Potential anti-neuroinflammatory triterpenoids isolated from Chinese acorns (Quercus serrata var. brevipetiolata) (Q113959805)

scientific article published on 26 September 2018

Language	Label	Description	Also known as
English	Potential anti-neuroinflammatory triterpenoids isolated from Chinese acorns (Quercus serrata var. brevipetiolata)	scientific article published on 26 September 2018

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instance of

scholarly article

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title

Potential anti-neuroinflammatory triterpenoids isolated from Chinese acorns (Quercus serrata var. brevipetiolata) (English)

1 reference

reference URL

http://api.crossref.org/works/10.1016%2Fj.jff.2018.09.022

main subject

Quercus serrata

object named as

Quercus serrata

2 references

[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,4aR,6aS,6bR,9S,10R,11R,12aR)-1,10,11-trihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate

1 reference

inferred from

reverse claim

[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,4aR,6aS,6bR,10R,11R,12aR)-1,10,11-trihydroxy-9,9-bis(hydroxymethyl)-2,2,6a,6b,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate

1 reference

inferred from

reverse claim

[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2R,4aS,6aS,6bR,9R,10R,11R,12aR)-1,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate

1 reference

inferred from

reverse claim

NCGC00179844-02_C36H58O11_1-O-[(2alpha,3beta,5xi,9xi,18xi,19alpha)-2,3,19,23-Tetrahydroxy-28-oxoolean-12-en-28-yl]-beta-D-glucopyranose

1 reference

inferred from

reverse claim

(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (1R,2R,4aS,6aS,6bR,9S,10R,11R,12aR)-1,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylate

1 reference

inferred from

reverse claim

XSXXFSZMJCUMKW-DYVAUQPQSA-N

1 reference

inferred from

reverse claim

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

1 reference

inferred from

reverse claim

(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (1S,4aR,6aS,6bR,9S,10S,12aR)-9-formyl-1,10-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,12a-pentamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylate

1 reference

inferred from

reverse claim

(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (1R,3aS,5aR,5bR,8R,9R,10R,11aR)-9,10-dihydroxy-8-(hydroxymethyl)-5a,5b,8,11a-tetramethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate

1 reference

1 reference

(1S,4aR,6aS,6bR,9S,10R,11R,12aR)-1,10,11-trihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid

1 reference

inferred from

reverse claim

(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (1R,2R,4aS,6aS,6bR,9S,10R,11R,12aR)-9-formyl-1,10,11-trihydroxy-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylate

1 reference

inferred from

reverse claim

(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (4aS,6aR,6bS,8aR,12S,14bR,16R,16aR)-12,16-dihydroxy-4a,6a,6b,11,11,14b-hexamethyl-2-propyl-2H,3H,4H,4bH,5H,6H,7H,8H,9H,10H,12H,12aH,14H,14aH,15H,16H,16aH-piceno[3,4-b]pyran-8a-carboxylate

1 reference

inferred from

reverse claim

(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl (1R,2R,4aS,6aS,6bR,9S,10S,11R,12aR)-1,9,11-trihydroxy-1,2,6a,6b,9,12a-hexamethyl-10-(3,4,5-trihydroxybenzoyloxy)-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylate

1 reference

inferred from

reverse claim

(1R,2R,4aS,6aS,6bR,9R,10R,11R,12aR)-1,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid

1 reference

inferred from

reverse claim

(1S,2R,4aS,6aS,6bR,9R,10R,11R,12aR)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid

1 reference

4

1 reference

reference URL

http://api.crossref.org/works/10.1016%2Fj.jff.2018.09.022

author name string

Yanqiong Lei

series ordinal

1

1 reference

reference URL

http://api.crossref.org/works/10.1016%2Fj.jff.2018.09.022

Yuying Huang

series ordinal

2

1 reference

reference URL

http://api.crossref.org/works/10.1016%2Fj.jff.2018.09.022

Yihai Wang

series ordinal

3

1 reference

reference URL

http://api.crossref.org/works/10.1016%2Fj.jff.2018.09.022

publication date

26 September 2018

1 reference

reference URL

http://api.crossref.org/works/10.1016%2Fj.jff.2018.09.022

published in

Journal of Functional Foods

1 reference

reference URL

http://api.crossref.org/works/10.1016%2Fj.jff.2018.09.022

volume

50

1 reference

reference URL

http://api.crossref.org/works/10.1016%2Fj.jff.2018.09.022

page(s)

18-25

1 reference

reference URL

http://api.crossref.org/works/10.1016%2Fj.jff.2018.09.022

cites work

Bioactive pentacyclic triterpenes from the stems of Combretum laxum.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.3390/MOLECULES13112717

Quadranosides VI-XI, six new triterpene glucosides from the seeds of Combretum quadrangulare

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.48.1114

Identifiers

DOI

10.1016/J.JFF.2018.09.022

1 reference

reference URL

http://api.crossref.org/works/10.1016%2Fj.jff.2018.09.022

Potential anti-neuroinflammatory triterpenoids isolated from Chinese acorns (Quercus serrata var. brevipetiolata) (Q113959805)

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Potential anti-neuroinflammatory triterpenoids isolated from Chinese acorns (Quercus serrata var. brevipetiolata) (Q113959805)

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