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Synthesis and Photolytic Assessment of Nitroindolinyl-Caged Calcium Ion Chelators †
Neuroactive amino acids derivatised at their carboxylate groups with a photolabile nitroindolinyl group are highly effective reagents for the sub-µs release of neuroactive amino acids in physiological solutions. However, the same does not apply in the case of calcium ion chelators. In this study, ni...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104977/ https://www.ncbi.nlm.nih.gov/pubmed/35565996 http://dx.doi.org/10.3390/molecules27092645 |
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author | Papageorgiou, George Corrie, John E. T. |
author_facet | Papageorgiou, George Corrie, John E. T. |
author_sort | Papageorgiou, George |
collection | PubMed |
description | Neuroactive amino acids derivatised at their carboxylate groups with a photolabile nitroindolinyl group are highly effective reagents for the sub-µs release of neuroactive amino acids in physiological solutions. However, the same does not apply in the case of calcium ion chelators. In this study, nitroindolinyl-caged BAPTA is found to be completely photostable, whereas nitroindolinyl-caged EDTA photolyses only when saturated with calcium ions. |
format | Online Article Text |
id | pubmed-9104977 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91049772022-05-14 Synthesis and Photolytic Assessment of Nitroindolinyl-Caged Calcium Ion Chelators † Papageorgiou, George Corrie, John E. T. Molecules Article Neuroactive amino acids derivatised at their carboxylate groups with a photolabile nitroindolinyl group are highly effective reagents for the sub-µs release of neuroactive amino acids in physiological solutions. However, the same does not apply in the case of calcium ion chelators. In this study, nitroindolinyl-caged BAPTA is found to be completely photostable, whereas nitroindolinyl-caged EDTA photolyses only when saturated with calcium ions. MDPI 2022-04-20 /pmc/articles/PMC9104977/ /pubmed/35565996 http://dx.doi.org/10.3390/molecules27092645 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Papageorgiou, George Corrie, John E. T. Synthesis and Photolytic Assessment of Nitroindolinyl-Caged Calcium Ion Chelators † |
title | Synthesis and Photolytic Assessment of Nitroindolinyl-Caged Calcium Ion Chelators † |
title_full | Synthesis and Photolytic Assessment of Nitroindolinyl-Caged Calcium Ion Chelators † |
title_fullStr | Synthesis and Photolytic Assessment of Nitroindolinyl-Caged Calcium Ion Chelators † |
title_full_unstemmed | Synthesis and Photolytic Assessment of Nitroindolinyl-Caged Calcium Ion Chelators † |
title_short | Synthesis and Photolytic Assessment of Nitroindolinyl-Caged Calcium Ion Chelators † |
title_sort | synthesis and photolytic assessment of nitroindolinyl-caged calcium ion chelators † |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9104977/ https://www.ncbi.nlm.nih.gov/pubmed/35565996 http://dx.doi.org/10.3390/molecules27092645 |
work_keys_str_mv | AT papageorgiougeorge synthesisandphotolyticassessmentofnitroindolinylcagedcalciumionchelators AT corriejohnet synthesisandphotolyticassessmentofnitroindolinylcagedcalciumionchelators |