(Q45953338)

18 December 2017

title

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

1 reference

18 December 2017

2''-O-alpha-L-Rhamnopyranostylquercitrin

1 reference

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

1 reference

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

1 reference

Kaempferol 3-(2-rhamnopyranosylrhamnopyranoside)

1 reference

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

1 reference

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

1 reference

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

1 reference

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

1 reference

Yu-Jen Kuo

1

1 reference

18 December 2017

Ping-Chun Hsiao

2

1 reference

18 December 2017

Li-Jie Zhang

3

1 reference

18 December 2017

Ming-Der Wu

4

1 reference

18 December 2017

Yu-Han Liang

5

1 reference

18 December 2017

Hsiu-O Ho

6

1 reference

18 December 2017

Yao-Haur Kuo

7

1 reference

18 December 2017

Journal of Natural Products

publication date

8 June 2009

3 references

16 September 2022

16 September 2022

1 reference

18 December 2017

volume

72

1 reference

18 December 2017

issue

6

1 reference

18 December 2017

page(s)

1097-1101

1 reference

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

1 reference

18 December 2017