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Probing the steric requirements of the γ-aminobutyric acid aminotransferase active site with fluorinated analogues of vigabatrin

We have synthesized three analogues of 4-amino-5-fluorohexanoic acids as potential inactivators of γ-aminobutyric acid aminotransferase (GABA-AT), which were designed to combine the potency of their shorter chain analogue, 4-amino-5-fluoropentanoic acid (AFPA), with the greater enzyme selectivity of...

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Detalhes bibliográficos
Main Authors: Juncosa, Jose I., Groves, Andrew P., Xia, Guoyao, Silverman, Richard B.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3563932/
https://ncbi.nlm.nih.gov/pubmed/23306054
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bmc.2012.12.009
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