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 48 citing articles:

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: 37

Development of novel indolin-2-one derivative incorporating thiazole moiety as DHFR and quorum sensing inhibitors: Synthesis, antimicrobial, and antibiofilm activities with molecular modelling study
Abdullah Yahya Abdullah Alzahrani, Yousry A. Ammar, Mohammed Abu‐Elghait, et al.
Bioorganic Chemistry (2021) Vol. 119, pp. 105571-105571
Closed Access | Times Cited: 59

In vitro enzymatic evaluation of some pyrazolo[1,5‐a]pyrimidine derivatives: Design, synthesis, antioxidant, anti‐diabetic, anti‐Alzheimer, and anti‐arthritic activities with molecular modeling simulation
Ashraf S. Hassan, Nesrin M. Morsy, Wael M. Aboulthana, et al.
Drug Development Research (2022) Vol. 84, Iss. 1, pp. 3-24
Closed Access | Times Cited: 55

Synthesis, characterization, thermal properties, antimicrobial evaluation, ADMET study, and molecular docking simulation of new mono Cu (II) and Zn (II) complexes with 2-oxoindole derivatives
Ahmed Ragab, Yousry A. Ammar, Ahmed Ezzat, et al.
Computers in Biology and Medicine (2022) Vol. 145, pp. 105473-105473
Closed Access | Times Cited: 49

Synthesis, characterization, and in vitro antibacterial activity of some new pyridinone and pyrazole derivatives with some in silico ADME and molecular modeling study
Khadija E. Saadon, Nadia M. H. Taha, N. A. Mahmoud, et al.
Journal of the Iranian Chemical Society (2022) Vol. 19, Iss. 9, pp. 3899-3917
Open Access | Times Cited: 46

Discovery of novel pyrazole and pyrazolo[1,5‐a]pyrimidine derivatives as cyclooxygenase inhibitors (COX‐1 and COX‐2) using molecular modeling simulation
Radwa Ayman, A. M. Radwan, Amira M. Elmetwally, et al.
Archiv der Pharmazie (2022) Vol. 356, Iss. 2
Closed Access | Times Cited: 44

Novel cyclohepta[b]thiophene derivative incorporating pyrimidine, pyridine, and chromene moiety as potential antimicrobial agents targeting DNA gyrase
Eman A. Fayed, Marwa Mohsen, Shimaa M. Abd El‐Gilil, et al.
Journal of Molecular Structure (2022) Vol. 1262, pp. 133028-133028
Closed Access | Times Cited: 37

A new exploration toward adamantane derivatives as potential anti‐MDR agents: Design, synthesis, antimicrobial, and radiosterilization activity as potential topoisomerase IV and DNA gyrase inhibitors
Ahmed Ragab, Moustafa S. Abusaif, Dina S. Aboul‐Magd, et al.
Drug Development Research (2022) Vol. 83, Iss. 6, pp. 1305-1330
Closed Access | Times Cited: 35

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

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: 20

Analgesic and anti-inflammatory activity of quinoxaline derivatives: Design synthesis and characterization
Geethavani Meka, Ramakrishna Chintakunta
Results in Chemistry (2023) Vol. 5, pp. 100783-100783
Open Access | Times Cited: 19

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: 9

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

Current strategies in design and synthesis of antifungals hybrid and chimeric diazine derivatives
Dumitrela Diaconu, Marius Savu, Catalina Ionica Ciobanu, et al.
Bioorganic & Medicinal Chemistry (2025) Vol. 119, pp. 118069-118069
Open Access

Synthesis, spectral characterization, antimicrobial evaluation and molecular docking studies of new Cu (II), Zn (II) thiosemicarbazone based on sulfonyl isatin
Ahmed Ezzat, Mahmoud Basseem I. Mohamed, Ammar M. Mahmoud, et al.
Journal of Molecular Structure (2021) Vol. 1251, pp. 132004-132004
Closed Access | Times Cited: 42

A novel of quinoxaline derivatives tagged with pyrrolidinyl scaffold as a new class of antimicrobial agents: Design, synthesis, antimicrobial activity, and molecular docking simulation
Mostafa M. Abdelgalil, Yousry A. Ammar, Gameel A. M. El‐Hag Ali, et al.
Journal of Molecular Structure (2022) Vol. 1274, pp. 134443-134443
Closed Access | Times Cited: 32

Development of new spiro[1,3]dithiine-4,11′-indeno[1,2-b]quinoxaline derivatives as S. aureus Sortase A inhibitors and radiosterilization with molecular modeling simulation
Ahmed Ragab, Moustafa S. Abusaif, Nirvana A. Gohar, et al.
Bioorganic Chemistry (2022) Vol. 131, pp. 106307-106307
Closed Access | Times Cited: 31

Design and Synthesis of 2-(4-Bromophenyl)Quinoline-4-Carbohydrazide Derivatives via Molecular Hybridization as Novel Microbial DNA-Gyrase Inhibitors
Hany M. Abd El‐Lateef, Ayman Abo Elmaaty, Lina M. A. Abdel Ghany, et al.
ACS Omega (2023) Vol. 8, Iss. 20, pp. 17948-17965
Open Access | Times Cited: 18

Design, synthesis, biological evaluation, and docking study of chromone-based phenylhydrazone and benzoylhydrazone derivatives as antidiabetic agents targeting α‐glucosidase
Meiyan Fan, Wei Yang, Lin Liu, et al.
Bioorganic Chemistry (2023) Vol. 132, pp. 106384-106384
Closed Access | Times Cited: 17

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