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 alky...

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Autores principales: Turjanski, A., Chaia, Z.D., Doctorovich, F., Estrin, D., Rosenstein, R., Piro, O.E.
Formato: Artículo publishedVersion
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
https://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_01082701_v56_n6_p682_Turjanski_oai
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Repositorio Digital de la Universidad de Buenos Aires (UBA) de Universidad de Buenos Aires
id I28-R145-paper_01082701_v56_n6_p682_Turjanski_oai
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spelling I28-R145-paper_01082701_v56_n6_p682_Turjanski_oai2024-08-16 Turjanski, A. Chaia, Z.D. Doctorovich, F. Estrin, D. Rosenstein, R. Piro, O.E. 2000 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. application/pdf http://hdl.handle.net/20.500.12110/paper_01082701_v56_n6_p682_Turjanski info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar Acta Crystallogr Sect C Cryst Struct Commun 2000;56(6):682-683 Aromatic compounds Conformations Crystal atomic structure Crystallization Derivatives Hydrogen bonds Molecular structure Nitrosomelatonin Hormones N-nitrosomelatonin info:eu-repo/semantics/article info:ar-repo/semantics/artículo info:eu-repo/semantics/publishedVersion https://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_01082701_v56_n6_p682_Turjanski_oai
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-145
collection Repositorio Digital de la Universidad de Buenos Aires (UBA)
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
https://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=artiaex&d=paper_01082701_v56_n6_p682_Turjanski_oai
work_keys_str_mv AT turjanskia nnitrosomelatonin
AT chaiazd nnitrosomelatonin
AT doctorovichf nnitrosomelatonin
AT estrind nnitrosomelatonin
AT rosensteinr nnitrosomelatonin
AT pirooe nnitrosomelatonin
_version_ 1809356808458862592

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