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Cheirolophus intybaceus

Cheirolophus intybaceus - 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 UUID643fd005a2746512716054
Scientific name Cheirolophus intybaceus
Authority (Lam.) Dostál
First published in Bot. J. Linn. Soc. 71(3): 274 (1976)

Description Top

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Synonyms Top

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Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Cheirolophus intybaceus subsp. intybaceus Unknown
Cheirolophus intybaceus subsp. lagunae (Olivares, Peris, Stübing & J.Martín) Mateo & M.B.Crespo Flora Montiber. 59: 90 (2015)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Northern Europe
      • Great Britain
    • Southwestern Europe
      • Corse
      • France
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000095505
INPN 90653
KEW urn:lsid:ipni.org:names:192734-1
The Plant List gcc-51686
Open Tree Of Life 404582
Observations.org 129384
NCBI Taxonomy 64995
IPNI 192734-1
iNaturalist 512436
GBIF 3097063
EPPO CENIN
EOL 6216465

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Environmental isolation explains Iberian genetic diversity in the highly homozygous model grass Brachypodium distachyon Marques I, Shiposha V, López-Alvarez D, Manzaneda AJ, Hernandez P, Olonova M, Catalán P BMC Evol Biol 15-Jun-2017
PMCID:PMC5472904
doi:10.1186/s12862-017-0996-x
PMID:28619047
The explosive radiation of Cheirolophus (Asteraceae, Cardueae) in Macaronesia Vitales D, Garnatje T, Pellicer J, Vallès J, Santos-Guerra A, Sanmartín I BMC Evol Biol 02-Jun-2014
PMCID:PMC4048045
doi:10.1186/1471-2148-14-118
PMID:24888240
Phylogeography sheds light on the central–marginal hypothesis in a Mediterranean narrow endemic plant Pouget M, Youssef S, Migliore J, Juin M, Médail F, Baumel A Ann Bot 20-Aug-2013
PMCID:PMC3806523
doi:10.1093/aob/mct183
PMID:23962409
Sesquiterpene lactones, lignans and aromatic esters from Cheirolophus species J.Alberto Marco, Juan F. Sanz-Cervera, Vicente Garcia-Lliso, Alfonso Susanna, Nuria Garcia-Jacas Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)89537-0

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(3aR,6R,7S,7aR)-6-ethenyl-7-(3-hydroxyprop-1-en-2-yl)-6-methyl-3-methylidene-2-oxo-4,5,7,7a-tetrahydro-3aH-1-benzofuran-4-yl] 2-(hydroxymethyl)prop-2-enoate 162880468 Click to see CC1(CC(C2C(C1C(=C)CO)OC(=O)C2=C)OC(=O)C(=C)CO)C=C 348.40 unknown https://doi.org/10.1016/S0031-9422(00)89537-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4S,6E,10Z,11aR)-10-(hydroxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-2-(hydroxymethyl)but-2-enoate 162951843 Click to see CC=C(CO)C(=O)OC1CC(=CCCC(=CC2C1C(=C)C(=O)O2)CO)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)89537-0
[(3aR,4S,6E,10Z,11aR)-10-(hydroxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-methylprop-2-enoate 162972447 Click to see CC1=CCCC(=CC2C(C(C1)OC(=O)C(=C)C)C(=C)C(=O)O2)CO 332.40 unknown https://doi.org/10.1016/S0031-9422(00)89537-0
Salonitenolide 5281498 Click to see CC1=CCCC(=CC2C(C(C1)O)C(=C)C(=O)O2)CO 264.32 unknown https://doi.org/10.1016/S0031-9422(00)89537-0
> Organic oxygen compounds / Organooxygen compounds / Enediols
Dihydro-caffeic acid 15847196 Click to see C1C(C=CC(=C1O)O)C=CC(=O)O 182.17 unknown https://doi.org/10.1016/S0031-9422(00)89537-0
> 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/S0031-9422(00)89537-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Axillarin 5281603 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O 346.30 unknown https://doi.org/10.1016/S0031-9422(00)89537-0
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/S0031-9422(00)89537-0
Jaceosidin 5379096 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown https://doi.org/10.1016/S0031-9422(00)89537-0

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