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Internal ID UUID643fd2384d1b3753677519
Scientific name Gamochaeta malvinensis
Authority (H.Koyama) T.R.Dudley
First published in Rhodora 83(836): 478 (1981): (1981)

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Synonyms Top

Scientific name Authority First published in
Gamochaeta affinis Cabrera Bol. Soc. Argent. Bot. 9: 363 (1961)
Gnaphalium malvinense H.Koyama Acta Phytotax. Geobot. 29: 84 (1978)

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Distribution (via POWO/KEW) Top

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- Doubtful data
- Extinct
- Introduced
- Native

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Database ID/link to page
World Flora Online wfo-0000121804
Tropicos 50160332
KEW urn:lsid:ipni.org:names:908751-1
The Plant List gcc-83007
Open Tree Of Life 7051319
IPNI 908751-1
iNaturalist 357435
GBIF 3139717

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
Title Authors Publication Released IDs
Flavonoids in the Flowers of<i>Gnaphalium affine</i>D. Don Yoichi Itakura, Taiji Imoto, Akio Kato, Kazuyoshi Yagishita Oxford University Press (OUP) 13-Apr-2016
doi:10.1080/00021369.1975.10861937
Flavonoids in the flowers of Gnaphalium affine D. Don. Yoichi ITAKURA, Taiji IMOTO, Akio KATO, Kazuyoshi YAGISHITA Oxford University Press (OUP) 13-Jul-2011
doi:10.1271/BBB1961.39.2237
South African plant extractives. Part III. Helichrysin, a new chalcone glucoside from a Helichrysum species Winifred G. Wright Royal Society of Chemistry (RSC) 23-Apr-2004
doi:10.1039/P19760001819
Insect antifeedant flavonoids from Gnaphalium affine D. Don. Morimoto M, Kumeda S, Komai K J Agric Food Chem 01-May-2000
doi:10.1021/JF990282Q
PMID:10820110

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1271/BBB1961.39.2237
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1080/00021369.1975.10861937
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1080/00021369.1975.10861937
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(E)-1-[2-hydroxy-6-methoxy-4-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one 162883181 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 448.40 unknown https://doi.org/10.1039/P19760001819
3,5,7-trihydroxy-2-[3-hydroxy-4-[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 163019481 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 464.40 unknown https://doi.org/10.1080/00021369.1975.10861937
5,7-dihydroxy-2-[3-hydroxy-4-[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 71774967 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown https://doi.org/10.1080/00021369.1975.10861937
Luteolin 4'-glucoside 12304737 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown https://doi.org/10.1080/00021369.1975.10861937
Quercetin-4'-o-glucoside 12442954 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 464.40 unknown https://doi.org/10.1080/00021369.1975.10861937
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 26339717 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1271/BBB1961.39.2237
Quercetin 3-O-rhamnoside 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1271/BBB1961.39.2237
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1271/BBB1961.39.2237
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,6-Dihydroxy-3,7-dimethoxyflavone 44259724 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=CC=C3)O)O 314.29 unknown https://doi.org/10.1021/JF990282Q
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Hydroxy-3,6,7,8-tetramethoxyflavone 44260046 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=CC=C3)OC)OC)OC 358.30 unknown https://doi.org/10.1021/JF990282Q
5-Hydroxyauranetin 11079623 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 388.40 unknown https://doi.org/10.1021/JF990282Q
Gardenin B 96539 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O 358.30 unknown https://doi.org/10.1021/JF990282Q
Tangeretin 68077 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC 372.40 unknown https://doi.org/10.1021/JF990282Q
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids
2',4,4',6'-Tetramethoxychalcone 5378566 Click to see COC1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2OC)OC)OC 328.40 unknown https://doi.org/10.1021/JF990282Q
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2',4-Dihydroxy-4',6'-dimethoxychalcone 6293081 Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=C(C=C2)O)O 300.30 unknown https://doi.org/10.1021/JF990282Q
2',4',4-Trihydroxy-6'-methoxychalcone 162957 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=C(C=C2)O)O)O 286.28 unknown https://doi.org/10.1021/JF990282Q
Flavokawain A 5355469 Click to see COC1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2OC)OC)O 314.30 unknown https://doi.org/10.1021/JF990282Q
Helichrysetin 6253344 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=C(C=C2)O)O)O 286.28 unknown https://doi.org/10.1021/JF990282Q

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