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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:

Development of adamantane scaffold containing 1,3,4-thiadiazole derivatives: Design, synthesis, anti-proliferative activity and molecular docking study targeting EGFR
Mohammed M. S. Wassel, Yousry A. Ammar, Gameel A. M. El‐Hag Ali, et al.
Bioorganic Chemistry (2021) Vol. 110, pp. 104794-104794
Closed Access | Times Cited: 51

Showing 26-50 of 51 citing articles:

EGFR as therapeutic target to develop new generation tyrosine kinase inhibitors against breast cancer: A critical review
Ruby Mariam Raju, Jeffin Joy A, Raghavendra Nulgumnalli Manjunathaiah, et al.
Results in Chemistry (2024) Vol. 7, pp. 101490-101490
Open Access | Times Cited: 3
Development and radiosterilization of new hydrazono‐quinoline hybrids as DNA gyrase and topoisomerase IV inhibitors: Antimicrobial and hemolytic activities against uropathogenic isolates with molecular docking study
Yousry A. Ammar, Jehan A. Micky, Dina S. Aboul‐Magd, et al.
Chemical Biology & Drug Design (2022) Vol. 101, Iss. 2, pp. 245-270
Closed Access | Times Cited: 18
Synthesis, characterization, biological evaluation and in silico studies of novel 1,3,4-thiadiazole derivatives as aromatase inhibitors
Sena Demiraran, Derya Osmani̇ye, Yusuf Özkay, et al.
Journal of Molecular Structure (2023) Vol. 1296, pp. 136903-136903
Closed Access | Times Cited: 10
Synthesis, characterization, molecular docking and molecular dynamics simulations of novel 2,5-disubstituted-1,3,4-thiadiazole derivatives as potential cholinesterase/monoamine oxidase dual inhibitors for Alzheimer’s disease
Amal A. AL-Sharabi, Asaf Evrim Evren, Begüm Nurpelin Sağlık, et al.
Journal of Biomolecular Structure and Dynamics (2023) Vol. 42, Iss. 23, pp. 13023-13041
Closed Access | Times Cited: 10
Nascent pharmacological advancement in adamantane derivatives
Aman Ragshaniya, Vijay Kumar, Ram Kumar Tittal, et al.
Archiv der Pharmazie (2023) Vol. 357, Iss. 3
Closed Access | Times Cited: 10
Antimicrobial evaluation, in silico ADMET prediction, molecular docking, and molecular electrostatic potential of pyrazole-isatin and pyrazole-indole hybrid molecules
Ashraf S. Hassan
Journal of the Iranian Chemical Society (2022) Vol. 19, Iss. 8, pp. 3577-3589
Closed Access | Times Cited: 16
Molecular Hybrid Design, Synthesis, In Vitro Cytotoxicity, In Silico ADME and Molecular Docking Studies of New Benzoate Ester-Linked Arylsulfonyl Hydrazones
Erdem Ergan, Reşit Çakmak, Eyüp Başaran, et al.
Molecules (2024) Vol. 29, Iss. 15, pp. 3478-3478
Open Access | Times Cited: 2
Synthesis, biological evaluation and molecular docking of new triphenylamine-linked pyridine, thiazole and pyrazole analogues as anticancer agents
Mohamed R. Elmorsy, Samar E. Mahmoud, Ahmed A. Fadda, et al.
BMC Chemistry (2022) Vol. 16, Iss. 1
Open Access | Times Cited: 13
Synthesis, biological evaluation and molecular docking studies of novel 1,3,4-thiadiazoles as potential anticancer agents and human carbonic anhydrase inhibitors
Sevgi Karakuş, Elif Başçıl, Fatih Tok, et al.
Molecular Diversity (2023)
Closed Access | Times Cited: 6
Design, Docking, Synthesis and Biological Evaluation of Novel Nicotinohydrazone Derivatives as Potential Butyrylcholinesterase Enzyme Inhibitor
Yusuf İslam Esmer, Ercan Çınar, Eyüp Başaran
ChemistrySelect (2022) Vol. 7, Iss. 33
Closed Access | Times Cited: 11
Synthesis, Biological Evaluation, and Docking Study of a New Series of Thiophene Derivatives Based on 3‐Oxobutanamidothiophene as an Anticancer Agent
Fatima S. Mehdhar, Ali Saeed, Ehab Abdel‐Latif, et al.
ChemistrySelect (2024) Vol. 9, Iss. 18
Closed 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
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
Design, synthesis, characterization, and antimicrobial evaluation of some new pyridine and chromene derivatives containing Lidocaine analogue
Abdullah Yahya Abdullah Alzahrani
Journal of Saudi Chemical Society (2023) Vol. 27, Iss. 2, pp. 101620-101620
Open Access | Times Cited: 2
Thiadiazoles

Royal Society of Chemistry eBooks (2024)
Closed Access
An efficient green synthesis and in vitro evaluation of novel adamantane-containing 4-thiazolidinone derivatives as anticancer agents
Mina Abkar Aras, Nahideh Jafari, Adeleh Moshtaghi Zonouz, et al.
Journal of Molecular Structure (2024) Vol. 1321, pp. 139708-139708
Closed Access
Design, Synthesis, Biological Evaluation and Molecular Docking Study of New 1,3,4‐Thiadiazole‐Based Compounds as EGFR Inhibitors
Marwa I. Serag, Samar S. Tawfik, Hassan M. Eisa, et al.
Drug Development Research (2024) Vol. 86, Iss. 1
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
Design and synthesis of N-formyl/carbothioamide based pyrazoline analogs using Pd(PPh3)4 catalyst: Cytotoxicity, apoptosis, and molecular docking studies
Manish Rana, Imran Ansari, Sumbul Jawed Khan, et al.
Journal of Organometallic Chemistry (2024), pp. 123369-123369
Closed Access
Sulfonylhydrazide Derivatives as Potential Anti-cancer Agents: Synthesis, In Vitro and In Silico Studies
Kholoud M Ibrahim, Doaa M. Elsisi, Yousry A. Ammar, et al.
The Protein Journal (2024)
Closed Access
Synthesis, antiproliferative and 4D-QSAR studies of thiadiazole derivatives bearing acrylamide moiety as EGFR inhibitors
Biying Cai, Tiansheng Zhao, Daogang Qin, et al.
SAR and QSAR in environmental research (2023) Vol. 34, Iss. 4, pp. 341-359
Closed Access | Times Cited: 1
Synthesis and Biological Evaluation of a Library of Sulfonamide Analogs of Memantine to Target Glioblastoma
John E. Philo, Jenna D. Caudle, Reema N. Moussa, et al.
ChemMedChem (2023) Vol. 18, Iss. 16
Closed Access | Times Cited: 1
Synthesis, Characterization, In vitro Antimicrobial Evaluation and Molecular Docking Studies of Pyrazole Based Pyrimidine and Pyrazolone Motifs
Nisheeth C. Desai, Ashvinkumar G. Khasiya, Bharti P. Dave, et al.
Anti-Infective Agents (2022) Vol. 20, Iss. 5
Closed Access | Times Cited: 1
New Bis-1,3,4-Thiadiazoles Based on Fumaric Acid: Preparation, Structure Elucidation, Antibacterial Activities, and Quantum-Chemical Studies
Halit Muğlu, Hasan Yakan, Ghaith Alabed Ibrayke Elefkhakry, et al.
Acta chimica slovenica (2023) Vol. 70, Iss. 2, pp. 247-260
Open Access
Synthesis of Novel Memantine and Rimantadine Derivatives as Promising Drug Candidates
Ya. K. Shtaitz, E. D. Ladin, Н. В. Словеснова, et al.
Russian Journal of General Chemistry (2023) Vol. 93, Iss. S1, pp. S100-S105
Closed Access

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