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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:
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: 29
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: 29
Showing 1-25 of 29 citing articles:
Emerging and Re-emerging Warheads for Targeted Covalent Inhibitors: An Update
Laura Hillebrand, Xiaojun Julia Liang, Ricardo Augusto Massarico Serafim, et al.
Journal of Medicinal Chemistry (2024) Vol. 67, Iss. 10, pp. 7668-7758
Closed Access | Times Cited: 37
Laura Hillebrand, Xiaojun Julia Liang, Ricardo Augusto Massarico Serafim, et al.
Journal of Medicinal Chemistry (2024) Vol. 67, Iss. 10, pp. 7668-7758
Closed Access | Times Cited: 37
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: 12
Guanghui Tang, Wei Wang, Chengjun Zhu, et al.
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 12
Closed Access | Times Cited: 12
Development of covalent inhibitors: Principle, design, and application in cancer
Lang Zheng, Yang Li, Defa Wu, et al.
MedComm – Oncology (2023) Vol. 2, Iss. 4
Open Access | Times Cited: 20
Lang Zheng, Yang Li, Defa Wu, et al.
MedComm – Oncology (2023) Vol. 2, Iss. 4
Open Access | Times Cited: 20
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: 13
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: 13
Tying the knot with lysine
Ana Koperniku, Nicholas A. Meanwell
Nature Reviews Chemistry (2024) Vol. 8, Iss. 4, pp. 235-237
Closed Access | Times Cited: 2
Ana Koperniku, Nicholas A. Meanwell
Nature Reviews Chemistry (2024) Vol. 8, Iss. 4, pp. 235-237
Closed Access | Times Cited: 2
Small Molecule-Induced Post-Translational Acetylation of Catalytic Lysine of Kinases in Mammalian Cells
Guanghui Tang, Xuan Wang, Huisi Huang, et al.
Journal of the American Chemical Society (2024) Vol. 146, Iss. 34, pp. 23978-23988
Closed Access | Times Cited: 2
Guanghui Tang, Xuan Wang, Huisi Huang, et al.
Journal of the American Chemical Society (2024) Vol. 146, Iss. 34, pp. 23978-23988
Closed Access | Times Cited: 2
Covalent fragment approaches targeting non-cysteine residues
Noémi Csorba, Péter Ábrányi‐Balogh, György M. Keserű
Trends in Pharmacological Sciences (2023) Vol. 44, Iss. 11, pp. 802-816
Open Access | Times Cited: 5
Noémi Csorba, Péter Ábrányi‐Balogh, György M. Keserű
Trends in Pharmacological Sciences (2023) Vol. 44, Iss. 11, pp. 802-816
Open Access | Times Cited: 5
Reactivity‐Tunable Fluorescent Platform for Selective and Biocompatible Modification of Cysteine or Lysine
Xiaojie Ren, Haokun Li, Hui Peng, et al.
Advanced Science (2024) Vol. 11, Iss. 31
Open Access | Times Cited: 1
Xiaojie Ren, Haokun Li, Hui Peng, et al.
Advanced Science (2024) Vol. 11, Iss. 31
Open Access | Times Cited: 1
Cell-active, irreversible covalent inhibitors that selectively target the catalytic lysine of EGFR by using fluorosulfate-based SuFEx chemistry
Guanghui Tang, Wei Wang, Xuan Wang, et al.
European Journal of Medicinal Chemistry (2023) Vol. 259, pp. 115671-115671
Closed Access | Times Cited: 5
Guanghui Tang, Wei Wang, Xuan Wang, et al.
European Journal of Medicinal Chemistry (2023) Vol. 259, pp. 115671-115671
Closed Access | Times Cited: 5
Kinase Inhibition via Small Molecule‐Induced Intramolecular Protein Cross‐Linking
Xuan Wang, Jie Sun, Huisi Huang, et al.
Angewandte Chemie (2024) Vol. 136, Iss. 28
Closed Access | Times Cited: 1
Xuan Wang, Jie Sun, Huisi Huang, et al.
Angewandte Chemie (2024) Vol. 136, Iss. 28
Closed Access | Times Cited: 1
Exploring the structural activity relationship of the Osimertinib: A covalent inhibitor of double mutant EGFRL858R/T790M tyrosine kinase for the treatment of Non-Small Cell Lung Cancer (NSCLC)
Bhatu R. Patil, Kunal V. Bhadane, Iqrar Ahmad, et al.
Bioorganic & Medicinal Chemistry (2024) Vol. 109, pp. 117796-117796
Closed Access | Times Cited: 1
Bhatu R. Patil, Kunal V. Bhadane, Iqrar Ahmad, et al.
Bioorganic & Medicinal Chemistry (2024) Vol. 109, pp. 117796-117796
Closed Access | Times Cited: 1
Aminomethyl Salicylaldehydes Lock onto a Surface Lysine by Forming an Extended Intramolecular Hydrogen Bond Network
Jacqueline Weaver, Gregory B. Craven, Linh Tram, et al.
Journal of the American Chemical Society (2024) Vol. 146, Iss. 35, pp. 24233-24237
Closed Access | Times Cited: 1
Jacqueline Weaver, Gregory B. Craven, Linh Tram, et al.
Journal of the American Chemical Society (2024) Vol. 146, Iss. 35, pp. 24233-24237
Closed Access | Times Cited: 1
Rationally designed BCR-ABL kinase inhibitors for improved leukemia treatment via covalent and pro-/dual-drug targeting strategies
Jie Sun, Liang Lou, Chengjun Zhu, et al.
Journal of Advanced Research (2024)
Open Access | Times Cited: 1
Jie Sun, Liang Lou, Chengjun Zhu, et al.
Journal of Advanced Research (2024)
Open Access | Times Cited: 1
Multitarget inhibitors/probes that target LRRK2 and AURORA A kinases noncovalently and covalently
Wei Wang, Xuan Wang, Guanghui Tang, et al.
Chemical Communications (2023) Vol. 59, Iss. 72, pp. 10789-10792
Closed Access | Times Cited: 3
Wei Wang, Xuan Wang, Guanghui Tang, et al.
Chemical Communications (2023) Vol. 59, Iss. 72, pp. 10789-10792
Closed Access | Times Cited: 3
Global Reactivity Profiling of the Catalytic Lysine in Human Kinome for Covalent Inhibitor Development
Guanghui Tang, Wei Wang, Chengjun Zhu, et al.
Angewandte Chemie (2024) Vol. 136, Iss. 12
Closed Access
Guanghui Tang, Wei Wang, Chengjun Zhu, et al.
Angewandte Chemie (2024) Vol. 136, Iss. 12
Closed Access
Kinase Inhibition via Small Molecule‐Induced Intramolecular Protein Cross‐Linking
Xuan Wang, Jie Sun, Huisi Huang, et al.
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 28
Closed Access
Xuan Wang, Jie Sun, Huisi Huang, et al.
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 28
Closed Access
Structure‐guided drug design targeting Abl kinase: how structure and regulation can assist in designing new drugs
Diego Martins, Philipe Oliveira Fernandes, Lucas A. Vieira, et al.
ChemBioChem (2024)
Closed Access
Diego Martins, Philipe Oliveira Fernandes, Lucas A. Vieira, et al.
ChemBioChem (2024)
Closed Access
Ethynylbenzaldehydes as novel reaction-based “turn-on” fluorescent probes for primary amine detection in solution, vapor, food, proteins, and live cells
Ajcharapan Tantipanjaporn, Jie‐Ren Deng, A. Chan, et al.
Sensors and Actuators B Chemical (2024), pp. 136673-136673
Closed Access
Ajcharapan Tantipanjaporn, Jie‐Ren Deng, A. Chan, et al.
Sensors and Actuators B Chemical (2024), pp. 136673-136673
Closed Access
Emerging Technologies for Epigenetic Drug Discovery
Royal Society of Chemistry eBooks (2024)
Closed Access
Royal Society of Chemistry eBooks (2024)
Closed Access
Mass Spectrometry and Chemical Biology Approaches for Deconvoluting Epigenetic Targets
Antony J. Burton, Ghaith M. Hamza, Anthony A. Iannetta, et al.
Royal Society of Chemistry eBooks (2024), pp. 50-83
Closed Access
Antony J. Burton, Ghaith M. Hamza, Anthony A. Iannetta, et al.
Royal Society of Chemistry eBooks (2024), pp. 50-83
Closed Access
Tuning isatoic anhydrides’ lysine ligation chemistry for bioconjugation and drug delivery
Sona Tiwari, Sathyapriya Senthil, Shweta Khanna, et al.
Cell Reports Physical Science (2024), pp. 102260-102260
Open Access
Sona Tiwari, Sathyapriya Senthil, Shweta Khanna, et al.
Cell Reports Physical Science (2024), pp. 102260-102260
Open Access
Global Profiling Lysine Reactivity and Ligandability with Oxidant‐Triggered Bioconjugation Chemistry
Mengya Zhou, Shengrong Li, Yi Tan, et al.
Angewandte Chemie International Edition (2024)
Closed Access
Mengya Zhou, Shengrong Li, Yi Tan, et al.
Angewandte Chemie International Edition (2024)
Closed Access
Global Profiling Lysine Reactivity and Ligandability with Oxidant‐Triggered Bioconjugation Chemistry
Mengya Zhou, Shengrong Li, Yi Tan, et al.
Angewandte Chemie (2024)
Closed Access
Mengya Zhou, Shengrong Li, Yi Tan, et al.
Angewandte Chemie (2024)
Closed Access
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
Bo Yuan, Yifan Feng, Mengyan Ma, et al.
Journal of Medicinal Chemistry (2024)
Closed Access
Chemical Dissection of Selective Myeloid Leukemia-1 Inhibitors: How They Were Found and Evolved
Lianzhou Wang, Yuxiang Chen, MeiZhi Zhang, et al.
European Journal of Medicinal Chemistry (2024) Vol. 283, pp. 117168-117168
Closed Access
Lianzhou Wang, Yuxiang Chen, MeiZhi Zhang, et al.
European Journal of Medicinal Chemistry (2024) Vol. 283, pp. 117168-117168
Closed Access