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:

Peptide‐based covalent inhibitors of protein–protein interactions
Felix M. Paulussen, Tom N. Grossmann
Journal of Peptide Science (2022) Vol. 29, Iss. 1
Open Access | Times Cited: 30

Showing 1-25 of 30 citing articles:

Peptide-Based Covalent Inhibitors Bearing Mild Electrophiles to Target a Conserved His Residue of the Bacterial Sliding Clamp
Guillaume Compain, Clément Monsarrat, Julie Blagojevic, et al.
JACS Au (2024) Vol. 4, Iss. 2, pp. 432-440
Open Access | Times Cited: 7

Design of Functional Globular β‐Sheet Miniproteins
Truc Lam Pham, Franziska Thomas
ChemBioChem (2024) Vol. 25, Iss. 7
Open Access | Times Cited: 6

Discovery of reactive peptide inhibitors of human papillomavirus oncoprotein E6
Xiyun Ye, Peiyuan Zhang, Jason Tao, et al.
Chemical Science (2023) Vol. 14, Iss. 44, pp. 12484-12497
Open Access | Times Cited: 15

A simple method for developing lysine targeted covalent protein reagents
Ronen Gabizon, Barr Tivon, Rambabu Reddi, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 15

Targeted Covalent Modification Strategies for Drugging the Undruggable Targets
Tomonori Tamura, Masaharu Kawano, Itaru Hamachi
Chemical Reviews (2025)
Closed Access

Rational Design of Stapled Covalent Peptide Modifiers of Oncoprotein E6 from Human Papillomavirus
Cole Emanuelson, Yuta Naro, Olivia Shade, et al.
ACS Chemical Biology (2025)
Open Access

Selection of Nucleotide-Encoded Mass Libraries of Macrocyclic Peptides for Inaccessible Drug Targets
Kilian Colas, Daniel Bindl, Hiroaki Suga
Chemical Reviews (2024) Vol. 124, Iss. 21, pp. 12213-12241
Open Access | Times Cited: 4

Non‐Canonical Amino Acids for Engineering Peptides and Proteins with new Functions
Kelly Zhi Qi Zhou, Richard Obexer
Israel Journal of Chemistry (2024)
Open Access | Times Cited: 3

SuFEx Chemistry Enables Covalent Assembly of a 280-kDa 18-Subunit Pore-Forming Complex
Lee Schnaider, Sophia K. Tan, Pratik Raj Singh, et al.
Journal of the American Chemical Society (2024) Vol. 146, Iss. 36, pp. 25047-25057
Closed Access | Times Cited: 3

Development of a β-lactamase activity assay for detecting ligand-protein interactions using an engineered split intein and β-lactamase
Hiroaki Hagiwara, E Fujii, Taisei Iwabuchi, et al.
Bulletin of the Chemical Society of Japan (2024) Vol. 97, Iss. 3
Closed Access | Times Cited: 2

Covalent Proximity Inducers
Nir London
Chemical Reviews (2024)
Open Access | Times Cited: 2

Electrophile Scanning Reveals Reactivity Hotspots for the Design of Covalent Peptide Binders
Nathalie M. Grob, Clint Remarcik, Simon L. Rössler, et al.
ACS Chemical Biology (2023) Vol. 19, Iss. 1, pp. 101-109
Closed Access | Times Cited: 6

bioTCIs: Middle-to-Macro Biomolecular Targeted Covalent Inhibitors Possessing Both Semi-Permanent Drug Action and Stringent Target Specificity as Potential Antibody Replacements
Jay Yang, Yudai Tabuchi, Riku Katsuki, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 4, pp. 3525-3525
Open Access | Times Cited: 5

Modulating Liquid–Liquid Phase Separation of Nck Adaptor Protein against Enteropathogenic Escherichia coli Infection
Min Liu, Chunjian Wu, Rui Wang, et al.
ACS Central Science (2023) Vol. 9, Iss. 12, pp. 2358-2368
Open Access | Times Cited: 4

Structure‐Based Design of Bicyclic Helical Peptides That Target the Oncogene β‐Catenin
Alejandro Yeste‐Vázquez, Felix M. Paulussen, Mathias Wendt, et al.
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 47
Open Access | Times Cited: 1

Slow-Binding and Covalent HDAC Inhibition: A New Paradigm?
Yasir S. Raouf, Carlos Moreno–Yruela
JACS Au (2024) Vol. 4, Iss. 11, pp. 4148-4161
Open Access | Times Cited: 1

From Protein Structures to Functional Biomimetics
Tom N. Grossmann, Canan Durukan
Synlett (2024)
Open Access

Synthesis of Noncoded Amino Acids Bearing a Salicylaldehyde Tag for the Design of Reversible‐Covalent Peptides
Mattia Mason, Beatrice Nava, Laura Belvisi, et al.
European Journal of Organic Chemistry (2024) Vol. 27, Iss. 22
Open Access

Process Development of a Macrocyclic Peptide Inhibitor of PD-L1
Subha Mukherjee, Amanda Rogers, Gardner S. Creech, et al.
The Journal of Organic Chemistry (2024) Vol. 89, Iss. 10, pp. 6651-6663
Closed Access

Reversibly Reactive Affinity Selection–Mass Spectrometry Enables Identification of Covalent Peptide Binders
Peiyuan Zhang, Xiyun Ye, John Wang, et al.
Journal of the American Chemical Society (2024) Vol. 146, Iss. 22, pp. 15627-15639
Closed Access

Covalent Flexible Peptide Docking in Drug Discovery: Current Challenges and Potential Interventions
Zineb Lafifi, Imane Bjij, Mahmoud E. S. Soliman
Deleted Journal (2024) Vol. 1, Iss. 2, pp. 15-15
Open Access

Structure‐Based Design of Bicyclic Helical Peptides That Target the Oncogene β‐Catenin
Alejandro Yeste‐Vázquez, Felix M. Paulussen, Mathias Wendt, et al.
Angewandte Chemie (2024) Vol. 136, Iss. 47
Open Access

Covalent Inhibitors of MAP Kinases
Surya K. De
Drug design and discovery (2024), pp. 159-189
Closed Access

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