This submission belongs to the session c. Bioorganic Chemistry and Natural Products of the event The 11th International Electronic Conference on Synthetic Organic Chemistry
Published date
30 Nov, 2007
Citation
Maria J. G. Fernandes, M. Sameiro T. Gonçalves, Susana P. G. Costa, Photocleavage Studies of γ-aminobutyric acid (GABA) Conjugates, in Proceedings of The 11th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2007, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-11-01338
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Photocleavage Studies of γ-aminobutyric acid (GABA) Conjugates
Maria J. G. Fernandes 1
M. Sameiro T. Gonçalves 1
Susana P. G. Costa 1
1. Centro de Química, Universidade do Minho, Campus de Gualtar, 4710-057 Braga, Portugal
Abstract
Polycyclic aromatic labels such as naphthalene and pyrene were coupled to the C- terminus of N-benzyloxycarbonyl protected -aminobutyric acid (GABA). The photophysical properties of the corresponding fluorescent conjugates were evaluated, as well as their behaviour towards photocleavage by irradiation in MeOH/HEPES buffer solution (80:20), in a photochemical reactor at different wavelengths (254, 300, 350 and 419 nm), followed by HPLC/UV monitoring.
Keywords
Naphthalene
Pyrene
-Aminobutyric acid (GABA)
Photocleavable protecting groups
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