Acylated flavonol glycosides from Eugenia jambolana leaves (Q43818995)

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title

Acylated flavonol glycosides from Eugenia jambolana leaves (English)

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

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[(2S,3R,4S,5S,6S)-6-[2-(3,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate

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3-O-methylellagic acid

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2-(3,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}chromen-4-one

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[(2S,3R,4S,5R,6S)-6-[2-(3,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate

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2,3-di-O-galloyl--d-glucose

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Myricetrin 4''-O-acetyl-2''-O-gallate

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3-(6-Deoxy-alpha-L-glucopyranosyloxy)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one

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[(2S,3R,4S,5S,6S)-6-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate

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[(2S,3S,4R,5R,6S)-5-acetyloxy-2-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4-hydroxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate

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

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[(2S,3R,4S,5R,6S)-6-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate

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myricetin 3-O-glucuronide

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Quercetin 3-(4-O-acetyl-alpha-L-rhamnopyranoside)

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Mahmoud II

1

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Marzouk MS

2

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Moharram FA

3

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El-Gindi MR

4

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Hassan AM

5

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publication date

December 2001

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16 September 2022

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volume

58

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issue

8

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page(s)

1239-1244

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Chemical Evaluation of Betula Species in Japan. II. Constituents of Betula platyphylla var. japonica.

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cites work

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https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900365-X

7 January 2021

A new flavonol glycoside gallate ester from Acer okamotoanum and its inhibitory activity against human immunodeficiency virus-1 (HIV-1) integrase

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900365-X

7 January 2021

Flavonol glycosides with acetyl substitution from Kalanchoe gracilis

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900365-X

7 January 2021

Flavonoid glycosides from Eugenia jambos

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https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900365-X

7 January 2021

A simple two-step purification of antidiabetic compounds from Eugenia jambolana fruit-pulp: proteolytic resistance and other properties

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900365-X

7 January 2021

Two macrocyclic hydrolysable tannin dimers from Eugenia uniflora

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https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900365-X

7 January 2021

New and rare flavonol glycosides from leaves of Syzygium samarangense

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https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900365-X

7 January 2021

High-performance Liquid Chromatographic/Electrospray Ionization Mass Spectrometric Screening for Polyphenolic Compounds ofEpilobium hirsutum—The Structure of the Unique Ellagitannin Epilobamide-A

1 reference

https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900365-X

7 January 2021

HPLC isolation and identification of flavonoids from white birch Betula pubescens leaves

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https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900365-X

7 January 2021

Flavonoids from Rhamnus pallasii

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https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900365-X

7 January 2021

Syzyginins A and B, two ellagitannins from Syzygium aromaticum

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https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900365-X

7 January 2021

Acetylated flavonol glycosides from Zingiber zerumbet

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https://api.crossref.org/works/10.1016%2FS0031-9422%2801%2900365-X

7 January 2021

10.1016/S0031-9422(01)00365-X

Identifiers

DOI

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27 November 2017

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