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@ARTICLE{Peinado:1037158,
author = {Peinado, Rafaela dos Santos and Saivish, Marielena Vogel
and Menezes, Gabriela de Lima and Fulco, Umberto Laino and
da Silva, Roosevelt Alves and Korostov, Karolina and Eberle,
Raphael Josef and Melo, Paulo A. and Nogueira, Maurício
Lacerda and Pacca, Carolina Colombelli and Arni, Raghuvir
Krishnaswamy and Coronado, Mônika Aparecida},
title = {{T}he search for an antiviral lead molecule to combat the
neglected emerging {O}ropouche virus},
journal = {Current research in microbial sciences},
volume = {6},
issn = {2666-5174},
address = {Amsterdam},
publisher = {Elsevier B.V.},
reportid = {FZJ-2025-00503},
pages = {100238 -},
year = {2024},
abstract = {Oropouche virus (OROV) is a member of the Peribunyaviridae
family and the causative agent of a dengue-like febrile
illness transmitted by mosquitoes. Although mild symptoms
generally occur, complications such as encephalitis and
meningitis may develop. A lack of proper diagnosis, makes it
a potential candidate for new epidemics and outbreaks like
other known arboviruses such as Dengue, Yellow Fever and
Zika virus. The study of natural molecules as potential
antiviral compounds is a promising alternative for antiviral
therapies. Wedelolactone (WDL) has been demonstrated to
inhibit some viral proteins and virus replication, making it
useful to target a wide range of viruses. In this study, we
report the in silico effects of WDL on the OROV N-terminal
polymerase and its potential inhibitory effects on several
steps of viral infection in mammalian cells in vitro, which
revealed that WDL indeed acts as a potential inhibitor
molecule against OROV infection.},
cin = {IBI-7},
ddc = {570},
cid = {I:(DE-Juel1)IBI-7-20200312},
pnm = {5241 - Molecular Information Processing in Cellular Systems
(POF4-524)},
pid = {G:(DE-HGF)POF4-5241},
typ = {PUB:(DE-HGF)16},
pubmed = {38745914},
UT = {WOS:001240427000001},
doi = {10.1016/j.crmicr.2024.100238},
url = {https://juser.fz-juelich.de/record/1037158},
}