Pereira Marcos D P, da Silva Tito, Aguiar Anna Caroline C, Oliva Glaucius, Guido Rafael V C, Yokoyama-Yasunaka Jenicer K U, Uliana Silvia R B, Lopes Lucia M X
Instituto de Química, Universidade Estadual Paulista, Araraquara - SP, Brasil.
Centro de Ciências Sociais, Saúde e Tecnologia, Universidade Federal do Maranhão, Imperatriz - MA, Brasil.
Planta Med. 2017 Jul;83(11):912-920. doi: 10.1055/s-0043-104776. Epub 2017 Mar 6.
This is a comparative study on the intraspecific chemical variability of species, collected in two different regions of Brazil, Biome Cerrado (semiarid) and Biome Amazônia (coastal). The use of GC-MS and statistical methods led to the identification of 56 compounds. A higher percentage of palmitone and germacrene-D in the hexanes extracts of the leaves of plants from these respective biomes was observed. Phytochemical studies on the extracts led to the isolation and identification of 19 known compounds, including lignans, neolignans, aristolochic acids, indole--carboline, and indole alkaloids. In addition, two new indole alkaloids, 3,4-dihydro-hyrtiosulawesine and 6--(-glucopyranosyl)hyrtiosulawesine, were isolated and a new neolignan, -eupomatenoid-7, was obtained in a mixture with its known isomer eupomatenoid-7. Their structures were determined by spectroscopic methods, mainly by 1D- and 2D-NMR. The occurrence of indole alkaloids is being described for the first time in the Aristolochiaceae family. Moreover, the susceptibility of intracellular amastigote and promastigote forms of to the alkaloids and eupomatenoid-7 were evaluated. This neolignan exhibited low activity against promastigotes (IC = 46 µM), while the alkaloids did not show inhibitory activity. The new alkaloid 6--(-glucopyranosyl)hyrtiosulawesine exhibited activity in the low micromolar range against , with an IC value of 5 µM and a selectivity index higher than 50.
这是一项关于在巴西两个不同地区采集的物种种内化学变异性的比较研究,这两个地区分别是生物群落塞拉多(半干旱)和生物群落亚马逊(沿海)。使用气相色谱 - 质谱联用仪(GC - MS)和统计方法鉴定出了56种化合物。在来自这些各自生物群落的植物叶片的己烷提取物中,观察到棕榈酮和杜松烯 - D的比例更高。对提取物进行的植物化学研究导致分离并鉴定出19种已知化合物,包括木脂素、新木脂素、马兜铃酸、吲哚 - β - 咔啉和吲哚生物碱。此外,分离出了两种新的吲哚生物碱,3,4 - 二氢 - 海替硫拉韦辛和6 - β - ( - 葡萄糖吡喃糖基)海替硫拉韦辛,并获得了一种新的新木脂素, - 优波马酮 - 7,它与其已知异构体优波马酮 - 7混合存在。它们的结构通过光谱方法确定,主要是通过一维和二维核磁共振(1D - 和2D - NMR)。马兜铃科中首次描述了吲哚生物碱的存在。此外,评估了细胞内无鞭毛体和前鞭毛体形式对生物碱和优波马酮 - 7的敏感性。这种新木脂素对前鞭毛体表现出低活性(IC = 46 μM),而生物碱未显示出抑制活性。新生物碱6 - β - ( - 葡萄糖吡喃糖基)海替硫拉韦辛对表现出低微摩尔范围的活性,IC值为5 μM,选择性指数高于50。