(Q44340752)

2 December 2017

title

Synthesis and antioxidant properties of a new lipophilic ascorbic acid analogue (English)

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2 December 2017

4

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2 December 2017

Philippe Cotelle

1

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2 December 2017

Nicole Cotelle

series ordinal

2

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2 December 2017

Elisabeth Teissier

series ordinal

3

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2 December 2017

language of work or name

English

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publication date

1 March 2003

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Bioorganic & Medicinal Chemistry

2 December 2017

published in

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2 December 2017

volume

11

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2 December 2017

issue

6

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2 December 2017

page(s)

1087-1093

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Lipid peroxidation: its mechanism, measurement, and significance

2 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

Antioxidant defense: vitamins E and C and carotenoids

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

Evidence from cancer intervention and biomarker studies and the development of biochemical markers

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

The effects of ascorbate and dehydroascorbate on the oxidation of low-density lipoprotein.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

Antioxidant properties of novel lipophilic ascorbic acid analogues

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

Novel 4,5-diaryl-3-hydroxy-2(5H)-furanones as anti-oxidants and anti-inflammatory agents.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

Novel antioxidant agents deriving from molecular combinations of vitamins C and E analogues: 3,4-dihydroxy-5(R)

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

Antioxidant activity and xanthine oxidase inhibition activity of reductic acid: ascorbic acid analogue

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

Synthesis and antitumor activities of novel pyrimidine derivatives of 2,3-O,O-dibenzyl-6-deoxy-L-ascorbic acid and 4,5-didehydro-5,6- dideoxy-L-ascorbic acid

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

Metabolic products of Aspergillus terreus. IX. Biosynthesis of butyrolactone derivatives isolated from strains IFO 8835 and 4100.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

Suillusin, a unique benzofuran from the mushroom Suillus granulatus

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

Antioxidant properties of hydroxy-flavones

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

New bis-catechols 5-lipoxygenase inhibitors

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

Antioxidant properties of di-tert-butylhydroxylated flavonoids

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

Continuous monitoring of in vitro oxidation of human low density lipoprotein

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

AM1-SM2 Calculations Model the Redox Potential of Nitroxyl Radicals Such as TEMPO.

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

A simplification of the protein assay method of Lowry et al. which is more generally applicable

1 reference

https://api.crossref.org/works/10.1016%2FS0968-0896%2802%2900446-7

7 January 2021

Studies on the metabolic products of Aspergillus terreus. III. Metabolites of the strain IFO 8835. 1.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.25.2593

Identifiers

DOI

10.1016/S0968-0896(02)00446-7

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2 December 2017

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