Design, Synthesis, and Molecular Evaluation of S(N)Ar-Reactive N-(6-Fluoro-3-Nitropyridin-2-yl)Isoquinolin-3-Amines as Covalent USP7 Inhibitors Reveals an Unconventional Binding Mode.
- DOI
- 10.1002/ardp.70053
- Published
- 2025 Aug
- Container
- Archiv der Pharmazie
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1002/ardp.70053,
title = {Design, Synthesis, and Molecular Evaluation of S(N)Ar-Reactive N-(6-Fluoro-3-Nitropyridin-2-yl)Isoquinolin-3-Amines as Covalent USP7 Inhibitors Reveals an Unconventional Binding Mode.},
author = {Ernst LN and Stahlecker J and Mier F and Serafim RAM and Wydra VR and Masberg B and Jaag SJ and Knappe C and Lämmerhofer M and Stehle T and Gehringer M and Boeckler FM},
year = {2025},
journal = {Archiv der Pharmazie},
doi = {10.1002/ardp.70053},
url = {https://doi.org/10.1002/ardp.70053}
}RIS
TY - JOUR TI - Design, Synthesis, and Molecular Evaluation of S(N)Ar-Reactive N-(6-Fluoro-3-Nitropyridin-2-yl)Isoquinolin-3-Amines as Covalent USP7 Inhibitors Reveals an Unconventional Binding Mode. AU - Ernst LN AU - Stahlecker J AU - Mier F AU - Serafim RAM AU - Wydra VR AU - Masberg B AU - Jaag SJ AU - Knappe C AU - Lämmerhofer M AU - Stehle T AU - Gehringer M AU - Boeckler FM PY - 2025 JO - Archiv der Pharmazie DO - 10.1002/ardp.70053 UR - https://doi.org/10.1002/ardp.70053 ER -
APA
LN, E., J, S., F, M., RAM, S., VR, W., B, M., SJ, J., C, K., M, L., T, S., M, G., & FM, B. (2025). Design, Synthesis, and Molecular Evaluation of S(N)Ar-Reactive N-(6-Fluoro-3-Nitropyridin-2-yl)Isoquinolin-3-Amines as Covalent USP7 Inhibitors Reveals an Unconventional Binding Mode.. Archiv der Pharmazie. https://doi.org/10.1002/ardp.70053
Source records
- pubmed · retrieved 2026-09-25T01:15:02.802Z