N-nitrosomelatonin

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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 chai...

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Detalles Bibliográficos
Autores principales:	Turjanski, A., Chaia, Z.D., Doctorovich, F., Estrin, D., Rosenstein, R., Piro, O.E.
Formato:	Artículo publishedVersion
Lenguaje:	Inglés
Publicado:	2000
Materias:	Aromatic compounds Conformations Crystal atomic structure Crystallization Derivatives Hydrogen bonds Molecular structure Nitrosomelatonin Hormones
Acceso en línea:	http://hdl.handle.net/20.500.12110/paper_01082701_v56_n6_p682_Turjanski
Aporte de:	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

id	paperaa:paper_01082701_v56_n6_p682_Turjanski
record_format	dspace
spelling	paperaa:paper_01082701_v56_n6_p682_Turjanski2023-06-12T16:46:33Z N-nitrosomelatonin Acta Crystallogr Sect C Cryst Struct Commun 2000;56(6):682-683 Turjanski, A. Chaia, Z.D. Doctorovich, F. Estrin, D. Rosenstein, R. Piro, O.E. Aromatic compounds Conformations Crystal atomic structure Crystallization Derivatives Hydrogen bonds Molecular structure Nitrosomelatonin Hormones 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. Fil:Turjanski, A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Chaia, Z.D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Doctorovich, F. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Estrin, D. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Rosenstein, R. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2000 info:eu-repo/semantics/article info:ar-repo/semantics/artículo info:eu-repo/semantics/publishedVersion application/pdf eng info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_01082701_v56_n6_p682_Turjanski
institution	Universidad de Buenos Aires
institution_str	I-28
repository_str	R-134
collection	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
language	Inglés
orig_language_str_mv	eng
topic	Aromatic compounds Conformations Crystal atomic structure Crystallization Derivatives Hydrogen bonds Molecular structure Nitrosomelatonin Hormones
spellingShingle	Aromatic compounds Conformations Crystal atomic structure Crystallization Derivatives Hydrogen bonds Molecular structure Nitrosomelatonin Hormones Turjanski, A. Chaia, Z.D. Doctorovich, F. Estrin, D. Rosenstein, R. Piro, O.E. N-nitrosomelatonin
topic_facet	Aromatic compounds Conformations Crystal atomic structure Crystallization Derivatives Hydrogen bonds Molecular structure Nitrosomelatonin Hormones
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.
format	Artículo Artículo publishedVersion
author	Turjanski, A. Chaia, Z.D. Doctorovich, F. Estrin, D. Rosenstein, R. Piro, O.E.
author_facet	Turjanski, A. Chaia, Z.D. Doctorovich, F. Estrin, D. Rosenstein, R. Piro, O.E.
author_sort	Turjanski, A.
title	N-nitrosomelatonin
title_short	N-nitrosomelatonin
title_full	N-nitrosomelatonin
title_fullStr	N-nitrosomelatonin
title_full_unstemmed	N-nitrosomelatonin
title_sort	n-nitrosomelatonin
publishDate	2000
url	http://hdl.handle.net/20.500.12110/paper_01082701_v56_n6_p682_Turjanski
work_keys_str_mv	AT turjanskia nnitrosomelatonin AT chaiazd nnitrosomelatonin AT doctorovichf nnitrosomelatonin AT estrind nnitrosomelatonin AT rosensteinr nnitrosomelatonin AT pirooe nnitrosomelatonin
_version_	1769810027462262784

N-nitrosomelatonin

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