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Centaurea clementei

Centaurea clementei - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fc79a9dd4f054285571
Scientific name Centaurea clementei
Authority Boiss. ex DC.
First published in Prodr. 7(1): 303 (1838)

Description Top

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Synonyms Top

Scientific name Authority First published in
Centaurea ragusina Clemente ex Boiss. Voy. Bot. Espagne 2: 346 (1840)
Colymbada clementei (Boiss.) Holub Folia Geobot. Phytotax. 7(3): 315 (1972)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Centaurea ragusina subsp. ragusina L.

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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No germination or propagation data was added yet.

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-0000015870
Tropicos 2726873
KEW urn:lsid:ipni.org:names:190230-1
The Plant List gcc-115356
Open Tree Of Life 489653
Observations.org 116292
NCBI Taxonomy 41516
IPNI 190230-1
iNaturalist 521556
GBIF 3127596
EPPO CENCL

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
Role of Some Food-Grade Synthesized Flavonoids on the Control of Ochratoxin A in Aspergillus carbonarius Ricelli A, De Angelis M, Primitivo L, Righi G, Sappino C, Antonioletti R Molecules 13-Jul-2019
PMCID:PMC6680773
doi:10.3390/molecules24142553
PMID:31337014
Anti-inflammatory activities of eleven Centaurea species occurring in the Carpathian Basin. Csupor D, Widowitz U, Blazsó G, Laczkó-Zöld E, Tatsimo JS, Balogh A, Boros K, Dankó B, Bauer R, Hohmann J Phytother Res 01-Apr-2013
doi:10.1002/PTR.4754
PMID:22674731
Evolution and biogeography of Centaurea section Acrocentron inferred from nuclear and plastid DNA sequence analyses Font M, Garcia-Jacas N, Vilatersana R, Roquet C, Susanna A Ann Bot 18-Feb-2009
PMCID:PMC2707886
doi:10.1093/aob/mcp022
PMID:19228702
Flavonoids from Centaurea clementei I. Gonzalez Collado, F. A. Macias, G. M. Massanet, F. Rodriguez Luis American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50041A020
Structure, chemistry and stereochemistry of clementeins, sesquiterpene lactones from centaurea clementei I. Gonzalez Collado, F.A. Macias, G.M. Massanet, F. Rodriguez Luis Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)87328-2
Structural determination of clementein, a new guaianolide isolated from Centaurea clementei Guillermo M. Massanet, Isidro G. Collado, Francisco A. Macías, Ferdinand Bohlmann, Jasmin Jakupovic Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)81732-3

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-4'-methyl-6,9-dimethylidene-2-oxospiro[3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-3,2'-oxetane]-4-yl) 2-(hydroxymethyl)prop-2-enoate 73089500 Click to see CC1CC2(O1)C3C(CC(=C)C4CC(C(=C)C4C3OC2=O)O)OC(=O)C(=C)CO 390.40 unknown https://doi.org/10.1016/S0040-4039(00)81732-3
https://doi.org/10.1016/S0040-4020(01)87328-2
(8-hydroxy-4',9-dimethyl-6-methylidene-2-oxospiro[4,5,6a,7,8,9,9a,9b-octahydro-3aH-azuleno[4,5-b]furan-3,2'-oxetane]-4-yl) 2-(hydroxymethyl)prop-2-enoate 162892512 Click to see CC1CC2(O1)C3C(CC(=C)C4CC(C(C4C3OC2=O)C)O)OC(=O)C(=C)CO 392.40 unknown https://doi.org/10.1016/S0040-4020(01)87328-2
[(3S,3aR,4S,4'R,6aR,8S,9aR,9bR)-8-hydroxy-4'-methyl-6,9-dimethylidene-2-oxospiro[3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-3,2'-oxetane]-4-yl] 2-(hydroxymethyl)prop-2-enoate 11760945 Click to see CC1CC2(O1)C3C(CC(=C)C4CC(C(=C)C4C3OC2=O)O)OC(=O)C(=C)CO 390.40 unknown https://doi.org/10.1016/S0040-4039(00)81732-3
https://doi.org/10.1016/S0040-4020(01)87328-2
[(3S,3aR,4S,4'R,6aR,8S,9aR,9bS)-8-hydroxy-4'-methyl-6,9-dimethylidene-2-oxospiro[3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-3,2'-oxetane]-4-yl] 2-(hydroxymethyl)prop-2-enoate 162883548 Click to see CC1CC2(O1)C3C(CC(=C)C4CC(C(=C)C4C3OC2=O)O)OC(=O)C(=C)CO 390.40 unknown https://doi.org/10.1016/S0040-4020(01)87328-2
[(3S,3aR,4S,4'R,6aR,8S,9S,9aR,9bR)-8-hydroxy-4',9-dimethyl-6-methylidene-2-oxospiro[4,5,6a,7,8,9,9a,9b-octahydro-3aH-azuleno[4,5-b]furan-3,2'-oxetane]-4-yl] 2-(hydroxymethyl)prop-2-enoate 101047284 Click to see CC1CC2(O1)C3C(CC(=C)C4CC(C(C4C3OC2=O)C)O)OC(=O)C(=C)CO 392.40 unknown https://doi.org/10.1016/S0040-4020(01)87328-2
[(3S,3aR,4S,4'S,6aR,8S,9aR,9bR)-8-hydroxy-4'-methyl-6,9-dimethylidene-2-oxospiro[3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-3,2'-oxetane]-4-yl] 2-(hydroxymethyl)prop-2-enoate 11025573 Click to see CC1CC2(O1)C3C(CC(=C)C4CC(C(=C)C4C3OC2=O)O)OC(=O)C(=C)CO 390.40 unknown https://doi.org/10.1016/S0040-4039(00)81732-3
https://doi.org/10.1016/S0040-4020(01)87328-2
[(3S,3aR,4S,4'S,6aR,8S,9aR,9bS)-8-hydroxy-4'-methyl-6,9-dimethylidene-2-oxospiro[3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-3,2'-oxetane]-4-yl] 2-(hydroxymethyl)prop-2-enoate 162883549 Click to see CC1CC2(O1)C3C(CC(=C)C4CC(C(=C)C4C3OC2=O)O)OC(=O)C(=C)CO 390.40 unknown https://doi.org/10.1016/S0040-4039(00)81732-3
[(3S,3aS,4S,4'R,6aR,8S,9S,9aR,9bS)-8-hydroxy-4',9-dimethyl-6-methylidene-2-oxospiro[4,5,6a,7,8,9,9a,9b-octahydro-3aH-azuleno[4,5-b]furan-3,2'-oxetane]-4-yl] 2-(hydroxymethyl)prop-2-enoate 162892513 Click to see CC1CC2(O1)C3C(CC(=C)C4CC(C(C4C3OC2=O)C)O)OC(=O)C(=C)CO 392.40 unknown https://doi.org/10.1016/S0040-4020(01)87328-2
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Scutellarein 5281697 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O 286.24 unknown https://doi.org/10.1021/NP50041A020
> 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/10.1021/NP50041A020
> 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/10.1021/NP50041A020
https://doi.org/10.1002/PTR.4754
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Negletein 471719 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O)O 284.26 unknown https://doi.org/10.1021/NP50041A020

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