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Cited by 648

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Transformation of arachidonic acid by rabbit polymorphonuclear leukocytes. Formation of a novel dihydroxyeicosatetraenoic acid.

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Borgeat, P., Samuelsson, B.·1979·Journal of Biological Chemistry

Abstract

A new metabolite of arachidonic acid, 5-D-(S),12-D-(R)-dihydroxy-6,8,10,14-eicosatetraenoic acid, was found upon incubation of the fatty acid with a suspension of rabbit peritoneal polymorphonuclear leukocytes collected 4 h after injection of glycogen into the peritoneal cavity. The yield of the dihydroxy acid was 0.5 to 2%. The compound possesses three conjugated double bonds and was found to be stereochemically pure at C-5 and C-12. Incubation of the cells with 8,11,14-eicosatrienoic acid did not lead to the formation of the analogous triunsaturated dihydroxy acid.

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Metadata

Authors
Borgeat, P., & Samuelsson, B.
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
1979-04
Volume
254
Issue
8
Pages
2643-2646
ISSN
0021-9258 (ISSN-L)
OpenAlex
W1631595783
Cited by
648
References
0
FWCI
21.29
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Transformation of arachidonic acid by rabbit polymorphonuclear leukocytes. Formation of a novel dihydroxyeicosatetraenoic acid. https://app.cochat.ai/papers/10.1016/s0021-9258(17)30120-5
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Borgeat, P., & Samuelsson, B. (1979). Transformation of arachidonic acid by rabbit polymorphonuclear leukocytes. Formation of a novel dihydroxyeicosatetraenoic acid. Journal of Biological Chemistry. https://doi.org/10.1016/s0021-9258(17)30120-5

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.