The absolute stereostructures of three rare D:B-friedobaccharane skeleton triterpenes from the leaves of Salacia chinensis (Q104993670)

From Wikidata

Jump to navigation Jump to search

scientific article published on 16 May 2008

edit

Language	Label	Description	Also known as
English	The absolute stereostructures of three rare D:B-friedobaccharane skeleton triterpenes from the leaves of Salacia chinensis	scientific article published on 16 May 2008

Statements

instance of

scholarly article

0 references

title

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

1 reference

reference URL

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

main subject

Salacia chinensis

1 reference

inferred from

reverse claim

(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

1 reference

inferred from

reverse claim

uvaol

1 reference

inferred from

reverse claim

(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

1 reference

inferred from

reverse claim

Epifriedelin

1 reference

inferred from

reverse claim

betulone

1 reference

inferred from

reverse claim

29-Nor-20-oxolupeol

1 reference

inferred from

reverse claim

(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

1 reference

inferred from

reverse claim

betulin

1 reference

inferred from

reverse claim

betulinic acid

1 reference

inferred from

reverse claim

erythrodiol

1 reference

inferred from

reverse claim

(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

1 reference

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

1 reference

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

1 reference

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

1 reference

inferred from

reverse claim

ursolic acid

1 reference

inferred from

reverse claim

Octandronol

1 reference

inferred from

reverse claim

(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

inferred from

reverse claim

oleanolic acid

1 reference

inferred from

reverse claim

lupan-3beta,20-diol

1 reference

inferred from

reverse claim

friedelin

1 reference

inferred from

reverse claim

(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

inferred from

reverse claim

author name string

Yi Zhang

series ordinal

1

1 reference

reference URL

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

Seikou Nakamura

series ordinal

2

1 reference

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

1 reference

stated in

Crossref

retrieved

16 September 2022

published in

Tetrahedron

1 reference

reference URL

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

volume

64

1 reference

reference URL

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

issue

30-31

1 reference

reference URL

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

page(s)

7347-7352

1 reference

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

stated in

COCI

retrieved

12 April 2024

reference URL

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

stated in

COCI

retrieved

12 April 2024

reference URL

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

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

1 reference

stated in

COCI

retrieved

12 April 2024

reference URL

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

1 reference

stated in

COCI

retrieved

12 April 2024

reference URL

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

1 reference

stated in

COCI

retrieved

12 April 2024

reference URL

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

stated in

COCI

retrieved

12 April 2024

reference URL

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

stated in

COCI

retrieved

12 April 2024

reference URL

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

Stereochemistry of Novel Triterpenes from Cynanchum hancokianum.

1 reference

stated in

COCI

retrieved

12 April 2024

reference URL

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

1 reference

stated in

COCI

retrieved

12 April 2024

reference URL

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

Identifiers

DOI

10.1016/J.TET.2008.05.054

0 references

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q104993670&oldid=2133558397"