(Q34505052)

2 August 2017

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title

Polyphenolics of Salvia--a review (English)

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luteolin-7-O-β-glucuronide

2 August 2017

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ChEBI release 2020-05-28

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Salvia blepharophylla

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Salvia lavandulifolia

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(2S,3S,4R,5S,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid

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1-[4-[(2S,3R,4S,5S,6R)-6-[[(2R,3S,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]ethanone

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UYOUXKDGHGVDEM-UBLZNYDLSA-N

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5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

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luteolin 3'-O-glucuronide

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[(2R,3S,4S,5S,6S)-3,4,5-trihydroxy-6-[7-hydroxy-5-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate

isosalvianolic acid C

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(2R,3R)-2-[4-[(E)-3-[(1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-hydroxyphenoxy]-3-(3,4-dihydroxyphenyl)-3-hydroxypropanoic acid

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(2S)-2-[(1S,2R)-3-[(1S)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-2-(3,4-dihydroxyphenyl)-7,8-dihydroxy-1,2-dihydronaphthalene-1-carbonyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid

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4-hydroxybenzoic acid

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apigenin 7-rutinoside

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5,3'-Dihydroxy-7,4'-dimethoxyflavanone

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3,3'-di-O-methylquercetin

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6-Hydroxyluteolin 7-glucoside

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1-Hydroxypinoresinol 1-O-glucoside

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2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

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(2R)-2-[(E)-3-[4-[(E)-1-carboxy-2-(3,4-dihydroxyphenyl)ethenoxy]-3-hydroxyphenyl]prop-2-enoyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid

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(E)-3-[3-[[(Z)-1-Carboxy-2-(3,4-dihydroxyphenyl)ethenyl]oxy]-4-hydroxyphenyl]propenoic acid 1-[(R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethyl] ester

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2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

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3',4',5,7-tetrahydroxy-3-methoxyflavone

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apigenin 7,4'-dimethyl ether

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5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

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7-(beta-D-Galactopyranosyloxy)-3',4',5-trihydroxy-3-methoxyflavone

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Quercetin4'-O-glucuronide

Dimethyl Lithospermate

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6,7-dimethoxy-2-(4-methoxyphenyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

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(1R,2S,6S,7R,8R,9R)-10-[(E)-3-[(1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-8-(3,4-dihydroxyphenyl)-2,6-dihydroxy-4-oxo-3-oxatricyclo[5.2.2.02,6]undec-10-ene-9-carboxylic acid

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(2R)-2-[(E)-3-[4-(6,7-dihydroxy-2-oxochromen-3-yl)oxy-3-hydroxyphenyl]prop-2-enoyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid

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(2R,3R)-4-[(1E)-3-[(1R)-1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxo-1-propen-1-yl]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-7-hydroxy-3-benzofurancarboxylic acid

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(2R)-2-[(E)-3-[2-[(E)-3-[(1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-1-(3,4-dihydroxyphenyl)-3-oxoprop-1-en-2-yl]-4,5-dihydroxyphenyl]prop-2-enoyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid

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3',5-Dihydroxy-4',7-dimethoxyflavone

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3-[(2S,3R,4R,5S,6S)-4,5-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one

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(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid

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2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

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(2S,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid

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5-hydroxy-7-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[4-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one

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(2R)-3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate

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7,3',4'-Tri-O-methylluteolin

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Benzenepropanoic acid, alpha,3,4-trihydroxy-, (aS)-

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2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

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(12R)-4,5,17-trihydroxy-11-oxo-2-oxatetracyclo[8.7.1.03,8.014,18]octadeca-1(17),3(8),4,6,9,14(18),15-heptaene-12-carboxylic acid

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5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one

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WLRPCCKPZVGSQJ-AVHNDQTMSA-N

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AFOQFWOYGIZHHU-QBMVVDGVSA-N

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5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2R,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one

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(2S)-2-[(1R,2R,3R,4R)-2-[(1R)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-3,4-bis(3,4-dihydroxyphenyl)cyclobutanecarbonyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid

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6,7,3',4'-Tetramethoxyflavone

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2-hydroxy-3-(3,4-dihydroxyphenyl)propanoic acid

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6-[3-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-3-(3,4-dihydroxyphenyl)cyclohex-5-ene-1,2,4-tricarboxylic acid

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3-({3-[(2-carboxyacetyl)oxy]-4,5-dihydroxy-6-{[7-hydroxy-2-(4-oxocyclohexa-2,5-dien-1-ylidene)-3-{[3,4,5-trihydroxy-6-({[3-(4-hydroxyphenyl)prop-2-enoyl]oxy}methyl)oxan-2-yl]oxy}chromen-5-yl]oxy}oxan-2-yl}methoxy)-3-oxopropanoic acid

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3-(3,4-Dihydroxyphenyl)-2-[3-(2,3,10-trihydroxybenzo[b][1]benzoxepin-7-yl)prop-2-enoyloxy]propanoic acid

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3-(3,4-Dihydroxyphenyl)-2-[3-[2-(3,4-dihydroxyphenyl)-7-hydroxy-1-benzofuran-4-yl]prop-2-enoyloxy]propanoic acid

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2-[3-[3-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethenoxy]-4-hydroxyphenyl]prop-2-enoyloxy]-3-(3,4-dihydroxyphenyl)propanoic acid

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6-[3-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-(3,4-dihydroxyphenyl)-2,3-dihydro-1,4-benzodioxine-3-carboxylic acid

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(+)-Lithospermic acid

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3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid

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N-Boc-amino-(3-thienyl)aceticacid

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2-[4-[3-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-hydroxyphenoxy]-3-(3,4-dihydroxyphenyl)-3-hydroxypropanoic acid

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2-[3-[4-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethenoxy]-3-hydroxyphenyl]prop-2-enoyloxy]-3-(3,4-dihydroxyphenyl)propanoic acid

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3-[2-[2-(3,4-Dihydroxyphenyl)ethenyl]-3,4-dihydroxyphenyl]prop-2-enoic acid

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3-(3,4-Dihydroxyphenyl)-2-[3-[4-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyloxy]propanoic acid

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Methyl 3-(3,4-dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoate

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Rosmarinus officinalis

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Yinrong Lu

1

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2 August 2017

L Yeap Foo

series ordinal

2

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2 August 2017

publication date

January 2002

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16 September 2022

24

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inferred from page(s)

published in

Phytochemistry

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2 August 2017

volume

59

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2 August 2017

issue

2

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2 August 2017

page(s)

117-140

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Flavone glycosides of Salvia triloba

2 August 2017

cites work

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7 January 2021

Phytochemical study of Salvia moorcroftiana

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7 January 2021

Salvianolic acid J, a depside from Salvia flava

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7 January 2021

Stereostructure of Salvianolic Acid B and Isolation of Salvianolic Acid C from Salvia miltiorrhiza

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7 January 2021

Salvianolic Acids D and E: Two New Depsides from Salvia miltiorrhiza

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7 January 2021

Flavonoids and Phenolic Acids of Sage: Influence of Some Agricultural Factors

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7 January 2021

[Flavones from Salvia officinalis L. 22. Components of Salvia off. L]

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7 January 2021

Structure elucidation and total synthesis of new tanshinones isolated from Salvia miltiorrhiza Bunge (Danshen)

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7 January 2021

Inhibitory effect of caffeic acid analogues isolated from Salviae Miltiorrhizae Radix against 1,1-diphenyl-2-picrylhydrazyl radical

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7 January 2021

Demonstration of the myocardial salvage effect of lithospermic acid B isolated from the aqueous extract of Salvia miltiorrhiza

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7 January 2021

Terpenoids and flavonoids from Salvia cyanescens

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7 January 2021

Flavonoids from Salvia texana

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7 January 2021

Terpenes and flavones of Salvia cardiophylla

1 reference

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7 January 2021

Preventive effect of lithospermate B from Salvia miltiorhiza on experimental hepatitis induced by carbon tetrachloride or D-galactosamine/lipopolysaccharide.

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7 January 2021

Flavonoids from Salvia syriaca

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7 January 2021

Endothelium-dependent vasodilator effects of the extract from Salviae Miltiorrhizae radix. A study on the identification of lithospermic acid B in the extracts.

1 reference

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7 January 2021

Hypotensive effects of lithospermic acid B isolated from the extract of Salviae miltiorrhizae Radix in the rat.

1 reference

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7 January 2021

Antioxidant effect ofSalvia miltiorrhiza

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7 January 2021

Comparative study of seventeen Salvia plants: aldose reductase inhibitory activity of water and MeOH extracts and liquid chromatography-mass spectrometry (LC-MS) analysis of water extracts

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7 January 2021

Isolation of inhibitors of adenylate cyclase from dan-shen, the root of Salvia miltiorrhiza

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7 January 2021

Structure of anthocyanins in scarlet, purple, and blue flowers of salvia

1 reference

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7 January 2021

Salvianolic Acid A, a New Depside from Roots of Salvia miltiorrhiza

1 reference

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7 January 2021

Protective action of seven natural phenolic compounds against peroxidative damage to biomembranes

1 reference

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7 January 2021

Rosmarinic acid derivatives from Salvia officinalis

1 reference

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7 January 2021

Flavonoid and phenolic glycosides from Salvia officinalis

1 reference

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7 January 2021

Salvianolic acid L, a potent phenolic antioxidant from Salvia officinalis

1 reference

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7 January 2021

Sagecoumarin, a novel caffeic acid trimer from Salvia officinalis

1 reference

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7 January 2021

Antibacterial activity studies of flavonoids from Salvia palaestina

1 reference

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7 January 2021

Production of Lithospermic Acid B and Rosmarinic Acid in Callus Tissue and Regenerated Plantlets of Salvia miltiorrhiza

1 reference

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7 January 2021

Tannins of Salvia officinalis and their changes during storage (author's transl)

1 reference

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7 January 2021

Metabolism of rosmarinic acid in rats

1 reference

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7 January 2021

Flavonoids from Salvia nicolsoniana

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900415-0

7 January 2021

An abietane diterpenoid from Salvia sapinae

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900415-0

7 January 2021

A secoisolariciresinol branched fatty diester from Salvia plebeia seed

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900415-0

7 January 2021

Structure of a secoisolariciresinol diester from Salvia plebeia seed

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900415-0

7 January 2021

Inhibition of collagen hydroxylation by lithospermic acid magnesium salt, a novel compound isolated from Salviae miltiorrhizae Radix

1 reference

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7 January 2021

Identification of malonated anthocyanins in the liliaceae and labiatae

1 reference

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7 January 2021

A blue pigment complex in flowers of Salvia patens

1 reference

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7 January 2021

Four New Caffeic Acid Metabolites, Yunnaneic Acids E-H, from Salvia yunnanensis.

1 reference

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7 January 2021

Isolation and Characterization of Yunnaneic Acids A−D, Four Novel Caffeic Acid Metabolites fromSalvia yunnanensis

1 reference

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7 January 2021

Aldose reductase inhibitory constituents of the root of Salvia miltiorhiza Bunge

1 reference

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7 January 2021

Constituents of Roots of Salvia deserta SCHANG. (Xinjiang-Danshen)

1 reference

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7 January 2021

Dimalonated anthocyanins from the flowers of Salvia splendens and S. coccinea

1 reference

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7 January 2021

Terpenoids and flavonoids from the aerial parts of Salvia candidissima

1 reference

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7 January 2021

Sesterterpenes and other constituents of Salvia yosgadensis

1 reference

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7 January 2021

A New Flavone from Salvia triloba L.f (Labiatae)

1 reference

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7 January 2021

Flavonoidal and other compounds of Salvia aethiopis

1 reference

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7 January 2021

Flavonoids of Salvia tomentosa (Labiatae)

1 reference

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7 January 2021

Further Flavones and Triterpenes and the New 6-Hydroxyluteolin 5-β-D-Glucoside From Salvia tomentosa

1 reference

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7 January 2021

Flavonoids and Terpenoids From Salvia verticillata and Salvia pinnata

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900415-0

7 January 2021

Diterpenoids from Salvia heldrichiana

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900415-0

7 January 2021

An abietane diterpene and two phenolics from Salvia forskahlei.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900415-0

7 January 2021

Flavonoid cellobiosides from Salvia uliginosa

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900415-0

7 January 2021

Isolation and structural elucidation of two new glycosides from sage (Salvia officinalis L.)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900415-0

7 January 2021

Antioxidative Phenolic Compounds from Sage (Salvia officinalis)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900415-0

7 January 2021

Antioxidative phenolic glycosides from sage (Salvia officinalis)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900415-0

7 January 2021

Untersuchungen über die Anthocyane. XI. Über das Anthocyan der rotblühenden Salviaarten

1 reference

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7 January 2021

Notes: Exudate Flavonoids of Some Salvia and a Trichostema Species

1 reference

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7 January 2021

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900415-0

1 reference

7 January 2021

Evaluation of Caffeic Acid Analogues using a Cultured Renal Epithelial Cell Line, LLC-PK<SUB>1</SUB>

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900415-0

7 January 2021

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1 reference

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1 reference

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7 January 2021

Antioxidative components of tanshen (Salvia miltiorhiza Bung)

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900415-0

7 January 2021

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1 reference

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1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900415-0

7 January 2021

10.1016/S0031-9422(01)00415-0

Identifiers

DOI

1 reference

2 August 2017

1 reference