Biologically active secondary metabolites from Ginkgo biloba (Q43992847)

28 November 2017

title

Biologically active secondary metabolites from Ginkgo biloba (English)

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

28 November 2017

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3-(6-O-alpha-L-Rhamnopyranosyl-beta-D-glucopyranosyloxy)-3',5,5',7-tetrahydroxy-4'-methoxyflavone

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

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GFXMZXPRAAYHIX-MDUOHGEWSA-N

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Kaempferol 3-O-glucosyl-(1->2)-rhamnoside

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9-Tert-butyl-7,9-dihydroxy-3,5,12-trioxatetracyclo[6.6.0.01,11.04,8]tetradecane-2,6,13-trione

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(+)-7-epi-Syringaresinol 4'-glucoside

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

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4-(3,4-Dihydroxy-2,2,6-trimethylcyclohexyl)but-3-en-2-one

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

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Episyringaresinol 4'-O-beta-D-glncopyranoside

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ginkgolide-B (CID 6324617)

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[6-[4,5-Dihydroxy-2-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-3-yl]oxy-6-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate

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3-[2-(4-Methoxyphenyl)-4-oxo-5,7-dihydroxy-4H-1-benzopyran-8-yl]-4-methoxybenzoic acid

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

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Kaempferol 3-O-beta-(6''-p-coumaroyl) glucopyranosyl (1 inverted exclamation marku2)-alpha-L-rhamnopyranoside

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Quercetin 3-O-beta-(6''-p-coumaroyl)glucopyranosyl(1 inverted exclamation marku2)-alpha-L-rhamnopyranoside

luteolin 3'-glucoside

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

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Quercetin 3-(2-glucosylrhamnoside)

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(E)-4-[(1R,3S,4S,6R)-3,4-dihydroxy-2,2,6-trimethylcyclohexyl]but-3-en-2-one

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Riaz A Khan

3

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Satoshi Takamatsu

object named as

Satoshi Takamatsu

5

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Erdal Bedir

object named as

Erdal Bedir

1

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Ikhlas A Khan

8

object named as

Ikhlas A Khan

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28 November 2017

Irem I Tatli

2

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28 November 2017

Jianping Zhao

4

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28 November 2017

Larry A Walker

6

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28 November 2017

Peter Goldman

7

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Journal of Agricultural and Food Chemistry

28 November 2017

language of work or name

English

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publication date

20 April 2002

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16 September 2022

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28 November 2017

volume

50

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issue

11

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28 November 2017

page(s)

3150-3155

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Use of on-flow LC/1H NMR for the study of an antioxidant fraction from Orophea enneandra and isolation of a polyacetylene, lignans, and a tocopherol derivative

28 November 2017

cites work

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24 October 2022

https://opencitations.net/index/coci/api/v1/citations/10.1021/NP980203P

Glycoric Acid Possessing a New 10-Normegastigmane Skeleton from Glycosmis arborea.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.44.1421

Constituents of the roots of Boerhaavia diffusa L. III. Identification of Ca2+ channel antagonistic compound from the methanol extract

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.39.1551

Identifiers

DOI

10.1021/JF011682S

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release_w5dbwa6nnngvrdqienyw6hryqm

28 November 2017

Fatcat ID

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https://api.fatcat.wiki/v0/release/w5dbwa6nnngvrdqienyw6hryqm

Fatcat

reference URL

mapped directly with Wikidata item

24 November 2022

based on heuristic

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