Arylboronic acids inhibit P2X7 receptor function and the acute inflammatory response
Author:
Funder
CNPq
FAPERJ
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Physiology
Link
http://link.springer.com/content/pdf/10.1007/s10863-019-09802-x.pdf
Reference73 articles.
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2. Allsopp RC, Dayl S, Schmid R, Evans RJ (2017) Unique residues in the ATP gated human P2X7 receptor define a novel allosteric binding pocket for the selective antagonist AZ10606120. Sci Rep 7:725
3. Asano T, Nakamura H, Uehara Y, Yamamoto Y (2004) Design, synthesis, and biological evaluation of aminoboronic acids as growth-factor receptor inhibitors of EGFR and VEGFR-1 tyrosine kinases. Chembiochem Eur J Chem Biol 5:483–490. https://doi.org/10.1002/cbic.200300748
4. Baas T (2012) Paradoxical P2X7. Sci-Bus Exch 5:512–512. https://doi.org/10.1038/scibx.2012.512
5. Baker SJ, Ding CZ, Akama T, Zhang Y-K, Hernandez V, Xia Y (2009) Therapeutic potential of boron-containing compounds. Future Med Chem 1:1275–1288. https://doi.org/10.4155/fmc.09.71
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