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Inositol Derivatives and Phenolic Compounds from the Roots of Taraxacum coreanum

In this study, the characterization of chemical constituents and biological activity of the roots of (Asteraceae) was attempted. Phytochemical investigation of the roots of led to the isolation of two new inositol derivatives, taraxinositols A ( ) and B ( ), and a new phenolic compound, taraxinol (...

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Published in:Molecules (Basel, Switzerland) Switzerland), 2017-08, Vol.22 (8), p.1349
Main Authors: Mo, Eun Jin, Ahn, Jong Hoon, Jo, Yang Hee, Kim, Seon Beom, Hwang, Bang Yeon, Lee, Mi Kyeong
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description In this study, the characterization of chemical constituents and biological activity of the roots of (Asteraceae) was attempted. Phytochemical investigation of the roots of led to the isolation of two new inositol derivatives, taraxinositols A ( ) and B ( ), and a new phenolic compound, taraxinol ( ), together with twenty known compounds including four inositol derivatives, -inositol-1,4-bis (4-hydroxybenzeneacetate) ( ), -inositol-1,5-bis(4- hydroxybenzeneacetate) ( ), -inositol-2,3-bis (4-hydroxybenzeneacetate) ( ) and -inositol- 1,2,3-tris (4-hydroxybenzeneacetate) ( ), nine phenolic compounds: -hydroxybenzaldehyde ( ), vanillin ( ), syringaldehyde ( ), vanillic acid ( ), 4-methoxyphenylacetic acid ( ), 4-hydroxy- phenylacetic acid methyl ester ( ), optivanin ( ), isoferulic acid ( ) and dihydroconiferyl alcohol ( ), four coumarins: nodakenetin ( ), decursinol ( ), prangol ( ) and isobyakangelicin ( ), and three lignans: syringaresinol-4'- -β-d-glucoside ( ), syringaresinol ( ), and pinoresinol ( ). The structures of isolated compounds were determined on the basis of spectroscopic analysis. Among the isolated compounds, vanillic acid, isoferulic acid and syringaresinol showed radical scavenging activity with IC values ranging from 30.4 to 75.2 μM.
doi_str_mv 10.3390/molecules22081349
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Phytochemical investigation of the roots of led to the isolation of two new inositol derivatives, taraxinositols A ( ) and B ( ), and a new phenolic compound, taraxinol ( ), together with twenty known compounds including four inositol derivatives, -inositol-1,4-bis (4-hydroxybenzeneacetate) ( ), -inositol-1,5-bis(4- hydroxybenzeneacetate) ( ), -inositol-2,3-bis (4-hydroxybenzeneacetate) ( ) and -inositol- 1,2,3-tris (4-hydroxybenzeneacetate) ( ), nine phenolic compounds: -hydroxybenzaldehyde ( ), vanillin ( ), syringaldehyde ( ), vanillic acid ( ), 4-methoxyphenylacetic acid ( ), 4-hydroxy- phenylacetic acid methyl ester ( ), optivanin ( ), isoferulic acid ( ) and dihydroconiferyl alcohol ( ), four coumarins: nodakenetin ( ), decursinol ( ), prangol ( ) and isobyakangelicin ( ), and three lignans: syringaresinol-4'- -β-d-glucoside ( ), syringaresinol ( ), and pinoresinol ( ). The structures of isolated compounds were determined on the basis of spectroscopic analysis. Among the isolated compounds, vanillic acid, isoferulic acid and syringaresinol showed radical scavenging activity with IC values ranging from 30.4 to 75.2 μM.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>28805750</pmid><doi>10.3390/molecules22081349</doi><oa>free_for_read</oa></addata></record>
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subjects Acids
Alcohols
antioxidant
Antioxidants - chemistry
Antioxidants - pharmacology
Biological activity
Chromatography, High Pressure Liquid - methods
Coumarins - chemistry
Furans - chemistry
Glucosides - chemistry
Humans
Hydroxybenzaldehydes
Inhibitory Concentration 50
Inositol
Inositol - chemistry
Inositol - isolation & purification
Inositol 1,4,5-trisphosphate receptors
Lignans
Lignans - chemistry
Magnetic Resonance Spectroscopy - methods
Phenol - chemistry
Phenol - isolation & purification
phenolic
Phenolic compounds
Phenols
Phenylacetic acid
Plant Extracts - chemistry
Plant Extracts - isolation & purification
Plant Roots - chemistry
Receptors, Scavenger - chemistry
Receptors, Scavenger - metabolism
Roots
Syringaldehyde
Taraxacum - chemistry
Taraxacum coreanum
Vanillic acid
Vanillin
title Inositol Derivatives and Phenolic Compounds from the Roots of Taraxacum coreanum
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