(Q104847867)

http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900106-x

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kaempferol-7-rhamnoside

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

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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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8-beta-D-Glucopyranosyl-5,7-dihydroxy-2-isopropylchromone

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

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

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

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

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

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3-[(2S,3S,4S,5S,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one

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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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2-(3,4-Dihydroxyphenyl)-5-hydroxy-3-methoxy-8,8-dimethyl-4h,8h-benzo[1,2-b:3,4-b']dipyran-4-one

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Hypericum sikokumontanum

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Hypericum triquetrifolium

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Hypericum tetrapterum

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Hypericum linarioides

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Hypericum laricifolium

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Hypericum curvisepalum

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Qing-Li Wu

1

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900106-x

Sheng-Ping Wang

2

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900106-x

Li-Jun Du

3

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900106-x

Shu-Ming Zhang

4

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900106-x

Jun-Shan Yang

5

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900106-x

Pei-Gen Xiao

6

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900106-x

publication date

November 1998

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16 September 2022

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900106-x

volume

49

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900106-x

issue

5

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http://api.crossref.org/works/10.1016%2Fs0031-9422%2898%2900106-x

page(s)

1417-1420

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cites work

Sarothralen A and B, new antibiotic compounds from Hypericum japonicum

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900106-X

7 January 2021

Saroaspidin A, B, and C: additional antibiotic compounds from Hypericum japonicum

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900106-X

7 January 2021

X-Ray crystal structure of sarothralin, a novel antibiotic compound from Hypericum japonicum

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900106-X

7 January 2021

Sarothralin G: A New Antimicrobial Compound fromHypericum japonicum

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900106-X

7 January 2021

A flavanonol rhamnoside from Hypericum japonicum

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900106-X

7 January 2021

An isopentenylated flavonol from Hypericum japonicum

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900106-X

7 January 2021

A dipeptide derivative fromHypericum japonicum

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900106-X

7 January 2021

A chromene from Hypericum japonicum☆

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900106-X

7 January 2021

A prenylated xanthone from cell suspension cultures of Hypericum patulum

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900106-X

7 January 2021

A chromone from Zanthoxylum species

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900106-X

7 January 2021

Weitere Phloroglucin- und alpha-Pyron-Derivate aus Helichrysum-Arten

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900106-X

7 January 2021

New antibacterial tetratriacontanol derivatives from Agave americana L.

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900106-X

7 January 2021

Seven prenylated flavonol glycosides from two Epimedium species

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900106-X

7 January 2021

13C-NMR-spektren natürlich vorkommender flavonoide

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900106-X

7 January 2021

HIV-1 reverse transcriptase inhibitory principles from Chamaesyce hyssopifolia

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https://api.crossref.org/works/10.1016%2FS0031-9422%2898%2900106-X

7 January 2021