New bioactive oxylipins formed by non-enzymatic free-radical-catalyzed pathways: the phytoprostanes (Q37605602)

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scientific article published on 30 September 2009

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English	New bioactive oxylipins formed by non-enzymatic free-radical-catalyzed pathways: the phytoprostanes	scientific article published on 30 September 2009

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scholarly article

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Europe PubMed Central

PubMed publication ID

19789901

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21 August 2017

review article

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Europe PubMed Central

title

New bioactive oxylipins formed by non-enzymatic free-radical-catalyzed pathways: the phytoprostanes (English)

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Europe PubMed Central

PubMed publication ID

19789901

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21 August 2017

author name string

Thierry Durand

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1

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Europe PubMed Central

PubMed publication ID

19789901

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21 August 2017

Valérie Bultel-Poncé

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2

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Europe PubMed Central

PubMed publication ID

19789901

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21 August 2017

Alexandre Guy

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3

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Europe PubMed Central

PubMed publication ID

19789901

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21 August 2017

Susanne Berger

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4

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Europe PubMed Central

PubMed publication ID

19789901

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21 August 2017

Martin J Mueller

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5

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Europe PubMed Central

PubMed publication ID

19789901

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21 August 2017

Jean-Marie Galano

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6

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Europe PubMed Central

PubMed publication ID

19789901

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21 August 2017

publication date

30 September 2009

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Europe PubMed Central

PubMed publication ID

19789901

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21 August 2017

published in

Lipids

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Europe PubMed Central

PubMed publication ID

19789901

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21 August 2017

volume

44

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Europe PubMed Central

PubMed publication ID

19789901

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21 August 2017

issue

10

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Europe PubMed Central

PubMed publication ID

19789901

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21 August 2017

page(s)

875-888

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Europe PubMed Central

PubMed publication ID

19789901

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21 August 2017

cites work

Synthesis of prostaglandin and phytoprostane B1 via regioselective intermolecular Pauson-Khand reactions

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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B1-phytoprostanes trigger plant defense and detoxification responses

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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General detoxification and stress responses are mediated by oxidized lipids through TGA transcription factors in Arabidopsis

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Analysis of oxidative stress and wound-inducible dinor isoprostanes F(1) (phytoprostanes F(1)) in plants

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Prostaglandins. IX. Synthesis of (+-)-prostaglandin E1, (+-)-11-deoxyprostaglandins E1,F1.alpha., and F1.beta., and (+-)-9-oxo-13-cis-prostenoic acid by conjugate addition of vinylcopper reagents

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https://pubmed.ncbi.nlm.nih.gov/19789901

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Immunomodulatory Mediators from Pollen Enhance the Migratory Capacity of Dendritic Cells and License Them for Th2 Attraction

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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F4-Isoprostanes: A Novel Class of Prostanoids Formed during Peroxidation of Docosahexaenoic Acid (DHA)

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https://pubmed.ncbi.nlm.nih.gov/19789901

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Beyond prostaglandins--chemistry and biology of cyclic oxygenated metabolites formed by free-radical pathways from polyunsaturated fatty acids

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https://pubmed.ncbi.nlm.nih.gov/19789901

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Evidence from heterologous expression of glutathione S-transferases A and A1 of the plaice (Pleuronectes platessa) that their endogenous role is in detoxification of lipid peroxidation products

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https://pubmed.ncbi.nlm.nih.gov/19789901

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Total synthesis of prostaglandins. II. Prostaglandin E 1

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Nomenclature of isoprostanes: a proposal.

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https://pubmed.ncbi.nlm.nih.gov/19789901

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Measurement of F(2)-isoprostanes as an index of oxidative stress in vivo

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Singlet oxygen is the major reactive oxygen species involved in photooxidative damage to plants.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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General strategy for the synthesis of B1 phytoprostanes, dinor isoprostanes, and analogs

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Biosynthesis of 14,15-dehydro-12-oxo-phytodienoic acid and related cyclopentenones via the phytoprostane D(1) pathway

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Biologically active oxidized lipids (phytoprostanes) in the plant diet and parenteral lipid nutrition

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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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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Total Synthesis of the Four Enantiomerically Pure Diasteroisomers of the Phytoprostanes E1Type II and of the 15-E2t-Isoprostanes

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Cyclopentenone isoprostanes induced by reactive oxygen species trigger defense gene activation and phytoalexin accumulation in plants

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Reactive electrophilic oxylipins: pattern recognition and signalling

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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A flexible synthesis of the phytoprostanes B1 type I and II.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Evidence for the formation of dinor isoprostanes E1 from alpha-linolenic acid in plants

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Intracellular Levels of Free Linolenic and Linoleic Acids Increase in Tomato Leaves in Response to Wounding

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Impact of cyclopentenone-oxylipins on the proteome of Arabidopsis thaliana

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Prostaglandins. X. Synthesis of prostaglandin models and prostaglandins by conjugage addition of a functionalized organocopper reagent

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Total synthesis of the eight diastereomers of the syn-anti-syn phytoprostanes F1 types I and II

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Flaxseed oil supplementation increases plasma F1-phytoprostanes in healthy men.

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12 December 2020

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Formation of isoprostane F(2)-like compounds (phytoprostanes F(1)) from alpha-linolenic acid in plants

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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The isoprostanoid pathway in plants

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Formation of reactive cyclopentenone compounds in vivo as products of the isoprostane pathway

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Archetype signals in plants: the phytoprostanes

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12 December 2020

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Immunomodulatory effects of aqueous birch pollen extracts and phytoprostanes on primary immune responses in vivo.

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Pollen-associated phytoprostanes inhibit dendritic cell interleukin-12 production and augment T helper type 2 cell polarization

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Formation of isoprostane-like compounds (neuroprostanes) in vivo from docosahexaenoic acid

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Oxylipin analysis methods

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Total synthesis and biological activity of 13,14-dehydro-12-oxo-phytodienoic acids (deoxy-J1-phytoprostanes).

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19789901

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12 December 2020

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Identifiers

DOI

10.1007/S11745-009-3351-1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19789901

retrieved

21 August 2017

PubMed publication ID

19789901

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19789901

retrieved

21 August 2017

ResearchGate publication ID

26856673

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