(Q58856127)

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Analysis of flavonol glycosides of thirteen Epilobium species (onagraceae) by LC-UV and thermospray LC-MS

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title

Analysis of flavonol glycosides of thirteen Epilobium species (onagraceae) by LC-UV and thermospray LC-MS (English)

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main subject

Epilobium parviflorum

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inferred from

reverse claim

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

1 reference

inferred from

reverse claim

(2S,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-2,3-dihydro-1-benzopyran-4-one

1 reference

inferred from

reverse claim

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

1 reference

inferred from

reverse claim

(2S,3R)-3-[(2S,3R,4R,5R)-5-[(1R)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one

1 reference

inferred from

reverse claim

(2S,3R)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one

1 reference

1 reference

[(2R,3R,4S,5R,6S)-6-[[(2S,3R)-5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate

1 reference

inferred from

reverse claim

(2S,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3-dihydrochromen-4-one

1 reference

inferred from

reverse claim

(2S,3R)-5,7-dihydroxy-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one

1 reference

inferred from

reverse claim

(2S,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3-dihydrochromen-4-one

1 reference

inferred from

reverse claim

(2S,3S,4S,5R,6R)-6-[[(2S,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

1 reference

inferred from

reverse claim

(2S,3S,4S,5R,6R)-6-[[(2S,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid

1 reference

inferred from

reverse claim

[(2R,3R,4S,5R,6S)-6-[[(2S,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate

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onagraceae

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based on heuristic

inferred from title

Chamaenerion dodonaei

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1 reference

1 reference

K. Hostettmann

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Jean-Luc Wolfender

series ordinal

object named as

J.L. Wolfender

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author name string

B. Ducrey

series ordinal

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A. Marston

series ordinal

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publication date

January 1995

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16 September 2022

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inferred from page(s)

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129-137

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cites work

Isolation of flavonoids from Populus nigra as delta 4-3-ketosteroid (5 alpha) reductase inhibitors

1 reference

24 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0031-9422(94)00629-8

Liquid chromatographic—thermospray mass spectrometric analysis of crude plant extracts containing phenolic and terpene glycosides

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24 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0031-9422(94)00629-8

24 October 2022

https://opencitations.net/index/coci/api/v1/citations/10.1016/0021-9673(93)83400-M

Liquid chromatographic—UV detection and liquid chromatographic—thermospray mass spectrometric analysis of Chironia (Gentianaceae) species

2 references

24 October 2022

https://opencitations.net/index/coci/api/v1/citations/10.1016/0021-9673(93)83401-D

24 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0031-9422(94)00629-8

Isolation of the antiphlogistic principle from Epilobium angustifolium

1 reference

24 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0031-9422(94)00629-8

Isolation and determination of flavonol glycosides from epilobium species

1 reference

24 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0031-9422(94)00629-8

Inhibition of human estrogen synthetase (aromatase) by flavones

1 reference

24 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0031-9422(94)00629-8

On the influence of the sugar moiety on the antigonadotropic activity of luteoline glycosides

1 reference

24 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0031-9422(94)00629-8

An improved high performance liquid chromatographic post-column derivatization procedure for the UV — Vis spectroscopic characterization of phenolic compounds

1 reference

27 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/0031-9422(94)00629-8

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DOI

10.1016/0031-9422(94)00629-8

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