Biosynthesis, isolation, and NMR analysis of leukotriene A epoxides: Substrate chirality as a determinant of the cis or trans epoxide confi guration

Journal of Lipid Research

Volumn 54, Issue 3, 2013, Pages 754-761

  Jin, Jing ^a   Zheng, Yuxiang ^a   Boeglin, William E ^a   Brash, Alan R ^a  

^a VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

15 lipoxygenase; 5 lipoxygenase; Hydroperoxy eicosatetraenoic acid; Nuclear magnetic resonance

Indexed keywords

15 HYDROPEROXYARACHIDONIC ACID; ARACHIDONATE 15 LIPOXYGENASE; ARACHIDONATE 5 LIPOXYGENASE; EPOXIDE; EPOXYEICOSATETRAENOATE; LEUKOTRIENE A EPOXIDE DERIVATIVE; LEUKOTRIENE DERIVATIVE; LIPOXYGENASE; LIPOXYGENASE I; RECOMBINANT ENZYME; UNCLASSIFIED DRUG;

ARABIDOPSIS; ARTICLE; BIOSYNTHESIS; CATALYSIS; CHEMICAL STRUCTURE; CHIRALITY; ENZYME MECHANISM; NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; SEPARATION TECHNIQUE;

EPOXY COMPOUNDS; GAS CHROMATOGRAPHY-MASS SPECTROMETRY; HUMANS; HYDROXYEICOSATETRAENOIC ACIDS; LEUKOTRIENE A4; LIPOXYGENASE; MAGNETIC RESONANCE SPECTROSCOPY; STEREOISOMERISM;

EID: 84874090777     PISSN: 00222275     EISSN: 15397262     Source Type: Journal    
DOI: 10.1194/jlr.M033746     Document Type: Article

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