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Centaurea thessala

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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 UUID643fcdbf48c4f834311670
Scientific name Centaurea thessala
Authority Hausskn.
First published in Mitt. Bot. Ver. Jena 5: 86. 1889

Description Top

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Synonyms Top

Scientific name Authority First published in
Centaurea orphanidea var. thessala (Hausskn.) Halácsy Bull. Herb. Boissier 6: 599 (1898)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Centaurea thessala subsp. drakiensis (Freyn & Sint.) T.Georgiadis Contrib. Phylogén. Centaurea L. (sect. Acrolophus (Cass.) DC.) en Grèce 68 (1980):.
Centaurea thessala subsp. thessala Hausskn.

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000075128
Tropicos 2700510
KEW urn:lsid:ipni.org:names:191778-1
The Plant List gcc-31827
Open Tree Of Life 3894165
IPNI 191778-1
iNaturalist 521829
GBIF 3128785
EOL 6217523

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)!
Title Authors Publication Released IDs
A Novel Eudesmanolide from Centaurea Thessala Hausskn. Ssp. Drakiensis (Freyn & Sint.) Georg Evanthia Georgiadou, Helen Skaltsa, Diamanto Lazari, Begoña Garcia, Catherine Harvala Informa UK Limited 07-Jul-2007
doi:10.1080/10575630008041227
Sesquiterpene lactones from Centaurea thessala and Centaurea attica. Antifungal activity. Skaltsa H, Lazari D, Panagouleas C, Georgiadou E, Garcia B, Sokovic M Phytochemistry 01-Dec-2000
doi:10.1016/S0031-9422(00)00254-5
PMID:11140522
Sesquiterpene Lactones from Centaurea Species: C. thessala subsp. drakiensis and C. attica subsp. attica. Skaltsa H, Lazari D, Georgiadou E, Kakavas S, Constantinidis T Planta Med 01-May-1999
doi:10.1055/S-2006-960801
PMID:17260267

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 / Phenanthrenes and derivatives / Phenanthroindolizidines
tylophoridicine F 44443383 Click to see COC1=CC2=C(C=C1)C3=C(C[N+]4(CCCC4C3O)[O-])C5=CC(=C(C=C52)OC)OC 395.40 unknown https://doi.org/10.1055/S-2006-960801
https://doi.org/10.1016/S0031-9422(00)00254-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
[(1S,2S,3R,4R,5S)-5-ethenyl-3-hydroxy-4-(3-hydroxyprop-1-en-2-yl)-2-(3-methoxy-3-oxoprop-1-en-2-yl)-5-methylcyclohexyl] (3S)-3,4-dihydroxy-2-methylidenebutanoate 162981478 Click to see CC1(CC(C(C(C1C(=C)CO)O)C(=C)C(=O)OC)OC(=O)C(=C)C(CO)O)C=C 410.50 unknown https://doi.org/10.1016/S0031-9422(00)00254-5
[5-Ethenyl-3-hydroxy-4-(3-hydroxyprop-1-en-2-yl)-2-(3-methoxy-3-oxoprop-1-en-2-yl)-5-methylcyclohexyl] 3,4-dihydroxy-2-methylidenebutanoate 45783166 Click to see CC1(CC(C(C(C1C(=C)CO)O)C(=C)C(=O)OC)OC(=O)C(=C)C(CO)O)C=C 410.50 unknown https://doi.org/10.1016/S0031-9422(00)00254-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(3aR,4S,6S,7R,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] (3S)-3,4-dihydroxy-2-methylidenebutanoate 162962883 Click to see CC1(CC(C2C(C1C(=C)CO)OC(=O)C2=C)OC(=O)C(=C)C(CO)O)C=C 378.40 unknown https://doi.org/10.1016/S0031-9422(00)00254-5
[(3aR,4S,6S,7R,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] (3S)-4-acetyloxy-3-hydroxy-2-methylidenebutanoate 163189150 Click to see CC(=O)OCC(C(=C)C(=O)OC1CC(C(C2C1C(=C)C(=O)O2)C(=C)CO)(C)C=C)O 420.50 unknown https://doi.org/10.1016/S0031-9422(00)00254-5
[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] 4-acetyloxy-3-hydroxy-2-methylidenebutanoate 78191539 Click to see CC(=O)OCC(C(=C)C(=O)OC1CC(C(C2C1C(=C)C(=O)O2)C(=C)CO)(C)C=C)O 420.50 unknown https://doi.org/10.1016/S0031-9422(00)00254-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,4S,5aR,6R,9S,9aS,9bR)-4,6-dihydroxy-5a-methyl-3-methylidene-2-oxo-4,5,6,7,8,9,9a,9b-octahydro-3aH-benzo[g][1]benzofuran-9-carbaldehyde 10707855 Click to see CC12CC(C3C(C1C(CCC2O)C=O)OC(=O)C3=C)O 280.32 unknown https://doi.org/10.1016/S0031-9422(00)00254-5
4,6-dihydroxy-5a-methyl-3-methylidene-2-oxo-4,5,6,7,8,9,9a,9b-octahydro-3aH-benzo[g][1]benzofuran-9-carbaldehyde 45783172 Click to see CC12CC(C3C(C1C(CCC2O)C=O)OC(=O)C3=C)O 280.32 unknown https://doi.org/10.1016/S0031-9422(00)00254-5
> 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] (3R)-4-acetyloxy-3-hydroxy-2-methylidenebutanoate 101688203 Click to see CC1=CCCC(=CC2C(C(C1)OC(=O)C(=C)C(COC(=O)C)O)C(=C)C(=O)O2)CO 420.50 unknown https://doi.org/10.1055/S-2006-960801
[(3aR,4S,6E,10Z,11aR)-10-(hydroxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (3S)-3,4-dihydroxy-2-methylidenebutanoate 52948006 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/10.1016/S0031-9422(00)00254-5
[(3aR,4S,6E,10Z,11aR)-10-(hydroxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (3S)-4-acetyloxy-3-hydroxy-2-methylidenebutanoate 22829100 Click to see CC1=CCCC(=CC2C(C(C1)OC(=O)C(=C)C(COC(=O)C)O)C(=C)C(=O)O2)CO 420.50 unknown https://doi.org/10.1016/S0031-9422(00)00254-5
[10-(Hydroxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 3,4-dihydroxy-2-methylidenebutanoate 91176 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/10.1016/S0031-9422(00)00254-5
[10-(Hydroxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 4-acetyloxy-3-hydroxy-2-methylidenebutanoate 73999085 Click to see CC1=CCCC(=CC2C(C(C1)OC(=O)C(=C)C(COC(=O)C)O)C(=C)C(=O)O2)CO 420.50 unknown https://doi.org/10.1055/S-2006-960801
https://doi.org/10.1016/S0031-9422(00)00254-5
https://doi.org/10.1080/10575630008041227
CID 10342082 10342082 Click to see CC1=CCCC(=CC2C(C(C1)OC(=O)C(=CCOC(=O)C)CO)C(=C)C(=O)O2)CO 420.50 unknown https://doi.org/10.1016/S0031-9422(00)00254-5
https://doi.org/10.1055/S-2006-960801
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/10.1080/10575630008041227
NCGC00385206-01_C20H26O7_(3aR,4S,10Z,11aR)-10-(Hydroxymethyl)-6-methyl-3-methylene-2-oxo-2,3,3a,4,5,8,9,11a-octahydrocyclodeca[b]furan-4-yl 3,4-dihydroxy-2-methylenebutanoate 138404438 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/10.1080/10575630008041227
> Organoheterocyclic compounds / Isobenzofurans
3-Furan-3-yl-3a,7-dimethyl-3a,4,5,6-tetrahydro-3H-isobenzofuran-1-one 500095 Click to see CC1=C2C(=O)OC(C2(CCC1)C)C3=COC=C3 232.27 unknown https://doi.org/10.1016/S0031-9422(00)00254-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
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/10.1080/10575630008041227
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/10.1080/10575630008041227
> 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/10.1080/10575630008041227

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