1H NMR characterization of the intermediate formed upon UV-A excitation of biopterin, neopterin and 6-hydroxymethylpterin in O2-free aqueous solutions
Pterins belong to a family of heterocyclic compounds present in a wide range of living systems and participate in relevant biological functions. Under anaerobic conditions, the unstable red intermediate generated by UV-A irradiation of biopterin, neopterin and 6-hydroxymethylpterin was identified by...
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todo:paper_00092614_v484_n4-6_p330_Vignoni2023-10-03T14:08:29Z 1H NMR characterization of the intermediate formed upon UV-A excitation of biopterin, neopterin and 6-hydroxymethylpterin in O2-free aqueous solutions Vignoni, M. Salum, M.L. Erra-Balsells, R. Thomas, A.H. Cabrerizo, F.M. Anaerobic conditions Aqueous solutions Biological functions Biopterin Heterocyclic compound Living systems Neopterin NMR analysis Nuclear magnetic resonance Pterins belong to a family of heterocyclic compounds present in a wide range of living systems and participate in relevant biological functions. Under anaerobic conditions, the unstable red intermediate generated by UV-A irradiation of biopterin, neopterin and 6-hydroxymethylpterin was identified by 1H NMR analysis, in alkaline D2O solutions, as 5,8-dihydro-6-formylpterin. © 2009 Elsevier B.V. All rights reserved. Fil:Erra-Balsells, 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_00092614_v484_n4-6_p330_Vignoni |
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Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
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Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
Anaerobic conditions Aqueous solutions Biological functions Biopterin Heterocyclic compound Living systems Neopterin NMR analysis Nuclear magnetic resonance |
spellingShingle |
Anaerobic conditions Aqueous solutions Biological functions Biopterin Heterocyclic compound Living systems Neopterin NMR analysis Nuclear magnetic resonance Vignoni, M. Salum, M.L. Erra-Balsells, R. Thomas, A.H. Cabrerizo, F.M. 1H NMR characterization of the intermediate formed upon UV-A excitation of biopterin, neopterin and 6-hydroxymethylpterin in O2-free aqueous solutions |
topic_facet |
Anaerobic conditions Aqueous solutions Biological functions Biopterin Heterocyclic compound Living systems Neopterin NMR analysis Nuclear magnetic resonance |
description |
Pterins belong to a family of heterocyclic compounds present in a wide range of living systems and participate in relevant biological functions. Under anaerobic conditions, the unstable red intermediate generated by UV-A irradiation of biopterin, neopterin and 6-hydroxymethylpterin was identified by 1H NMR analysis, in alkaline D2O solutions, as 5,8-dihydro-6-formylpterin. © 2009 Elsevier B.V. All rights reserved. |
format |
JOUR |
author |
Vignoni, M. Salum, M.L. Erra-Balsells, R. Thomas, A.H. Cabrerizo, F.M. |
author_facet |
Vignoni, M. Salum, M.L. Erra-Balsells, R. Thomas, A.H. Cabrerizo, F.M. |
author_sort |
Vignoni, M. |
title |
1H NMR characterization of the intermediate formed upon UV-A excitation of biopterin, neopterin and 6-hydroxymethylpterin in O2-free aqueous solutions |
title_short |
1H NMR characterization of the intermediate formed upon UV-A excitation of biopterin, neopterin and 6-hydroxymethylpterin in O2-free aqueous solutions |
title_full |
1H NMR characterization of the intermediate formed upon UV-A excitation of biopterin, neopterin and 6-hydroxymethylpterin in O2-free aqueous solutions |
title_fullStr |
1H NMR characterization of the intermediate formed upon UV-A excitation of biopterin, neopterin and 6-hydroxymethylpterin in O2-free aqueous solutions |
title_full_unstemmed |
1H NMR characterization of the intermediate formed upon UV-A excitation of biopterin, neopterin and 6-hydroxymethylpterin in O2-free aqueous solutions |
title_sort |
1h nmr characterization of the intermediate formed upon uv-a excitation of biopterin, neopterin and 6-hydroxymethylpterin in o2-free aqueous solutions |
url |
http://hdl.handle.net/20.500.12110/paper_00092614_v484_n4-6_p330_Vignoni |
work_keys_str_mv |
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