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Internal ID UUID643fd1bd3640e476275532
Scientific name Centaurea cuneifolia
Authority Sm.
First published in Fl. Graec. Prodr. 2(1): 198 (1813)

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Centaurea cuneifolia subsp. pallida (Friv.) Hayek Repert. Spec. Nov. Regni Veg. Beih. 30(2): 763 (1931)

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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
  • Europe
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Romania
      • Turkey-in-Europe
      • Yugoslavia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000117798
Tropicos 2700402
KEW urn:lsid:ipni.org:names:190299-1
The Plant List gcc-79149
Open Tree Of Life 992160
Observations.org 116299
NCBI Taxonomy 1048535
IPNI 190299-1
iNaturalist 521766
GBIF 3127971
EOL 6216052

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)!
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Title Authors Publication Released IDs
Overview of the anti-inflammatory effects, pharmacokinetic properties and clinical efficacies of arctigenin and arctiin from Arctium lappa L Gao Q, Yang M, Zuo Z Acta Pharmacol Sin 26-Apr-2018
PMCID:PMC5943914
doi:10.1038/aps.2018.32
PMID:29698388
Anti-Inflammatory properties of Salograviolide A purified from Lebanese plant Centaurea ainetensis Al-Saghir J, Al-Ashi R, Salloum R, Saliba NA, Talhouk RS, Homaidan FR BMC Complement Altern Med 23-Sep-2009
PMCID:PMC2761300
doi:10.1186/1472-6882-9-36
PMID:19775456
Chemical constituents of Centaurea cadmea C. Karamenderes, E. Bedir, H. Abou-Gazar, I. A. Khan Springer Science and Business Media LLC 23-Feb-2008
doi:10.1007/S10600-007-0232-9
Flavonoids of Centaurea cuneifolia. Oksüz S, Halfon B, Terem B Planta Med 01-Feb-1988
doi:10.1055/S-2006-962352
PMID:17265218
Chemical Constituents of Centaurea brugueriana. Rustaiyan A, Niknejad A, Aynehchi Y Planta Med 01-Mar-1982
doi:10.1055/S-2007-971441
PMID:17402113

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 / 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/10.1055/S-2007-971441
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
Cnicin 5281435 Click to see CC1=CCCC(=CC2C(C(C1)OC(=O)C(=C)C(CO)O)C(=C)C(=O)O2)CO 378.40 unknown https://doi.org/10.1007/S10600-007-0232-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1055/S-2007-971441
https://doi.org/10.1007/S10600-007-0232-9
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1055/S-2006-962352
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-2007-971441
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/S10600-007-0232-9
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/S10600-007-0232-9
https://doi.org/10.1055/S-2007-971441
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide 5280862 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 300.26 unknown https://doi.org/10.1055/S-2007-971441
> 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/10.1055/S-2007-971441
https://doi.org/10.1007/S10600-007-0232-9
https://doi.org/10.1055/S-2006-962352
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupatilin 5273755 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 344.30 unknown https://doi.org/10.1055/S-2006-962352
https://doi.org/10.1055/S-2007-971441
https://doi.org/10.1007/S10600-007-0232-9
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/10.1007/S10600-007-0232-9
https://doi.org/10.1055/S-2007-971441
https://doi.org/10.1055/S-2006-962352
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1055/S-2006-962352
Salvigenin 161271 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown https://doi.org/10.1055/S-2006-962352
https://doi.org/10.1055/S-2007-971441
https://doi.org/10.1007/S10600-007-0232-9

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