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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:

Discovery of Highly Potent p53-MDM2 Antagonists and Structural Basis for Anti-Acute Myeloid Leukemia Activities
Yijun Huang, Siglinde Wolf, Barbara Beck, et al.
ACS Chemical Biology (2014) Vol. 9, Iss. 3, pp. 802-811
Open Access | Times Cited: 40

Showing 1-25 of 40 citing articles:

Indoles as therapeutics of interest in medicinal chemistry: Bird's eye view
Navriti Chadha, Om Silakari
European Journal of Medicinal Chemistry (2017) Vol. 134, pp. 159-184
Closed Access | Times Cited: 515
Medicinal chemistry of indole derivatives: Current to future therapeutic prospectives
Archana Kumari, Rajesh K. Singh
Bioorganic Chemistry (2019) Vol. 89, pp. 103021-103021
Closed Access | Times Cited: 433
Multicomponent Reactions, Union of MCRs and Beyond
Tryfon Zarganes‐Tzitzikas, Ajay L. Chandgude, Alexander Dömlingꝉ
The Chemical Record (2015) Vol. 15, Iss. 5, pp. 981-996
Open Access | Times Cited: 244
Hot spot-based design of small-molecule inhibitors for protein–protein interactions
Wenxing Guo, John A. Wisniewski, Haitao Ji
Bioorganic & Medicinal Chemistry Letters (2014) Vol. 24, Iss. 11, pp. 2546-2554
Open Access | Times Cited: 138
Impaired Notch Signaling Leads to a Decrease in p53 Activity and Mitotic Catastrophe in Aged Muscle Stem Cells
Ling Liu, Gregory W. Charville, Tom H. Cheung, et al.
Cell stem cell (2018) Vol. 23, Iss. 4, pp. 544-556.e4
Open Access | Times Cited: 131
Discovery of Novel Spiro[3H-indole-3,2′-pyrrolidin]-2(1H)-one Compounds as Chemically Stable and Orally Active Inhibitors of the MDM2–p53 Interaction
Andreas Gollner, Dorothea Rudolph, Heribert Arnhof, et al.
Journal of Medicinal Chemistry (2016) Vol. 59, Iss. 22, pp. 10147-10162
Closed Access | Times Cited: 107
Small-molecule MDM2/X inhibitors and PROTAC degraders for cancer therapy: advances and perspectives
Yuan Fang, Guochao Liao, Bin Yu
Acta Pharmaceutica Sinica B (2020) Vol. 10, Iss. 7, pp. 1253-1278
Open Access | Times Cited: 79
Organocatalytic Asymmetric Synthesis of Spiro-oxindole Piperidine Derivatives That Reduce Cancer Cell Proliferation by Inhibiting MDM2–p53 Interaction
Ming-Cheng Yang, Cheng Peng, Hua Huang, et al.
Organic Letters (2017) Vol. 19, Iss. 24, pp. 6752-6755
Closed Access | Times Cited: 85
Efficient Isocyanide-less Isocyanide-Based Multicomponent Reactions
Constantinos G. Neochoritis, Silvia Stotani, Bhupendra Mishra, et al.
Organic Letters (2015) Vol. 17, Iss. 8, pp. 2002-2005
Open Access | Times Cited: 67
Rational drug design, synthesis, and biological evaluation of novel chiral tetrahydronaphthalene-fused spirooxindole as MDM2-CDK4 dual inhibitor against glioblastoma
Biao Wang, Peng Fu, Wei Huang, et al.
Acta Pharmaceutica Sinica B (2019) Vol. 10, Iss. 8, pp. 1492-1510
Open Access | Times Cited: 66
Cytotoxic Effect of YH239-EE and Its Enantiomer on MCF7 Cell Line
Hany Akeel Al-Hussaniy, Mohammed AL-Zobaidy
Asian Pacific Journal of Cancer Prevention (2024) Vol. 25, Iss. 6, pp. 2133-2138
Open Access | Times Cited: 4
Development of MDM2‐Targeting PROTAC for Advancing Bone Regeneration
Seongkeun Jeong, Jae‐Kook Cha, Wasim Ahmed, et al.
Advanced Science (2025)
Open Access
Artificial Macrocycles by Ugi Reaction and Passerini Ring Closure
Eman M. M. Abdelraheem, Katarzyna Kurpiewska, Justyna Kalinowska‐Tłuścik, et al.
The Journal of Organic Chemistry (2016) Vol. 81, Iss. 19, pp. 8789-8795
Open Access | Times Cited: 42
Two‐Step Synthesis of Complex Artificial Macrocyclic Compounds
Rudrakshula Madhavachary, Eman M. M. Abdelraheem, Arianna Rossetti, et al.
Angewandte Chemie International Edition (2017) Vol. 56, Iss. 36, pp. 10725-10729
Open Access | Times Cited: 41
Which Three-Dimensional Characteristics Make Efficient Inhibitors of Protein–Protein Interactions?
Mélaine A. Kuenemann, Laura M. L. Bourbon, Céline M. Labbé, et al.
Journal of Chemical Information and Modeling (2014) Vol. 54, Iss. 11, pp. 3067-3079
Closed Access | Times Cited: 38
A Unique Mdm2-Binding Mode of the 3-Pyrrolin-2-one- and 2-Furanone-Based Antagonists of the p53-Mdm2 Interaction
Ewa Surmiak, Aleksandra Twarda‐Clapa, Krzysztof M. Zak, et al.
ACS Chemical Biology (2016) Vol. 11, Iss. 12, pp. 3310-3318
Open Access | Times Cited: 32
Macrocycles: MCR synthesis and applications in drug discovery
Eman M. M. Abdelraheem, Shabnam Shaabani, Alexander Dömlingꝉ
Drug Discovery Today Technologies (2018) Vol. 29, pp. 11-17
Open Access | Times Cited: 31
Artificial Macrocycles
Eman M. M. Abdelraheem, Shabnam Shaabani, Alexander Dömlingꝉ
Synlett (2018) Vol. 29, Iss. 09, pp. 1136-1151
Open Access | Times Cited: 28
Inhibitors of the Ubiquitin-Mediated Signaling Pathway Exhibit Broad-Spectrum Antiviral Activities against New World Alphaviruses
Niloufar A. Boghdeh, Brittany McGraw, Michael D. Barrera, et al.
Viruses (2023) Vol. 15, Iss. 3, pp. 655-655
Open Access | Times Cited: 8
Discovery of a Potent Allosteric Kinase Modulator by Combining Computational and Synthetic Methods
Edwin Kroon, Jörg O. Schulze, Evelyn Süß, et al.
Angewandte Chemie International Edition (2015) Vol. 54, Iss. 47, pp. 13933-13936
Open Access | Times Cited: 26
Molecular Probing of the HPV-16 E6 Protein Alpha Helix Binding Groove with Small Molecule Inhibitors
Anne Rietz, Dino P. Petrov, Matthew Bartolowits, et al.
PLoS ONE (2016) Vol. 11, Iss. 2, pp. e0149845-e0149845
Open Access | Times Cited: 26
Prospective virtual screening for novel p53–MDM2 inhibitors using ultrafast shape recognition
Sachin Patil, Pedro J. Ballester, Cassidy R. Kerezsi
Journal of Computer-Aided Molecular Design (2014) Vol. 28, Iss. 2, pp. 89-97
Closed Access | Times Cited: 24
Scaffold hopping via ANCHOR.QUERY: β-lactams as potent p53-MDM2 antagonists
Shabnam Shaabani, Constantinos G. Neochoritis, Aleksandra Twarda‐Clapa, et al.
MedChemComm (2017) Vol. 8, Iss. 5, pp. 1046-1052
Open Access | Times Cited: 23
Absolute Binding Free Energy Calculations for Highly Flexible Protein MDM2 and Its Inhibitors
Nidhi Singh, Wenjin Li
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 13, pp. 4765-4765
Open Access | Times Cited: 19
Fragment-Based Library Generation for the Discovery of a Peptidomimetic p53-Mdm4 Inhibitor
André Boltjes, Yijun Huang, Rob van de Velde, et al.
ACS Combinatorial Science (2014) Vol. 16, Iss. 8, pp. 393-396
Open Access | Times Cited: 20
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