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Pyrrolopyrimidine based CSF1R inhibitors: Attempted departure from Flatland.
Eur J Med Chem. 2024 Feb 5;265:116053. doi: 10.1016/j.ejmech.2023.116053. Epub 2023 Dec 17.
Eur J Med Chem. 2024.
PMID: 38141285
Free article.
Synthesis and Development of Highly Selective Pyrrolo[2,3-d]pyrimidine CSF1R Inhibitors Targeting the Autoinhibited Form.
Aarhus TI, Bjørnstad F, Wolowczyk C, Larsen KU, Rognstad L, Leithaug T, Unger A, Habenberger P, Wolf A, Bjørkøy G, Pridans C, Eickhoff J, Klebl B, Hoff BH, Sundby E.
Aarhus TI, et al.
J Med Chem. 2023 May 25;66(10):6959-6980. doi: 10.1021/acs.jmedchem.3c00428. Epub 2023 May 16.
J Med Chem. 2023.
PMID: 37191268
Free PMC article.
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A highly selective purine-based inhibitor of CSF1R potently inhibits osteoclast differentiation.
Aarhus TI, Eickhoff J, Klebl B, Unger A, Boros J, Choidas A, Zischinsky ML, Wolowczyk C, Bjørkøy G, Sundby E, Hoff BH.
Aarhus TI, et al.
Eur J Med Chem. 2023 Jul 5;255:115344. doi: 10.1016/j.ejmech.2023.115344. Epub 2023 Apr 28.
Eur J Med Chem. 2023.
PMID: 37141705
Free article.
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Potent and selective EGFR inhibitors based on 5-aryl-7H-pyrrolopyrimidin-4-amines.
Reiersølmoen AC, Aarhus TI, Eckelt S, Nørsett KG, Sundby E, Hoff BH.
Reiersølmoen AC, et al. Among authors: aarhus ti.
Bioorg Chem. 2019 Jul;88:102918. doi: 10.1016/j.bioorg.2019.102918. Epub 2019 Apr 11.
Bioorg Chem. 2019.
PMID: 30999245
Free article.
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