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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 30 citing articles:

Design and Synthesis of Novel Antimicrobial Agents
Zeinab Breijyeh, Rafik Karaman
Antibiotics (2023) Vol. 12, Iss. 3, pp. 628-628
Open Access | Times Cited: 68
Development of novel pyrazole, imidazo[1,2-b]pyrazole, and pyrazolo[1,5-a]pyrimidine derivatives as a new class of COX-2 inhibitors with immunomodulatory potential
Radwa Ayman, Moustafa S. Abusaif, A. M. Radwan, et al.
European Journal of Medicinal Chemistry (2023) Vol. 249, pp. 115138-115138
Closed Access | Times Cited: 41
Insight into divergent chemical modifications of chitosan biopolymer: Review
Elsayed M. Elnaggar, Moustafa S. Abusaif, Yasser M. Abdel-Baky, et al.
International Journal of Biological Macromolecules (2024) Vol. 277, pp. 134347-134347
Closed Access | Times Cited: 15
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: 25
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: 24
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: 24
Innovation of 6-sulfonamide-2H-chromene derivatives as antidiabetic agents targeting α-amylase, α-glycosidase, and PPAR-γ inhibitors with in silico molecular docking simulation
Hamdy Khamees Thabet, Ahmed Ragab, Mohd Imran, et al.
RSC Advances (2024) Vol. 14, Iss. 22, pp. 15691-15705
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: 10
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 | Times Cited: 1
Unveiling the multifaceted bioactivity of copper(ii)–Schiff base complexes: a comprehensive study of antioxidant, anti-bacterial, anti-inflammatory, enzyme inhibition and cytotoxic potentials with DFT insights
T.M. Dhanya, M.R. Prathapachandra Kurup, K.J. Rajimon, et al.
Dalton Transactions (2025)
Closed Access | Times Cited: 1
Novel Water-soluble quinoxaline-2,3-dione-6-sulfohydrazide derivatives as efficient acid corrosion inhibitors: Design, characterization, experimental, and theoretical studies
Moustafa S. Abusaif, Amira M. Hyba, Yousry A. Ammar, et al.
Journal of the Taiwan Institute of Chemical Engineers (2023) Vol. 153, pp. 105207-105207
Closed Access | Times Cited: 21
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: 7
Evaluation of novel compounds as anti-bacterial or anti-virulence agents
Brankica Filipić, Dušan Ušjak, Martina Hrast Rambaher, et al.
Frontiers in Cellular and Infection Microbiology (2024) Vol. 14
Open Access | Times Cited: 6
Design, green synthesis, and quorum sensing quenching potential of novel 2-oxo-pyridines containing a thiophene/furan scaffold and targeting a LasR gene on P. aeruginosa
Yousry A. Ammar, Ahmed Ragab, M.A. Migahed, et al.
RSC Advances (2023) Vol. 13, Iss. 39, pp. 27363-27384
Open Access | Times Cited: 14
Discovery of new thiazolidin-4-one and thiazole nucleus incorporation sulfaguanidine scaffold as new class of antimicrobial agents: Design, synthesis, in silico ADMET, and docking simulation
Ola A. Abu Ali, Ahmed Ragab, Yousry A. Ammar, et al.
Journal of Molecular Structure (2025), pp. 141879-141879
Closed Access
Unveiling a novel pyrazolopyrimidine scaffold as a dual COX-2/5-LOX inhibitor with immunomodulatory potential: Design, synthesis, target prediction, anti-inflammatory activity, and ADME-T with docking simulation
Ahmed Ragab, Radwa Ayman, Mohamed A. Salem, et al.
European Journal of Medicinal Chemistry (2025) Vol. 290, pp. 117499-117499
Closed Access
Recent advances in the synthesis, reaction, and bio-evaluation potential of purines as precursor pharmacophores in chemical reactions: a review
Ahmed Ragab
RSC Advances (2025) Vol. 15, Iss. 5, pp. 3607-3645
Open Access
Unveiling the antitumor potential of novel N-(substituted-phenyl)-8-methoxycoumarin-3-carboxamides as dual inhibitors of VEGFR2 kinase and cytochrome P450 for targeted treatment of hepatocellular carcinoma
Eman M. Radwan, Eman Abo-Elabass, Atef E. Abd El-Baky, et al.
Frontiers in Chemistry (2023) Vol. 11
Open Access | Times Cited: 10
Synthesis, characterization, and biological target prediction of novel 1,3-dithiolo[4,5-b]quinoxaline and thiazolo[4,5-b]quinoxaline derivatives
M. S. A. El‐Gaby, Yousry A. Ammar, Mostafa A. Ismail, et al.
Heterocyclic Communications (2023) Vol. 29, Iss. 1
Open Access | Times Cited: 10
Green synthesis of some new azolopyrimidines as antibacterial agents based on thiophene-chalcone
Salwa Magdy Eldaly, Nadia H. Metwally
Synthetic Communications (2024) Vol. 54, Iss. 5, pp. 348-370
Closed Access | Times Cited: 3
Chemistry of heterocycles as carbonic anhydrase inhibitors: A pathway to novel research in medicinal chemistry review
Anjaneyulu Bendi, Taruna, Rajni Rajni, et al.
Archiv der Pharmazie (2024) Vol. 357, Iss. 7
Closed Access | Times Cited: 3
Photocatalytic activity of co‐doped NPs based on ZnO as a new class of anti‐microbial agents: Synthesis, characterization, kinetics, isotherm, and in silico molecular docking simulation
Mohga Basseem, Abeer A. Emam, Fatma H. Kamal, et al.
Applied Organometallic Chemistry (2023) Vol. 37, Iss. 10
Open Access | Times Cited: 8
One-pot synthesis of pyrazolo[4,3-d]thiazole derivatives containing α-aminophosphonate as potential Mur A inhibitors against MDR pathogens with radiosterilization and molecular modeling simulation
Ahmed Ragab, Seham A. Ibrahim, Dina S. Aboul‐Magd, et al.
RSC Advances (2023) Vol. 13, Iss. 49, pp. 34756-34771
Open Access | Times Cited: 8
Antibacterial and Antifungal Pyrazoles Based on Different Construction Strategies
Muneeb Ur Rehman, Fang He, Xi Shu, et al.
European Journal of Medicinal Chemistry (2024) Vol. 282, pp. 117081-117081
Closed Access | Times Cited: 2
Exploration of 3‐aryl pyrazole‐tethered sulfamoyl carboxamides as carbonic anhydrase inhibitors
Ojaswitha Ommi, Niccolò Paoletti, Alessandro Bonardi, et al.
Archiv der Pharmazie (2023) Vol. 356, Iss. 11
Closed Access | Times Cited: 5
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