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.

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Showing 1-25 of 49 citing articles:

In vitro biological studies and computational prediction-based analyses of pyrazolo[1,5-a]pyrimidine derivatives
Abdulrahman A. Almehizia, Wael M. Aboulthana, Ahmed M. Naglah, et al.
RSC Advances (2024) Vol. 14, Iss. 12, pp. 8397-8408
Open Access | Times Cited: 12

Antioxidant Activity, Molecular Docking and Quantum Studies of New Bis‐Schiff Bases Based on Benzyl Phenyl Ketone Moiety
Rashid Ahmad, Aftab Alam, Momin Khan, et al.
ChemistrySelect (2023) Vol. 8, Iss. 35
Closed Access | Times Cited: 28

A new class of anti-proliferative activity and apoptotic inducer with molecular docking studies for a novel of 1,3-dithiolo[4,5-b]quinoxaline derivatives hybrid with a sulfonamide moiety
Mostafa A. Ismail, Moustafa S. Abusaif, M. S. A. El‐Gaby, et al.
RSC Advances (2023) Vol. 13, Iss. 18, pp. 12589-12608
Open Access | Times Cited: 22

Discovery a novel of thiazolo[3,2-a]pyridine and pyrazolo[3,4-d]thiazole derivatives as DNA gyrase inhibitors; design, synthesis, antimicrobial activity, and some in-silico ADMET with molecular docking study
Hazem Ali Mohamed, Yousry A. Ammar, Gameel A. M. Elhagali, et al.
Journal of Molecular Structure (2023) Vol. 1287, pp. 135671-135671
Closed Access | Times Cited: 22

Evaluation of the anti-proliferative activity of 2-oxo-pyridine and 1′H-spiro-pyridine derivatives as a new class of EGFRWt and VEGFR-2 inhibitors with apoptotic inducers
Reham R. Raslan, Yousry A. Ammar, Sawsan A. Fouad, et al.
RSC Advances (2023) Vol. 13, Iss. 15, pp. 10440-10458
Open Access | Times Cited: 21

Synthesis, in silico ADMET prediction analysis, and pharmacological evaluation of sulfonamide derivatives tethered with pyrazole or pyridine as anti-diabetic and anti-Alzheimer's agents
Nagwa M. Abdelazeem, Wael M. Aboulthana, Ashraf S. Hassan, et al.
Saudi Pharmaceutical Journal (2024) Vol. 32, Iss. 5, pp. 102025-102025
Open Access | Times Cited: 10

Explore new quinoxaline pharmacophore tethered sulfonamide fragments as in vitro α‐glucosidase, α‐amylase, and acetylcholinesterase inhibitors with ADMET and molecular modeling simulation
Ahmed Ragab, Mohamed A. Salem, Yousry A. Ammar, et al.
Drug Development Research (2024) Vol. 85, Iss. 4
Closed Access | Times Cited: 8

Novel isatin–triazole based thiosemicarbazones as potential anticancer agents: synthesis, DFT and molecular docking studies
Alia Mushtaq, Rabbia Asif, Waqar Ahmed Humayun, et al.
RSC Advances (2024) Vol. 14, Iss. 20, pp. 14051-14067
Open Access | Times Cited: 7

Bioactive Fused Pyrazoles Inspired by the Adaptability of 5-Aminopyrazole Derivatives: Recent Review
Dana M. Odeh, Mohanad Odeh, Taghrid S. Hafez, et al.
Molecules (2025) Vol. 30, Iss. 2, pp. 366-366
Open Access

Three Novel Schiff Bases Based on Ninhydrin: Synthesis, Characterization, DFT, Anticancer, Antibacterial and Molecular Docking Studies
Lakshmi V. Menon, E. Manoj
Journal of Molecular Structure (2025), pp. 141497-141497
Closed Access

Target based synthesis, medicinal evaluation and in silico modeling of thiazole incorporating bis-Schiff bases: Ligands protein interaction against α amylase and α glucosidase insight
Shoaib Khan, Tayyiaba Iqbal, Rafaqat Hussain, et al.
Journal of the Indian Chemical Society (2025), pp. 101609-101609
Closed Access

Assessment of the In Vitro Biological Activities of Schiff Base-Synthesized Copper Oxide Nanoparticles as an Anti-Diabetic, Anti-Alzheimer, and Anti-Cancer Agent
Abdulrahman A. Almehizia, Ahmed M. Naglah, Sadeem S. Aljafen, et al.
Pharmaceutics (2025) Vol. 17, Iss. 2, pp. 180-180
Open Access

Design, Synthesis and In vitro Antitubercular Effect of New Chalcone Derivatives Coupled with 1,2,3‐Triazoles: A Computational Docking Techniques
Kumaraswamy Sadineni, Sravanthi Basireddy, Tejeswara Rao Allaka, et al.
Chemistry & Biodiversity (2024) Vol. 21, Iss. 5
Closed Access | Times Cited: 5

Design, synthesis and in silico molecular docking evaluation of novel 1,2,3-triazole derivatives as potent antimicrobial agents
Sudhakar Reddy Baddam, Mahesh Kumar Avula, Raghunadh Akula, et al.
Heliyon (2024) Vol. 10, Iss. 7, pp. e27773-e27773
Open Access | Times Cited: 5

Discovery of novel 6-(piperidin-1-ylsulfonyl)-2H-chromenes targeting α-glucosidase, α-amylase, and PPAR-γ: Design, synthesis, virtual screening, and anti-diabetic activity for type 2 diabetes mellitus
Hamdy Khamees Thabet, Moustafa S. Abusaif, Mohd Imran, et al.
Computational Biology and Chemistry (2024) Vol. 111, pp. 108097-108097
Closed Access | Times Cited: 5

Discovery of new anti-diabetic potential agents based on paracetamol incorporating sulfa-drugs: Design, synthesis, α-amylase, and α-glucosidase inhibitors with molecular docking simulation
Hamdy Khamees Thabet, Ahmed Ragab, Mohd Imran, et al.
European Journal of Medicinal Chemistry (2024) Vol. 275, pp. 116589-116589
Closed Access | Times Cited: 4

Metal Complexes with Schiff Bases as Antimicrobials and Catalysts
Domenico Iacopetta, Jessica Ceramella, Alessia Catalano, et al.
Inorganics (2023) Vol. 11, Iss. 8, pp. 320-320
Open Access | Times Cited: 12

Graph theoretical analysis, pharmacoinformatics and molecular docking investigation of Chalcone-Schiff base hybrids as Cyclin-Dependent kinase inhibitors
Praveen Sekar, Sathishkumar Arivanantham, Pavithra Jaishankar, et al.
Research in Pharmacy (2024)
Open Access | Times Cited: 2

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