Geris Regina, Rodrigues-Fo Edson, Garcia da Silva Heloísa Helena, Garcia da Silva Ionizete
Instituto de Química, Universidade Federal da Bahia, Rua Barão de Geremoabo s/n, Ondina, Salvador - BA, 41950-350, Brasil.
Chem Biodivers. 2008 Feb;5(2):341-5. doi: 10.1002/cbdv.200890032.
The mosquito Aedes aegypti is an increasing problem of public health, being the vector responsible for dengue and Yellow Fever in tropical and subtropical regions. The aim of this work was to determine the potential larvicidal activity of a series of meroterpenoids, compounds 1-7, previously obtained fungal secondary metabolites from Penicillium sp., against the third-instar larvae of A. aegypti. The lethal concentrations (LC(50) and LC(90)) of 1-7 were evaluated 24 h after exposure. Dehydroaustin (4) was the most active meroterpenoid in the series, with an LC(50) value of 2.9 ppm, making it an attractive natural insecticide.
埃及伊蚊是一个日益严重的公共卫生问题,它是热带和亚热带地区登革热和黄热病的传播媒介。本研究的目的是确定一系列半萜类化合物(化合物1 - 7)的潜在杀幼虫活性,这些化合物是先前从青霉菌中获得的真菌次级代谢产物,用于对抗埃及伊蚊的三龄幼虫。在接触24小时后评估了1 - 7的致死浓度(LC50和LC90)。脱氢奥斯汀(4)是该系列中活性最高的半萜类化合物,LC50值为2.9 ppm,使其成为一种有吸引力的天然杀虫剂。