(Q39422932)

11 September 2017

title

Inhibitory effects of polyphenols toward HCV from the mangrove plant Excoecaria agallocha L. (English)

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(2S,3R,4R,5R,6S)-2-{[(2R,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl]oxy}-6-methyloxane-3,4,5-triol

11 September 2017

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(6,7,8,11,12,13,22,23-Octahydroxy-3,16-dioxo-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-21-yl) 3,4,5-trihydroxybenzoate

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[(1R,19R,21S,22R,23R)-6,7,8,11,12,13,22-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl] 3,4,5-trihydroxybenzoate

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[(2R,3R,4R,5R,6S)-5-hydroxy-3,4,6-tris[(3,4,5-trihydroxybenzoyl)oxy]tetrahydropyran-2-yl]methyl 3,4,5-trihydroxybenzoate

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3-(6-O-Galloyl-beta-D-glucopyranosyloxy)-3',4',5,5',7-pentahydroxyflavone

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[6,7,8,11,12,13,23-Heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-22-yl] 3,4,5-trihydroxybenzoate

(+)-Catechin 3-glucoside

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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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[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-(hydroxymethyl)-2-methoxyphenoxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate

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(2R,3R,4S,5S,6R)-2-[(4-hydroxy-3,5-dimethoxyphenyl)methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

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[(1S,7S,9R,18R,19S,21R,22S)-7,8,8,12,13,22-hexahydroxy-21-(hydroxymethyl)-3,6,16-trioxo-2,17,20,23-tetraoxapentacyclo[16.3.1.17,11.04,9.010,15]tricosa-4,10,12,14-tetraen-19-yl] 3,4,5-trihydroxybenzoate

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[(1S,19R,21S,22R,23R)-6,7,8,11,12,13,23-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-22-yl] 3,4,5-trihydroxybenzoate

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1,2,6-Trigalloyl-beta-D-glucopyranose

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Epicatechin 3-glucoside

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[(1R,19R,21S,22R,23R)-6,7,8,11,12,13,22-heptahydroxy-16-oxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl] 3,4,5-trihydroxybenzoate

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3,4-dihydroxybenzoic acid

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1,2,6-Trigalloyl glucose

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6,7,14-Trihydroxy-13-(3,4,5-trihydroxyoxan-2-yl)oxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione

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2-{[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-3-yl]oxy}-6-methyloxane-3,4,5-triol

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.beta-Penta-O-galloyl-D-glucose

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(6-{[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl)methyl 3,4,5-trihydroxybenzoate

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Quercetin 3-O-(6''-galloyl)-beta-D-galactopyranoside

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Quercetin 3-O-(6''-galloyl)-beta-D-glucopyranoside

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[5-Hydroxy-3,4,6-tris[(3,4,5-trihydroxybenzoyl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate

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Quercetin 3-O-(6 inverted exclamation mark inverted exclamation mark-galloyl)-|A-D-glucopyranoside

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catechin-7-O-glucoside

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Ellagic acid 4-O-xylopyranoside

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flavan-3,3',4',5,5',7-hexol

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4

Peter Proksch

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11 September 2017

Yongxin Li

1

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11 September 2017

Shanjiang Yu

series ordinal

2

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11 September 2017

Dong Liu

series ordinal

3

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11 September 2017

Wenhan Lin

series ordinal

5

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Bioorganic & Medicinal Chemistry Letters

11 September 2017

language of work or name

English

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publication date

January 2012

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16 September 2022

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11 September 2017

volume

22

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11 September 2017

issue

2

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11 September 2017

page(s)

1099-1102

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Antibacterial substances in japanese green tea extract against Streptococcus mutans, a cariogenic bacterium.

11 September 2017

cites work

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1271/BBB1961.53.2307

Two new galloylglucosides from the leaves of Mallotus furetianus

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.52.776

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.36.2940

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.34.1039

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.37.2063

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.29.2862

Identifiers

DOI

10.1016/J.BMCL.2011.11.109

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11 September 2017

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