Potential Insecticidal Activity of Steroidal C-17 Pyrazolinyl Derivatives

Detalhes bibliográficos
Autor(a) principal: Fan,Ning-Juan
Data de Publicação: 2015
Outros Autores: Gao,Jin-Ming, Tang,Jiang-Jiang
Tipo de documento: Relatório
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532015000200389
Resumo: Agrochemical research, over the last two decades, has resulted in the discovery of chemically novel insecticides, of which steroids-based compounds that mimic the action of hormones have been considered as safe insecticides. In this study, eight steroidal C-17 pyrazolinyl derivatives were resynthesized through molecular hybridization and their insecticidal activities against 4thinstar larvae of Mythimna separate were evaluated. These results showed that some compounds exhibited significant insecticidal activities and the susceptibility assays were expressed as the median lethal dose (LD50), of which one of the compounds exerted the most potent insecticidal activity (LD50 = 296 µg g-1), comparable to that of the natural product insecticide, celangulatin V (LD50 = 260 µg g-1). This strategy led to a promising candidate for the development of new steroidal insecticidal agents.
id SBQ-2_eafacc18f09e15afd8189dab8ecf0a99
oai_identifier_str oai:scielo:S0103-50532015000200389
network_acronym_str SBQ-2
network_name_str Journal of the Brazilian Chemical Society (Online)
repository_id_str
spelling Potential Insecticidal Activity of Steroidal C-17 Pyrazolinyl Derivativessteroidprogesteronepyrazolineinsecticidal activityAgrochemical research, over the last two decades, has resulted in the discovery of chemically novel insecticides, of which steroids-based compounds that mimic the action of hormones have been considered as safe insecticides. In this study, eight steroidal C-17 pyrazolinyl derivatives were resynthesized through molecular hybridization and their insecticidal activities against 4thinstar larvae of Mythimna separate were evaluated. These results showed that some compounds exhibited significant insecticidal activities and the susceptibility assays were expressed as the median lethal dose (LD50), of which one of the compounds exerted the most potent insecticidal activity (LD50 = 296 µg g-1), comparable to that of the natural product insecticide, celangulatin V (LD50 = 260 µg g-1). This strategy led to a promising candidate for the development of new steroidal insecticidal agents.Sociedade Brasileira de Química2015-02-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532015000200389Journal of the Brazilian Chemical Society v.26 n.2 2015reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20140248info:eu-repo/semantics/openAccessFan,Ning-JuanGao,Jin-MingTang,Jiang-Jiangeng2015-10-26T00:00:00Zoai:scielo:S0103-50532015000200389Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2015-10-26T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Potential Insecticidal Activity of Steroidal C-17 Pyrazolinyl Derivatives
title Potential Insecticidal Activity of Steroidal C-17 Pyrazolinyl Derivatives
spellingShingle Potential Insecticidal Activity of Steroidal C-17 Pyrazolinyl Derivatives
Fan,Ning-Juan
steroid
progesterone
pyrazoline
insecticidal activity
title_short Potential Insecticidal Activity of Steroidal C-17 Pyrazolinyl Derivatives
title_full Potential Insecticidal Activity of Steroidal C-17 Pyrazolinyl Derivatives
title_fullStr Potential Insecticidal Activity of Steroidal C-17 Pyrazolinyl Derivatives
title_full_unstemmed Potential Insecticidal Activity of Steroidal C-17 Pyrazolinyl Derivatives
title_sort Potential Insecticidal Activity of Steroidal C-17 Pyrazolinyl Derivatives
author Fan,Ning-Juan
author_facet Fan,Ning-Juan
Gao,Jin-Ming
Tang,Jiang-Jiang
author_role author
author2 Gao,Jin-Ming
Tang,Jiang-Jiang
author2_role author
author
dc.contributor.author.fl_str_mv Fan,Ning-Juan
Gao,Jin-Ming
Tang,Jiang-Jiang
dc.subject.por.fl_str_mv steroid
progesterone
pyrazoline
insecticidal activity
topic steroid
progesterone
pyrazoline
insecticidal activity
description Agrochemical research, over the last two decades, has resulted in the discovery of chemically novel insecticides, of which steroids-based compounds that mimic the action of hormones have been considered as safe insecticides. In this study, eight steroidal C-17 pyrazolinyl derivatives were resynthesized through molecular hybridization and their insecticidal activities against 4thinstar larvae of Mythimna separate were evaluated. These results showed that some compounds exhibited significant insecticidal activities and the susceptibility assays were expressed as the median lethal dose (LD50), of which one of the compounds exerted the most potent insecticidal activity (LD50 = 296 µg g-1), comparable to that of the natural product insecticide, celangulatin V (LD50 = 260 µg g-1). This strategy led to a promising candidate for the development of new steroidal insecticidal agents.
publishDate 2015
dc.date.none.fl_str_mv 2015-02-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/report
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format report
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532015000200389
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532015000200389
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.5935/0103-5053.20140248
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.26 n.2 2015
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
_version_ 1750318176974929920