Novel indole-type glucosinolates from woad (Isatis tinctoria L.) (Q59504320)

[(Z)-[(3R)-3-hydroxy-1-{[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}pent-4-en-1-ylidene]amino]oxysulfonic acid

1 reference

[(Z)-[(3R)-3-({2-[(3S)-2-hydroxy-3H-indol-3-yl]acetyl}oxy)-1-{[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}pent-4-en-1-ylidene]amino]oxysulfonic acid

1 reference

[(Z)-[(3R)-3-({2-[(3S)-2,3-dihydroxyindol-3-yl]acetyl}oxy)-1-{[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}pent-4-en-1-ylidene]amino]oxysulfonic acid

1 reference

1 reference

[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1Z)-2-(1H-indol-3-yl)-N-sulfooxyethanimidothioate

1 reference

[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1Z)-N-sulfooxypent-4-enimidothioate

1 reference

[(Z)-[2-(4-hydroxy-1H-indol-3-yl)-1-{[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino]oxysulfonic acid

1 reference

1 reference

[(Z)-[2-(1-methoxyindol-3-yl)-1-{[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanyl}ethylidene]amino]oxysulfonic acid

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3-Butenylglucosinolate

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Nicolas Fabre

2

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Sabine Montaut

object named as

Sabine Montaut

4

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author name string

Antoine Fréchard

1

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Christophe Péan

3

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Marie-Thérèse Fauvel

5

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Patrick Rollin

6

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Isabelle Fourasté

The chemical diversity and distribution of glucosinolates and isothiocyanates among plants

7

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publication date

December 2001

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16 September 2022

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42

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page(s)

9015-9017

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issue

51

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cites work

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https://api.crossref.org/works/10.1016%2FS0040-4039%2801%2902015-9

7 January 2021

Bioactive organosulfur phytochemicals in Brassica oleracea vegetables--a review

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4039%2801%2902015-9

7 January 2021

A comparison of the individual and collective effects of four glucosinolate breakdown products from brussels sprouts on induction of detoxification enzymes

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4039%2801%2902015-9

7 January 2021

Comprehensive chromatographic and spectroscopic methods for the separation and identification of intact glucosinolates

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4039%2801%2902015-9

7 January 2021

Three glucosinolates from seeds of Brassica juncea

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4039%2801%2902015-9

7 January 2021

Isolation of Four New Indole-3-acetic Acid (IAA) Oxidative Metabolites, a Pair of Diasteromers 5-O-β-D-glucopyranosyl 3,5-Dihydroxy-2-indolinone-3-acetic Acid and 5-O-β-D-cellobiosyl 3,5-Dihydroxy-2-indolinone-3-acetic Acid from Rice Bran

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4039%2801%2902015-9

7 January 2021

Metabolism of indole-3-acetic acid in Arabidopsis.

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4039%2801%2902015-9

7 January 2021

Free and conjugated indole-3-acetic Acid in developing bean seeds

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4039%2801%2902015-9

7 January 2021

Metabolism of indole-3-acetic acid by orange (Citrus sinensis) flavedo tissue during fruit development

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4039%2801%2902015-9

7 January 2021

Flavonol oligosaccharides from the seeds of Aesculus hippocastanum

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4039%2801%2902015-9

7 January 2021