Understanding the degradation of electrochemically-generated reactive drug metabolites by quantitative NMR.
about
Unexpected benzimidazole ring formation from a quinoneimide species in the presence of ammonium acetate as supporting electrolyte used in the coupling of electrochemistry with mass spectrometry.(19)F NMR-, ESR-, and vis-NIR-spectroelectrochemical study of the unconventional reduction behaviour of a perfluoroalkylated fullerene: dimerization of the C70(CF3)10(-) radical anionPhase I and phase II reductive metabolism simulation of nitro aromatic xenobiotics with electrochemistry coupled with high resolution mass spectrometry.Metabolism of a sea lamprey pesticide by fish liver enzymes part B: method development and application in quantification of TFM metabolites formed in vivo.Metabolism of a sea lamprey pesticide by fish liver enzymes part A: identification and synthesis of TFM metabolites.
P2860
Understanding the degradation of electrochemically-generated reactive drug metabolites by quantitative NMR.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
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2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
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2013年學術文章
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name
Understanding the degradation ...... tabolites by quantitative NMR.
@en
Understanding the degradation ...... tabolites by quantitative NMR.
@nl
type
label
Understanding the degradation ...... tabolites by quantitative NMR.
@en
Understanding the degradation ...... tabolites by quantitative NMR.
@nl
prefLabel
Understanding the degradation ...... tabolites by quantitative NMR.
@en
Understanding the degradation ...... tabolites by quantitative NMR.
@nl
P1433
P1476
Understanding the degradation ...... tabolites by quantitative NMR.
@en
P2093
Patrick Giraudeau
P304
P356
10.1016/J.TALANTA.2013.07.026
P407
P577
2013-07-19T00:00:00Z