Synthesis and computational simulation of new phosphorilated sulfoximines with insecticidal activity

Autores
Bellozas Reinhard, M.E.; Licastrode, S.A.
Año de publicación
2000
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
New organophosphorus insecticides of dialkylsulphoximines derived with activity upon acetylcholinesterase were synthesized. The obtained compounds were characterized by NMR and IR, and anticholinesterase activity and toxicity was measured. A simulation through computer was done in order to establish the relationship between structure and activity.
Fuente
Molecules 2000;5(3):602-604
Materia
acetylcholinesterase
insecticide
organophosphorus compound
sulfoximine
unclassified drug
computer simulation
conference paper
infrared radiation
insecticidal activity
measurement
nuclear magnetic resonance
phosphorylation
structure analysis
toxicity
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/2.5/ar
Repositorio
Biblioteca Digital (UBA-FCEN)
Institución
Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
OAI Identificador
paperaa:paper_14203049_v5_n3_p602_BellozasReinhard
Acceder
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oai_identifier_str paperaa:paper_14203049_v5_n3_p602_BellozasReinhard
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling Synthesis and computational simulation of new phosphorilated sulfoximines with insecticidal activityBellozas Reinhard, M.E.Licastrode, S.A.acetylcholinesteraseinsecticideorganophosphorus compoundsulfoximineunclassified drugcomputer simulationconference paperinfrared radiationinsecticidal activitymeasurementnuclear magnetic resonancephosphorylationstructure analysistoxicityNew organophosphorus insecticides of dialkylsulphoximines derived with activity upon acetylcholinesterase were synthesized. The obtained compounds were characterized by NMR and IR, and anticholinesterase activity and toxicity was measured. A simulation through computer was done in order to establish the relationship between structure and activity.2000info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p602_BellozasReinhardMolecules 2000;5(3):602-604reponame:Biblioteca Digital (UBA-FCEN)instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesinstacron:UBA-FCENenginfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/2.5/ar2025-11-06T09:39:39Zpaperaa:paper_14203049_v5_n3_p602_BellozasReinhardInstitucionalhttps://digital.bl.fcen.uba.ar/Universidad públicaNo correspondehttps://digital.bl.fcen.uba.ar/cgi-bin/oaiserver.cgiana@bl.fcen.uba.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:18962025-11-06 09:39:41.002Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv Synthesis and computational simulation of new phosphorilated sulfoximines with insecticidal activity
title Synthesis and computational simulation of new phosphorilated sulfoximines with insecticidal activity
spellingShingle Synthesis and computational simulation of new phosphorilated sulfoximines with insecticidal activity
Bellozas Reinhard, M.E.
acetylcholinesterase
insecticide
organophosphorus compound
sulfoximine
unclassified drug
computer simulation
conference paper
infrared radiation
insecticidal activity
measurement
nuclear magnetic resonance
phosphorylation
structure analysis
toxicity
title_short Synthesis and computational simulation of new phosphorilated sulfoximines with insecticidal activity
title_full Synthesis and computational simulation of new phosphorilated sulfoximines with insecticidal activity
title_fullStr Synthesis and computational simulation of new phosphorilated sulfoximines with insecticidal activity
title_full_unstemmed Synthesis and computational simulation of new phosphorilated sulfoximines with insecticidal activity
title_sort Synthesis and computational simulation of new phosphorilated sulfoximines with insecticidal activity
dc.creator.none.fl_str_mv Bellozas Reinhard, M.E.
Licastrode, S.A.
author Bellozas Reinhard, M.E.
author_facet Bellozas Reinhard, M.E.
Licastrode, S.A.
author_role author
author2 Licastrode, S.A.
author2_role author
dc.subject.none.fl_str_mv acetylcholinesterase
insecticide
organophosphorus compound
sulfoximine
unclassified drug
computer simulation
conference paper
infrared radiation
insecticidal activity
measurement
nuclear magnetic resonance
phosphorylation
structure analysis
toxicity
topic acetylcholinesterase
insecticide
organophosphorus compound
sulfoximine
unclassified drug
computer simulation
conference paper
infrared radiation
insecticidal activity
measurement
nuclear magnetic resonance
phosphorylation
structure analysis
toxicity
dc.description.none.fl_txt_mv New organophosphorus insecticides of dialkylsulphoximines derived with activity upon acetylcholinesterase were synthesized. The obtained compounds were characterized by NMR and IR, and anticholinesterase activity and toxicity was measured. A simulation through computer was done in order to establish the relationship between structure and activity.
description New organophosphorus insecticides of dialkylsulphoximines derived with activity upon acetylcholinesterase were synthesized. The obtained compounds were characterized by NMR and IR, and anticholinesterase activity and toxicity was measured. A simulation through computer was done in order to establish the relationship between structure and activity.
publishDate 2000
dc.date.none.fl_str_mv 2000
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p602_BellozasReinhard
url http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p602_BellozasReinhard
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/2.5/ar
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/2.5/ar
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv Molecules 2000;5(3):602-604
reponame:Biblioteca Digital (UBA-FCEN)
instname:Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron:UBA-FCEN
reponame_str Biblioteca Digital (UBA-FCEN)
collection Biblioteca Digital (UBA-FCEN)
instname_str Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
instacron_str UBA-FCEN
institution UBA-FCEN
repository.name.fl_str_mv Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales
repository.mail.fl_str_mv ana@bl.fcen.uba.ar
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score 12.976206

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