Photorelease of glycine and beta-alanine from (7-bromocoumarin-4-yl)methyl cages

The synthesis of a new 7-bromo-4-(chloromethyl)-coumarin to be used as cage for the release of bioactive molecules is presented. Ester cages of two neurotransmitter amino acids, glycine and β-alanine, were also synthetized. These neurotransmitters were chosen as models due to their biological releva...

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Bibliographic Details
Main Author: Conceição, Rafaela C. O. (author)
Other Authors: Costa, Susana P. G. (author), Gonçalves, M. Sameiro T. (author)
Format: conferencePaper
Language:eng
Published: 2015
Subjects:
Online Access:http://hdl.handle.net/1822/49322
Country:Portugal
Oai:oai:repositorium.sdum.uminho.pt:1822/49322
Description
Summary:The synthesis of a new 7-bromo-4-(chloromethyl)-coumarin to be used as cage for the release of bioactive molecules is presented. Ester cages of two neurotransmitter amino acids, glycine and β-alanine, were also synthetized. These neurotransmitters were chosen as models due to their biological relevance. The glycine and β-alanine ester conjugates, in methanol/HEPES buffer (80:20), were irradiated at 254, 300, 350 and 419 nm in a Rayonet RPR-100 photochemical reactor and the photolysis process was followed by HPLC with UV detection. These results were compared with those previously obtained by our research group when 4-chloromethyl-coumarin was used in the photorelease of glycine and β-alanine.