(Q44565445)

4 December 2017

title

Acylated flavonoid and phenylethanoid glycosides from Marrubium velutinum (English)

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SAXAVBJEDNTTOS-VAEKSEKFSA-N

4 December 2017

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[2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate

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Chrysoeriol 7-O-(3'',6''-di-O-E-p-coumaroyl)-beta-D-glucopyranoside

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3''-O-(4-Hydroxycinnamoyl)cosmosiin

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isorhamnetin 3-O-glucoside

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6''-O-beta-D-Glucopyranosylmartynoside

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[(2S,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-[[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate

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[(2R,3R,4S,5R,6S)-3,5-dihydroxy-6-{[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy}-4-{[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}oxan-2-yl]methyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

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SZACDOIDSPMWRE-SEAGDCMCSA-N

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[(2S,3S,4R,5S,6R)-3,5-dihydroxy-6-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxy-4-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate

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HLELABHGAXFZDU-NANSPCQOSA-N

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Isorhamnetin 3-glucoside

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[(2R,3S,4S,5R,6S)-6-{[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl (2E)-3-(4-hydroxyphenyl)prop-2-enoate

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HLELABHGAXFZDU-UQCUAMOISA-N

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(1S,4aR,5S,7R,7aR)-7-methyl-1-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4a,5,7-triol

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[(2R,3R,4R,5R,6R)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

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

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QFUYJSDAALMTEV-WOMSQKRTSA-N

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

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XLDOANLTPPTGQN-ZLJNPLPMSA-N

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SZACDOIDSPMWRE-ZFNPRWKESA-N

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[(2R,3R,4S,5S,6S)-3,5-dihydroxy-6-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxy-4-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate

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Quercetin 3-O-(6''-acetyl-glucoside)

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

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1

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4 December 2017

2

Helen Skaltsa

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4 December 2017

3

Jörg Heilmann

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4 December 2017

Otto Sticher

4

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4 December 2017

language of work or name

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September 2003

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16 September 2022

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4 December 2017

volume

64

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4 December 2017

issue

2

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4 December 2017

page(s)

655-660

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Phenylpropanoid glycosides from Marrubium alysson

4 December 2017

cites work

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https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Phenylethanoid glycosides from Globularia trichosantha

1 reference

https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Stachysetin, a diapigenin-7-glucoside-p,p′-dihydroxy-truxinate from Stachys aegyptiaca

1 reference

https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Structure of Forsythoside B, an Antibacterial Principal of Forsythia koreana Stems

1 reference

https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Structures of magnolosides B and C, novel phenylpropanoid glycosides with allopyranose as core the sugar unit.

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https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Two tyrosinase inhibiting flavonol glycosides from Buddleia coriacea

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https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Nine phenethyl alcohol glycosides from Stachys sieboldii

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https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Flavonoid lactates from leaves of Marrubium vulgare

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https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Flower Pigments. Flavonoids from Argemone mexicana linn. (Papaveraceae)

1 reference

https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Anisofolin-A, a New Acylated Flavone Glucoside from Anisomeles ovata R. Br.

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https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Chemical constituents from Marrubium alysson.

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https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Preperegrinine, a prefuranic labdane diterpene from Marrubium friwaldskyanum

1 reference

https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Isolation and pharmacological activity of phenylpropanoid esters from Marrubium vulgare

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https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Marruboside, a new phenylethanoid glycoside from Marrubium vulgare L.

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https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

A phenylpropanoid glycoside from Ballota nigra

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https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Isolierung und Konstitution des Echinacosids, eines Glykosids aus den Wurzeln von Echinacea angustifolia D. C. 6. Mitteilung über antibakterielle Stoffe

1 reference

https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Distribution of 6-hydroxy-, 6-methoxy- and 8-hydroxyflavone glycosides in the labiatae, the scrophulariaceae and related families

1 reference

https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Flavonoid p-coumaroylglucosides and 8-hydroxyflavone allosylglucosides in some labiatae

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https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Quercetin-3-(O-acetyl)-β-d-glucopyranosid in Plummera floribunda und Helenium hoopesii

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https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

Phenylethanoid and lignan glycosides from Verbascum thapsus

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https://api.crossref.org/works/10.1016/S0031-9422(03)00242-5

7 January 2021

10.1016/S0031-9422(03)00242-5

Identifiers

DOI

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4 December 2017

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