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:

Structural and functional insight into thiazolidinone derivatives as novel candidates for anticancer drug design: in vitro biological and in-silico strategies
Pervaiz Ali Channar, Mubashir Aziz, Syeda Abida Ejaz, et al.
Journal of Biomolecular Structure and Dynamics (2021) Vol. 41, Iss. 3, pp. 942-953
Closed Access | Times Cited: 13

Showing 13 citing articles:

Identification and molecular mechanism of novel 5-alkenyl-2-benzylaminothiazol-4(5H)-one analogs as anti-melanogenic and antioxidant agents
Min Kyung Kang, Dahye Yoon, Hee Jin Jung, et al.
Bioorganic Chemistry (2023) Vol. 140, pp. 106763-106763
Closed Access | Times Cited: 10

In-silico Investigations of quinine and quinidine as potential Inhibitors of AKR1B1 and AKR1B10: Functional and structural characterization
Syeda Abida Ejaz, Amna Saeed, Pervez Rashid Birmani, et al.
PLoS ONE (2022) Vol. 17, Iss. 10, pp. e0271602-e0271602
Open Access | Times Cited: 9

Cytotoxicity assays for cancer drug screening: methodological insights and considerations for reliable assessment in drug discovery
Gul-e-Saba Chaudhry, Zeenia, Naila Safdar, et al.
Brazilian Journal of Biology (2024) Vol. 84
Open Access | Times Cited: 1

Synthesis of Oleanolic Acid-Dithiocarbamate Conjugates and Evaluation of Their Broad-Spectrum Antitumor Activities
Liyao Tang, Yan Zhang, Jinrun Xu, et al.
Molecules (2023) Vol. 28, Iss. 3, pp. 1414-1414
Open Access | Times Cited: 4

Design, Synthesis, Anticancer Evaluation and Molecular Modeling Studies of New Thiazolidinone‐Benzoate Scaffold as EGFR Inhibitors, Cell Cycle Interruption and Apoptosis Inducers in HepG2
Salwa Magdy Eldaly, Dalia Salama Zakaria, Nadia H. Metwally
Chemistry & Biodiversity (2023) Vol. 20, Iss. 10
Closed Access | Times Cited: 4

Evaluation of anticancer potential of tetracene-5,12-dione (A01) and pyrimidine-2,4-dione (A02) via caspase 3 and lactate dehydrogenase cytotoxicity investigations
Mubashir Aziz, Muhammad Sarfraz, Muhammad Ibrahim, et al.
PLoS ONE (2023) Vol. 18, Iss. 12, pp. e0292455-e0292455
Open Access | Times Cited: 3

Starting a new chapter on class Ia ribonucleotide reductases
Talya S. Levitz, Catherine L. Drennan
Current Opinion in Structural Biology (2022) Vol. 77, pp. 102489-102489
Open Access | Times Cited: 5

Synthesis and antitumor evaluation of glycyrrhetinic acid‐dithiocarbamate hybrids
Jiahong Su, Xingyue Wang, Sha Li, et al.
Archiv der Pharmazie (2024) Vol. 358, Iss. 1
Closed Access

Evaluation of mechanical features and antibacterial potential of fluoroquinolone against β-ketoacyl-ACP synthases (FabB, FabF & FabH) via computational approaches
Syeda Abida Ejaz, Mubashir Aziz, Tanveer A. Wani, et al.
Archives of Biochemistry and Biophysics (2023) Vol. 744, pp. 109674-109674
Closed Access | Times Cited: 1

Repurposing of Strychnine as the Potential Inhibitors of Aldo–keto Reductase Family 1 Members B1 and B10: Computational Modeling and Pharmacokinetic Analysis
Muhammad Sarfraz, Mubashir Aziz, Saira Afzal, et al.
The Protein Journal (2023) Vol. 43, Iss. 2, pp. 207-224
Closed Access | Times Cited: 1

A comprehensive computational approach for the identification of structure-based potential pharmacological candidates as selective AKR1B1 and AKR1B10 inhibitors: repurposing of purine alkaloids for the treatment of cancer
Mubashir Aziz, Syeda Abida Ejaz, Nissren Tamam, et al.
Journal of Biomolecular Structure and Dynamics (2022) Vol. 41, Iss. 16, pp. 7892-7912
Closed Access | Times Cited: 2

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