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Onopordum corymbosum

Onopordum corymbosum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fcaecbaf62866124362
Scientific name Onopordum corymbosum
Authority Willk.
First published in Linnaea 30: 108 (1859-61)

Description Top

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Synonyms Top

Scientific name Authority First published in
Onopordum tauricum subsp. corymbosum (Willk.) Nyman Nyman, Consp. Fl. Eur. 1879. 403 1879
Onopordum tauricum subsp. humile (Loscos) Rouy Rouy in Bull. Soc. Bot. France 43. 1896. 591 1896

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000042318
INPN 110249
KEW urn:lsid:ipni.org:names:235272-1
The Plant List gcc-140933
Open Tree Of Life 5144245
Observations.org 120128
IPNI 235272-1
iNaturalist 513646
GBIF 3094918
EPPO ONRCO
EOL 6245335

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

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, flavonolignans and a phenylpropanoid from Onopordon corymbosum M. Luz Cardona, Begon˜a Garcia, Jost R. Pedro, Jorge F. Sinisterra Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85131-X
Sesquiterpene lactones and an elemane derivative from Onopordon corymbosum Ma Luz Cardona, Begoña Garcia, Jose R. Pedro, Jorge F. Sinisterra Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80228-6

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
> Lignans, neolignans and related compounds / Flavonolignans
Hydnocarpin 5489114 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO)O 464.40 unknown https://doi.org/10.1016/0031-9422(90)85131-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(3aS,4R,6R,7S,7aS)-6-ethenyl-4-hydroxy-7-(3-hydroxyprop-1-en-2-yl)-6-methyl-3-methylidene-4,5,7,7a-tetrahydro-3aH-1-benzofuran-2-one 133554346 Click to see CC1(CC(C2C(C1C(=C)CO)OC(=O)C2=C)O)C=C 264.32 unknown https://doi.org/10.1016/0031-9422(89)80228-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Elemacarmanin 13891365 Click to see CC1(CC(C(C(C1C(=C)CO)O)C(=C)C(=O)OC)OC(=O)C(=C)CO)C=C 380.40 unknown https://doi.org/10.1016/0031-9422(89)80228-6
> 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/10.1016/0031-9422(90)85131-X
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/10.1016/0031-9422(90)85131-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/0031-9422(90)85131-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown https://doi.org/10.1016/0031-9422(90)85131-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1016/0031-9422(90)85131-X
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown https://doi.org/10.1016/0031-9422(90)85131-X

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