Scientific name	Authority	First published in
Melanoloma pullatum	(L.) Fourr.	Fourr. in Ann. Soc. Linn. Lyon, ser. 2 17. 1869. 96 1869
Centaurea pullata var. claryi	(Debeaux) Batt.
Centaurea pullata var. zatii	Maubert
Centaurea pullata subsp. claryi	(Debeaux) Batt.
Centaurea pullata var. pullata	L.
Centaurea pullata var. minor	Ball

Common names Top

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Filter by language:

Language	Common/alternative name
Arabic	قنطريون متفجع
Japanese	チェンタウレア・プッラータ
Kabyle	Ǧuz
Malayalam	സെന്റൗറിയ പുല്ലാറ്റ

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Centaurea pullata subsp. baetica	Talavera	Lagascalia 12(2): 274 (1984) (1984)
Centaurea pullata subsp. pullata	L.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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

Africa click to expand
- Northern Africa
  - Algeria
  - Egypt
  - Morocco
  - Tunisia

Europe click to expand
- Southeastern Europe
  - Italy
  - Sicilia
  - Turkey-in-Europe
- Southwestern Europe
  - France
  - Portugal
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000138368
Tropicos	2702207
INPN	89681
KEW	urn:lsid:ipni.org:names:191381-1
The Plant List	gcc-99015
Open Tree Of Life	852757
Observations.org	140207
NCBI Taxonomy	347528
NBN Atlas	NBNSYS0200003483
IPNI	191381-1
iNaturalist	82650
GBIF	3127841
Freebase	/m/012cf8sj
EPPO	CENPU
Wikipedia	Centaurea_pullata

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

Ecological and Syntaxonomic Analysis of the Communities of Glebionis coronaria and G. discolor (Malvion neglectae) in the European Mediterranean Area

Cano E, Cano-Ortiz A, Quinto Canas R, Piñar Fuentes JC, Rodrigues Meireles C, Raposo M, Pinto Gomes C, Laface VL, Spampinato G, Musarella CM

Plants (Basel)

20-Feb-2024

PMCID:	PMC10934477
doi:	10.3390/plants13050568
PMID:	38475415

Diploid Nuclei Occur throughout the Life Cycles of Pucciniales Fungi

Talhinhas P, Carvalho R, Tavares S, Ribeiro T, Azinheira H, Ramos AP, Silva MD, Monteiro M, Loureiro J, Morais-Cecílio L

Microbiol Spectr

08-Jun-2023

PMCID:	PMC10433954
doi:	10.1128/spectrum.01532-23
PMID:	37289058

Wild Edible Plants of Andalusia: Traditional Uses and Potential of Eating Wild in a Highly Diverse Region

Benítez G, Molero-Mesa J, González-Tejero MR

Plants (Basel)

07-Mar-2023

PMCID:	PMC10051205
doi:	10.3390/plants12061218
PMID:	36986907

Genotyping-by-Sequencing and Morphology Revealed the Role of Polyploidization and Hybridization in the Diversification of the Centaurea aspera L. Complex of Section Seridia (Juss.) DC. (Asteraceae)

Merle H, Garmendia A, Ferriol M

Plants (Basel)

25-Jul-2022

PMCID:	PMC9332712
doi:	10.3390/plants11151919
PMID:	35893623

Morphologic, genetic, and biogeographic continua among subspecies hinder the conservation of threatened taxa: the case of Centaurea aspera ssp. scorpiurifolia (Asteraceae)

Garmendia A, Merle H, Sanía M, López C, Ferriol M

Sci Rep

18-Jan-2022

PMCID:	PMC8766572
doi:	10.1038/s41598-022-04934-4
PMID:	35042932

Plant DNA Barcode as a Tool for Root Identification in Hypogea: The Case of the Etruscan Tombs of Tarquinia (Central Italy)

Isola D, Bartoli F, Langone S, Ceschin S, Zucconi L, Caneva G

Plants (Basel)

03-Jun-2021

PMCID:	PMC8228792
doi:	10.3390/plants10061138
PMID:	34205139

Local Factors Rather than the Landscape Context Explain Species Richness and Functional Trait Diversity and Responses of Plant Assemblages of Mediterranean Cereal Field Margins

Pallavicini Y, Bastida F, Hernández-Plaza E, Petit S, Izquierdo J, Gonzalez-Andujar JL

Plants (Basel)

22-Jun-2020

PMCID:	PMC7356665
doi:	10.3390/plants9060778
PMID:	32580354

Efficacy of some natural compounds as antifungal agents

Vengurlekar S, Sharma R, Trivedi P

Pharmacogn Rev

01-Jul-2012

PMCID:	PMC3459460
doi:	10.4103/0973-7847.99942
PMID:	23055634

A novel sesquiterpene lactone from Centaurea pullata: structure elucidation, antimicrobial activity, and prediction of pharmacokinetic properties.

Djeddi S, Karioti A, Sokovic M, Koukoulitsa C, Skaltsa H

Bioorg Med Chem

01-Apr-2008

doi:	10.1016/J.BMC.2008.01.056
PMID:	18280170

Minor sesquiterpene lactones from Centaurea pullata and their antimicrobial activity.

Djeddi S, Karioti A, Sokovic M, Stojkovic D, Seridi R, Skaltsa H

J Nat Prod

01-Nov-2007

doi:	10.1021/NP070125I
PMID:	17979247

Polyacetylenverbindungen, CXVII. Neue Polyine der Gattung <i>Centaurea</i> L.

Ferdinand Bohlmann, Käthe‐Marie Rode, Christa Zdero

Wiley

08-Jun-2007

doi:	10.1002/CBER.19660991121

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

Flavonoids of the Aerial Part of Centaurea pullata

K. Medjroubi, S. Mezhoud, F. Benayache, E. Seguin, F. Tillequin

Springer Science and Business Media LLC

26-Jul-2005

doi:	10.1007/S10600-005-0117-8

Sesquiterpene lactones from Centaurea pullata

Fadila Benayache, Samir Benayache, Kamel Medjroubi, Georges Massiott, Paul Aclinou, Bohdan Drodz, Gerard Nowaks

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(92)80477-V

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
2-[(1S,2S)-1-[5-[(1R)-1-(2-hydroxyphenyl)prop-2-enyl]-2,4-dimethoxyphenoxy]-1-phenylpropan-2-yl]-5-methoxycyclohexa-2,5-diene-1,4-dione	163036242	Click to see CC(C1=CC(=O)C(=CC1=O)OC)C(C2=CC=CC=C2)OC3=C(C=C(C(=C3)C(C=C)C4=CC=CC=C4O)OC)OC	540.60	unknown	https://doi.org/10.1002/CBER.19660991121
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
(3E,5E,11E)-trideca-1,3,5,11-tetraen-7,9-diyne	5352698	Click to see CC=CC#CC#CC=CC=CC=C	168.23	unknown	https://doi.org/10.1002/CBER.19660991121
1,3,5,11-Tridecatetraene-7,9-diyne	150169	Click to see CC=CC#CC#CC=CC=CC=C	168.23	unknown	https://doi.org/10.1002/CBER.19660991121
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
(5E,7E,13E)-pentadeca-5,7,13-trien-9,11-diynal	14412232	Click to see CC=CC#CC#CC=CC=CCCCC=O	212.29	unknown	https://doi.org/10.1002/CBER.19660991121
(5E,7E)-pentadeca-5,7-dien-9,11,13-triynal	14412236	Click to see CC#CC#CC#CC=CC=CCCCC=O	210.27	unknown	https://doi.org/10.1002/CBER.19660991121
(6E,8E,14E)-hexadeca-6,8,14-trien-10,12-diynal	14412233	Click to see CC=CC#CC#CC=CC=CCCCCC=O	226.31	unknown	https://doi.org/10.1002/CBER.19660991121
(7E,9E,11E,13E)-hexadeca-7,9,11,13-tetraenal	14412223	Click to see CCC=CC=CC=CC=CCCCCCC=O	232.36	unknown	https://doi.org/10.1002/CBER.19660991121
(7E,9E,15E)-heptadeca-7,9,15-trien-11,13-diynal	14412234	Click to see CC=CC#CC#CC=CC=CCCCCCC=O	240.34	unknown	https://doi.org/10.1002/CBER.19660991121
(8E,10E,12E,14E)-heptadeca-8,10,12,14-tetraenal	14412224	Click to see CCC=CC=CC=CC=CCCCCCCC=O	246.40	unknown	https://doi.org/10.1002/CBER.19660991121
Heptadeca-7,9,15-trien-11,13-diynal	85626732	Click to see CC=CC#CC#CC=CC=CCCCCCC=O	240.34	unknown	https://doi.org/10.1002/CBER.19660991121
Heptadeca-8,10,12,14-tetraenal	85627034	Click to see CCC=CC=CC=CC=CCCCCCCC=O	246.40	unknown	https://doi.org/10.1002/CBER.19660991121
Hexadeca-6,8,14-trien-10,12-diynal	85626892	Click to see CC=CC#CC#CC=CC=CCCCCC=O	226.31	unknown	https://doi.org/10.1002/CBER.19660991121
Pentadeca-5,7-dien-9,11,13-triynal	85626930	Click to see CC#CC#CC#CC=CC=CCCCC=O	210.27	unknown	https://doi.org/10.1002/CBER.19660991121
Pentadeca-5,7,13-trien-9,11-diynal	71436965	Click to see CC=CC#CC#CC=CC=CCCCC=O	212.29	unknown	https://doi.org/10.1002/CBER.19660991121
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
6-Ethenyl-4-hydroxy-7-(3-hydroxyprop-1-en-2-yl)-3,6-dimethyl-3,3a,4,5,7,7a-hexahydro-1-benzofuran-2-one	14162546	Click to see CC1C2C(CC(C(C2OC1=O)C(=C)CO)(C)C=C)O	266.33	unknown	https://doi.org/10.1016/J.BMC.2008.01.056
Melitensin	14162547	Click to see CC1C2C(CC(C(C2OC1=O)C(=C)CO)(C)C=C)O	266.33	unknown	https://doi.org/10.1016/J.BMC.2008.01.056
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(3S,3aR,4S,6S,7R,7aR)-6-ethenyl-7-(3-hydroxyprop-1-en-2-yl)-3,6-dimethyl-2-oxo-3,3a,4,5,7,7a-hexahydro-1-benzofuran-4-yl] 4-hydroxy-2-methylidenebutanoate	25113751	Click to see CC1C2C(CC(C(C2OC1=O)C(=C)CO)(C)C=C)OC(=O)C(=C)CCO	364.40	unknown	https://doi.org/10.1016/J.BMC.2008.01.056
[6-Ethenyl-7-(3-hydroxyprop-1-en-2-yl)-3,6-dimethyl-2-oxo-3,3a,4,5,7,7a-hexahydro-1-benzofuran-4-yl] 4-hydroxy-2-methylidenebutanoate	163030047	Click to see CC1C2C(CC(C(C2OC1=O)C(=C)CO)(C)C=C)OC(=O)C(=C)CCO	364.40	unknown	https://doi.org/10.1016/J.BMC.2008.01.056
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3S,3aR,4S,5aR,6R,9S,9aS,9bR)-4,6-dihydroxy-3,5a-dimethyl-2-oxo-3,3a,4,5,6,7,8,9,9a,9b-decahydrobenzo[g][1]benzofuran-9-carbaldehyde	44567329	Click to see CC1C2C(CC3(C(CCC(C3C2OC1=O)C=O)O)C)O	282.33	unknown	https://doi.org/10.1016/J.BMC.2008.01.056
(3S,3aR,4S,5aR,6R,9S,9bR)-4,6-dihydroxy-3,5a-dimethyl-2-oxo-3,3a,4,5,6,7,8,9,9a,9b-decahydrobenzo[g][1]benzofuran-9-carbaldehyde	163006665	Click to see CC1C2C(CC3(C(CCC(C3C2OC1=O)C=O)O)C)O	282.33	unknown	https://doi.org/10.1016/J.BMC.2008.01.056
(3S,3aR,4S,5aR,9R,9bR)-4-hydroxy-3,5a-dimethyl-2-oxo-3,3a,4,5,6,7,8,9,9a,9b-decahydrobenzo[g][1]benzofuran-9-carbaldehyde	44567330	Click to see CC1C2C(CC3(CCCC(C3C2OC1=O)C=O)C)O	266.33	unknown	https://doi.org/10.1016/J.BMC.2008.01.056
(3S,3aR,4S,5aR,9S,9aS,9bR)-4-hydroxy-3,5a-dimethyl-2-oxo-3,3a,4,5,6,7,8,9,9a,9b-decahydrobenzo[g][1]benzofuran-9-carbaldehyde	162943118	Click to see CC1C2C(CC3(CCCC(C3C2OC1=O)C=O)C)O	266.33	unknown	https://doi.org/10.1016/J.BMC.2008.01.056
(9-Formyl-6-hydroxy-3,5a-dimethyl-2-oxo-3,3a,4,5,6,7,8,9,9a,9b-decahydrobenzo[g][1]benzofuran-4-yl) 4-hydroxy-2-methylidenebutanoate	74218162	Click to see CC1C2C(CC3(C(CCC(C3C2OC1=O)C=O)O)C)OC(=O)C(=C)CCO	380.40	unknown	https://doi.org/10.1021/NP070125I https://doi.org/10.1016/J.BMC.2008.01.056
[(3S,3aR,4S,5aR,6R,9R,9aS,9bR)-9-formyl-6-hydroxy-3,5a-dimethyl-2-oxo-3,3a,4,5,6,7,8,9,9a,9b-decahydrobenzo[g][1]benzofuran-4-yl] 4-hydroxy-2-methylidenebutanoate	162939508	Click to see CC1C2C(CC3(C(CCC(C3C2OC1=O)C=O)O)C)OC(=O)C(=C)CCO	380.40	unknown	https://doi.org/10.1021/NP070125I https://doi.org/10.1016/J.BMC.2008.01.056
[(3S,3aR,4S,5aR,6R,9S,9aS,9bR)-9-formyl-6-hydroxy-3,5a-dimethyl-2-oxo-3,3a,4,5,6,7,8,9,9a,9b-decahydrobenzo[g][1]benzofuran-4-yl] 4-hydroxy-2-methylidenebutanoate	162939507	Click to see CC1C2C(CC3(C(CCC(C3C2OC1=O)C=O)O)C)OC(=O)C(=C)CCO	380.40	unknown	https://doi.org/10.1021/NP070125I https://doi.org/10.1016/J.BMC.2008.01.056
4-Hydroxy-3,5a-dimethyl-2-oxo-3,3a,4,5,6,7,8,9,9a,9b-decahydrobenzo[g][1]benzofuran-9-carbaldehyde	75072420	Click to see CC1C2C(CC3(CCCC(C3C2OC1=O)C=O)C)O	266.33	unknown	https://doi.org/10.1016/J.BMC.2008.01.056
4,6-Dihydroxy-3,5a-dimethyl-2-oxo-3,3a,4,5,6,7,8,9,9a,9b-decahydrobenzo[g][1]benzofuran-9-carbaldehyde	75072419	Click to see CC1C2C(CC3(C(CCC(C3C2OC1=O)C=O)O)C)O	282.33	unknown	https://doi.org/10.1016/J.BMC.2008.01.056
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3S,3aR,4S,6E,10Z,11aR)-4-hydroxy-10-(hydroxymethyl)-3,6-dimethyl-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-2-one	38349578	Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)O	266.33	unknown	https://doi.org/10.1016/J.BMC.2008.01.056
(3S,3aR,4S,6E,11aR)-4-hydroxy-10-(hydroxymethyl)-3,6-dimethyl-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-2-one	163004748	Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)O	266.33	unknown	https://doi.org/10.1016/J.BMC.2008.01.056
[(3S,3aR,4S,6E,10Z,11aR)-10-(hydroxymethyl)-3,6-dimethyl-2-oxo-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-4-yl] (3R)-3,4-dihydroxy-2-methylidenebutanoate	162933862	Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)OC(=O)C(=C)C(CO)O	380.40	unknown	https://doi.org/10.1021/NP070125I
[(3S,3aR,4S,6E,10Z,11aR)-10-(hydroxymethyl)-3,6-dimethyl-2-oxo-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-4-yl] (3S)-3,4-dihydroxy-2-methylidenebutanoate	162933863	Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)OC(=O)C(=C)C(CO)O	380.40	unknown	https://doi.org/10.1016/0031-9422(92)80477-V https://doi.org/10.1016/J.BMC.2008.01.056
[(3S,3aR,4S,6E,10Z,11aR)-10-(hydroxymethyl)-3,6-dimethyl-2-oxo-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-4-yl] 4-hydroxy-2-methylidenebutanoate	163087128	Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)OC(=O)C(=C)CCO	364.40	unknown	https://doi.org/10.1021/NP070125I https://doi.org/10.1016/0031-9422(92)80477-V https://doi.org/10.1016/J.BMC.2008.01.056
[(3S,3aR,4S,6Z,10E,11aR)-4-acetyloxy-3,6-dimethyl-2-oxo-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-10-yl]methyl acetate	101634636	Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)COC(=O)C)C)OC(=O)C	350.40	unknown	https://doi.org/10.1016/J.BMC.2008.01.056
[10-(hydroxymethyl)-3,6-dimethyl-2-oxo-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-4-yl] 3,4-dihydroxy-2-methylidenebutanoate	74218926	Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)OC(=O)C(=C)C(CO)O	380.40	unknown	https://doi.org/10.1016/J.BMC.2008.01.056 https://doi.org/10.1016/0031-9422(92)80477-V https://doi.org/10.1021/NP070125I
[10-(hydroxymethyl)-3,6-dimethyl-2-oxo-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-4-yl] 4-acetyloxy-2-(hydroxymethyl)but-2-enoate	74218161	Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)OC(=O)C(=CCOC(=O)C)CO	422.50	unknown	https://doi.org/10.1016/J.BMC.2008.01.056 https://doi.org/10.1021/NP070125I
[10-(hydroxymethyl)-3,6-dimethyl-2-oxo-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-4-yl] 4-hydroxy-2-methylidenebutanoate	74218927	Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)OC(=O)C(=C)CCO	364.40	unknown	https://doi.org/10.1016/0031-9422(92)80477-V https://doi.org/10.1021/NP070125I https://doi.org/10.1016/J.BMC.2008.01.056
11beta13-Dihydrocnicin	44445511	Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)OC(=O)C(=C)C(CO)O	380.40	unknown	https://doi.org/10.1016/0031-9422(92)80477-V
8alpha-O-(4-acetoxy-5-hydroxyangeloyl)-11beta,13-dihydrocnicin	24178997	Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)OC(=O)C(=CCOC(=O)C)CO	422.50	unknown	https://doi.org/10.1016/J.BMC.2008.01.056 https://doi.org/10.1021/NP070125I
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
8-Tetradecene-11,13-diyn-2-one, (8Z)-	11528546	Click to see CC(=O)CCCCCC=CCC#CC#C	202.29	unknown	https://doi.org/10.1002/CBER.19660991121
Tetradeca-8-en-11,13-diyn-2-one	72996063	Click to see CC(=O)CCCCCC=CCC#CC#C	202.29	unknown	https://doi.org/10.1002/CBER.19660991121
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxy-3-methylchromone	22978769	Click to see CC1=COC2=CC(=CC(=C2C1=O)O)O	192.17	unknown	https://doi.org/10.1016/J.BMC.2008.01.056
> Organoheterocyclic compounds / Dihydrofurans
5-nona-4,6,8-trien-2-ynylidene-2H-furan	129682079	Click to see C=CC=CC=CC#CC=C1C=CCO1	184.23	unknown	https://doi.org/10.1002/CBER.19660991121
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
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/10.1007/S10600-005-0117-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Fastigenin	162464	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O	344.30	unknown	https://doi.org/10.1007/S10600-005-0117-8

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Centaurea pullata

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top