N-nitrosomelatonin

Autores
Turjanski, Adrián; Chaia, Zulema Débora; Doctorovich, Fabio; Estrin, Dario; Rosenstein, Ruth; Piro, Oscar Enrique
Año de publicación
2000
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The title compound, N-[2-(5-methoxy-1-nitroso-1H-indol-3-yl)ethyl]acetamide, C13H15N3O3, an N-nitroso derivative of melatonin, crystallizes in the monoclinic C2/c space group. The molecules are arranged in such a way that the aromatic rings are in a planar conformation, with the alkylamide side chains in a different plane, at a dihedral angle of 108.60 (6)°. The alkylamide chains are interconnected by hydrogen bonds, constituting an infinite array.
Facultad de Ciencias Exactas
Materia
Física
Cristalografía
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/83310
Acceder
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oai_identifier_str oai:sedici.unlp.edu.ar:10915/83310
network_acronym_str SEDICI
repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling N-nitrosomelatoninTurjanski, AdriánChaia, Zulema DéboraDoctorovich, FabioEstrin, DarioRosenstein, RuthPiro, Oscar EnriqueFísicaCristalografíaThe title compound, N-[2-(5-methoxy-1-nitroso-1H-indol-3-yl)ethyl]acetamide, C13H15N3O3, an N-nitroso derivative of melatonin, crystallizes in the monoclinic C2/c space group. The molecules are arranged in such a way that the aromatic rings are in a planar conformation, with the alkylamide side chains in a different plane, at a dihedral angle of 108.60 (6)°. The alkylamide chains are interconnected by hydrogen bonds, constituting an infinite array.Facultad de Ciencias Exactas2000info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf682-683http://sedici.unlp.edu.ar/handle/10915/83310enginfo:eu-repo/semantics/altIdentifier/issn/0108-2701info:eu-repo/semantics/altIdentifier/doi/10.1107/S010827010000456Xinfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-10-15T11:07:47Zoai:sedici.unlp.edu.ar:10915/83310Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-15 11:07:47.307SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv N-nitrosomelatonin
title N-nitrosomelatonin
spellingShingle N-nitrosomelatonin
Turjanski, Adrián
Física
Cristalografía
title_short N-nitrosomelatonin
title_full N-nitrosomelatonin
title_fullStr N-nitrosomelatonin
title_full_unstemmed N-nitrosomelatonin
title_sort N-nitrosomelatonin
dc.creator.none.fl_str_mv Turjanski, Adrián
Chaia, Zulema Débora
Doctorovich, Fabio
Estrin, Dario
Rosenstein, Ruth
Piro, Oscar Enrique
author Turjanski, Adrián
author_facet Turjanski, Adrián
Chaia, Zulema Débora
Doctorovich, Fabio
Estrin, Dario
Rosenstein, Ruth
Piro, Oscar Enrique
author_role author
author2 Chaia, Zulema Débora
Doctorovich, Fabio
Estrin, Dario
Rosenstein, Ruth
Piro, Oscar Enrique
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv Física
Cristalografía
topic Física
Cristalografía
dc.description.none.fl_txt_mv The title compound, N-[2-(5-methoxy-1-nitroso-1H-indol-3-yl)ethyl]acetamide, C13H15N3O3, an N-nitroso derivative of melatonin, crystallizes in the monoclinic C2/c space group. The molecules are arranged in such a way that the aromatic rings are in a planar conformation, with the alkylamide side chains in a different plane, at a dihedral angle of 108.60 (6)°. The alkylamide chains are interconnected by hydrogen bonds, constituting an infinite array.
Facultad de Ciencias Exactas
description The title compound, N-[2-(5-methoxy-1-nitroso-1H-indol-3-yl)ethyl]acetamide, C13H15N3O3, an N-nitroso derivative of melatonin, crystallizes in the monoclinic C2/c space group. The molecules are arranged in such a way that the aromatic rings are in a planar conformation, with the alkylamide side chains in a different plane, at a dihedral angle of 108.60 (6)°. The alkylamide chains are interconnected by hydrogen bonds, constituting an infinite array.
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
Articulo
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://sedici.unlp.edu.ar/handle/10915/83310
url http://sedici.unlp.edu.ar/handle/10915/83310
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/0108-2701
info:eu-repo/semantics/altIdentifier/doi/10.1107/S010827010000456X
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/4.0/
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.format.none.fl_str_mv application/pdf
682-683
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
instacron:UNLP
reponame_str SEDICI (UNLP)
collection SEDICI (UNLP)
instname_str Universidad Nacional de La Plata
instacron_str UNLP
institution UNLP
repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
repository.mail.fl_str_mv alira@sedici.unlp.edu.ar
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score 13.22299

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