School of Biological and Chemical Sciences, University of Galway, University Road, Galway H91 TK33, Ireland.
Fundación MEDINA, Centro de Excelencia en Investigación de Medicamentos Innovadores en Andalucía Avda. del Conocimiento 34, Edificio Centro de Desarrollo Farmacéutico y Alimentario, Parque Tecnológico de Ciencias de la Salud, 18016 Granada, Spain.
J Nat Prod. 2024 Apr 26;87(4):906-913. doi: 10.1021/acs.jnatprod.3c01186. Epub 2024 Mar 2.
The chemical diversity of annelids, particularly those belonging to the class Sipuncula, remains largely unexplored. However, as part of a Marine Biodiscovery program in Ireland, the peanut worm emerged as a promising source of unique metabolites. The purification of the MeOH/CHCl extract of this species led to the isolation of six new linear guanidine amides, named phascolosomines A-F (-). NMR analysis allowed for the elucidation of their structures, all of which feature a terminal guanidine, central amide linkage, and a terminal isobutyl group. Notably, these guanidine amides were present in unusually high concentrations, comprising ∼3% of the dry mass of the organism. The primary concentration of the phascolosomines in the viscera is similar to that previously identified in linear amides from sipunculid worms and marine fireworms. The compounds from sipunculid worms have been hypothesized to be toxins, while those from fireworms are reported to be defensive irritants. However, screening of the newly isolated compounds for inhibitory bioactivity showed no significant inhibition in any of the assays conducted.
环节动物的化学多样性,特别是属于星虫类的那些,仍然在很大程度上未被探索。然而,作为爱尔兰海洋生物发现计划的一部分,花生蠕虫成为了独特代谢产物的有前途的来源。对该物种的 MeOH/CHCl 提取物进行纯化,导致分离出六种新的线性胍酰胺,命名为 phascolosomines A-F(-)。NMR 分析阐明了它们的结构,所有这些结构都具有末端胍基、中心酰胺键和末端异丁基。值得注意的是,这些胍酰胺以异常高的浓度存在,占生物体干重的约 3%。phascolosomines 在内脏中的主要浓度与先前在星虫和海洋火蠕虫中的线性酰胺中鉴定的浓度相似。来自星虫的化合物被假设为毒素,而来自火蠕虫的化合物则被报道为防御性刺激物。然而,对新分离的化合物进行抑制生物活性筛选,在进行的任何测定中均未显示出显著抑制作用。