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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:

Multicomponent reaction for the synthesis of new 1,3,4-thiadiazole-thiazolidine-4-one molecular hybrids as promising antidiabetic agents through α-glucosidase and α-amylase inhibition
Lalitha Gummidi, Nagaraju Kerru, Oluwakemi Ebenezer, et al.
Bioorganic Chemistry (2021) Vol. 115, pp. 105210-105210
Closed Access | Times Cited: 49

Showing 26-50 of 49 citing articles:

Exploring the Antimicrobial and Antitubercular Potential of 1-Thia-4-azaspiro[4.5]decan-3-one Derivatives: Synthesis, Molecular Docking, and MD Simulations
Parth P. Patel, Navin B. Patel, Manesh S. Tople, et al.
Journal of Molecular Structure (2024), pp. 141107-141107
Closed Access | Times Cited: 1
Synthesis, characterization, crystallographic, binding, in silico and antidiabetic studies of novel 2,4-thiazolidinedione-phenothiazine molecular hybrids
Manasa A. Doddagaddavalli, Veerendra Kumar A. Kalalbandi, J. Seetharamappa
Journal of Molecular Structure (2022) Vol. 1276, pp. 134625-134625
Closed Access | Times Cited: 9
Recent advances in the synthesis of five-membered heterocycles via multicomponent and domino reactions (from 2017 to 2022)
Vahideh Zadsirjan
Advances in heterocyclic chemistry (2023), pp. 1-126
Closed Access | Times Cited: 4
Synthesis, Biological Evaluation, Molecular Docking and Kinetic Investigation of New 2,4,5‐Trisubstituted Imidazole Derivatives as Antidiabetic Agents
Pawan Kumar, Bindu Syal, Pule Seboletswe, et al.
ChemistrySelect (2023) Vol. 8, Iss. 31
Open Access | Times Cited: 4
Fluorenone–thiazolidine-4-one scaffolds as antidiabetic and antioxidant agents: design, synthesis, X-ray crystal structures, and binding and computational studies
Manasa A. Doddagaddavalli, Veerendra Kumar A. Kalalbandi, Tejas R. Naik, et al.
New Journal of Chemistry (2023) Vol. 47, Iss. 28, pp. 13581-13599
Closed Access | Times Cited: 3
α‐Amylase Inhibitors Based on Thiazolidinone Skeleton: A Promising Approach in Diabetes Management
Rahul Singh, Jayant Sindhu, Parvin Kumar, et al.
ChemistrySelect (2023) Vol. 8, Iss. 48
Closed Access | Times Cited: 3
Synthesis and Anticancer Evaluation of New Thiazole and Thiadiazole Derivatives Bearing Acetanilide Moiety
Ali El‐Rayyes, Ahbarah M. Soliman, Ali Saeed
Russian Journal of General Chemistry (2022) Vol. 92, Iss. 10, pp. 2132-2144
Open Access | Times Cited: 6
Improving Regulation of Polymeric Proanthocyanidins and Tea Polyphenols against Postprandial Hyperglycemia via Acid-Catalyzed Transformation
Yì Wáng, Xinlei Xu, Jianle Chen, et al.
Journal of Agricultural and Food Chemistry (2022) Vol. 70, Iss. 16, pp. 5218-5227
Closed Access | Times Cited: 5
Design, synthesis, and screening for the antiproliferative activity of new 1,3,4-thiadiazole scaffold linked to substituted phenacyl derivatives and disulfides
Yang Liu, Junjie Li, Xuguang Liu, et al.
Journal of Sulfur Chemistry (2022) Vol. 43, Iss. 4, pp. 426-442
Closed Access | Times Cited: 5
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
Synthesis and antiproliferative evaluation of novel 1,3,4-thiadiazole-S-alkyl derivatives based on quinazolinone
Yanle Men, Zi‐Jian Li, Hongying Wang, et al.
Phosphorus, sulfur, and silicon and the related elements (2023) Vol. 198, Iss. 7, pp. 591-601
Closed Access | Times Cited: 2
Synthesis of 1,2,3‐triazole‐1,3,4‐thiadiazole hybrids as novel α‐glucosidase inhibitors by in situ azidation/click assembly
Hariom Kumar, Manoj Dhameja, Sirisha Kurella, et al.
Archiv der Pharmazie (2023) Vol. 356, Iss. 8
Closed Access | Times Cited: 2
Crystal structure of (E)-3-(benzylideneamino)-2-phenylthiazolidin-4-one, C16H14N2OS
Pule Seboletswe, Sizwe J. Zamisa, Gobind Kumar, et al.
Zeitschrift für Kristallographie - New Crystal Structures (2024) Vol. 239, Iss. 3, pp. 343-345
Open Access
In vitro β–glucuronidase and in silico molecular docking studies of thiazole-fused-thiadiazole derivatives prepared through molecular-iodine promoted [3+2] oxidative cyclization
Imran Khan, Wajid Rehman, Rafaqat Hussain, et al.
Journal of Molecular Structure (2024) Vol. 1308, pp. 138097-138097
Closed Access
Synthesis, Binding and Docking Studies of Indole‐1,3,4‐Thiadiazole Derivatives As Potent Α‐Amylase and Lox Inhibitors
Manasa A. Doddagaddavalli, Umesha Katrahalli, Shrinivas D. Joshi, et al.
ChemistrySelect (2024) Vol. 9, Iss. 19
Closed Access
Development and assessment of novel pyrazole–thiadiazol hybrid derivatives as VEGFR-2 inhibitors: design, synthesis, anticancer activity evaluation, molecular docking, and molecular dynamics simulation
Gresa Halimi, Derya Osmani̇ye, Yusuf Özkay, et al.
Zeitschrift für Naturforschung C (2024) Vol. 79, Iss. 9-10, pp. 291-304
Closed Access
Thiadiazoles

Royal Society of Chemistry eBooks (2024)
Closed Access
Machine learning based QSAR model for therapeutically active candidate drugs with thiazolidinedione (TZD) scaffold
Irina Ghosh, Komal Singh, Venkatesan Jayaprakash, et al.
Journal of Research in Pharmacy (2024) Vol. 28(4), Iss. 28(4), pp. 1135-1151
Open Access
In-silico Study of Molecular Docking and Dynamics Simulations for N-Substituted Thiazolidinones Derived from (R)-Carvone Targeting PPAR-γ Protein: Synthesis and Characterization
Yassine Riadi, Ammar A. Razzak Mahmood, Mohammed H. Geesi, et al.
Polycyclic aromatic compounds (2024), pp. 1-26
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
Benzylidenehydrazine Derivatives: Synthesis, Antidiabetic Evaluation, Antioxidation, Mode Of Inhibition, DFT And Molecular Docking Studies
Parvesh Singh, Pule Seboletswe, Gobind Kumar, et al.
Chemistry & Biodiversity (2024)
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
Synthesis, Antifungal Activity and Molecular Docking Study of 1,3,4-Thiadiazole-Urea Compounds Containing gem-Dimethylcyclopropane Ring Structure
Yucheng Cui, Mei-Hua Chen, Lin Guishan, et al.
Chinese Journal of Organic Chemistry (2022) Vol. 42, Iss. 11, pp. 3784-3784
Open Access | Times Cited: 3
Novel Approach for the Synthesis of 2, 5-disubstituted 1, 3, 4-thiadiazoles from Benzothiohydrazides and Ethylbenzimidate
S. V. Shobha, Kemparajegowda, Swamy Savvemala Girimanchanaika, et al.
Letters in Organic Chemistry (2023) Vol. 20, Iss. 11, pp. 1070-1076
Closed Access
Vetting of New 2,5-Bis (2,2,2-trifluoroethoxy) Phenyl-Linked 1,3-Thiazolidine-4-one Derivatives as AURKA and VEGFR-2 Inhibitor Antiglioma Agents Assisted with In Vitro and In Silico Studies
Sathyanarayana D. Shankara, Arun M. Isloor, Pavan K. Jayaswamy, et al.
ACS Omega (2023) Vol. 8, Iss. 46, pp. 43596-43609
Open Access
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