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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:

Design, synthesis and biological evaluation of novel α-acyloxy carboxamides via Passerini reaction as caspase 3/7 activators
Mohammed Salah Ayoup, Yasmin Wahby, Hamida Abdel‐Hamid, et al.
European Journal of Medicinal Chemistry (2019) Vol. 168, pp. 340-356
Closed Access | Times Cited: 46

Showing 1-25 of 46 citing articles:

Two decades of recent advances of Ugi reactions: synthetic and pharmaceutical applications
Manar Ahmed Fouad, Hamida Abdel‐Hamid, Mohammed Salah Ayoup
RSC Advances (2020) Vol. 10, Iss. 70, pp. 42644-42681
Open Access | Times Cited: 139
Caspase‐3: A primary target for natural and synthetic compounds for cancer therapy
Poonam Yadav, Ramakant Yadav, Shweta Jain, et al.
Chemical Biology & Drug Design (2021) Vol. 98, Iss. 1, pp. 144-165
Closed Access | Times Cited: 114
Multicomponent Reaction-Assisted Drug Discovery: A Time- and Cost-Effective Green Approach Speeding Up Identification and Optimization of Anticancer Drugs
Giovanni Graziano, Angela Stefanachi, Marialessandra Contino, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 7, pp. 6581-6581
Open Access | Times Cited: 42
Caspase-3 Activators as Anticancer Agents
Nitin Srivastava, Anil K. Saxena
Current Protein and Peptide Science (2023) Vol. 24, Iss. 10, pp. 783-804
Closed Access | Times Cited: 26
Molecular hybridization design and synthesis of novel spirooxindole-based MDM2 inhibitors endowed with BCL2 signaling attenuation; a step towards the next generation p53 activators
Gehad Lotfy, Yasmine M. Abdel Aziz, Mohamed M. Said, et al.
Bioorganic Chemistry (2021) Vol. 117, pp. 105427-105427
Open Access | Times Cited: 44
The structure – Activity correlation in the family of dicationic imidazolium surfactants: Antimicrobial properties and cytotoxic effect
Alexandra D. Voloshina, Syumbelya Gumerova, Аnastasiia S. Sapunova, et al.
Biochimica et Biophysica Acta (BBA) - General Subjects (2020) Vol. 1864, Iss. 12, pp. 129728-129728
Closed Access | Times Cited: 47
Antimicrobial and cytotoxic effects of ammonium derivatives of diterpenoids steviol and isosteviol
Alexandra D. Voloshina, Аnastasiia S. Sapunova, Natalia Kulik, et al.
Bioorganic & Medicinal Chemistry (2020) Vol. 32, pp. 115974-115974
Closed Access | Times Cited: 43
Repurposing 1,2,4-oxadiazoles as SARS-CoV-2 PLpro inhibitors and investigation of their possible viral entry blockade potential
Mohammed Salah Ayoup, Mariam M. ElShafey, Hamida Abdel‐Hamid, et al.
European Journal of Medicinal Chemistry (2023) Vol. 252, pp. 115272-115272
Open Access | Times Cited: 13
Structure-based design and optimization of pyrimidine- and 1,2,4-triazolo[4,3-a]pyrimidine-based matrix metalloproteinase-10/13 inhibitors via Dimroth rearrangement towards targeted polypharmacology
El Sayed H. El Ashry, Laila F. Awad, Mohamed Teleb, et al.
Bioorganic Chemistry (2020) Vol. 96, pp. 103616-103616
Closed Access | Times Cited: 39
Beyond direct Nrf2 activation; reinvestigating 1,2,4-oxadiazole scaffold as a master key unlocking the antioxidant cellular machinery for cancer therapy
Mohammed Salah Ayoup, Marwa M. Abu‐Serie, Hamida Abdel‐Hamid, et al.
European Journal of Medicinal Chemistry (2021) Vol. 220, pp. 113475-113475
Closed Access | Times Cited: 29
Halting Tumor Progression via Novel Non-Hydroxamate Triazole-Based Mannich Bases MMP-2/9 Inhibitors; Design, Microwave-Assisted Synthesis, and Biological Evaluation
Fawzia Faleh Albelwi, Mohamed Teleb, Marwa M. Abu‐Serie, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 19, pp. 10324-10324
Open Access | Times Cited: 27
Cobalt polygalacturonates and the pharmacological composition based on them: Preparation, properties and cytotoxicity
С. Т. Минзанова, E. V. Chekunkov, А. В. Хабибуллина, et al.
International Journal of Biological Macromolecules (2025), pp. 140377-140377
Closed Access
Strong Hydrogen Bond Donating Solvents Accelerate the Passerini Three-Component Reaction
Claudio Ferdeghini, Minghui Wu, Prabhat Ranjan, et al.
The Journal of Organic Chemistry (2025)
Open Access
Combating oxi-inflamm-aging: Passerini adducts tethered with 1,2,3-triazoles for enhanced antioxidant defense and 5-LOX inhibition
Mohammed Salah Ayoup, Magdy Rashwan, Saied M. Soliman, et al.
RSC Medicinal Chemistry (2025)
Closed Access
Dual VEGFR-2/PIM-1 kinase inhibition towards surmounting the resistance to antiangiogenic agents via hybrid pyridine and thienopyridine-based scaffolds: Design, synthesis and biological evaluation
Ola H. Rizk, Mohamed Teleb, Marwa M. Abu‐Serie, et al.
Bioorganic Chemistry (2019) Vol. 92, pp. 103189-103189
Closed Access | Times Cited: 35
Battle tactics against MMP-9; discovery of novel non-hydroxamate MMP-9 inhibitors endowed with PI3K/AKT signaling attenuation and caspase 3/7 activation via Ugi bis-amide synthesis
Mohammed Salah Ayoup, Manar Ahmed Fouad, Hamida Abdel‐Hamid, et al.
European Journal of Medicinal Chemistry (2019) Vol. 186, pp. 111875-111875
Closed Access | Times Cited: 34
Diverse Biological Activity of Benzofuroxan/Sterically Hindered Phenols Hybrids
Elena Chugunova, Э. М. Гибадуллина, Kirill Matylitsky, et al.
Pharmaceuticals (2023) Vol. 16, Iss. 4, pp. 499-499
Open Access | Times Cited: 10
Microdroplet Chemistry Accelerating a Three-Component Passerini Reaction for α-Acyloxy Carboxamide Synthesis
Yikang Wu, Heyong Cheng, Jiayao Li, et al.
The Journal of Organic Chemistry (2023) Vol. 88, Iss. 15, pp. 11186-11196
Closed Access | Times Cited: 9
Halting colorectal cancer metastasis via novel dual nanomolar MMP-9/MAO-A quinoxaline-based inhibitors; design, synthesis, and evaluation
Mohammed Salah Ayoup, Marwa M. Abu‐Serie, Laila F. Awad, et al.
European Journal of Medicinal Chemistry (2021) Vol. 222, pp. 113558-113558
Closed Access | Times Cited: 23
Two decades of recent advances of Passerini reactions: synthetic and potential pharmaceutical applications
Yasmin Wahby, Hamida Abdel‐Hamid, Mohammed Salah Ayoup
New Journal of Chemistry (2021) Vol. 46, Iss. 4, pp. 1445-1468
Closed Access | Times Cited: 22
Synthesis, characterization of new heterocyclic compound: pyrazolyl hydrazino quinoxaline derivative: 3-[5-(hydroxy1methyl)-1-phenylpyrazol-3-yl]-2-[2, 4, 5-trimethoxybenzylidine] hydrazonyl-quinoxaline of potent antimicrobial, antioxidant, antiviral, and antitumor activity
Eman R. Sallam, S.F. Aboulnaga, Ahmed Samy, et al.
Journal of Molecular Structure (2022) Vol. 1271, pp. 133983-133983
Closed Access | Times Cited: 15
Synthesis, anticancer evaluation and molecular docking of new benzothiazole scaffolds targeting FGFR-1
Eman A. Abd El‐Meguid, Eman M. Mohi El-Deen, Gaber O. Moustafa, et al.
Bioorganic Chemistry (2021) Vol. 119, pp. 105504-105504
Closed Access | Times Cited: 19
Highlighting multicomponent reactions as an efficient and facile alternative route in the chemical synthesis of organic-based molecules: a tremendous growth in the past 5 years
Reagan L. Mohlala, Thompho Jason Rashamuse, E. Mabel Coyanis
Frontiers in Chemistry (2024) Vol. 12
Open Access | Times Cited: 2
Efficient synthesis, biological evaluation, and docking study of isatin based derivatives as caspase inhibitors
Loghman Firoozpour, Lixin Gao, Setareh Moghimi, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry (2020) Vol. 35, Iss. 1, pp. 1674-1684
Open Access | Times Cited: 16
Nature-inspired new isoindole-based Passerini adducts as efficient tumor-selective apoptotic inducers via caspase-3/7 activation
Mohammed Salah Ayoup, Ahmed Farag Mansour, Hamida Abdel‐Hamid, et al.
European Journal of Medicinal Chemistry (2022) Vol. 245, pp. 114865-114865
Closed Access | Times Cited: 10
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