Synthesis of Flavonols and Assessment of Their Biological Activity as Anticancer Agents
作者:Yu-Hui Hsieh、Pei-Hsuan Hsu、Anren Hu、Yang-Je Cheng、Tzenge-Lien Shih、Jih-Jung Chen
DOI:10.3390/molecules29092041
日期:——
A series of flavanols were synthesized to assess their biological activity against human non-small cell lung cancer cells (A549). Among the sixteen synthesized compounds, it was observed that compounds 6k (3.14 ± 0.29 µM) and 6l (0.46 ± 0.02 µM) exhibited higher potency compared to 5-fluorouracil (5-Fu, 4.98 ± 0.41 µM), a clinical anticancer drug which was used as a positive control. Moreover, compound
合成了一系列黄烷醇以评估其针对人非小细胞肺癌细胞(A549)的生物活性。在十六种合成的化合物中,观察到化合物 6k (3.14 ± 0.29 µM) 和 6l (0.46 ± 0.02 µM) 与临床抗癌药物 5-氟尿嘧啶 (5-Fu,4.98 ± 0.41 µM) 相比表现出更高的效力,用作阳性对照。此外,化合物6l(4'-溴黄酮醇)通过线粒体和caspase-3依赖性途径显着诱导A549细胞凋亡。因此,化合物6I可被开发为治疗或预防肺癌的候选物。