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:

The Bioactivity of Thiazolidin-4-Ones: A Short Review of the Most Recent Studies
Dominika Mech, Antonina Kurowska, Nazar Trotsko
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 21, pp. 11533-11533
Open Access | Times Cited: 40

Showing 1-25 of 40 citing articles:

In vitro and in vivo evaluation of the antimicrobial, antioxidant, cytotoxic, hemolytic activities and in silico POM/DFT/DNA-binding and pharmacokinetic analyses of new sulfonamide bearing thiazolidin-4-ones
Sangar Ali Hassan, Dara Muhammed Aziz, Media Noori Abdullah, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 42, Iss. 7, pp. 3747-3763
Closed Access | Times Cited: 28

Synthesis of novel pyrido[2,3-d]pyrimidine-thiazolidine-1,2,3-triazoles: Potent EGFR targeting anticancer agents
Sandhya Rani Bandi, Ravikumar Kapavarapu, Rambabu Palabindela, et al.
Journal of Molecular Structure (2023) Vol. 1294, pp. 136451-136451
Closed Access | Times Cited: 17

Synthesis, Characterization, Molecular Docking and in vitro Biological Studies of Thiazolidin‐4‐one Derivatives as Anti‐Breast‐Cancer Agents
Halil Şenol, Ahmet Gökhan Ağgül, Sezen Atasoy
ChemistrySelect (2023) Vol. 8, Iss. 20
Closed Access | Times Cited: 15

Thiazolidine-2,4-dione framework containing spiropyrrolidine-oxindole and 1,2,3-triazole scaffold: synthesis, in vitro α-amylase inhibition and in silico studies
Meenakshi Duhan, Rahul Singh, Meena Devi, et al.
New Journal of Chemistry (2023) Vol. 47, Iss. 11, pp. 5399-5412
Closed Access | Times Cited: 10

New Thiazolidine-4-One Derivatives as SARS-CoV-2 Main Protease Inhibitors
Antonella Messore, Paolo Malune, Elisa Patacchini, et al.
Pharmaceuticals (2024) Vol. 17, Iss. 5, pp. 650-650
Open Access | Times Cited: 2

Molecular modeling and cytotoxic activity of newly synthesized benzothiazole-thiazole conjugates
Wael M. Alamoudi
Journal of Saudi Chemical Society (2024) Vol. 28, Iss. 4, pp. 101897-101897
Open Access | Times Cited: 2

New 4-thiazolidinone-based molecules Les-2769 and Les-3266 as possible PPARγ modulators
Monika Bar, Bartosz Skóra, Anna Tabęcka-Łonczyńska, et al.
Bioorganic Chemistry (2022) Vol. 128, pp. 106075-106075
Open Access | Times Cited: 13

Green design and synthesis of some novel thiazolidinone appended benzothiazole–triazole hybrids as antimicrobial agents
Bhaskar Dwivedi, Diksha Bhardwaj, Deepika Choudhary
RSC Advances (2024) Vol. 14, Iss. 12, pp. 8341-8352
Open Access | Times Cited: 1

Ultrasound-assisted synthesis of 4-thiazolidinone Schiff bases and their antioxidant, α-glucosidase, α-amylase inhibition, mode of inhibition and computational studies
Pule Seboletswe, Gobind Kumar, Lungisani Kubone, et al.
Medicinal Chemistry Research (2024) Vol. 33, Iss. 9, pp. 1578-1597
Open Access | Times Cited: 1

Anticancer Potential of Compounds Bearing Thiazolidin-4-one Scaffold: Comprehensive Review
Dalbir Singh, Mona Piplani, Harsha Kharkwal, et al.
Pharmacophore (2023) Vol. 14, Iss. 1, pp. 56-70
Open Access | Times Cited: 4

Anticancer 5‐arylidene‐2‐(4‐hydroxyphenyl)aminothiazol‐4(5H)‐ones as tubulin inhibitors
Jiřı́ Řehulka, Ivanna Subtel’na, Anna Kryshchyshyn, et al.
Archiv der Pharmazie (2022) Vol. 355, Iss. 12
Closed Access | Times Cited: 8

5-Arylmethylidene-2-iminothiazolidin-4-ones in the synthesis of novel dispiro-fused oxindolepyrrolidineiminothiazolidinones
Alexei N. Izmest’ev, Andrey А. Streltsov, Ангелина Н. Кравченко, et al.
Chemistry of Heterocyclic Compounds (2023) Vol. 59, Iss. 4-5, pp. 309-316
Closed Access | Times Cited: 3

Design, Synthesis, Anticancer and Antimicrobial Studies of 2‐Phenylthiazolidin‐4‐one Glycinamide Conjugates
Dalbir Singh, A.K. Aggarwal, Rajiv M. Patel, et al.
ChemistrySelect (2023) Vol. 8, Iss. 42
Closed Access | Times Cited: 3

A comprehensive review on the antidiabetic attributes of thiazolidine‐4‐ones: Synthetic strategies and structure–activity relationships
Tathagata Pradhan, Ojasvi Gupta, Vivek Kumar, et al.
Archiv der Pharmazie (2022) Vol. 356, Iss. 2
Closed Access | Times Cited: 5

(2Z,5Z)-5-((3-(Benzofuran-2-yl)-1-phenyl-1H-pyrazol-4-yl)methylene)-2-((4-methoxyphenyl)imino)-3-phenylthiazolidin-4-one
Bakr F. Abdel-Wahab, Hanan A. Mohamed, Benson M. Kariuki, et al.
Molbank (2023) Vol. 2023, Iss. 2, pp. M1665-M1665
Open Access | Times Cited: 2

Thiazolidin-4-Ones as a Promising Scaffold in the Development of Antibiofilm Agents—A Review
Nazar Trotsko
International Journal of Molecular Sciences (2023) Vol. 25, Iss. 1, pp. 325-325
Open Access | Times Cited: 2

Molecular Docking, Synthesis, Characterization and Antimicrobial Evaluation of 5-methylthiazolidine-4-ones
Sarmad Saadi Hussein, Karima F. Ali, Fouad A. Al-Saady, et al.
Al Mustansiriyah Journal of Pharmaceutical Sciences (2024) Vol. 24, Iss. 2, pp. 163-177
Open Access

Discovery of structural diversity guided steroidal thiazolidin-4-one derivatives as potential cytotoxic agents targeting CDK1
Fei Yang, Yong Min, Kui Li, et al.
Journal of Saudi Chemical Society (2024) Vol. 28, Iss. 3, pp. 101860-101860
Open Access

Silver(I) Octanuclear Complexes Containing N′-(4-Oxotiazolidin-2-Iliden)picolinohydrazonamide and Nitrate as Bridge Ligands. An Example of Solvatomorphism?
Isabel García‐Santos, Julia Krümpelmann, Manuel Saa, et al.
Inorganic Chemistry (2024) Vol. 63, Iss. 20, pp. 9221-9236
Open Access

Synthesis, Characterization, Molecular Docking, and Preliminary Antimicrobial Evaluation of Thiazolidinone Derivatives
Sarmad Saadi Hussein, Karima F. Ali, Fouad A. Al-Saady
Deleted Journal (2024) Vol. 9, Iss. 2
Open Access

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