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  1. 1.
    0579447 - ÚOCHB 2025 RIV GB eng J - Journal Article
    Misehe, Mbilo - Šála, Michal - Matoušová, Marika - Hercík, Kamil - Kocek, Hugo - Chalupská, Dominika - Chaloupecká, Ema - Hájek, Miroslav - Bouřa, Evžen - Mertlíková-Kaiserová, Helena - Nencka, Radim
    Design, synthesis and evaluation of novel thieno[2,3d]pyrimidine derivatives as potent and specific RIPK2 inhibitors.
    Bioorganic and Medicinal Chemistry Letters. Roč. 97, January (2024), č. článku 129567. ISSN 0960-894X. E-ISSN 1464-3405
    R&D Projects: GA MZd(CZ) NU20-05-00472; GA MŠMT(CZ) LX22NPO5103
    Grant - others:AV ČR(CZ) StrategieAV21/25
    Program: StrategieAV
    Institutional support: RVO:61388963
    Keywords : kinase inhibitor * thieno [2,3d] pyrimidine derivative * receptor-interacting protein kinase 2 * RIPK2 * NOD
    OECD category: Medicinal chemistry
    Impact factor: 2.7, year: 2022
    Method of publishing: Open access
    https://doi.org/10.1016/j.bmcl.2023.129567
    Permanent Link: https://hdl.handle.net/11104/0348249
    FileDownloadSizeCommentaryVersionAccess
    10.1016j.bmcl.2023.129567.pdf11.6 MBPublisher’s postprintopen-access
     
     
  2. 2.
    0574898 - ÚOCHB 2024 RIV NL eng J - Journal Article
    Misehe, Mbilo - Matoušová, Marika - Dvořáková, Alexandra - Hercík, Kamil - Škach, Kryštof - Chalupská, Dominika - Dejmek, Milan - Šála, Michal - Hájek, Miroslav - Bouřa, Evžen - Mertlíková-Kaiserová, Helena - Nencka, Radim
    Exploring positions 6 and 7 of a quinazoline-based scaffold leads to changes in selectivity and potency towards RIPK2/3 kinases.
    European Journal of Medicinal Chemistry. Roč. 260, November (2023), č. článku 115717. ISSN 0223-5234. E-ISSN 1768-3254
    R&D Projects: GA MŠMT(CZ) LX22NPO5103; GA MZd(CZ) NU20-05-00472
    Institutional support: RVO:61388963
    Keywords : kinase inhibitor * quinazoline derivatives * RIPK2 * NOD * inflammation * RIPK3
    OECD category: Medicinal chemistry
    Impact factor: 6.7, year: 2022
    Method of publishing: Open access
    https://doi.org/10.1016/j.ejmech.2023.115717
    Permanent Link: https://hdl.handle.net/11104/0344824
    FileDownloadSizeCommentaryVersionAccess
    10.1016j.ejmech.2023.115717.pdf04.4 MBPublisher’s postprintopen-access
     
     
  3. 3.
    0562658 - ÚOCHB 2023 RIV GB eng J - Journal Article
    Misehe, Mbilo - Klíma, Martin - Matoušová, Marika - Chalupská, Dominika - Dejmek, Milan - Šála, Michal - Mertlíková-Kaiserová, Helena - Bouřa, Evžen - Nencka, Radim
    Structure-based design and modular synthesis of novel PI4K class II inhibitors bearing a 4-aminoquinazoline scaffold.
    Bioorganic and Medicinal Chemistry Letters. Roč. 76, November (2022), č. článku 129010. ISSN 0960-894X. E-ISSN 1464-3405
    R&D Projects: GA MŠMT(CZ) EF16_019/0000729; GA MZd(CZ) NU20-05-00472
    Institutional support: RVO:61388963
    Keywords : phosphatidylinositol 4-kinase class II * PI4K2A inhibitor * quinazoline derivative * SAR investigation * ATP-binding site
    OECD category: Biochemistry and molecular biology
    Impact factor: 2.7, year: 2022
    Method of publishing: Limited access
    https://doi.org/10.1016/j.bmcl.2022.129010
    Permanent Link: https://hdl.handle.net/11104/0334914
     

    Research data: PDB
     


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