Instituto de Pesquisa em Fármacos e Medicamentos, Universidade Federal da Paraíba, João Pessoa 58051-900, PB, Brazil.
Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador 40296-710, BA, Brazil.
Fitoterapia. 2020 Sep;145:104632. doi: 10.1016/j.fitote.2020.104632. Epub 2020 May 22.
This current study presents the phytochemical analysis of Croton velutinus, describing phenylpropanoids obtained from this species. The fractionation of the roots hexane extract led to the isolation of four new phenylpropanoids derivatives, velutines A-D (1-4) and three known (5-7). Their structures were established based on spectroscopic (1D-2D NMR; HRMS and IR) analysis. Cytotoxic, trypanocidal and anti-inflammatory activities of compounds 1-7 were evaluated. Only compounds 2 and 5 showed cytotoxic activity against cancer cell lines (B16F10, HL-60, HCT116, MCF-7 and HepG2), with IC values ranging from 6.8 to 18.3 μM and 11.1 to 18.3 μM, respectively. Compounds 2 and 5 also showed trypanocidal activity against bloodstream trypomastigotes with EC values of 9.0 and 9.58 μM, respectively. Finally, the anti-inflammatory potential of these compounds was evaluated on cultures of activated macrophages. All compounds exhibited concentration-dependent suppressive activity on the production of nitrite and IL-1β by macrophages stimulated with LPS and IFN-γ. These results indicate phenylpropanoids esters (2 and 5) from C. velutinus as promising cytotoxic, trypanocidal and anti-inflammatory candidates that warrants further studies.
本研究对巴豆 velutinus 的植物化学进行了分析,描述了从该物种中获得的苯丙烷类化合物。对根的正己烷提取物进行分级分离,得到了四个新的苯丙烷类衍生物,即 velutines A-D(1-4)和三个已知化合物(5-7)。根据光谱(1D-2D NMR;HRMS 和 IR)分析确定了它们的结构。对化合物 1-7 的细胞毒性、抗锥虫活性和抗炎活性进行了评价。只有化合物 2 和 5 对癌细胞系(B16F10、HL-60、HCT116、MCF-7 和 HepG2)表现出细胞毒性活性,IC 值范围分别为 6.8 至 18.3μM 和 11.1 至 18.3μM。化合物 2 和 5 对血腔锥虫也表现出抗锥虫活性,EC 值分别为 9.0 和 9.58μM。最后,评估了这些化合物在激活巨噬细胞培养物中的抗炎潜力。所有化合物对 LPS 和 IFN-γ 刺激的巨噬细胞中硝酸盐和 IL-1β 的产生均表现出浓度依赖性抑制活性。这些结果表明,来自 C. velutinus 的苯丙烷酯(2 和 5)具有作为有前途的细胞毒性、抗锥虫和抗炎候选物的潜力,值得进一步研究。