(Q46792818)

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Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of Saussureosides A and B from Saussurea medusa

scientific article published in November 2005

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scholarly article

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/16272724

Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of Saussureosides A and B from Saussurea medusa (English)

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/16272724

Saussurea medusa

1 reference

tricosanoic acid

1 reference

1 reference

1 reference

Apigenin 7-rutinoside

1 reference

1 reference

1 reference

eleutheroside B

1 reference

octadec-9-enoic acid

1 reference

(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

1 reference

DL-phenylalanine

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luteolin-4'-O-beta-D-glucopyranoside

1 reference

1 reference

1 reference

1 reference

1 reference

methyl chlorogenate

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Quercetin 3-alloside

1 reference

Luteolin 4'-glucoside

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(+)-pinoresinol

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apigenin 7-rutinoside

1 reference

(2S,3R,4S,5S,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-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

1 reference

5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

1 reference

1 reference

(+)-syringaresinol beta-D-glucoside

1 reference

(+)-syringaresinol

1 reference

octadeca-9,12-dienoic acid

1 reference

Saussureosides A

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Flaxseeds extract

1 reference

Luteolin 7-rutinoside

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alpha-linolenic acid

1 reference

(2R,3R,4S,5S,6R)-2-[(Z)-hex-3-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

1 reference

5-hydroxy-2-(4-hydroxy-3-methoxy-phenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-chromen-4-one

1 reference

methyl (1S,3R,4S,5R)-4-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,3,5-trihydroxycyclohexane-1-carboxylate

1 reference

1 reference

1 reference

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

Chrysoeriol 7-O-glucoside

1 reference

4-Methoxybenzyl beta-D-glucopyranoside

1 reference

1 reference

1 reference

Apigenin-4'-glucoside

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benzyl β-D-glucoside

1 reference

phenylethyl beta-D-glucopyranoside

1 reference

1 reference

1 reference

1 reference

Neochlorogenic acid methyl ester

1 reference

octadeca-9,12,15-trienoic acid

1 reference

1 reference

1 reference

1 reference

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

1 reference

1 reference

1 reference

1 reference

1 reference

(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-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1 reference

Saussureosides B

1 reference

homovanillyl alcohol

1 reference

1 reference

Matairesinoside

1 reference

5,7-dihydroxy-2-[4-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one

1 reference

1 reference

secoisolariciresinol

1 reference

Saussurea costus

1 reference

Saussurea pulchella

1 reference

Saussurea amara

1 reference

Saussurea involucrata

1 reference

Toshio Morikawa

4

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/16272724

author name string

Haihui Xie

1

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/16272724

Tao Wang

2

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/16272724

Hisashi Matsuda

3

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/16272724

Masayuki Yoshikawa

5

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/16272724

Tadato Tani

6

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/16272724

language of work or name

1 reference

Chemical & Pharmaceutical Bulletin

publication date

2005

1 reference

16 September 2022

full work available at URL

https://www.jstage.jst.go.jp/article/cpb/53/11/53_11_1416/_pdf

1 reference

19 March 2024

https://api.unpaywall.org/v2/10.1248/cpb.53.1416?email=unpaywall_01@example.com

Chemical & Pharmaceutical Bulletin

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/16272724

53

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/16272724

1416-1422

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/16272724

11

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/16272724

online access status

1 reference

19 March 2024

https://api.unpaywall.org/v2/10.1248/cpb.53.1416?email=unpaywall_01@example.com

access restriction status

1 reference

based on heuristic

inferred from online access status

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Identifiers

10.1248/CPB.53.1416

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/16272724

1 reference

Europe PubMed Central

25 December 2017

http://europepmc.org/abstract/MED/16272724

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