Počet záznamů: 1  

Kinetic Target-Guided Synthesis of Small-Molecule G-Quadruplex Stabilizers

  1. 1.
    0537196 - ÚOCHB 2021 RIV DE eng J - Článek v odborném periodiku
    Pomeislová, Alice - Vrzal, Lukáš - Kozák, Jaroslav - Dobiaš, Juraj - Hubálek, Martin - Dvořáková, H. - Reyes Gutierrez, Paul Eduardo - Teplý, Filip - Veverka, Václav
    Kinetic Target-Guided Synthesis of Small-Molecule G-Quadruplex Stabilizers.
    ChemistryOpen. Roč. 9, č. 12 (2020), s. 1236-1250. ISSN 2191-1363. E-ISSN 2191-1363
    Grant CEP: GA ČR(CZ) GA17-04393S; GA MŠMT(CZ) LO1304; GA MŠMT(CZ) LK11205; GA MŠMT(CZ) EF16_019/0000729
    Institucionální podpora: RVO:61388963
    Klíčová slova: anticancer therapy * click chemistry * G-quadruplex * NMR * secondary structures
    Obor OECD: Organic chemistry
    Impakt faktor: 2.911, rok: 2020
    Způsob publikování: Open access
    https://doi.org/10.1002/open.202000261

    The formation of a G‐quadruplex motif in the promoter region of the c‐MYC protooncogene prevents its expression. Accordingly, G‐quadruplex stabilization by a suitable ligand may be a viable approach for anticancer therapy. In our study, we used the 4‐(4‐methylpiperazin‐1‐yl)aniline molecule, previously identified as a fragment library screen hit, as a template for the SAR‐guided design of a new small library of clickable fragments and subjected them to click reactions, including kinetic target‐guided synthesis in the presence of a G‐quadruplex forming oligonucleotide Pu24. We tested the clickable fragments and products of click reactions for their G‐quadruplex stabilizing activity and determined their mode of binding to the c‐MYC G‐quadruplex by NMR spectroscopy. The enhanced stabilizing potency of click products in biology assays (FRET, Polymerase extension assay) matched the increased yields of in situ click reactions. In conclusion, we identified the newly synthesized click products of bis‐amino derivatives of 4‐(4‐methylpiperazin‐1‐yl)aniline as potent stabilizers of c‐MYC G‐quadruplex, and their further evolution may lead to the development of an efficient tool for cancer treatment.
    Trvalý link: http://hdl.handle.net/11104/0316292

     
     
Počet záznamů: 1  

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