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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:

Synthesis of new substituted pyridine derivatives as potent anti-liver cancer agents through apoptosis induction: In vitro, in vivo, and in silico integrated approaches
Ahmed T. A. Boraei, Elsayed H. Eltamany, Imran Ali, et al.
Bioorganic Chemistry (2021) Vol. 111, pp. 104877-104877
Closed Access | Times Cited: 55

Showing 1-25 of 55 citing articles:

Synthesis, in vitro thymidine phosphorylase inhibitory activity and molecular docking study of novel pyridine-derived bis-oxadiazole bearing bis-schiff base derivatives
Rafaqat Hussain, Wajid Rehman, Fazal Rahim, et al.
Arabian Journal of Chemistry (2023) Vol. 16, Iss. 6, pp. 104773-104773
Open Access | Times Cited: 49
Topo II inhibition and DNA intercalation by new phthalazine-based derivatives as potent anticancer agents: design, synthesis, anti-proliferative, docking, and in vivo studies
Mohamed M. Khalifa, Ahmed A. Al‐Karmalawy, Eslam B. Elkaeed, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2021) Vol. 37, Iss. 1, pp. 299-314
Open Access | Times Cited: 60
Exploration of novel VEGFR2 tyrosine kinase inhibitors via design and synthesis of new alkylated indolyl-triazole Schiff bases for targeting breast cancer
Mohamed S. Nafie, Ahmed T. A. Boraei
Bioorganic Chemistry (2022) Vol. 122, pp. 105708-105708
Closed Access | Times Cited: 54
Design and synthesis of novel benzoazoninone derivatives as potential CBSIs and apoptotic inducers: In Vitro, in Vivo, molecular docking, molecular dynamics, and SAR studies
Mohamed M. Hammouda, Ayman Abo Elmaaty, Mohamed S. Nafie, et al.
Bioorganic Chemistry (2022) Vol. 127, pp. 105995-105995
Closed Access | Times Cited: 39
PIM1 alleviated liver oxidative stress and NAFLD by regulating the NRF2/HO-1/NQO1 pathway
Kai Yang, Xiaoxiao Yu, Zihao Guo, et al.
Life Sciences (2024) Vol. 349, pp. 122714-122714
Closed Access | Times Cited: 9
Bioactive 2-pyridone-containing heterocycle syntheses using multicomponent reactions
Diana Hurtado-Rodríguez, Angélica Salinas-Torres, Hugo Rojas, et al.
RSC Advances (2022) Vol. 12, Iss. 54, pp. 34965-34983
Open Access | Times Cited: 31
Synthesis of novel mono- and bis-pyrazolylthiazole derivatives as anti-liver cancer agents through EGFR/HER2 target inhibition
Mostafa E. Salem, Esraa M. Mahrous, Eman A. Ragab, et al.
BMC Chemistry (2023) Vol. 17, Iss. 1
Open Access | Times Cited: 17
Synthesis of novel bioactive pyrido[2,3-d]pyrimidine derivatives with potent cytotoxicity through apoptosis as PIM-1 kinase inhibitors
Eman S. Tantawy, Mohamed S. Nafie, Hesham A. Morsy, et al.
RSC Advances (2024) Vol. 14, Iss. 16, pp. 11098-11111
Open Access | Times Cited: 7
Design and synthesis of novel rigid dibenzo[ b,f ]azepines through ring closure technique as promising anticancer candidates against leukaemia and acting as selective topoisomerase II inhibitors and DNA intercalators
Mohammed Farrag El‐Behairy, Walaa Hamada Abd‐Allah, Mohamed M. Khalifa, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2023) Vol. 38, Iss. 1
Open Access | Times Cited: 15
Synthesis and SARs study of novel spiro‐oxindoles as potent antiproliferative agents with CDK‐2 inhibitory activities
Refaah M. Al-Jassas, Mohammad Shahidul Islam, Abdullah Mohammed Al‐Majid, et al.
Archiv der Pharmazie (2023) Vol. 356, Iss. 8
Closed Access | Times Cited: 14
Nicotinonitrile-derived apoptotic inducers: Design, synthesis, X-ray crystal structure and Pim kinase inhibition
Shaimaa M. Aboukhatwa, Amera O. Ibrahim, Hiroshi Aoyama, et al.
Bioorganic Chemistry (2022) Vol. 129, pp. 106126-106126
Closed Access | Times Cited: 17
Synthesis, topology, molecular docking and dynamics studies of o -phenylenediamine derivative
T. Sankar Ganesan, N. Elangovan, Munusamy Thirumavalavan, et al.
Journal of Biomolecular Structure and Dynamics (2024), pp. 1-20
Closed Access | Times Cited: 3
Potent EGFR/PARP-1 inhibition by spirooxindole-triazole hybrids for targeted liver cancer therapy
Mohamed S. Nafie, M. Ali, Moayad Abdullah Alwehaibi, et al.
RSC Advances (2025) Vol. 15, Iss. 1, pp. 58-74
Open Access
Novel zerumbone-secondary amide hybrids: ultrasonic synthesis, cytotoxic evaluation, molecular docking and in silico ADMET studies
Phạm Thế Chính, Pham Thi Tham, Vũ Thị Kim Liên, et al.
RSC Advances (2025) Vol. 15, Iss. 12, pp. 8986-8998
Open Access
Anticancer potential of nicotinonitrile derivatives as PIM-1 kinase inhibitors through apoptosis: in vitro and in vivo studies
Syed Mahtab Ali, Mohamed S. Nafie, Huda Fahmy Farag, et al.
Medicinal Chemistry Research (2025) Vol. 34, Iss. 5, pp. 1074-1088
Closed Access
Ultrasound-Assisted Synthesis of Polyfunctionalized Pyridine Derivatives Catalyzed by Silica-Supported Perchloric Acid: In Vitro Anticancer Studies and Molecular Docking
N. Hussain Basha, T. Jagadish, Parasuraman Karthikeyan, et al.
Russian Journal of Bioorganic Chemistry (2025) Vol. 51, Iss. 2, pp. 932-946
Closed Access
In Vitro and In Vivo Studies of Anti-Lung Cancer Activity of Artemesia judaica L. Crude Extract Combined with LC-MS/MS Metabolic Profiling, Docking Simulation and HPLC-DAD Quantification
Marwa S. Goda, Mohamed S. Nafie, Basma Awad, et al.
Antioxidants (2021) Vol. 11, Iss. 1, pp. 17-17
Open Access | Times Cited: 22
Synthesis of Novel Phthalazinedione-Based Derivatives with Promising Cytotoxic, Anti-bacterial, and Molecular Docking Studies as VEGFR2 Inhibitors
Samir M. El Rayes, Gaber El Enany, Imran Ali, et al.
ACS Omega (2022) Vol. 7, Iss. 30, pp. 26800-26811
Open Access | Times Cited: 16
Tailored horseshoe-shaped nicotinonitrile scaffold as dual promising c-Met and Pim-1 inhibitors: Design, synthesis, SAR and in silico study
Samy Mohamady, Ahmed Khalil, Bassem H. Naguib, et al.
Bioorganic Chemistry (2023) Vol. 143, pp. 106988-106988
Closed Access | Times Cited: 9
Microbubble-enhanced HIFU therapy for vascularized tumors using Levovist contrast agent
Hossein Azizi Sormoli, Afsaneh Mojra, Ghassem Heidarinejad
International Journal of Mechanical Sciences (2023) Vol. 257, pp. 108569-108569
Closed Access | Times Cited: 8
Preparation, DFT calculations, docking studies, antioxidant, and anticancer properties of new pyrazole and pyridine derivatives
Zineddine Zebbiche, Güldeniz Şekerci, Houssem Boulebd, et al.
Journal of Biochemical and Molecular Toxicology (2022) Vol. 36, Iss. 9
Closed Access | Times Cited: 14
Synthesis of New Bioactive Indolyl-1,2,4-Triazole Hybrids As Dual Inhibitors for EGFR/PARP-1 Targeting Breast and Liver Cancer Cells
Mohamed F. Youssef, Mohamed S. Nafie, Eid E. Salama, et al.
ACS Omega (2022) Vol. 7, Iss. 49, pp. 45665-45677
Open Access | Times Cited: 13
A review: Biological activities of novel cyanopyridine derivatives
Yurou Wu, Tao Wu, Yong Huang
Archiv der Pharmazie (2023) Vol. 356, Iss. 7
Closed Access | Times Cited: 7
Synthesis of novel phthalazine-based derivatives with potent cytotoxicity against HCT-116 cells through apoptosis and VEGFR2 inhibition
Donia El Sayed, Samir M. El Rayes, Hamdy A.M. Soliman, et al.
RSC Advances (2024) Vol. 14, Iss. 19, pp. 13027-13043
Open Access | Times Cited: 2
Development of a selective COX-2 inhibitor: from synthesis to enhanced efficacy via nano-formulation
Marwa Elewa, Mohamed Shehda, Pierre A. Hanna, et al.
RSC Advances (2024) Vol. 14, Iss. 45, pp. 32721-32732
Open Access | Times Cited: 2
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