Graduate Program in Chemistry, Department of Chemistry, Federal University of Espírito Santo, UFES, Vitória, 29075-910, Brazil.
Department of Pharmacology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, 05508-000, Brazil.
Chem Biodivers. 2024 Oct;21(10):e202400943. doi: 10.1002/cbdv.202400943. Epub 2024 Sep 14.
Paeonol is a broadly studied natural product due to its many biological activities. Using a methodology previously employed by our research group, 11 derivatives of paeonol were synthesized (seven of them are unpublished compounds), including four ethers and seven benzofurans. Additionally, we determined the crystal structure of one of these ether derivatives (1 a) and of five benzofuran derivatives (2 a, 2 b, 2 c, 2 f and 2 g) by single crystal X-ray diffraction. To continue studying the cytotoxicity of this natural product and its derivatives, all compounds were tested against two cancer cell lines, HCT116 and MCF-7. Compounds 2 b, 2 e, and 2 g were considered active against the colorectal adenocarcinoma cells HCT116 (Growth inhibition >60 %). Compound 2 e showed an IC of 0.2 μM and was selected for further analysis, results reinforce its anticancer potential.
丹皮酚是一种广泛研究的天然产物,因为它具有许多生物活性。使用我们研究小组以前采用的方法,合成了 11 种丹皮酚衍生物(其中 7 种为未发表的化合物),包括 4 种醚类和 7 种苯并呋喃类化合物。此外,我们通过单晶 X 射线衍射确定了其中一种醚类衍生物(1a)和五种苯并呋喃类衍生物(2a、2b、2c、2f 和 2g)的晶体结构。为了继续研究这种天然产物及其衍生物的细胞毒性,我们将所有化合物都对两种癌细胞系 HCT116 和 MCF-7 进行了测试。化合物 2b、2e 和 2g 被认为对结直肠腺癌细胞 HCT116 具有活性(生长抑制率>60%)。化合物 2e 表现出 0.2μM 的 IC,被选中进行进一步分析,结果证实了其抗癌潜力。