(Q104993670)

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The absolute stereostructures of three rare D:B-friedobaccharane skeleton triterpenes from the leaves of Salacia chinensis

scientific article published on 16 May 2008

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The absolute stereostructures of three rare D:B-friedobaccharane skeleton triterpenes from the leaves of Salacia chinensis (English)

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http://api.crossref.org/works/10.1016%2Fj.tet.2008.05.054

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(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-1-(3-hydroxyprop-1-en-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-hexadecahydrocyclopenta[a]chrysen-9-ol

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(1R,3aR,5S,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-5,9-diol

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(3S,4aR,6aR,6aS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6a,8a,11,12,14b-octamethyl-2,3,4a,5,6,8,9,10,11,12,12a,13,14,14a-tetradecahydro-1H-picen-3-ol

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(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bS)-1-acetyl-3a,5a,5b,8,8,11a-hexamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one

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inferred from

reverse claim

(4R,4aS,6aS,6aS,6bR,8aR,12aR,13R,14aS,14bS)-13-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

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inferred from

reverse claim

(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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inferred from

reverse claim

(2S,4aS,4bR,6aS,8S,10aR,10bS)-8-[(E)-4-hydroxy-4-methylpent-2-enyl]-1,1,4b,6a,8,10a-hexamethyl-3,4,4a,5,6,7,9,10,10b,11-decahydro-2H-chrysen-2-ol

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(1R,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14aR,14bS)-1,2,4a,6a,6b,9,9,12a-octamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-hexadecahydropicene-2,10-diol

1 reference

inferred from

reverse claim

(2S,4aS,4bR,6aS,8S,10aR,10bS)-8-[(3R)-3-hydroxy-4-methylpent-4-enyl]-1,1,4b,6a,8,10a-hexamethyl-3,4,4a,5,6,7,9,10,10b,11-decahydro-2H-chrysen-2-ol

1 reference

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1 reference

(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bS)-1-(3-hydroxyprop-1-en-2-yl)-3a,5a,5b,8,8,11a-hexamethyl-tetradecahydro-1H-cyclopenta[a]chrysen-9-one

1 reference

Yi Zhang

1

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reference URL

http://api.crossref.org/works/10.1016%2Fj.tet.2008.05.054

Seikou Nakamura

series ordinal

2

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reference URL

http://api.crossref.org/works/10.1016%2Fj.tet.2008.05.054

Tao Wang

series ordinal

3

1 reference

reference URL

http://api.crossref.org/works/10.1016%2Fj.tet.2008.05.054

Hisashi Matsuda

series ordinal

4

1 reference

reference URL

http://api.crossref.org/works/10.1016%2Fj.tet.2008.05.054

Masayuki Yoshikawa

series ordinal

5

1 reference

reference URL

http://api.crossref.org/works/10.1016%2Fj.tet.2008.05.054

publication date

July 2008

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16 September 2022

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http://api.crossref.org/works/10.1016%2Fj.tet.2008.05.054

volume

64

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reference URL

http://api.crossref.org/works/10.1016%2Fj.tet.2008.05.054

page(s)

7347-7352

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reference URL

http://api.crossref.org/works/10.1016%2Fj.tet.2008.05.054

issue

30-31

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reference URL

http://api.crossref.org/works/10.1016%2Fj.tet.2008.05.054

cites work

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

1 reference

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

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12 April 2024

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Absolute structures of new megastigmane glycosides, foliasalaciosides E(1), E(2), E(3), F, G, H, and I from the leaves of Salacia chinensis

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.56.547

3-epicabraleahydroxylactone and other triterpenoids from camellia oil and their inhibitory effects on Epstein-Barr virus activation

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.52.153

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

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12 April 2024

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

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

Stereochemistry of Novel Triterpenes from Cynanchum hancokianum.

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12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.39.2271

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

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DOI

10.1016/J.TET.2008.05.054

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(Q104993670)

The absolute stereostructures of three rare D:B-friedobaccharane skeleton triterpenes from the leaves of Salacia chinensis

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