A comprehensive metabolite profiling of Isatis tinctoria leaf extracts (Q33442716)

26 July 2017

A comprehensive metabolite profiling of Isatis tinctoria leaf extracts (English)

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(9Z,12Z,15Z)-(S)-2-Hydroxy-3-(((2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)propyl octadeca-9,12,15-trienoate

26 July 2017

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N-formylanthranilic acid

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indole-3-carboxaldehyde

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2'-hydroxy-1'H-[2,3'-biindol]-3-one

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3'-hydroxy-1'H-[2,2'-biindol]-3-one

10-Hydroxyphaeophorbide

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(10E,12E,14E,16S)-16-hydroxy-9-oxooctadeca-10,12,14-trienoic acid

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5-Hydroxy-2-oxyindole

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indole-3-acetonitrile

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2-(1H-indol-3-ylmethylidene)-1H-indol-3-one

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(9R,10E,12Z,15Z)-9-hydroxyoctadeca-10,12,15-trienoic acid

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2'-hydroxy-1'H-[3,3'-biindol]-2-one

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(2E)-2-(1H-indol-3-ylmethylidene)-1H-indol-3-one

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(11E)-11-eicosenoic acid

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2-[3-[(2E)-2-(3-oxo-1H-indol-2-ylidene)indol-3-yl]-1H-indol-2-yl]indol-3-one

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(10E,12E,14E,16R)-16-hydroxy-9-oxooctadeca-10,12,14-trienoic acid

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(9E,12Z)-linoleic acid

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(10E)-9-oxooctadeca-10,12,15-trienoic acid

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(10E,12Z,15Z)-9-oxooctadeca-10,12,15-trienoic acid

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octadeca-9,12-dienoic acid

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2-[3-[2-(3-oxo-1H-indol-2-ylidene)indol-3-yl]-1H-indol-2-yl]indol-3-one

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[3,3'-biindolylidene]-2,2'-diol

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3

Matthias Hamburger

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26 July 2017

Tobias Mohn

1

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PubMed ID

19467550

retrieved

26 July 2017

Inken Plitzko

series ordinal

2

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26 July 2017

May 2009

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full work available at URL

Crossref

retrieved

16 September 2022

https://edoc.unibas.ch/953/1/Dissertation_Tobias_Mohn.pdf

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19 March 2024

https://api.unpaywall.org/v2/10.1016/j.phytochem.2009.04.019?email=unpaywall_01@example.com

published in

Phytochemistry

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26 July 2017

70

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924-934

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26 July 2017

7

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https://api.unpaywall.org/v2/10.1016/j.phytochem.2009.04.019?email=unpaywall_01@example.com

26 July 2017

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19 March 2024

access restriction status

open access

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based on heuristic

inferred from online access status

cites work

Biotransformation of Pinoresinol Diglucoside to Mammalian Lignans by Human Intestinal Microflora, and Isolation of Enterococcus faecalis Strain PDG-1 Responsible for the Transformation of (+)-Pinoresinol to (+)-Lariciresinol

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.51.508

Medicinal foodstuffs. XIV. On the bioactive constituents of moroheiya. (2): New fatty acids, corchorifatty acids A, B, C, D, E, and F, from the leaves of Corchorus olitorius L. (Tiliaceae): structures and inhibitory effect on NO production in mouse

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.46.1008

Identifiers

DOI

10.1016/J.PHYTOCHEM.2009.04.019

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26 July 2017

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