(Q86677426)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24203404%20AND%20SRC:MED&resulttype=core&format=json

29 February 2020

title

Mass spectrometric analysis of four regioisomers of F2-isoprostanes formed by free radical oxidation of arachidonic acid (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24203404%20AND%20SRC:MED&resulttype=core&format=json

29 February 2020

author name string

R J Waugh

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24203404%20AND%20SRC:MED&resulttype=core&format=json

29 February 2020

R C Murphy

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24203404%20AND%20SRC:MED&resulttype=core&format=json

29 February 2020

publication date

1 May 1996

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24203404%20AND%20SRC:MED&resulttype=core&format=json

Journal of the American Society for Mass Spectrometry

29 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24203404%20AND%20SRC:MED&resulttype=core&format=json

29 February 2020

volume

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24203404%20AND%20SRC:MED&resulttype=core&format=json

29 February 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24203404%20AND%20SRC:MED&resulttype=core&format=json

29 February 2020

page(s)

490-499

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24203404%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1016/1044-0305(95)00709-1

29 February 2020

exact match

0 references

cites work

Free radical-induced generation of isoprostanes in vivo. Evidence for the formation of D-ring and E-ring isoprostanes.

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Isoleukotrienes are biologically active free radical products of lipid peroxidation

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Evidence that the F2-isoprostane, 8-epi-prostaglandin F2 alpha, is formed in vivo

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Fast atom bombardment and collision-induced dissociation of prostaglandins and thromboxanes: Some examples of charge remote fragmentation

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Cyclooxygenase-dependent formation of the isoprostane, 8-epi prostaglandin F2 alpha

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Glomerular actions of a free radical-generated novel prostaglandin, 8-epi-prostaglandin F2 alpha, in the rat. Evidence for interaction with thromboxane A2 receptors

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Quantification of noncyclooxygenase derived prostanoids as a marker of oxidative stress

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A series of prostaglandin F2-like compounds are produced in vivo in humans by a non-cyclooxygenase, free radical-catalyzed mechanism.

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Formation of novel non-cyclooxygenase-derived prostanoids (F2-isoprostanes) in carbon tetrachloride hepatotoxicity. An animal model of lipid peroxidation

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Mass spectrometry of prostanoids: F2-isoprostanes produced by non-cyclooxygenase free radical-catalyzed mechanism

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12 December 2020

Role of prostaglandin endoperoxides in the serum thiobarbituric acid reaction

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The F2-isoprostane, 8-epi-prostaglandin F2 alpha, a potent agonist of the vascular thromboxane/endoperoxide receptor, is a platelet thromboxane/endoperoxide receptor antagonist

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Analysis of hydroxy fatty acids as pentafluorobenzyl ester, trimethylsilyl ether derivatives by electron ionization gas chromatography/mass spectrometry

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The isoprostanes: novel markers of lipid peroxidation and potential mediators of oxidant injury

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12 December 2020