Labdane diterpenoid glycosides from Alpinia densespicata and their nitric oxide inhibitory activities in macrophages. (Q45953338)

18 December 2017

title

Labdane diterpenoid glycosides from Alpinia densespicata and their nitric oxide inhibitory activities in macrophages. (English)

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18 December 2017

2''-O-alpha-L-Rhamnopyranostylquercitrin

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1 reference

4-[(2S,6aR,8S,10aS)-8-hydroxy-7,7,10a-trimethyl-2,4,5,6,6a,8,9,10-octahydro-1H-benzo[f]isochromen-2-yl]-2H-furan-5-one

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4-[(2R,4S,4aS,6aR,8S,10aR,10bR)-8-{[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1H-naphtho[2,1-c]pyran-2-yl]-5H-furan-2-one

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Kaempferol 3-(2-rhamnopyranosylrhamnopyranoside)

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1 reference

3-[(2R,6aS,8S,10aS)-8-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-7,7,10a-trimethyl-2,4,5,6,6a,8,9,10-octahydro-1H-benzo[f]isochromen-2-yl]-2H-furan-5-one

1 reference

4-[(2S,6aR,8S,10aS)-8-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-7,7,10a-trimethyl-2,4,5,6,6a,8,9,10-octahydro-1H-benzo[f]isochromen-2-yl]-2H-furan-5-one

1 reference

1 reference

[(2R,3S,4S,5R,6R)-6-{[(2R,4S,4aS,6aR,8S,10aR,10bR)-4-hydroxy-7,7,10a-trimethyl-2-(5-oxo-2H-furan-3-yl)-decahydro-1H-naphtho[2,1-c]pyran-8-yl]oxy}-3,4-dihydroxy-5-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]methyl acetate

1 reference

[(2R,3S,4S,5R,6R)-6-{[(2R,4aR,6aR,8S,10aR,10bS)-4-hydroxy-7,7,10a-trimethyl-2-(2-oxo-5H-furan-3-yl)-decahydro-1H-naphtho[2,1-c]pyran-8-yl]oxy}-3,4-dihydroxy-5-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]methyl acetate

1 reference

1 reference

4-[(2S,4R,4aS,6aR,8S,10aS,10bS)-8-{[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1H-naphtho[2,1-c]pyran-2-yl]-5H-furan-2-one

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2-(2,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

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3-[(2S,6aS,8S,10aS)-8-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-7,7,10a-trimethyl-2,4,5,6,6a,8,9,10-octahydro-1H-benzo[f]isochromen-2-yl]-2H-furan-5-one

1 reference

(2S,3R,4R,5R,6S)-2-{[(2R,3R,4S,5S,6R)-2-{[(2R,3S,3aR,5aR,7S,9aR,9bR)-3-hydroxy-6,6,9a-trimethyl-2-(prop-1-en-2-yl)-decahydro-1H-cyclopenta[a]naphthalen-7-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

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3-[(2R,4aR,6aR,8S,10aR,10bR)-8-{[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1H-naphtho[2,1-c]pyran-2-yl]-5H-furan-2-one

1 reference

[(2R,3S,4S,5R,6R)-6-{[(2S,4R,4aS,6aR,8S,10aS,10bS)-4-hydroxy-7,7,10a-trimethyl-2-(5-oxo-2H-furan-3-yl)-decahydro-1H-naphtho[2,1-c]pyran-8-yl]oxy}-3,4-dihydroxy-5-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]methyl acetate

1 reference

(2S,3R,4R,5R,6S)-2-{[(2R,3R,4S,5S,6R)-2-{[(2R,3S,3aR,5aR,7S,9aR,9bR)-3-hydroxy-2-(3-hydroxyprop-1-en-2-yl)-6,6,9a-trimethyl-decahydro-1H-cyclopenta[a]naphthalen-7-yl]oxy}-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

1 reference

3-[(2R,6aR,8S,10aS)-8-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-7,7,10a-trimethyl-2,4,5,6,6a,8,9,10-octahydro-1H-benzo[f]isochromen-2-yl]-2H-furan-5-one

1 reference

4-[(2R,6aR,8S,10aS)-8-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-7,7,10a-trimethyl-2,4,5,6,6a,8,9,10-octahydro-1H-benzo[f]isochromen-2-yl]-2H-furan-5-one

1 reference

3-[(2S,6aR,8S,10aS)-8-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-7,7,10a-trimethyl-2,4,5,6,6a,8,9,10-octahydro-1H-benzo[f]isochromen-2-yl]-2H-furan-5-one

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Yu-Jen Kuo

1

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18 December 2017

Ping-Chun Hsiao

2

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18 December 2017

Li-Jie Zhang

3

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18 December 2017

Ming-Der Wu

4

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18 December 2017

Yu-Han Liang

5

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18 December 2017

Hsiu-O Ho

6

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18 December 2017

Yao-Haur Kuo

7

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18 December 2017

Journal of Natural Products

publication date

8 June 2009

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16 September 2022

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18 December 2017

volume

72

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18 December 2017

issue

6

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18 December 2017

page(s)

1097-1101

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18 December 2017

1′-Acetoxychavicol Acetate as a Potent Inhibitor of Tumor Promoter-induced Epstein-Barr Virus Activation fromLanguas gaianga, a Traditional Thai Condiment

cites work

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1271/BBB.57.1344

Anti-platelet aggregation triterpene saponins from the galls of Sapindus mukorossi

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.1248/CPB.55.1412

Identifiers

DOI

10.1021/NP900019N

1 reference

18 December 2017

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18 December 2017