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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:

Enhanced Suppression of a Protein–Protein Interaction in Cells Using Small-Molecule Covalent Inhibitors Based on an N-Acyl-N-alkyl Sulfonamide Warhead
Tsuyoshi Ueda, Tomonori Tamura, Masaharu Kawano, et al.
Journal of the American Chemical Society (2021) Vol. 143, Iss. 12, pp. 4766-4774
Open Access | Times Cited: 56

Showing 1-25 of 56 citing articles:

Recent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials
Xin Xie, Tingting Yu, Xiang Li, et al.
Signal Transduction and Targeted Therapy (2023) Vol. 8, Iss. 1
Open Access | Times Cited: 163
Emerging and Re-emerging Warheads for Targeted Covalent Inhibitors: An Update
Laura Hillebrand, Xiaojun Julia Liang, Ricardo A. M. Serafim, et al.
Journal of Medicinal Chemistry (2024) Vol. 67, Iss. 10, pp. 7668-7758
Closed Access | Times Cited: 49
Inhibition of Autophagy by a Small Molecule through Covalent Modification of the LC3 Protein
Shijie Fan, Liyan Yue, Wei Wan, et al.
Angewandte Chemie International Edition (2021) Vol. 60, Iss. 50, pp. 26105-26114
Open Access | Times Cited: 68
2-Ethynylbenzaldehyde-Based, Lysine-Targeting Irreversible Covalent Inhibitors for Protein Kinases and Nonkinases
Peng Chen, Guanghui Tang, Chengjun Zhu, et al.
Journal of the American Chemical Society (2023) Vol. 145, Iss. 7, pp. 3844-3849
Closed Access | Times Cited: 32
Platform Reagents Enable Synthesis of Ligand-Directed Covalent Probes: Study of Cannabinoid Receptor 2 in Live Cells
Miroslav Kosar, David A. Sykes, Alexander E. G. Viray, et al.
Journal of the American Chemical Society (2023) Vol. 145, Iss. 28, pp. 15094-15108
Closed Access | Times Cited: 23
Global Reactivity Profiling of the Catalytic Lysine in Human Kinome for Covalent Inhibitor Development
Guanghui Tang, Wei Wang, Chengjun Zhu, et al.
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 12
Closed Access | Times Cited: 14
Targeted Covalent Modification Strategies for Drugging the Undruggable Targets
Tomonori Tamura, Masaharu Kawano, Itaru Hamachi
Chemical Reviews (2025)
Closed Access | Times Cited: 1
Recent progress in covalent warheads for in vivo targeting of endogenous proteins
Naoya Shindo, Akio Ojida
Bioorganic & Medicinal Chemistry (2021) Vol. 47, pp. 116386-116386
Open Access | Times Cited: 44
Sulfamate Acetamides as Self-Immolative Electrophiles for Covalent Ligand-Directed Release Chemistry
Rambabu Reddi, Adi Rogel, Ronen Gabizon, et al.
Journal of the American Chemical Society (2023) Vol. 145, Iss. 6, pp. 3346-3360
Open Access | Times Cited: 22
Lysine-Reactive N-Acyl-N-aryl Sulfonamide Warheads: Improved Reaction Properties and Application in the Covalent Inhibition of an Ibrutinib-Resistant BTK Mutant
Masaharu Kawano, Syunsuke Murakawa, Kenji Higashiguchi, et al.
Journal of the American Chemical Society (2023) Vol. 145, Iss. 48, pp. 26202-26212
Closed Access | Times Cited: 15
Discovering covalent inhibitors of protein–protein interactions from trillions of sulfur(VI) fluoride exchange-modified oligonucleotides
Zichen Qin, Kaining Zhang, Ping He, et al.
Nature Chemistry (2023) Vol. 15, Iss. 12, pp. 1705-1714
Closed Access | Times Cited: 13
Luminol anchors improve the electrochemical-tyrosine-click labelling of proteins
Sébastien Depienne, Dimitri Álvarez‐Dorta, Mikaël Croyal, et al.
Chemical Science (2021) Vol. 12, Iss. 46, pp. 15374-15381
Open Access | Times Cited: 28
Ligand‐Directed Chemistry for Protein Labeling for Affinity‐Based Protein Analysis
Seiji Sakamoto, Itaru Hamachi
Israel Journal of Chemistry (2023) Vol. 63, Iss. 3-4
Closed Access | Times Cited: 12
Recent progress of chemical methods for lysine site-selective modification of peptides and proteins
Jian Li, Jinjin Chen, Qi-Long Hu, et al.
Chinese Chemical Letters (2024), pp. 110126-110126
Closed Access | Times Cited: 4
Formation of mono- and dual-labelled antibody fragment conjugates via reversible site-selective disulfide modification and proximity induced lysine reactivity
Ioanna A. Thanasi, Nathalie Bouloc, Clíona McMahon, et al.
Chemical Science (2025)
Open Access
A Protein Cleavage Platform Based on Selective Formylation at Cysteine Residues
Naoki Zenmyo, Yuya Matsumoto, Akihiro YASUDA, et al.
Journal of the American Chemical Society (2025)
Closed Access
Targeted Degradation of ZBP1 with Covalent PROTACs for Anti‐Inflammatory Treatment of Infections
Riming Huang, Yusi Hu, Yifan Wang, et al.
Angewandte Chemie International Edition (2025)
Closed Access
Targeted Degradation of ZBP1 with Covalent PROTACs for Anti‐Inflammatory Treatment of Infections
Riming Huang, Yusi Hu, Yifan Wang, et al.
Angewandte Chemie (2025)
Closed Access
A dimeric proteomimetic prevents SARS-CoV-2 infection by dimerizing the spike protein
Bhavesh Khatri, Ishika Pramanick, Sameer Kumar Malladi, et al.
Nature Chemical Biology (2022) Vol. 18, Iss. 10, pp. 1046-1055
Open Access | Times Cited: 17
Ynamide Coupling Reagent for the Chemical Cross-Linking of Proteins in Live Cells
Shengrong Li, Chengjun Zhu, Qian Zhao, et al.
ACS Chemical Biology (2023) Vol. 18, Iss. 6, pp. 1405-1415
Closed Access | Times Cited: 10
N-Acyl-N-alkyl/aryl Sulfonamide Chemistry Assisted by Proximity for Modification and Covalent Inhibition of Endogenous Proteins in Living Systems
Tomonori Tamura, Itaru Hamachi
Accounts of Chemical Research (2024)
Closed Access | Times Cited: 3
O-Cyanobenzaldehydes Irreversibly Modify Both Buried and Exposed Lysine Residues in Live Cells
Huan Ling, Lin Li, Liping Duan, et al.
Journal of the American Chemical Society (2025)
Closed Access
Discovery of MK-4688: an Efficient Inhibitor of the HDM2–p53 Protein–Protein Interaction
Michael H. Reutershan, Michelle R. Machacek, Michael D. Altman, et al.
Journal of Medicinal Chemistry (2021) Vol. 64, Iss. 21, pp. 16213-16241
Closed Access | Times Cited: 19
Inverse Drug Discovery identifies weak electrophiles affording protein conjugates
Gabriel M. Kline, Karina Nugroho, Jeffery W. Kelly
Current Opinion in Chemical Biology (2022) Vol. 67, pp. 102113-102113
Open Access | Times Cited: 13
Lysine-Targeted Covalent Inhibitors of PI3Kδ Synthesis and Screening by In Situ Interaction Upgradation
Bo Yuan, Yifan Feng, Mengyan Ma, et al.
Journal of Medicinal Chemistry (2024)
Closed Access | Times Cited: 2
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