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Internal ID UUID643fc8f609966057627585
Scientific name Centaurea spruneri
Authority Boiss. & Heldr.
First published in 132 1846

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Synonyms Top

Scientific name Authority First published in
Colymbada spruneri (Boiss.) Holub Folia Geobot. Phytotax. 7(3): 316 (1972)
Centaurea fraasii Sch.Bip. ex Nyman Consp. Fl. Eur. 2: 429 (1879)
Centaurea spruneriana Halácsy Bull. Herb. Boissier vi. 640
Centaurea saxicola var. spruneriana Sch.Bip. Sch. Bip. in Flora 25, Beibl. 1. 1842. 160 1842

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Centaurea spruneri subsp. guicciardii (Boiss.) Hayek Repert. Spec. Nov. Regni Veg. Beih. 30(2): 749. 1931 (1931)

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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-0000026624
KEW urn:lsid:ipni.org:names:191665-1
The Plant List gcc-125730
Open Tree Of Life 7613439
Observations.org 145619
IPNI 191665-1
iNaturalist 521536
GBIF 3128884
EOL 6217414

Genomes (via NCBI) Top

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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
Antimicrobial activity of secondary metabolites isolated from Centaurea spruneri Boiss.& Heldr. Ana Ciric, Anastasia Karioti, Jasmina Glamoclija, Marina Sokovic, Helen Skaltsa National Library of Serbia 11-Jan-2011
doi:10.2298/JSC100127008C

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.2298/JSC100127008C
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3-Hydroxy-4-methoxybenzoic acid 12575 Click to see COC1=C(C=C(C=C1)C(=O)O)O 168.15 unknown https://doi.org/10.2298/JSC100127008C
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown https://doi.org/10.2298/JSC100127008C
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.2298/JSC100127008C
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.2298/JSC100127008C
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.2298/JSC100127008C

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