Post-Graduate Program in Natural and Synthetic Bioactive Products, Federal University of Paraíba, João Pessoa 58051-900, Brazil.
Post-Graduate Program in Development and Innovation of Drugs and Medicines, Federal University of Paraíba, João Pessoa 58051-900, Brazil.
Molecules. 2023 May 10;28(10):4009. doi: 10.3390/molecules28104009.
Chalcones are direct precursors in the biosynthesis of flavonoids. They have an α,β-unsaturated carbonyl system which gives them broad biological properties. Among the biological properties exerted by chalcones, their ability to suppress tumors stands out, in addition to their low toxicity. In this perspective, the present work explores the role of natural and synthetic chalcones and their anticancer activity in vitro reported in the last four years from 2019 to 2023. Moreover, we carried out a partial least square (PLS) analysis of the biologic data reported for colon adenocarcinoma lineage HCT-116. Information was obtained from the Web of Science database. Our in silico analysis identified that the presence of polar radicals such as hydroxyl and methoxyl contributed to the anticancer activity of chalcones derivatives. We hope that the data presented in this work will help researchers to develop effective drugs to inhibit colon adenocarcinoma in future works.
查耳酮是类黄酮生物合成的直接前体。它们具有α,β-不饱和羰基系统,使其具有广泛的生物学特性。在查耳酮发挥的生物学特性中,其抑制肿瘤的能力尤为突出,而且其毒性较低。从这个角度来看,本工作探讨了天然和合成查耳酮及其在体外的抗癌活性,这些活性是 2019 年至 2023 年的过去四年中报道的。此外,我们对报道的结肠腺癌系 HCT-116 的生物数据进行了偏最小二乘(PLS)分析。信息来自 Web of Science 数据库。我们的计算机分析表明,羟基和甲氧基等极性自由基的存在有助于查耳酮衍生物的抗癌活性。我们希望本工作中提供的数据将有助于研究人员在未来的工作中开发出有效的抑制结肠腺癌的药物。