(Q44631035)

4 December 2017

Biological activities of Salacia chinensis originating in Thailand: the quality evaluation guided by alpha-glucosidase inhibitory activity (English)

1 reference

6b-(Hydroxymethyl)-4,4a,6a,8a,11,11,14a-heptamethyl-1,2,4,5,6,6a,8,9,10,12,12a,13,14,14b-tetradecahydropicene-3,7-dione

4 December 2017

0 references

Salacia chinensis

2 references

1 reference

1 reference

1 reference

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

1 reference

20,21-Dihydroxy-5,8,11,14,17,24-hexamethyl-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracosane-11-carboxylic acid

1 reference

D:A-Friedooleanan-3-one, 29-hydroxy-, (20alpha)-

1 reference

21-Hydroxy-5,8,11,14,17,24-hexamethyl-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracosane-11-carboxylic acid

1 reference

3,9-Dihydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione

1 reference

3,9-dihydroxy-4,6a,6b,8a,11,14a-hexamethyl-9,11,12,12a,13,14-hexahydro-8H-picene-2,7,10-trione

1 reference

22-Hydroxy-3-oxoolean-12-en-29-oic acid

1 reference

1 reference

5-Methoxyisolariciresinol

1 reference

1 reference

1 reference

4,10,11-trihydroxy-2,4a,6a,6a,9,14a-hexamethyl-2,4,5,6,6b,7,8,13,14,14b-decahydro-1H-picen-3-one

1 reference

4,10-Dihydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylic acid

1 reference

11-hydroxy-2,4a,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-2-carboxylic acid

1 reference

7-hydroxy-11-(hydroxymethyl)-4,4a,6a,6b,8a,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one

1 reference

1 reference

4,4,6a,6b,8a,11,11,14b-Octamethyl-1,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-octadecahydro-2H-picen-3-one

1 reference

3-Hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione

1 reference

7-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one

1 reference

[4,12-Diacetyloxy-6-(acetyloxymethyl)-5-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate

1 reference

1 reference

1,3,6,7-Tetrahydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one

1 reference

1 reference

6-Hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,4,5,6,6a,8,9,10,12,12a,13,14,14b-tetradecahydropicene-3,7-dione

1 reference

4,10-dihydroxy-1,4a,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-2-carboxylic acid

1 reference

22-Hydroxy-3-oxo-12-ursen-30-oic acid

1 reference

[5,12-Diacetyloxy-6-(acetyloxymethyl)-4-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate

1 reference

4,11-Dihydroxy-2,4a,6a,6a,9,14a-hexamethyl-1,2,4,5,6,6b,7,8,11,12,12a,13,14,14b-tetradecahydropicene-3,10-dione

1 reference

6

1 reference

4 December 2017

Masayuki Yoshikawa

1

1 reference

4 December 2017

Yutana Pongpiriyadacha

2

1 reference

4 December 2017

Akinobu Kishi

3

1 reference

4 December 2017

Tadashi Kageura

4

1 reference

4 December 2017

Tao Wang

5

1 reference

4 December 2017

Hisashi Matsuda

7

1 reference

4 December 2017

language of work or name

Japanese

0 references

publication date

1 October 2003

1 reference

full work available at URL

4 December 2017

https://www.jstage.jst.go.jp/article/yakushi/123/10/123_10_871/_pdf

1 reference

19 March 2024

https://api.unpaywall.org/v2/10.1248/yakushi.123.871?email=unpaywall_01@example.com

published in

Journal of the Pharmaceutical Society of Japan

1 reference

4 December 2017

123

1 reference

4 December 2017

10

1 reference

4 December 2017

871-880

1 reference

https://api.unpaywall.org/v2/10.1248/yakushi.123.871?email=unpaywall_01@example.com

4 December 2017

1 reference

19 March 2024

access restriction status

open access

1 reference

based on heuristic

inferred from online access status

cites work

Protein glycation inhibitors from thyme (Thymus vulgaris)

2 references

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1271/BBB.59.2018

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

A micromethod for the assay of aldose reductase, its application to pancreatic islets

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

Polyphenol constituents from Salacia species: quantitative analysis of mangiferin with alpha-glucosidase and aldose reductase inhibitory activities

2 references

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/YAKUSHI.121.371

Structures of new friedelane-type triterpenes and eudesmane-type sesquiterpene and aldose reductase inhibitors from Salacia chinensis

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

Salacia reticulata and its polyphenolic constituents with lipase inhibitory and lipolytic activities have mild antiobesity effects in rats

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

Absolute stereostructure of potent alpha-glucosidase inhibitor, Salacinol, with unique thiosugar sulfonium sulfate inner salt structure from Salacia reticulata

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

A modified procedure for the rapid preparation of efficiently transporting vesicles from small intestinal brush border membranes. Their use in investigating some properties of d-glucose and choline transport systems

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

Kotalanol, a potent alpha-glucosidase inhibitor with thiosugar sulfonium sulfate structure, from antidiabetic ayurvedic medicine Salacia reticulata

2 references

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.46.1339

Protein glycation, diabetes, and aging

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

Structural requirements of flavonoids and related compounds for aldose reductase inhibitory activity

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

Structural requirements of flavonoids for nitric oxide production inhibitory activity and mechanism of action

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

Hepatoprotective and antioxidative properties of Salacia reticulata: preventive effects of phenolic constituents on CCl4-induced liver injury in mice

2 references

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/BPB.25.72

Salacinol, potent antidiabetic principle with unique thiosugar sulfonium sulfate structure from the Ayurvedic traditional medicine Salacia reticulata in Sri Lanka and India

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

Antioxidant constituents from rhubarb: structural requirements of stilbenes for the activity and structures of two new anthraquinone glucosides

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

Proanthocyanidins of Salacia chinensis Linn

1 reference

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

Antidiabetic principles of natural medicines. IV. Aldose reductase and qlpha-glucosidase inhibitors from the roots of Salacia oblonga Wall. (Celastraceae): structure of a new friedelane-type triterpene, kotalagenin 16-acetate

2 references

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.47.1725

Structures of new friedelane- and norfriedelane-type triterpenes and polyacylated eudesmane-type sesquiterpene from Salacia chinensis LINN. (S. prinoides DC., Hippocrateaceae) and radical scavenging activities of principal constituents

2 references

12 April 2024

https://opencitations.net/index/api/v1/references/10.1248/YAKUSHI.123.871

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.51.1051

Identifiers

DOI

10.1248/YAKUSHI.123.871

1 reference

release_xzu2xpxwp5botp67jgn4nugciq

4 December 2017

1 reference

https://api.fatcat.wiki/v0/release/xzu2xpxwp5botp67jgn4nugciq

Fatcat

reference URL

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference