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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| Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_01082701_v56_n6_p682_Turjanski |
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todo:paper_01082701_v56_n6_p682_Turjanski2023-10-03T14:57:49Z N-nitrosomelatonin 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. JOUR 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) |
| 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 |
JOUR |
| 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 |
| 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_ |
1807322877930766336 |