(Q44596821)

4 December 2017

title

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

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(1R,4S,5R,8S,11R,13R,14S,17R,18S,21R,24R)-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

4 December 2017

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(6aS,6bS,8aS,11R,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione

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(2S,4S,4aR,6aS,6bR,8aR,10S,12aR,12bR,14bS)-4,10-dihydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-2-carboxylic acid

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3beta,22beta-Dihydroxyolean-12-en-29-oic acid

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[(1S,2S,4R,5S,6R,7R,9R,12S)-5,12-diacetyloxy-6-(acetyloxymethyl)-4-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate

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

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(+)-8-Methoxyisolariciresinol

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(4R,4aS,6aS,6bR,8aS,11R,12aR,12bS,14aS,14bS)-11-(hydroxymethyl)-4,4a,6b,8a,11,12b,14a-heptamethyl-tetradecahydro-1H-picen-3-one

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(6S,7S,8R)-8-(4-hydroxy-3-methoxyphenyl)-6,7-bis(hydroxymethyl)-1,3-dimethoxy-5,6,7,8-tetrahydronaphthalen-2-ol

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15alpha-Hydroxyfriedelan-3-one

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(4R,4aR,6aS,6aS,6bR,7S,8aR,11R,12aR,14aS,14bR)-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

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(2R,4S,4aR,6aR,6aS,6bR,8aR,12aR,14bS)-4-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-2-carboxylic acid

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Triptotriterpenic acid C

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(4R,4aR,6aS,6aS,6bR,8aR,12aR,14aS,14bR)-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

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Toshio Morikawa

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4 December 2017

Akinobu Kishi

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4 December 2017

Yutana Pongpiriyadacha

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4 December 2017

Hisashi Matsuda

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4 December 2017

Masayuki Yoshikawa

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Journal of Natural Products

4 December 2017

publication date

29 August 2003

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16 September 2022

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4 December 2017

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4 December 2017

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4 December 2017

page(s)

1191-1196

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

4 December 2017

cites work

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12 April 2024

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

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

1 reference

12 April 2024

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

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

1 reference

12 April 2024

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

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

1 reference

12 April 2024

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

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

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12 April 2024

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

Identifiers

DOI

10.1021/NP0301543

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release_qiwkltmhcvfwzado5m2vy4xukq

4 December 2017

Fatcat ID

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https://api.fatcat.wiki/v0/release/qiwkltmhcvfwzado5m2vy4xukq

Fatcat

reference URL

mapped directly with Wikidata item

24 November 2022

based on heuristic

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