Movatterモバイル変換

Jump to content

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

From Wikidata

scientific article

Language	Label	Description	Also known as
default for all languages	No label defined
English	Inhibitory effects of polyphenols toward HCV from the mangrove plant Excoecaria agallocha L.	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Excoecaria agallocha

1 reference

1 reference

(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

(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

1 reference

[(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

[(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

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

1 reference

(+)-Catechin 3-glucoside

1 reference

1 reference

catechin 7-glucoside

1 reference

[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

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

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

1 reference

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

1 reference

[(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

Excoecariphenol D

1 reference

Excoecariphenol C

1 reference

(+)-gallocatechin

1 reference

1 reference

[(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

1 reference

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

1 reference

Epicatechin 3-glucoside

1 reference

[(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

3,4-dihydroxybenzoic acid

1 reference

excoecariphenol A

1 reference

1 reference

1 reference

1,2,6-Trigalloyl glucose

1 reference

1 reference

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

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

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

1 reference

1 reference

(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

chebulagic acid

1 reference

pentagalloylglucose

1 reference

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

1 reference

1 reference

Excoecariphenol B

1 reference

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

1 reference

1 reference

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

1 reference

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

1 reference

catechin-7-O-glucoside

1 reference

Ellagic acid 4-O-xylopyranoside

1 reference

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

1 reference

Chebulagic acid

1 reference

4

object named as

Peter Proksch

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

author name string

Yongxin Li

1

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Shanjiang Yu

2

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Dong Liu

3

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

Wenhan Lin

5

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

publication date

January 2012

1 reference

16 September 2022

language of work or name

0 references

Bioorganic & Medicinal Chemistry Letters

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

22

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

1099-1102

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

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

1 reference

12 April 2024

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

Two new galloylglucosides from the leaves of Mallotus furetianus

1 reference

12 April 2024

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

12 April 2024

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

12 April 2024

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

12 April 2024

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

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

1 reference

12 April 2024

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

Identifiers

10.1016/J.BMCL.2011.11.109

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 September 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q39422932&oldid=2133356528"

[8]ページ先頭

©2009-2025 Movatter.jp