N-nitrosomelatonin

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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Autores principales: Turjanski, Adrián Gustavo, Chaia, Zulema Débora, Doctorovich, Fabio Ariel, Estrin, Dario Ariel, Rosenstein, Ruth Estela
Publicado: 2000
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01082701_v56_n6_p682_Turjanski
http://hdl.handle.net/20.500.12110/paper_01082701_v56_n6_p682_Turjanski
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id paper:paper_01082701_v56_n6_p682_Turjanski
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spelling paper:paper_01082701_v56_n6_p682_Turjanski2023-06-08T15:10:39Z N-nitrosomelatonin Turjanski, Adrián Gustavo Chaia, Zulema Débora Doctorovich, Fabio Ariel Estrin, Dario Ariel Rosenstein, Ruth Estela 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 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01082701_v56_n6_p682_Turjanski 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)
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, Adrián Gustavo
Chaia, Zulema Débora
Doctorovich, Fabio Ariel
Estrin, Dario Ariel
Rosenstein, Ruth Estela
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.
author Turjanski, Adrián Gustavo
Chaia, Zulema Débora
Doctorovich, Fabio Ariel
Estrin, Dario Ariel
Rosenstein, Ruth Estela
author_facet Turjanski, Adrián Gustavo
Chaia, Zulema Débora
Doctorovich, Fabio Ariel
Estrin, Dario Ariel
Rosenstein, Ruth Estela
author_sort Turjanski, Adrián Gustavo
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 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01082701_v56_n6_p682_Turjanski
http://hdl.handle.net/20.500.12110/paper_01082701_v56_n6_p682_Turjanski
work_keys_str_mv AT turjanskiadriangustavo nnitrosomelatonin
AT chaiazulemadebora nnitrosomelatonin
AT doctorovichfabioariel nnitrosomelatonin
AT estrindarioariel nnitrosomelatonin
AT rosensteinruthestela nnitrosomelatonin
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