(Q77749601)

English

Hepatoprotective, superoxide scavenging, and antioxidative activities of aromatic constituents from the bark of Betula platyphylla var. japonica

scientific article published on 01 November 1998

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9873651%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

Hepatoprotective, superoxide scavenging, and antioxidative activities of aromatic constituents from the bark of Betula platyphylla var. japonica (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9873651%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

Betula platyphylla

1 reference

Betula platyphylla var. japonica

1 reference

1 reference

1 reference

(2S,3S,4S,5S,6S)-2-[[(1R,2S,3S)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

Catechin 7-xyloside

1 reference

(2R,3S,4S,5R,6R)-2-[[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(2S)-4-(4-hydroxyphenyl)butan-2-yl]oxyoxane-3,4,5-triol

1 reference

(E)-1,7-bis(4-hydroxyphenyl)hept-4-en-3-one

1 reference

1 reference

(2S,3S,4S,5S,6S)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

2-[[7-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

(2R,3R,4R,5R,6R)-2-[(3R)-1,7-bis(4-hydroxyphenyl)heptan-3-yl]oxy-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]oxane-3,4,5-triol

1 reference

1 reference

(+)-lyoniresinol-3-alpha-O-beta-D-glucopyranoside

1 reference

(2R,3R,4S,5S,6R)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

Epirhododendrin

1 reference

(2R,3R,4R,5R,6R)-2-[(3S,5S)-5-hydroxy-1,7-bis(4-hydroxyphenyl)heptan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

(2R,3R,4R,5R,6R)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(2R)-4-(4-hydroxyphenyl)butan-2-yl]oxyoxane-3,4,5-triol

1 reference

(5S)-1,7-bis(4-hydroxyphenyl)-5-[(2R,3R,4R,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3S)-3,4,4-trihydroxyoxolan-2-yl]oxymethyl]oxan-2-yl]oxyheptan-3-one

1 reference

(+)-catechin 7-O-beta-D-xyloside

1 reference

alpha-tocopherol

1 reference

1 reference

Platyphylloside

1 reference

butylated hydroxytoluene

1 reference

(2R,3R,4S,5S,6R)-2-[[(1R,2S,3S)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

(2R,3S,4S,5R,6R)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(2R)-4-(4-hydroxyphenyl)butan-2-yl]oxyoxane-3,4,5-triol

1 reference

1 reference

1 reference

1 reference

1 reference

(2R,3R,4R,5R,6R)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(2S)-4-(4-hydroxyphenyl)butan-2-yl]oxyoxane-3,4,5-triol

1 reference

(2R,3R,4R,5R,6R)-2-[(3S,5R)-5-hydroxy-1,7-bis(4-hydroxyphenyl)heptan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

1,7-bis(4-hydroxyphenyl)hept-4-en-3-one

1 reference

2,6-di-tert-butyl-4-methoxyphenol

1 reference

(5S)-1,7-bis(4-hydroxyphenyl)-5-[(2R,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-3-one

1 reference

(2R,3R,4R,5R,6R)-2-[[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(2R)-4-(4-hydroxyphenyl)butan-2-yl]oxyoxane-3,4,5-triol

1 reference

(2R,3R,4S,5S,6R)-2-[(3R)-1,7-bis(4-hydroxyphenyl)heptan-3-yl]oxy-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]oxane-3,4,5-triol

1 reference

author name string

H Matsuda

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9873651%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

A Ishikado

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9873651%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

N Nishida

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9873651%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

K Ninomiya

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9873651%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

H Fujiwara

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9873651%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

Y Kobayashi

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9873651%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

M Yoshikawa

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9873651%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

publication date

November 1998

1 reference

16 September 2022

Bioorganic & Medicinal Chemistry Letters

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9873651%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9873651%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

21

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9873651%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

2939-2944

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9873651%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

Two new triterpenes from Betula platyphylla

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Absolute Configuration of Platyphylloside and (−)-Centrolobol

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Phenolic glucosides from Parabenzoin praecox

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

New Lignan Glucosides from Stemmadenia minima*

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Arylbutanoid and diarylheptanoid glycosides from inner bark of Betula pendula

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Rhododendrol glycosides and phenyl glucoside esters from inner bark of Betula pubescens

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Indonesian Medicinal Plants. XII. Four Isomeric Lignan-Glucosides from the Bark of Aegle marmelos (Rutaceae).

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Chemical Evaluation of Betula Species in Japan. I. Constituents of Betula ermanii.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Chemical Evaluation of Betula Species in Japan. II. Constituents of Betula platyphylla var. japonica.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A new triterpene, betulafolienpentaol, from Betula platyphylla

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Chemical Evaluation of Betula Species in Japan. V. Constituents of Betula ovalifolia.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Chemical Evaluation of Betula Species in Japan. VI. Constituents of Betula schmidtii.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

[Bioactive constituents of Chinese natural medicines. III. Absolute stereostructures of new dihydroflavonols, hovenitins I, II, and III, isolated from hoveniae semen seu fructus, the seed and fruit of Hovenia dulcis THUNB. (Rhamnaceae): inhibitory e

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Bioactive saponins and glycosides. VIII. Notoginseng (1): new dammarane-type triterpene oligoglycosides, notoginsenosides-A, -B, -C, and -D, from the dried root of Panax notoginseng (Burk.) F.H. Chen

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

New hepatoprotective saponins, bupleurosides III, VI, IX, and XIII, from Chinese Bupleuri Radix: Structure-requirements for the cytoprotective activity in primary cultured rat hepatocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Scorzonerosides A, B, and C, novel triterpene oligoglycosides with hepatoprotective effect from Chinese Bupleuri Radix, the roots of Bupleurum scorzonerifolium Willd

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Inhibitory effect and action mechanism of sesquiterpenes from Zedoariae Rhizoma on D-galactosamine/lipopolysaccharide-induced liver injury

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Tumor necrosis factor is a terminal mediator in galactosamine/endotoxin-induced hepatitis in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2898%2900528-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0960-894X(98)00528-9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9873651%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9873651%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

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