Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/44064

TítuloPhotoactivatable prodrugs of butyric acid based on new coumarin fused oxazole heterocycles
Autor(es)Soares, Ana M. S.
Hungerford, Graham
Costa, Susana P. G.
Gonçalves, M. Sameiro T.
Palavras-chaveProdrugs
Coumarins
Oxazoles
Butyric acid
Photocleavable protecting groups
Photolysis
Data2017
EditoraElsevier 1
RevistaDyes and Pigments
CitaçãoA. M. S. Soares, G. Hungerford, S. P. G. Costa M. S. T. Gonçalves, “Photoactivatable prodrugs of butyric acid based on new coumarin fused oxazole heterocycles”, Dyes and Pigments, 2017, 137, 91-100.
Resumo(s)New coumarin fused oxazoles were investigated as photosensitive units for carboxylic acid groups using butyric acid as a model compound. 6-Oxo-6H-benzopyrano[6,7-d]oxazol-8-yl)methyl derivatives possessing various (hetero)aromatic substituents at position 2 of the heterocyclic system were used in the synthesis of ester conjugates of butyric acid. Photolysis at selected wavelengths in methanol/HEPES buffer (80:20) solutions, monitored by HPLC/UV and 1H NMR, produced the complete release of butyric acid. The shorter irradiation times for cleavage at longer wavelengths occurred for the conjugate with a 4-oxo-4H-benzopyran-2-yl substituent and thus (6-oxo-2-(4-oxo-4H-benzopyran-2-yl)-6H-benzopyrano[6,7-d]oxazol-8-yl)methyl has potential as a candidate photosensitive moiety for butyric acid prodrugs.
TipoArtigo
URIhttps://hdl.handle.net/1822/44064
DOI10.1016/j.dyepig.2016.10.001
ISSN0143-7208
Arbitragem científicayes
AcessoAcesso aberto
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