(Q79793878)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18986199%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

title

Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18986199%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

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(2R,3R,4R,5S,6R)-5-[4-[(2R,3S,4S)-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-(hydroxymethyl)oxolan-2-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-2,3,4-triol

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(2R,3R)-3-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2-(hydroxymethyl)-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one

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4-[3-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol

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caffeic acid methyl ester

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(2S,3R,4S,5R,6S)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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(3R,4R)-3-hydroxy-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-[[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl]oxolan-2-one

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4-[[(3R,4R,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol

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(2S,3S)-2-[(4-hydroxy-3-methoxyphenyl)methyl]-3-[[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl]cyclopentan-1-one

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(E)-4-hydroxy-3-methoxycinnamaldehyde

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(2S,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol

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(R)-1,2-Bis(3-methoxy-4-hydroxyphenyl)-3-hydroxy-1-propanone

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2beta-[3-Methoxy-4-(beta-D-glucopyranosyloxy)phenyl]-4alpha-(4-hydroxy-3-methoxybenzyl)tetrahydrofuran-3alpha-methanol

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(3S,4S)-3-hydroxy-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-[[3-methoxy-4-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl]oxolan-2-one

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(2S)-2,3-Dihydro-2beta-(4-hydroxy-3,5-dimethoxyphenyl)-3alpha-(hydroxymethyl)-9H-pyrano[2,3-f]-1,4-benzodioxin-9-one

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(2R)-2-[bis(4-hydroxy-3-methoxyphenyl)methyl]-3-(hydroxymethyl)butane-1,4-diol

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(+)-syringaresinol beta-D-glucoside

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3-(3,4-dihydroxy-5-methoxyphenyl)prop-2-enal

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6-Demethoxycleomiscosin A

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4-[(3R,3aS,6R,6aS)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol

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(2S,3S,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-6-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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(2R,3R)-2-(hydroxymethyl)-3-[3-methoxy-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one

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5'-Demethoxydaphneticin

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4-[(3R,3aR,6R,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol

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4-[[(3R,4R,5S)-5-ethoxy-4-[(4-hydroxy-3-methoxy-phenyl)methyl]tetrahydrofuran-3-yl]methyl]-2-methoxy-phenol

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4-[(2R,3R,4S,5S)-5-(4-hydroxy-3-methoxyphenyl)-3,4-bis(hydroxymethyl)oxolan-2-yl]-2-methoxyphenol

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Episyringaresinol 4'-O-beta-D-glncopyranoside

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(2R)-1,2-bis(3,4-dihydroxyphenyl)-3-hydroxypropan-1-one

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(2S,3R,4S,5R,6R)-2-[4-[(3R,3aS,6R,6aS)-6-[3-methoxy-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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(3S,4S)-4-[(3,4-dimethoxyphenyl)methyl]-3-[[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl]oxolan-2-one

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methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate

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(2S,3S)-2-(hydroxymethyl)-3-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one

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3-Hydroxy-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one

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4,4'-[[(2S,3R,4R)-2-Butoxytetrahydrofuran-3,4-diyl]bismethylene]bis(2-methoxyphenol)

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(2S,3S)-2-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-(hydroxymethyl)-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one

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(2S,3R,4S,5S,6R)-2-[4-[(3R,3aS,6R,6aS)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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6-[(1S,2R)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-5,7-dimethoxy-3,4-dihydronaphthalene-2-carbaldehyde

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4-[[(3R,4R,5R)-5-butoxy-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]methyl]-2-methoxyphenol

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(6R,7S,8S)-8-(4-hydroxy-3-methoxyphenyl)-6,7-bis(hydroxymethyl)-3-methoxy-5,6,7,8-tetrahydronaphthalen-2-ol

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(1R,2R)-guaiacylglycerol

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(2S,3R,4R)-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-ol

5-Hydroxyconiferaldehyde

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[(1R)-3aalpha,4,6,6aalpha-Tetrahydro-1H,3H-furo[3,4-c]furan-1alpha,4alpha-diyl]bis(2-methoxy-4,1-phenylene)bis(beta-D-glucopyranoside)

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(-)-Pinoresinol glucoside

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(3S,4R)-4-[(3,4-dimethoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one

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(2R,3R,4R)-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-ol

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(2S,3R,4S,5R,6R)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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(3R,4S)-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one

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(2S,3R,4S,5R,6R)-2-[4-[(3R,3aS,6R,6aS)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one

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(-)-syringaresinol O,O'-bis(beta-D-glucoside)

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3-(4-Hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one

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Daphne pseudomezereum

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6

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18986199%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

author name string

Shuang Liang

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18986199%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Yun-Heng Shen

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18986199%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Jun-Mian Tian

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18986199%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Zhi-Jun Wu

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18986199%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Hui-Zi Jin

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18986199%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Shi-Kai Yan

7

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18986199%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

publication date

6 November 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18986199%20AND%20SRC:MED&resulttype=core&format=json

Journal of Natural Products

25 December 2019

published in

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18986199%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

volume

71

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18986199%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

issue

11

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25 December 2019

page(s)

1902-1905

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18986199%20AND%20SRC:MED&resulttype=core&format=json

Studies on the constituents of the bark of Kalopanax pictus Nakai.

25 December 2019

cites work

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.39.865

Isolation and Characterization of Phenolic Compounds from Magnoliae Cortex Produced in China.

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.39.2024

Studies on the constituents of Clematis species. VI. The constituents of Clematis stans Sieb. et Zucc

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.43.2187

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

1 reference

12 April 2024

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

Tracheolospermum. II Lignans from Trachelospermum asiaticum.

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.34.4340

The constituents of Eucommia ulmoides OLIV. II. Isolation and structures of three new lignan glycosides.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.33.3651

Studies on the constituents of Cistanchis Herba. V. Isolation and structures of two new phenylpropanoid glycosides, cistanosides E and F.

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.33.1452

The constituents of Eucommia ulmoides Oliv. I. Isolation of (+)-medioresinol di-O-.BETA.-D-glucopyranoside.

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.31.2993

Identifiers

DOI

10.1021/NP8004166

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18986199%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

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