
Chemistry of Heterocyclic Compounds (2024) Vol. 60, Iss. 3-4, pp. 190-195
Closed Access
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
Safety assessment of novel oxadiazole derivatives in acute and sub-acute toxicity studies
Syeda Rida Zainab, Jehanzeb Khan, Humaira Nadeem, et al.
Naunyn-Schmiedeberg s Archives of Pharmacology (2024)
Closed Access
Synthesis and spectral characteristics of N -(2,2,2-trichloro-1-((5-(R-amino)-1,3,4-thiadiazol-2-yl)amino)ethyl)carboxamides
Valeriia V. Pavlova, Pavlo V. Zadorozhnii, Aleksey B. Ryabitsky, et al.
Synthetic Communications (2024) Vol. 54, Iss. 23, pp. 2076-2087
Closed Access
Evaluation of 1,3,4-thiadiazole and 1,3-thiazolidine-4-one binary molecules against the SARS-CoV-2 receptor: DFT study, PASS prediction, ADMET analysis, molecular docking, and ADMET optimization
Fariba Heidarizadeh, Sadegh Saadati, Elham Rostami
Materials chemistry horizons. (2024) Vol. 3, Iss. 2, pp. 1-23
Open Access
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