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Design, synthesis and evaluation of novel thieno[2,3d]pyrimidine derivatives as potent and specific RIPK2 inhibitors.
Bioorg Med Chem Lett. 2024 Jan 1;97:129567. doi: 10.1016/j.bmcl.2023.129567. Epub 2023 Nov 24.
Bioorg Med Chem Lett. 2024.
PMID: 38008339
Free article.
Exploring positions 6 and 7 of a quinazoline-based scaffold leads to changes in selectivity and potency towards RIPK2/3 kinases.
Misehe M, Matoušová M, Dvořáková A, Hercík K, Škach K, Chalupská D, Dejmek M, Šála M, Hájek M, Boura E, Mertlíková-Kaiserová H, Nencka R.
Misehe M, et al.
Eur J Med Chem. 2023 Nov 15;260:115717. doi: 10.1016/j.ejmech.2023.115717. Epub 2023 Aug 9.
Eur J Med Chem. 2023.
PMID: 37598483
Free article.
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Structure-based design and modular synthesis of novel PI4K class II inhibitors bearing a 4-aminoquinazoline scaffold.
Misehe M, Klima M, Matoušová M, Chalupská D, Dejmek M, Šála M, Mertlíková-Kaiserová H, Boura E, Nencka R.
Misehe M, et al.
Bioorg Med Chem Lett. 2022 Nov 15;76:129010. doi: 10.1016/j.bmcl.2022.129010. Epub 2022 Sep 29.
Bioorg Med Chem Lett. 2022.
PMID: 36184029
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