Autor: |
Clowes, Samuel R., Ali, Yusuf, Astley, Olivia R., Răsădean, Dora M., Pantoş, G. Dan |
Předmět: |
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Zdroj: |
Molecules; Nov2023, Vol. 28 Issue 21, p7291, 19p |
Abstrakt: |
G-quadruplexes (G4s) have been identified as a potential alternative chemotherapy target. A series of eight β-amino acid derived naphthalenediimides (NDI) were screened against a series of oncogenic G4 sequences: c-KIT1, h-TELO, and TBA. Three sets of enantiomers were investigated to further our understanding of the effect of point chirality on G4 stabilisation. Enantioselective binding behaviour was observed with both c-KIT1 and h-TELO. Docking studies using GNINA and UV-vis titrations were employed to better understand this selective binding behaviour. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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