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Provedor de dados:  ArchiMer
País:  France
Título:  Structure Elucidation, Relative LC–MS Response and In Vitro Toxicity of Azaspiracids 7–10 Isolated from Mussels (Mytilus edulis)
Autores:  Kilcoyne, Jane
Twiner, Michael J.
Mccarron, Pearse
Crain, Sheila
Giddings, Sabrina D.
Foley, Barry
Rise, Frode
Hess, Philipp
Willdns, Alistair L.
Miles, Christopher O.
Data:  2015-05
Ano:  2015
Palavras-chave:  Azaspiracid
Structure confirmation
LC-MS molar response
NMR
Mass spectrometry
Purification
Jurkat T
Toxicity
Resumo:  Azaspiracids (AZAs) are marine biotoxins produced by dinoflagellates that can accumulate in shellfish, which if consumed can lead to poisoning events. AZA7–10, 7–10, were isolated from shellfish and their structures, previously proposed on the basis of only LC–MS/MS data, were confirmed by NMR spectroscopy. Purified AZA4–6, 4–6, and 7–10 were accurately quantitated by qNMR and used to assay cytotoxicity with Jurkat T lymphocyte cells for the first time. LC–MS(MS) molar response studies performed using isocratic and gradient elution in both selected ion monitoring and selected reaction monitoring modes showed that responses for the analogues ranged from 0.3 to 1.2 relative to AZA1, 1. All AZA analogues tested were cytotoxic to Jurkat T lymphocyte cells in a time- and concentration-dependent manner; however, there were distinct differences in their EC50 values, with the potencies for each analogue being: AZA6 > AZA8 > AZA1 > AZA4 ≈ AZA9 > AZA5 ≈ AZA10. This data contributes to the understanding of the structure–activity relationships of AZAs.
Tipo:  Text
Idioma:  Inglês
Identificador:  http://archimer.ifremer.fr/doc/00269/38059/36190.pdf

DOI:10.1021/acs.jafc.5b01320

http://archimer.ifremer.fr/doc/00269/38059/
Editor:  Amer Chemical Soc
Relação:  info:eu-repo/grantAgreement/EC/FP7/221117/EU//ALGETOX
Formato:  application/pdf
Fonte:  Journal Of Agricultural And Food Chemistry (0021-8561) (Amer Chemical Soc), 2015-05 , Vol. 63 , N. 20 , P. 5083-5091
Direitos:  2015 American Chemical Society

info:eu-repo/semantics/openAccess

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