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PMID: 16417352 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

Convergent oxygenation of arachidonic acid by 5-lipoxygenase and cyclooxygenase-2.

Journal of the American Chemical Society ·Vol. 128 ·No. 3 ·2006-01-25 ·Pages 720-1

Schneider C, Boeglin WE, Yin H, Stec DF, Voehler M

Abstract

5-Lipoxygenase and cyclooxygenase-2 (COX-2) initiate the biosynthesis of distinct families of mediators from arachidonic acid (leukotrienes and prostaglandins, respectively) and are each the target of anti-inflammatory medications. Here we show that the product of 5-lipoxygenase, 5S-hydroxyeicosatetraenoic acid, is selectively and efficiently triply oxygenated by COX-2, implicating a cross-pathway interaction. The product is a unique diendoperoxide, potentially representing the parent compound of a novel group of lipid mediators.

MeSH Terms
Arachidonate 5-Lipoxygenase/chemistry,metabolism Arachidonic Acid/chemistry,metabolism Cyclooxygenase 2/chemistry,metabolism Nuclear Magnetic Resonance, Biomolecular Oxidation-Reduction
Chemicals
Arachidonic Acid Arachidonate 5-Lipoxygenase Cyclooxygenase 2
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Schneider Claus
Department of Pharmacology, Division of Clinical Pharmacology, 23rd Avenue South at Pierce, Vanderbilt University Medical School, Nashville, Tennessee 37232, USA. [email protected]
Boeglin William E
Yin Huiyong
Stec Donald F
Voehler Markus
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12 references, click to expand
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Article Info
Journal
Journal of the American Chemical Society
Abbr.
J Am Chem Soc
ISSN
0002-7863
Published
2006-01-25
Pages
720-1
Language
English
Region
United States
NLM ID
7503056
PMCID
PMC2532595
Subset
IM
Grants
NIGMS NIH HHS · R01 GM053638 · United States
NIGMS NIH HHS · R01 GM053638-07 · United States
NIGMS NIH HHS · GM53638 · United States
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