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Stizolophus coronopifolius

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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 UUID643fce2bd29f4133414851
Scientific name Stizolophus coronopifolius
Authority Cass.
First published in Dict. Sci. Nat., ed. 2. 51: 51 (1827)

Description Top

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Synonyms Top

Scientific name Authority First published in
Centaurea reticulata M.Bieb. ex Willd. Sp. Pl., ed. 4 , 3: 2287 (1803)
Centaurea coronopifolia Lam. Encycl. 1: 667 (1785)
Centaurea exaltata Adams Beitr. Naturk. i. 74

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
  • 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-0000078970
Tropicos 2732456
KEW urn:lsid:ipni.org:names:251697-1
The Plant List gcc-35561
Open Tree Of Life 1036517
Observations.org 122696
NCBI Taxonomy 145831
IPNI 251697-1
iNaturalist 632897
GBIF 3141525

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
Lessons from Plectocephalus (Compositae, Cardueae-Centaureinae): ITS disorientation in annuals and Beringian dispersal as revealed by molecular analyses Susanna A, Galbany-Casals M, Romaschenko K, Barres L, Martín J, Garcia-Jacas N Ann Bot 28-Jun-2011
PMCID:PMC3143048
doi:10.1093/aob/mcr138
PMID:21712295
Phylogeny of Rhaponticum (Asteraceae, Cardueae–Centaureinae) and Related Genera Inferred from Nuclear and Chloroplast DNA Sequence Data: Taxonomic and Biogeographic Implications HIDALGO O, GARCIA-JACAS N, GARNATJE T, SUSANNA A Ann Bot 01-May-2006
PMCID:PMC2803413
doi:10.1093/aob/mcl029
PMID:16495316
Flavonoids of Stizolophus coronopifolius É. T. Oganesyan, S. F. Dzhumyrko Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563832
Sesquiterpene lactones from centaurea coronopifolia Sevil Öksüz, Hatice Ayyildiz Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)85520-X
Structure revision and cytotoxicity of the germacranolide, stizolicin, from Stizolophus balsamitus (Asteraceae). Cassady JM, Bean MFz K, McLaughlin JL, Aynehchi Y Experientia 15-Sep-1984
doi:10.1007/BF01946442
PMID:6468618

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 / Germacranolides and derivatives
(4,8-Dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-10-yl) 4-hydroxy-3-methylbut-2-enoate 163080545 Click to see CC1=CCCC2(C(O2)C3C(C(C1)OC(=O)C=C(C)CO)C(=C)C(=O)O3)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)85520-X
(9-Hydroxy-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-10-yl) 3-methylbut-2-enoate 162919418 Click to see CC1=CCCC2(C(O2)C3C(C(C1O)OC(=O)C=C(C)C)C(=C)C(=O)O3)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)85520-X
(9-Hydroxy-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-10-yl) 4-hydroxy-3-methylbut-2-enoate 538679 Click to see CC1=CCCC2(C(O2)C3C(C(C1O)OC(=O)C=C(C)CO)C(=C)C(=O)O3)C 378.40 unknown https://doi.org/10.1016/S0031-9422(00)85520-X
[(1S,2S,4R,7E,10S,11R)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-10-yl] (E)-4-hydroxy-2-(hydroxymethyl)but-2-enoate 16399773 Click to see CC1=CCCC2(C(O2)C3C(C(C1)OC(=O)C(=CCO)CO)C(=C)C(=O)O3)C 378.40 unknown https://doi.org/10.1016/S0031-9422(00)85520-X
[(1S,2S,4R,7E,10S,11R)-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-10-yl] (E)-4-hydroxy-3-methylbut-2-enoate 163080546 Click to see CC1=CCCC2(C(O2)C3C(C(C1)OC(=O)C=C(C)CO)C(=C)C(=O)O3)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)85520-X
[(1S,2S,4R,7E,9S,10R,11R)-9-hydroxy-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-10-yl] (E)-4-hydroxy-3-methylbut-2-enoate 163185788 Click to see CC1=CCCC2(C(O2)C3C(C(C1O)OC(=O)C=C(C)CO)C(=C)C(=O)O3)C 378.40 unknown https://doi.org/10.1016/S0031-9422(00)85520-X
[(1S,2S,4R,7E,9S,10R,11R)-9-hydroxy-4,8-dimethyl-12-methylidene-13-oxo-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-10-yl] 3-methylbut-2-enoate 162919419 Click to see CC1=CCCC2(C(O2)C3C(C(C1O)OC(=O)C=C(C)C)C(=C)C(=O)O3)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)85520-X
CID 6441532 6441532 Click to see CC1=CCCC2(C(O2)C3C(C(C1)OC(=O)C(=CCO)CO)C(=C)C(=O)O3)C 378.40 unknown https://doi.org/10.1007/BF01946442
Stizolicin 15089249 Click to see CC1=CCCC2(C(O2)C3C(C(C1)OC(=O)C(=CCO)CO)C(=C)C(=O)O3)C 378.40 unknown https://doi.org/10.1016/S0031-9422(00)85520-X
> 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/10.1016/S0031-9422(00)85520-X
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)85520-X
Urs-12-en-3beta-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)85520-X
> Phenylpropanoids and polyketides / Coumarins and derivatives
3-Hydroxy-9-[[6-hydroxy-2-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-3-yl]oxy]-10-methoxybenzo[c]chromen-6-one 163009793 Click to see COC1=C(C=CC2=C1OC(C2OC3=C(C4=C(C=C3)C(=O)OC5=C4C=CC(=C5)O)OC)CO)O 452.40 unknown https://doi.org/10.1016/S0031-9422(00)85520-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-5-hydroxy-3,6-dimethoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74978471 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC4C(C(C(C(O4)CO)O)O)O 508.40 unknown https://doi.org/10.1016/S0031-9422(00)85520-X
Axillaroside 101243893 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC4C(C(C(C(O4)CO)O)O)O 508.40 unknown https://doi.org/10.1016/S0031-9422(00)85520-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/10.1007/BF00563832
> 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)85520-X
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1016/S0031-9422(00)85520-X
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)85520-X

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