From retrospective assessment to prospective decisions in natural product isolation: HPLC-SPE-NMR analysis of Carthamus oxyacantha (Q34068783)

30 July 2017

title

From retrospective assessment to prospective decisions in natural product isolation: HPLC-SPE-NMR analysis of Carthamus oxyacantha (English)

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octadeca-9,11-dienoic acid

30 July 2017

main subject

Carthamus oxyacanthus

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(2S,3R,4S,5R,6R)-2-[2-[(3R,5R,6R,9R)-9-hydroxy-6-methyl-10-methylidenespiro[4.5]decan-3-yl]propan-2-yloxy]-6-methyloxane-3,4,5-triol

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(4R)-4-hydroxynon-2-enoic acid

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rel-(2R,5S,10S)-6,10-Dimethyl-2-[(1-methyl-1-beta-D-fucopyranosyloxy)ethyl]spiro[4.5]dec-6-en-8-one

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13-Oxo-9,11-octadecadienoic acid

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octadeca-9,12-dienoic acid

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(2S,3R,4S,5R,6R)-2-[2-[(3S,5S,6R)-6,10-dimethylspiro[4.5]dec-9-en-3-yl]propan-2-yloxy]-6-methyloxane-3,4,5-triol

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rel-(4S,5S,7R)-1,4-Dimethyl-7-[(1-methyl-1-beta-D-fucopyranosyloxy)ethyl]spiro[4.4]non-1-ene-2-carbaldehyde

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9-hydroxy-10,12-octadecadienoic acid

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(3R,5R,6R)-6-methyl-10-methylidene-3-[2-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxypropan-2-yl]spiro[4.5]decan-9-one

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(2Z,4R)-hydroxynon-2-enoic acid

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(9Z,11Z)-9,11-octadecadienoic acid

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9-hydroxy-10E,12Z-octadecadienoic acid

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(2S,3R,4S,5R,6R)-2-[2-[(3R,5R,6R,9R)-9-hydroperoxy-6-methyl-10-methylidenespiro[4.5]decan-3-yl]propan-2-yloxy]-6-methyloxane-3,4,5-triol

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(9E,11E)-13-oxooctadeca-9,11-dienoic acid

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(3S)-4-[(3,4-dimethoxyphenyl)methyl]-3-hydroxy-3-[[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl]oxolan-2-one

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4-(beta-D-glucopyranosyloxy)-3-methoxybenzoic acid

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(11E)-13-oxooctadeca-9,11-dienoic acid

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Jeweled distaff thistle

object named as

Carthamus oxyacantha

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2-[2-(6,10-Dimethylspiro[4.5]dec-9-en-3-yl)propan-2-yloxy]-6-methyloxane-3,4,5-triol

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6-Methyl-10-methylidene-3-[2-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxypropan-2-yl]spiro[4.5]decan-9-one

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2-[2-(9-Hydroperoxy-6-methyl-10-methylidenespiro[4.5]decan-3-yl)propan-2-yloxy]-6-methyloxane-3,4,5-triol

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2-[2-(9-Hydroxy-6-methyl-10-methylidenespiro[4.5]decan-3-yl)propan-2-yloxy]-6-methyloxane-3,4,5-triol

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Kenneth T Johansen

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30 July 2017

Sileshi G Wubshet

series ordinal

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30 July 2017

Nils T Nyberg

series ordinal

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Jerzy W Jaroszewski

series ordinal

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30 July 2017

publication date

7 November 2011

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Journal of Natural Products

30 July 2017

published in

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30 July 2017

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30 July 2017

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30 July 2017

page(s)

2454-2461

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Advances in Techniques for Profiling Crude Extracts and for the Rapid Identificationof Natural Products: Dereplication, Quality Control and Metabolomics

30 July 2017

cites work

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Modern approaches in the search for new lead antiparasitic compounds from higher plants

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24 October 2022

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Vetispirane sesquiterpene glucosides from flue-cured virginia tobacco: structure, absolute stereochemistry, and synthesis. X-Ray structure of the p-bromobenzenesulphonate of one of the derived aglycones

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COCI

reference URL

Accelerated Dereplication of Natural Products, Supported by Reference Libraries

5 March 2023

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COCI

reference URL

Natürlich vorkommende Terpen-Derivate, 74 Notiz über ein neues Sesquiterpen-Glycosid aus Carthamus oxyacantha

8 July 2023

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9 March 2024

https://opencitations.net/index/api/v1/citations/10.1002/CBER.19761091224

New sesquiterpene hydroperoxides with trypanocidal activity from Pogostemon cablin

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.52.1495

Tracheolospermum. II Lignans from Trachelospermum asiaticum.

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.34.4340

Lignans of Trachelospermum asiaticum var. intermedium. I.Isolation and Structures of Arctiin, Matairesinoside and Tracheloside

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.20.2710

Identifiers

DOI

10.1021/NP200780M

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30 July 2017

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