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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:

2,5-Disubstituted furan derivatives containing 1,3,4-thiadiazole moiety as potent α-glucosidase and E. coli β-glucuronidase inhibitors
Yasheng Li, Min He, Tao‐Shun Zhou, et al.
European Journal of Medicinal Chemistry (2021) Vol. 216, pp. 113322-113322
Closed Access | Times Cited: 21

Showing 21 citing articles:

Synthesis and biological evaluation of indole derivatives containing thiazolidine-2,4-dione as α-glucosidase inhibitors with antidiabetic activity
Chunmei Hu, Bingwen Liang, Jinping Sun, et al.
European Journal of Medicinal Chemistry (2023) Vol. 264, pp. 115957-115957
Closed Access | Times Cited: 44
Thiazolidine-2,4-dione derivatives as potential α-glucosidase inhibitors: Synthesis, inhibitory activity, binding interaction and hypoglycemic activity
Mengyue Li, Jinping Sun, Bingwen Liang, et al.
Bioorganic Chemistry (2024) Vol. 144, pp. 107177-107177
Closed Access | Times Cited: 24
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
Inhibition of α-glucosidase by trilobatin and its mechanism: kinetics, interaction mechanism and molecular docking
Ming He, Yuhan Zhai, Yu‐Qing Zhang, et al.
Food & Function (2021) Vol. 13, Iss. 2, pp. 857-866
Closed Access | Times Cited: 33
Flavone-1,2,3-triazole derivatives as potential α-glucosidase inhibitors: Synthesis, enzyme inhibition, kinetic analysis and molecular docking study
Manoj Dhameja, Hariom Kumar, Sirisha Kurella, et al.
Bioorganic Chemistry (2022) Vol. 127, pp. 106028-106028
Closed Access | Times Cited: 21
PROTACs in the Management of Prostate Cancer
Yedla Poornachandra, Ahmad O. Babalghith, Vindhya Vasini Andra, et al.
Molecules (2023) Vol. 28, Iss. 9, pp. 3698-3698
Open Access | Times Cited: 13
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
Synthesis of 7-azaindole based carbohydrazides and 1,3,4-oxadiazoles; Antioxidant activity, α-glucosidase inhibition properties and docking study
Samet İzgi, İbrahim F. Sengul, Engin Şahin, et al.
Journal of Molecular Structure (2021) Vol. 1247, pp. 131343-131343
Closed Access | Times Cited: 18
2,5-Disubstituted furan derivatives containing imidazole, triazole or tetrazole moiety as potent α-glucosidase inhibitors
Min He, Yuanjing Li, Jiang Shao, et al.
Bioorganic Chemistry (2022) Vol. 131, pp. 106298-106298
Closed Access | Times Cited: 9
Rapid in situ generation of 2-(halomethyl)-5-phenylfuran and nucleophilic addition in a microflow reactor
Yuma Matsuura, Shinichiro Fuse
Organic & Biomolecular Chemistry (2024) Vol. 22, Iss. 17, pp. 3448-3452
Open Access | Times Cited: 1
Synthesis, Properties, and Biological Applications of 1,3,4-Thiadiazoles
Kalyani Sonawane, Rushikesh Said, Navnath T. Hatvate
Royal Society of Chemistry eBooks (2024), pp. 163-223
Closed Access | Times Cited: 1
Novel coumarin-thiazolidine-2,4-dione hybrids as potential α-glucosidase inhibitors: Synthesis and bioactivity evaluation
Bingwen Liang, Jianping Li, Simin Wu, et al.
Journal of Molecular Structure (2024), pp. 140481-140481
Closed Access | Times Cited: 1
Exploring gabosine and chlorogentisyl alcohol derivatives from a marine-derived fungus as EcGUS inhibitors with informatic assisted approaches
Yichao Ge, Yihan Ma, Meilu Zhao, et al.
European Journal of Medicinal Chemistry (2022) Vol. 242, pp. 114699-114699
Closed Access | Times Cited: 8
Gaining deeper insights into 2,5-disubstituted furan derivatives as potent α-glucosidase inhibitors and discovery of putative targets associated with diabetes diseases using an integrative computational approach
Wahyu Eko Prasetyo, Triana Kusumaningsih, Fajar Rakhman Wibowo
Structural Chemistry (2022) Vol. 34, Iss. 2, pp. 519-538
Closed Access | Times Cited: 5
Thiadiazoles

Royal Society of Chemistry eBooks (2024)
Closed Access
Design, synthesis, and biological evaluation of (thio)urea derivatives as potent Escherichia coli β -glucuronidase inhibitors
Keren Xu, Leyi Ying, Ti‐Ti Ying, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2024) Vol. 39, Iss. 1
Open Access
Anti-Alzheimer’s Potency of Rich Phenylethanoid Glycosides Extract from Marrubium vulgare L.: In Vitro and In Silico Studies
Mahmoud Emam, Samah A. El-Newary, Hanan Y. Aati, et al.
Pharmaceuticals (2024) Vol. 17, Iss. 10, pp. 1282-1282
Open Access
An Explicative Review of Thiadiazole: Medicinal Chemistry Aspects
A. MISHRA, Ekta Khare, Dinesh Chandra
Oriental Journal Of Chemistry (2024) Vol. 40, Iss. 6, pp. 1796-1808
Open Access
Discovery of a series of 5-phenyl-2-furan derivatives containing 1,3-thiazole moiety as potent Escherichia coli β-glucuronidase inhibitors
Tao‐Shun Zhou, Lulu He, Jing He, et al.
Bioorganic Chemistry (2021) Vol. 116, pp. 105306-105306
Closed Access | Times Cited: 3
Fragment-Based Dynamic Combinatorial Chemistry for Identification of Selective α-Glucosidase Inhibitors
Wu Yao, Changming Liu, Lei Hu
ACS Medicinal Chemistry Letters (2022) Vol. 13, Iss. 11, pp. 1791-1796
Open Access | Times Cited: 2
Five-membered ring systems: furans and benzofurans
Halina Kwiecień
Progress in heterocyclic chemistry (2023), pp. 209-253
Closed Access
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