Synthesis and bioactivity of teasterone and typhasterol analogs

Autores
Ramírez, J.A.; Mancusso, R.; Sarno, S.; Galagovsky, L.R.
Año de publicación
2000
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Four brassinosteroids analogs of homoteasterone and homotyphasterol bearing 5α-OH and 5α-F groups have been synthesized and their bioactivities evaluated.
Fil:Ramírez, J.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
Fuente
Molecules 2000;5(3):367-369
Materia
brassinosteroid
bioassay
chemical analysis
conference paper
synthesis
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_p367_Ramirez
Acceder
id BDUBAFCEN_141e47ca2f720dc55ad337989e1b3d7d
oai_identifier_str paperaa:paper_14203049_v5_n3_p367_Ramirez
network_acronym_str BDUBAFCEN
repository_id_str 1896
network_name_str Biblioteca Digital (UBA-FCEN)
spelling Synthesis and bioactivity of teasterone and typhasterol analogsRamírez, J.A.Mancusso, R.Sarno, S.Galagovsky, L.R.brassinosteroidbioassaychemical analysisconference papersynthesisFour brassinosteroids analogs of homoteasterone and homotyphasterol bearing 5α-OH and 5α-F groups have been synthesized and their bioactivities evaluated.Fil:Ramírez, J.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.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_p367_RamirezMolecules 2000;5(3):367-369reponame: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/ar2025-11-06T09:39:58Zpaperaa:paper_14203049_v5_n3_p367_RamirezInstitucionalhttps://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 09:39:59.442Biblioteca Digital (UBA-FCEN) - Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturalesfalse
dc.title.none.fl_str_mv Synthesis and bioactivity of teasterone and typhasterol analogs
title Synthesis and bioactivity of teasterone and typhasterol analogs
spellingShingle Synthesis and bioactivity of teasterone and typhasterol analogs
Ramírez, J.A.
brassinosteroid
bioassay
chemical analysis
conference paper
synthesis
title_short Synthesis and bioactivity of teasterone and typhasterol analogs
title_full Synthesis and bioactivity of teasterone and typhasterol analogs
title_fullStr Synthesis and bioactivity of teasterone and typhasterol analogs
title_full_unstemmed Synthesis and bioactivity of teasterone and typhasterol analogs
title_sort Synthesis and bioactivity of teasterone and typhasterol analogs
dc.creator.none.fl_str_mv Ramírez, J.A.
Mancusso, R.
Sarno, S.
Galagovsky, L.R.
author Ramírez, J.A.
author_facet Ramírez, J.A.
Mancusso, R.
Sarno, S.
Galagovsky, L.R.
author_role author
author2 Mancusso, R.
Sarno, S.
Galagovsky, L.R.
author2_role author
author
author
dc.subject.none.fl_str_mv brassinosteroid
bioassay
chemical analysis
conference paper
synthesis
topic brassinosteroid
bioassay
chemical analysis
conference paper
synthesis
dc.description.none.fl_txt_mv Four brassinosteroids analogs of homoteasterone and homotyphasterol bearing 5α-OH and 5α-F groups have been synthesized and their bioactivities evaluated.
Fil:Ramírez, J.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
description Four brassinosteroids analogs of homoteasterone and homotyphasterol bearing 5α-OH and 5α-F groups have been synthesized and their bioactivities evaluated.
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_p367_Ramirez
url http://hdl.handle.net/20.500.12110/paper_14203049_v5_n3_p367_Ramirez
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):367-369
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
_version_ 1848046098459918336
score 12.976206

Publicaciones similares