Inhibitory effects of polyphenols toward HCV from the mangrove plant Excoecaria agallocha L. (Q39422932)

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Language	Label	Description	Also known as
English	Inhibitory effects of polyphenols toward HCV from the mangrove plant Excoecaria agallocha L.	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22196120

retrieved

11 September 2017

title

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

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22196120

retrieved

11 September 2017

main subject

polyphenol

1 reference

based on heuristic

inferred from title

mangrove

1 reference

based on heuristic

inferred from title

Excoecaria agallocha

1 reference

inferred from

reverse claim

catechins

1 reference

inferred from

reverse claim

(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

1 reference

inferred from

reverse claim

(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

1 reference

inferred from

reverse claim

Tercatain

1 reference

inferred from

reverse claim

[(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

1 reference

inferred from

reverse claim

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

1 reference

inferred from

reverse claim

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

1 reference

inferred from

reverse claim

(+)-Catechin 3-glucoside

1 reference

inferred from

reverse claim

CID 338147

1 reference

inferred from

reverse claim

Catechin 7-glucoside

1 reference

inferred from

reverse claim

[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

1 reference

inferred from

reverse claim

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

1 reference

inferred from

reverse claim

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

1 reference

inferred from

reverse claim

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

1 reference

inferred from

reverse claim

[(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

1 reference

inferred from

reverse claim

Excoecariphenol D

1 reference

inferred from

reverse claim

Excoecariphenol C

1 reference

inferred from

reverse claim

(+)-gallocatechin

1 reference

inferred from

reverse claim

corilagin

1 reference

inferred from

reverse claim

[(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

1 reference

inferred from

reverse claim

Furosin

1 reference

inferred from

reverse claim

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

1 reference

inferred from

reverse claim

Epicatechin 3-glucoside

1 reference

inferred from

reverse claim

[(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

1 reference

inferred from

reverse claim

3,4-dihydroxybenzoic acid

1 reference

inferred from

reverse claim

excoecariphenol A

1 reference

inferred from

reverse claim

ethyl gallate

1 reference

inferred from

reverse claim

Geraniin

1 reference

inferred from

reverse claim

1,2,6-Trigalloyl glucose

1 reference

inferred from

reverse claim

gallic acid

1 reference

inferred from

reverse claim

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

1 reference

inferred from

reverse claim

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

1 reference

inferred from

reverse claim

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

1 reference

inferred from

reverse claim

hyperoside

1 reference

inferred from

reverse claim

(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

1 reference

inferred from

reverse claim

chebulagic acid

1 reference

inferred from

reverse claim

pentagalloylglucose

1 reference

inferred from

reverse claim

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

1 reference

inferred from

reverse claim

isoquercetin

1 reference

inferred from

reverse claim

Excoecariphenol B

1 reference

inferred from

reverse claim

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

1 reference

inferred from

reverse claim

(+)-catechin

1 reference

inferred from

reverse claim

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

1 reference

inferred from

reverse claim

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

1 reference

inferred from

reverse claim

catechin-7-O-glucoside

1 reference

inferred from

reverse claim

Ellagic acid 4-O-xylopyranoside

1 reference

inferred from

reverse claim

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

1 reference

inferred from

reverse claim

Chebulagic acid

1 reference

inferred from

reverse claim

author

Peter Proksch

series ordinal

4

object named as

Peter Proksch

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22196120

retrieved

11 September 2017

author name string

Yongxin Li

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22196120

retrieved

11 September 2017

Shanjiang Yu

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22196120

retrieved

11 September 2017

Dong Liu

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22196120

retrieved

11 September 2017

Wenhan Lin

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22196120

retrieved

11 September 2017

language of work or name

English

0 references

publication date

January 2012

1 reference

stated in

Crossref

retrieved

16 September 2022

published in

Bioorganic & Medicinal Chemistry Letters

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22196120

retrieved

11 September 2017

volume

22

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22196120

retrieved

11 September 2017

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22196120

retrieved

11 September 2017

page(s)

1099-1102

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22196120

retrieved

11 September 2017

cites work

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

1 reference

stated in

COCI

retrieved

12 April 2024

reference URL

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

Two new galloylglucosides from the leaves of Mallotus furetianus

1 reference

stated in

COCI

retrieved

12 April 2024

reference URL

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

Tannins and related polyphenols of euphorbiaceous plants. IV. Euphorbins A and B, novel dimeric dehydroellagitannins from Euphorbia hirta L.

1 reference

stated in

COCI

retrieved

12 April 2024

reference URL

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

Tannins and related compounds. XLII. Isolation and characterization of four new hydrolyzable tannins, terflavins A and B, tergallagin and tercatain from the leaves of Terminalia catappa L.

1 reference

stated in

COCI

retrieved

12 April 2024

reference URL

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

Tannins and related compounds. LXXXIV. Isolation and characterization of five new hydrolyzable tannins from the bark of Mallotus japonicus

1 reference

stated in

COCI

retrieved

12 April 2024

reference URL

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

Tannins and related compounds. I. Rhubarb (1).

1 reference

stated in

COCI

retrieved

12 April 2024

reference URL

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

Identifiers

DOI

10.1016/J.BMCL.2011.11.109

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22196120

retrieved

11 September 2017

PubMed publication ID

22196120

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22196120

retrieved

11 September 2017

ResearchGate publication ID

51921994

0 references

 

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