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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:

Synthesis and biological evaluation of novel xanthine derivatives as potential apoptotic antitumor agents
Mohamed Hisham, Bahaa G. M. Youssif, Essam Eldin A. Osman, et al.
European Journal of Medicinal Chemistry (2019) Vol. 176, pp. 117-128
Closed Access | Times Cited: 73

Showing 26-50 of 73 citing articles:

Synthesis and SARs study of novel spiro‐oxindoles as potent antiproliferative agents with CDK‐2 inhibitory activities
Refaah Mousa Al‐Jassas, Mohammad Shahidul Islam, Abdullah Mohammed Al‐Majid, et al.
Archiv der Pharmazie (2023) Vol. 356, Iss. 8
Closed Access | Times Cited: 13
New Thiazolyl-Pyrazoline Derivatives as Potential Dual EGFR/HER2 Inhibitors: Design, Synthesis, Anticancer Activity Evaluation and In Silico Study
Mariam M. Fakhry, Amr A. Mattar, Marwa Alsulaimany, et al.
Molecules (2023) Vol. 28, Iss. 21, pp. 7455-7455
Open Access | Times Cited: 13
Acetic Acid Mediated for One-Pot Synthesis of Novel Pyrazolyl s-Triazine Derivatives for the Targeted Therapy of Triple-Negative Breast Tumor Cells (MDA-MB-231) via EGFR/PI3K/AKT/mTOR Signaling Cascades
Ihab Shawish, Assem Barakat, Ali Aldalbahi, et al.
Pharmaceutics (2022) Vol. 14, Iss. 8, pp. 1558-1558
Open Access | Times Cited: 19
Design, Synthesis, and Anti-Proliferative Action of Purine/Pteridine-Based Derivatives as Dual Inhibitors of EGFR and BRAFV600E
Samar El‐Kalyoubi, Hesham A. M. Gomaa, Elshimaa M. N. Abdelhafez, et al.
Pharmaceuticals (2023) Vol. 16, Iss. 5, pp. 716-716
Open Access | Times Cited: 10
Characterization of covalent inhibitors that disrupt the interaction between the tandem SH2 domains of SYK and FCER1G phospho-ITAM
Frances M. Bashore, V.L. Katis, Yuhong Du, et al.
PLoS ONE (2024) Vol. 19, Iss. 2, pp. e0293548-e0293548
Open Access | Times Cited: 3
Design and synthesis of some new imidazole-morpholine-1,2,4-oxadiazole hybrids as EGFR targeting in vitro anti-breast cancer agents
Praveen kumar Kannekanti, Satheesh Kumar Nukala, Srinivas Bandari, et al.
Journal of Molecular Structure (2024) Vol. 1310, pp. 138209-138209
Closed Access | Times Cited: 3
Anticancer potential and structure activity studies of purine and pyrimidine derivatives: an updated review
T. K. MANNA, Sumit Maji, M. Mondal A. Maity, et al.
Molecular Diversity (2024) Vol. 29, Iss. 1, pp. 817-848
Closed Access | Times Cited: 3
One-Pot Synthesis of 1-Thia-4-azaspiro[4.4/5]alkan-3-ones via Schiff Base: Design, Synthesis, and Apoptotic Antiproliferative Properties of Dual EGFR/BRAFV600E Inhibitors
Lamya H. Al-Wahaibi, Essmat M. El‐Sheref, Mohamed M. Hammouda, et al.
Pharmaceuticals (2023) Vol. 16, Iss. 3, pp. 467-467
Open Access | Times Cited: 9
Synthesis and Anti-Breast Cancer Potency of Mono- and Bis-(pyrazolyl[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine) Derivatives as EGFR/CDK-2 Target Inhibitors
Mostafa E. Salem, Esraa M. Mahrous, Eman A. Ragab, et al.
ACS Omega (2023) Vol. 8, Iss. 38, pp. 35359-35369
Open Access | Times Cited: 9
Novel urea linked ciprofloxacin-chalcone hybrids having antiproliferative topoisomerases I/II inhibitory activities and caspases-mediated apoptosis
Hamada H. H. Mohammed, Samar H. Abbas, Alaa M. Hayallah, et al.
Bioorganic Chemistry (2020) Vol. 106, pp. 104422-104422
Closed Access | Times Cited: 26
Design, synthesis and in silico insights of new 7,8-disubstituted-1,3-dimethyl-1H-purine-2,6(3H,7H)-dione derivatives with potent anticancer and multi-kinase inhibitory activities
Abdalla R. Mohamed, Ahmed M. El Kerdawy, Riham F. George, et al.
Bioorganic Chemistry (2020) Vol. 107, pp. 104569-104569
Closed Access | Times Cited: 24
Design and synthesis of new pyranoquinolinone heteroannulated to triazolopyrimidine of potential apoptotic antiproliferative activity
Mohamed Ramadan, Mohamed Abd Elaziz, Yaseen A. M. M. Elshaier, et al.
Bioorganic Chemistry (2020) Vol. 105, pp. 104392-104392
Open Access | Times Cited: 23
The design and synthesis of potent benzimidazole derivatives via scaffold hybridization and evaluating their antiproliferative and proapoptotic activity against breast and lung cancer cell lines
Mohamed Saleh Elgawish, Mohamed S. Nafie, Asmaa S. A. Yassen, et al.
New Journal of Chemistry (2022) Vol. 46, Iss. 9, pp. 4239-4256
Closed Access | Times Cited: 14
Novel anthraquinone amide derivatives as potential Glyoxalase-I inhibitors
Mohammed Al-Akeedi, Manal Al-Najdawi, Qosay Al-Balas, et al.
Journal of Medicine and Life (2024) Vol. 17, Iss. 1, pp. 87-98
Open Access | Times Cited: 2
Designing of xanthine-based DPP-4 inhibitors: a structure-guided alignment dependent Multifacet 3D-QSAR modeling, and molecular dynamics simulation study
Priya Bisht, Priyadarshi Gautam, Arka Bhattacharya, et al.
Journal of Biomolecular Structure and Dynamics (2024), pp. 1-25
Closed Access | Times Cited: 2
Rational design of novel potential EGFR inhibitors by 3D-QSAR, molecular docking, molecular dynamics simulation, and pharmacokinetics studies
Khalil El Khatabi, Reda El-Mernissi, Youness Moukhliss, et al.
Chemical Data Collections (2022) Vol. 39, pp. 100851-100851
Closed Access | Times Cited: 12
Novel indazole derivatives as potent apoptotic antiproliferative agents by multi-targeted mechanism: Synthesis and biological evaluation
Firas Obaid Arhema Frejat, Hongjin Zhai, Yaquan Cao, et al.
Bioorganic Chemistry (2022) Vol. 126, pp. 105922-105922
Closed Access | Times Cited: 12
Pyrazolyl-s-triazine with indole motif as a novel of epidermal growth factor receptor/cyclin-dependent kinase 2 dual inhibitors
Ihab Shawish, Mohamed S. Nafie, Assem Barakat, et al.
Frontiers in Chemistry (2022) Vol. 10
Open Access | Times Cited: 11
Rational Design, Synthesis and Biological Evaluation of Novel Pyrazoline-Based Antiproliferative Agents in MCF-7 Cancer Cells
Mariam M. Fakhry, Kazem Mahmoud, Mohamed S. Nafie, et al.
Pharmaceuticals (2022) Vol. 15, Iss. 10, pp. 1245-1245
Open Access | Times Cited: 10
Design, synthesis, and modelling study of new 1,2,3‐triazole/chalcone hybrids with antiproliferative action as epidermal growth factor receptor inhibitors
Mohamed T.‐E. Maghraby, Ola I. A. Salem, Bahaa G. M. Youssif, et al.
Chemical Biology & Drug Design (2022) Vol. 101, Iss. 3, pp. 749-759
Closed Access | Times Cited: 10
Design and synthesis of new quinoline-ester/-amide derivatives as potent antiproliferative agent targeting EGFR and BRAFV600E kinases
Aliaa M. Mohassab, Heba A. Hassan, Hesham A. Abou‐Zied, et al.
Journal of Molecular Structure (2023) Vol. 1297, pp. 136953-136953
Closed Access | Times Cited: 5
The Fundamental Role of Oxime and Oxime Ether Moieties in Improving the Physicochemical and Anticancer Properties of Structurally Diverse Scaffolds
Jean Fotie, Caitlyn M. Matherne, Jasmine B. Mather, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 23, pp. 16854-16854
Open Access | Times Cited: 5
KinomeMETA: meta-learning enhanced kinome-wide polypharmacology profiling
Qun Ren, Ning Qu, Jingjing Sun, et al.
Briefings in Bioinformatics (2023) Vol. 25, Iss. 1
Open Access | Times Cited: 5
Synthesis, spectroscopic analysis, quantum chemical calculations and in silico biological activity studies of a new series of 8-aryl xanthine
Mustafa Tuğfan Bilkan, Hamsa Abdullah Najeeb, Ayşe Halıç Poslu, et al.
Journal of Molecular Structure (2024) Vol. 1302, pp. 137485-137485
Closed Access | Times Cited: 1
Design and Synthesis of (2-oxo-1,2-Dihydroquinolin-4-yl)-1,2,3-triazole Derivatives via Click Reaction: Potential Apoptotic Antiproliferative Agents
Essmat M. El‐Sheref, Mohammed A. I. Elbastawesy, Alan B. Brown, et al.
Molecules (2021) Vol. 26, Iss. 22, pp. 6798-6798
Open Access | Times Cited: 12

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