Flavonoids and bioactive coumarins of Tordylium apulum (Q104847482)

http://api.crossref.org/works/10.1016/s0031-9422(98)50018-1

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

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kaempferol 3-O-neohesperidoside

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

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Narcissoside, >=95% (HPLC)

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[(2S,3S,4R,5S,6R)-4-acetyloxy-6-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-5-hydroxy-2-methyloxan-3-yl] acetate

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

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2-[(8S,9R)-9-hydroxy-2-oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl]propan-2-yl acetate

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[(2R,3R,4R,5S,6R)-4-acetyloxy-6-[[(2S,3R,4R,5S,6R)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-5-hydroxy-2-methyloxan-3-yl] acetate

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

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Columbianetin acetate

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5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3S,4R,5R,6R)-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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6

Kurt Hostettmann

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http://api.crossref.org/works/10.1016/s0031-9422(98)50018-1

author name string

Constantinos Kofinas

1

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http://api.crossref.org/works/10.1016/s0031-9422(98)50018-1

Ioanna Chinou

2

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http://api.crossref.org/works/10.1016/s0031-9422(98)50018-1

Anargiros Loukis

3

1 reference

http://api.crossref.org/works/10.1016/s0031-9422(98)50018-1

Catherine Harvala

4

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http://api.crossref.org/works/10.1016/s0031-9422(98)50018-1

Marc Maillard

5

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http://api.crossref.org/works/10.1016/s0031-9422(98)50018-1

publication date

June 1998

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16 September 2022

5

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inferred from page(s)

published in

Phytochemistry

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http://api.crossref.org/works/10.1016/s0031-9422(98)50018-1

volume

48

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http://api.crossref.org/works/10.1016/s0031-9422(98)50018-1

issue

4

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page(s)

637-641

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http://api.crossref.org/works/10.1016/s0031-9422(98)50018-1

cites work

Composition and Antibacterial Activity of the Essential Oil of Tordylium apulum L.

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7 January 2021

Constituents of Umbelliferous Plants. XIV. Coumarins of Peucedanum oreoselinum (L.) Moench

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7 January 2021

Coumarins XIV: high-resolution mass spectra of 3',4'-disubstituted 3',4'-dihydroseselins

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https://api.crossref.org/works/10.1016/S0031-9422(98)50018-1

7 January 2021

Eupafolin Rhamnosides fron Kalanchoe gracilis

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https://api.crossref.org/works/10.1016/S0031-9422(98)50018-1

7 January 2021

Flavonol glycosides with acetyl substitution from Kalanchoe gracilis

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https://api.crossref.org/works/10.1016/S0031-9422(98)50018-1

7 January 2021

Flavone and flavonol glycosides from Calluna vulgaris

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7 January 2021

Sagittatins A and B, Flavonoid Glycosides of Epimedium sagittatum Herbs1

1 reference

https://api.crossref.org/works/10.1016/S0031-9422(98)50018-1

7 January 2021

Flavonol 3-O-triglycosides from Actinidia species

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https://api.crossref.org/works/10.1016/S0031-9422(98)50018-1

7 January 2021

Biosynthesis of angular furanocoumarins.

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https://api.crossref.org/works/10.1016/S0031-9422(98)50018-1

7 January 2021

[Coumarins from chinese crude drug "She Huangzi," the fruits of Cnidium sp. and from Cnidium japonicum Miq]

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https://api.crossref.org/works/10.1016/S0031-9422(98)50018-1

7 January 2021