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Internal ID UUID643fcf0ca783e850479598
Scientific name Centaurea kotschyi
Authority (Boiss.) Hayek
First published in Centaur. Exsicc. Crit. Fasc. 3: 140. 1921 , fide G. Wagenitz

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Synonyms Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Centaurea kotschyi subsp. floccosa (Boiss.) Greuter Willdenowia 33(1): 55 (2003) (2003)
Centaurea kotschyi subsp. kotschyi (Boiss. & Heldr.) Hayek
Centaurea kotschyi subsp. persica (Boiss.) Greuter Willdenowia 33(1): 55 (2003) (2003)

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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
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Western Asia
      • Iran
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000086857
Tropicos 2729490
KEW urn:lsid:ipni.org:names:190819-1
The Plant List gcc-43240
Open Tree Of Life 717417
NCBI Taxonomy 75631
IPNI 190819-1
iNaturalist 1111597
GBIF 3128685

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
Structures, Sources, Identification/Quantification Methods, Health Benefits, Bioaccessibility, and Products of Isorhamnetin Glycosides as Phytonutrients Wang H, Chen L, Yang B, Du J, Chen L, Li Y, Guo F Nutrients 18-Apr-2023
PMCID:PMC10143801
doi:10.3390/nu15081947
PMID:37111165
Fire disturbance effects on plant taxonomic and functional β‐diversity mediated by topographic exposure Abedi M, Omidipour R, Hosseini SV, Bahalkeh K, Gross N Ecol Evol 25-Jan-2022
PMCID:PMC8796949
doi:10.1002/ece3.8552
PMID:35127050
A Review on Antidiabetic Activity of Centaurea spp.: A New Approach for Developing Herbal Remedies Fattaheian-Dehkordi S, Hojjatifard R, Saeedi M, Khanavi M Evid Based Complement Alternat Med 05-Jul-2021
PMCID:PMC8275385
doi:10.1155/2021/5587938
PMID:34285703
Cynaropicrin: A Comprehensive Research Review and Therapeutic Potential As an Anti-Hepatitis C Virus Agent Elsebai MF, Mocan A, Atanasov AG Front Pharmacol 08-Dec-2016
PMCID:PMC5143615
doi:10.3389/fphar.2016.00472
PMID:28008316
Potential Use of Turkish Medicinal Plants in the Treatment of Various Diseases Ozkan G, Kamiloglu S, Ozdal T, Boyacioglu D, Capanoglu E Molecules 25-Feb-2016
PMCID:PMC6273156
doi:10.3390/molecules21030257
PMID:26927038
Centaurea Revisited: A Molecular Survey of the Jacea Group GARCIA-JACAS N, UYSAL T, ROMASHCHENKO K, SUÁREZ-SANTIAGO VN, ERTUĞRUL K, SUSANNA A Ann Bot 01-Oct-2006
PMCID:PMC2806161
doi:10.1093/aob/mcl157
PMID:16873424
Guaianolides from Centaurea kotschyi Sevil Oksuz, Ersan Putun Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(83)80180-0

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 / Sesquiterpene lactones / Guaianolides and derivatives
(8-Hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl) 2,3-dihydroxy-2-methylpropanoate 75072485 Click to see CC(CO)(C(=O)OC1CC(=C)C2CC(C(=C)C2C3C1C(=C)C(=O)O3)O)O 364.40 unknown https://doi.org/10.1016/0031-9422(83)80180-0
(8-Hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl) 3-chloro-2-hydroxy-2-methylpropanoate 71439502 Click to see CC(CCl)(C(=O)OC1CC(=C)C2CC(C(=C)C2C3C1C(=C)C(=O)O3)O)O 382.80 unknown https://doi.org/10.1016/0031-9422(83)80180-0
[(3aR,4S,6aR,8S,9aR,9bR)-8-hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] (2R)-3-chloro-2-hydroxy-2-methylpropanoate 162931220 Click to see CC(CCl)(C(=O)OC1CC(=C)C2CC(C(=C)C2C3C1C(=C)C(=O)O3)O)O 382.80 unknown https://doi.org/10.1016/0031-9422(83)80180-0
[(3aR,4S,6aR,8S,9aR,9bR)-8-hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] (2S)-2,3-dihydroxy-2-methylpropanoate 163038682 Click to see CC(CO)(C(=O)OC1CC(=C)C2CC(C(=C)C2C3C1C(=C)C(=O)O3)O)O 364.40 unknown https://doi.org/10.1016/0031-9422(83)80180-0
Cynaropicrin 119093 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)OC(=O)C(=C)CO 346.40 unknown https://doi.org/10.1016/0031-9422(83)80180-0
Deacylcynaropicrin 3084544 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)O 262.30 unknown https://doi.org/10.1016/0031-9422(83)80180-0
Desacylcynaropicrin 13943205 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)O 262.30 unknown https://doi.org/10.1016/0031-9422(83)80180-0
Saupirin 181128 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)OC(=O)C(=C)CO 346.40 unknown https://doi.org/10.1016/0031-9422(83)80180-0

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