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:

Discovery of novel dual acetylcholinesterase and butyrylcholinesterase inhibitors using machine learning and structure-based drug design
Manish Tripathi, Bhagwati Bhardwaj, Digambar Kumar Waiker, et al.
Journal of Molecular Structure (2023) Vol. 1286, pp. 135517-135517
Closed Access | Times Cited: 14

Showing 14 citing articles:

Design, Synthesis, and Biological Investigation of Quinazoline Derivatives as Multitargeting Therapeutics in Alzheimer’s Disease Therapy
Akash Verma, Digambar Kumar Waiker, Neha Singh, et al.
ACS Chemical Neuroscience (2024) Vol. 15, Iss. 4, pp. 745-771
Closed Access | Times Cited: 8

Design, Synthesis, and Biological Evaluation of Piperazine and N-Benzylpiperidine Hybrids of 5-Phenyl-1,3,4-oxadiazol-2-thiol as Potential Multitargeted Ligands for Alzheimer’s Disease Therapy
Digambar Kumar Waiker, Akash Verma, Akhilesh Akhilesh, et al.
ACS Chemical Neuroscience (2023) Vol. 14, Iss. 11, pp. 2217-2242
Closed Access | Times Cited: 19

Design and development of benzyl piperazine linked 5-phenyl-1,2,4-triazole-3-thione conjugates as potential agents to combat Alzheimer’s disease
Pidugu Venkata Ravi Kiran, Digambar Kumar Waiker, Akash Verma, et al.
Bioorganic Chemistry (2023) Vol. 139, pp. 106749-106749
Closed Access | Times Cited: 16

Enhanced in silico QSAR-based screening of butyrylcholinesterase inhibitors using multi-feature selection and machine learning
D. Sharmistha, M Prabha, Ravi Kiran, et al.
SAR and QSAR in environmental research (2025), pp. 1-21
Closed Access

Research progress and perspectives of dual-target inhibitors
Xiaojing Pang, Wenyan Xu, Jing Liang, et al.
European Journal of Medicinal Chemistry (2025) Vol. 289, pp. 117453-117453
Closed Access

Novel Stannoxane-Based Cage: Development, Biological Activity, Computational and DNA Interaction Studies
Kaleem Ullah, Saqib Ali, Saba Naz, et al.
Journal of Molecular Structure (2025), pp. 141931-141931
Closed Access

Investigation of Pivalic Acid-Derived Organotin(IV) Carboxylates: Synthesis, Structural Insights, Interaction with Biomolecules, and Computational Studies
Kaleem Ullah, Saqib Ali, Ali Haider, et al.
Journal of Molecular Structure (2024), pp. 140444-140444
Closed Access | Times Cited: 4

Design, synthesis, and biological evaluation of some 2-(3-oxo-5,6-diphenyl-1,2,4-triazin-2(3H)-yl)-N-phenylacetamide hybrids as MTDLs for Alzheimer's disease therapy
Digambar Kumar Waiker, Akash Verma, T A Gajendra, et al.
European Journal of Medicinal Chemistry (2024) Vol. 271, pp. 116409-116409
Closed Access | Times Cited: 2

Unleashing the Future: The Revolutionary Role of Machine Learning and Artificial Intelligence in Drug Discovery
Manoj Kumar Yadav, Vandana Dahiya, Manish Tripathi, et al.
European Journal of Pharmacology (2024) Vol. 985, pp. 177103-177103
Closed Access | Times Cited: 2

A Series of Novel 1-H-isoindole-1,3(2H)-dione Derivatives as Acetylcholinesterase and Butyrylcholinesterase Inhibitors: In Silico, Synthesis and In Vitro Studies
Edward Krzyżak, Aleksandra Marciniak, Dominika Szkatuła, et al.
Molecules (2024) Vol. 29, Iss. 15, pp. 3528-3528
Open Access | Times Cited: 1

First Examples of Phosphoric Anhydride-Promoted O- and N-Acylation
Yu. M. Shafran, T. А. Поспелова
Russian Journal of General Chemistry (2023) Vol. 93, Iss. 12, pp. 3021-3033
Closed Access

First examples of phosphoric anhydride mediated O- and N-acylation
Yu. M. Shafran, T. А. Поспелова
Журнал Общей Химии (2023) Vol. 93, Iss. 12, pp. 1807-1821
Closed Access

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