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5-Ethyl-4a-methoxy-1,3-dimethyl-4a,5-dihydrobenzo[g]pteridine-2,4(1H,3H)dione
The title compound, C(15)H(18)N(4)O(3), was formed by the reaction of methanol with 5-ethyl-1,3-dimethylalloxazinium perchlorate. Its structure mimics those of possible flavin intermediates in flavoenzymes. The heterocyclic rings are substituted with methyl, ethyl and methoxy groups. The central...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969355/ https://www.ncbi.nlm.nih.gov/pubmed/21582825 http://dx.doi.org/10.1107/S1600536809020856 |
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author | Ménová, Petra Eigner, Václav Cibulka, Radek Čejka, Jan Dvořáková, Hana |
author_facet | Ménová, Petra Eigner, Václav Cibulka, Radek Čejka, Jan Dvořáková, Hana |
author_sort | Ménová, Petra |
collection | PubMed |
description | The title compound, C(15)H(18)N(4)O(3), was formed by the reaction of methanol with 5-ethyl-1,3-dimethylalloxazinium perchlorate. Its structure mimics those of possible flavin intermediates in flavoenzymes. The heterocyclic rings are substituted with methyl, ethyl and methoxy groups. The central tricyclic skeleton is bent due to the presence of an sp (3) C atom. There are weak intermolecular C—H⋯O interactions in the structure, forming a three-dimensional network. |
format | Text |
id | pubmed-2969355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29693552010-12-30 5-Ethyl-4a-methoxy-1,3-dimethyl-4a,5-dihydrobenzo[g]pteridine-2,4(1H,3H)dione Ménová, Petra Eigner, Václav Cibulka, Radek Čejka, Jan Dvořáková, Hana Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(15)H(18)N(4)O(3), was formed by the reaction of methanol with 5-ethyl-1,3-dimethylalloxazinium perchlorate. Its structure mimics those of possible flavin intermediates in flavoenzymes. The heterocyclic rings are substituted with methyl, ethyl and methoxy groups. The central tricyclic skeleton is bent due to the presence of an sp (3) C atom. There are weak intermolecular C—H⋯O interactions in the structure, forming a three-dimensional network. International Union of Crystallography 2009-06-10 /pmc/articles/PMC2969355/ /pubmed/21582825 http://dx.doi.org/10.1107/S1600536809020856 Text en © Ménová et al. 2009 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Organic Papers Ménová, Petra Eigner, Václav Cibulka, Radek Čejka, Jan Dvořáková, Hana 5-Ethyl-4a-methoxy-1,3-dimethyl-4a,5-dihydrobenzo[g]pteridine-2,4(1H,3H)dione |
title | 5-Ethyl-4a-methoxy-1,3-dimethyl-4a,5-dihydrobenzo[g]pteridine-2,4(1H,3H)dione |
title_full | 5-Ethyl-4a-methoxy-1,3-dimethyl-4a,5-dihydrobenzo[g]pteridine-2,4(1H,3H)dione |
title_fullStr | 5-Ethyl-4a-methoxy-1,3-dimethyl-4a,5-dihydrobenzo[g]pteridine-2,4(1H,3H)dione |
title_full_unstemmed | 5-Ethyl-4a-methoxy-1,3-dimethyl-4a,5-dihydrobenzo[g]pteridine-2,4(1H,3H)dione |
title_short | 5-Ethyl-4a-methoxy-1,3-dimethyl-4a,5-dihydrobenzo[g]pteridine-2,4(1H,3H)dione |
title_sort | 5-ethyl-4a-methoxy-1,3-dimethyl-4a,5-dihydrobenzo[g]pteridine-2,4(1h,3h)dione |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969355/ https://www.ncbi.nlm.nih.gov/pubmed/21582825 http://dx.doi.org/10.1107/S1600536809020856 |
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