Figueiredo Joana, Carreira-Barral Israel, Lourenço Pedro, Miranda André, Lopes-Nunes Jéssica, Quesada Roberto, Laranjo Mafalda, Mergny Jean-Louis, Cruz Carla
CICS-UBI - Health Sciences Research Centre, University of Beira Interior, Av. Infante D. Henrique, 6200-506, Covilhã, Portugal.
Departamento de Química, Facultad de Ciencias, Universidad de Burgos, 09001, Burgos, Spain.
ChemMedChem. 2025 Feb 16;20(4):e202400591. doi: 10.1002/cmdc.202400591. Epub 2024 Nov 21.
Novel 1,10-phenanthroline-2,9-bistriazoles derivatives have been synthesized by copper-catalyzed azide/alkyne cycloaddition reactions and assessed for their ability to bind and stabilize G-quadruplex (G4) structures. Ten novel compounds were evaluated using Förster resonance energy transfer (FRET) melting, circular dichroism (CD), and fluorescence spectroscopy on several G4 sequences. Biophysical characterization led to the identification of compounds 4 a, 4 b, and 5 b as good G4 ligands of KRAS G4 sequences. The impact on cell viability of all derivatives was also assessed, revealing weak effects. However, compound 2 a exhibited cytotoxicity activity on A549 and H1299 cancer cells and low cytotoxicity towards MRC-5 non-malignant cells MRC-5 not connected with its G4-binding ability. Flow cytometry showed that 2 a induced a cell viability decrease in S and G2/M phases for A549 and H1299; thus, more studies should be performed to explore the proteins involved in cell cycle regulation.
通过铜催化的叠氮化物/炔烃环加成反应合成了新型1,10-菲咯啉-2,9-双三唑衍生物,并评估了它们结合和稳定G-四链体(G4)结构的能力。使用Förster共振能量转移(FRET)熔解、圆二色性(CD)和荧光光谱对10种新型化合物在几个G4序列上进行了评估。生物物理表征确定化合物4a、4b和5b是KRAS G4序列的良好G4配体。还评估了所有衍生物对细胞活力的影响,结果显示影响较弱。然而,化合物2a对A549和H1299癌细胞表现出细胞毒性活性,而对MRC-5非恶性细胞的细胞毒性较低,且这与它的G4结合能力无关。流式细胞术显示,2a导致A549和H1299细胞在S期和G2/M期的细胞活力下降;因此,应进行更多研究以探索参与细胞周期调控的蛋白质。