Scientific name	Authority	First published in
Centaurea nathadzeae	Sosn.	Zametki Sist. Geogr. Rast. 21: 58 (1959)
Centaurea bella	Trautv.	Bull. Acad. Sci. St. Petersb. 10: 394. 1866
Centaurea bella subsp. nathadzeae	(Sosn.) Djindjolia	Zametki Sist. Geogr. Rast. 44-45: 141 (2005)
Centaurea svanetica	Mardal.	Bot. Zhurn. (Moscow & Leningrad) 70(2): 265 (1985)

Common names Top

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Language	Common/alternative name
Belarusian	васілёк прыгожы

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Caucasus
  - Transcaucasus

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000005453
KEW	urn:lsid:ipni.org:names:1015919-1
The Plant List	gcc-105250
Open Tree Of Life	350270
NCBI Taxonomy	146595
IPNI	1015919-1
iNaturalist	1196715
GBIF	3137947
Wikipedia	Psephellus_bellus

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

Antibacterial Activity of a Phenylpropanoid from the Root Extract of Carduus leptacanthus Fresen

Dagne A, Degu S, Abebe A, Bisrat D

J Trop Med

06-Sep-2023

PMCID:	PMC10499531
doi:	10.1155/2023/4983608
PMID:	37711213

The Evaluation of Phenolic Acids and Flavonoids Content and Antiprotozoal Activity of Eryngium Species Biomass Produced by Biotechnological Methods

Kikowska M, Chanaj-Kaczmarek J, Derda M, Budzianowska A, Thiem B, Ekiert H, Szopa A

Molecules

07-Jan-2022

PMCID:	PMC8781403
doi:	10.3390/molecules27020363
PMID:	35056679

Antifungal Activity of the Sesquiterpene Lactones from Psephellus bellus

Nawrot J, Adamski Z, Kamińska-Kolat B, Kubisiak-Rzepczyk H, Kroma A, Nowak G, Gornowicz-Porowska J

Plants (Basel)

09-Jun-2021

PMCID:	PMC8227665
doi:	10.3390/plants10061180
PMID:	34207928

Phytotherapy Perspectives for Treating Fungal Infections, Migraine, Sebhorreic Dermatitis and Hyperpigmentations with the Plants of the Centaureinae Subtribe (Asteraceae)

Nawrot J, Gornowicz-Porowska J, Nowak G

Molecules

15-Nov-2020

PMCID:	PMC7696306
doi:	10.3390/molecules25225329
PMID:	33203185

In vitro activity of Camellia sinensis (green tea) against trophozoites and cysts of Acanthamoeba castellanii

Fakae LB, Stevenson CW, Zhu XQ, Elsheikha HM

Int J Parasitol Drugs Drug Resist

02-Jun-2020

PMCID:	PMC7281304
doi:	10.1016/j.ijpddr.2020.05.001
PMID:	32512260

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

Detection Progress of Selected Drugs in TLC

Pyka A

Biomed Res Int

16-Jan-2014

PMCID:	PMC3914296
doi:	10.1155/2014/732078
PMID:	24551853

Sesquiterpene lactones. XXXVI. Sesquiterpene lactones in several subgenera of the genus Centaurea L.

Gerard Nowak, Miroslaw Holub, Miloš Buděšĺnský

Polish Botanical Society

12-Apr-2013

doi:	10.5586/ASBP.1989.008

Isolation and chromatography of 15-deoxyrepin and 25 other sesquiterpene lactones from Centaurea bella Trautv

Gerard Nowak

Polish Botanical Society

08-Apr-2013

doi:	10.5586/ASBP.1993.006

Syringin in some species of the subtribe Centaureinae of the Asteraceae

Joanna Cis, Gerard Nowak, Małgorzata Horoszkiewicz-Hassan, Wanda Kisiel

Polish Botanical Society

08-Apr-2013

doi:	10.5586/ASBP.2003.013

Chromatography of twentysix sesquiterpene lactones fromCentaurea bella

G. Nowak

Springer Science and Business Media LLC

09-Dec-2005

doi:	10.1007/BF02277519

Further sesquiterpene lactones of Centaurea bella

Włodzimierz M. Daniewski, Gerard Nowak

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(92)80134-Z

A chemotaxonomic study of sesquiterpene lactones from subtribe centaureinae of the compositae

Gerard Nowak

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(92)83281-3

Sesquiterpene Lactones of Centaurea salonitana

Włodzimierz M. Daniewski, Gerard Nowak, Elzbieta Pankowska, Theodore Georgiadis, Eugenia Routsi, Urszula Rychlewska, Beata Szczepańska

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(93)80027-P

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(4-Hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-7-yl) 2-methylpropanoate	162875629	Click to see CC(C)C(=O)OC1CC(=C)C2C1C(=C)CC(C3C2OC(=O)C3=C)O	332.40	unknown	https://doi.org/10.1016/0031-9422(93)80027-P
(7,8-Dihydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl) 2-methylprop-2-enoate	162922039	Click to see CC(=C)C(=O)OC1CC(=C)C2C(C3C1C(=C)C(=O)O3)C(=C)C(C2O)O	346.40	unknown	https://doi.org/10.1016/0031-9422(92)83281-3 https://doi.org/10.1007/BF02277519 https://doi.org/10.5586/ASBP.1993.006
(8-Hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-7-yl) 2-methylpropanoate	163027187	Click to see CC(C)C(=O)OC1C2C(C3C(CCC2=C)C(=C)C(=O)O3)C(=C)C1O	332.40	unknown	https://doi.org/10.1016/0031-9422(93)80027-P
[(3aR,4S,6aR,7R,8R,9aR,9bR)-4,8-dihydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-7-yl] 2-methylbutanoate	102058100	Click to see CCC(C)C(=O)OC1C2C(C3C(C(CC2=C)O)C(=C)C(=O)O3)C(=C)C1O	362.40	unknown	https://doi.org/10.5586/ASBP.1993.006 https://doi.org/10.1007/BF02277519 https://doi.org/10.1016/0031-9422(92)83281-3
[(3aR,4S,6aR,7R,8R,9aR,9bR)-4,8-dihydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-7-yl] 2-methylpropanoate	102058101	Click to see CC(C)C(=O)OC1C2C(C3C(C(CC2=C)O)C(=C)C(=O)O3)C(=C)C1O	348.40	unknown	https://doi.org/10.5586/ASBP.1993.006 https://doi.org/10.1007/BF02277519 https://doi.org/10.1016/0031-9422(92)83281-3
[(3aR,4S,6aR,7S,9aR,9bR)-4-hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-7-yl] 2-methylpropanoate	162875630	Click to see CC(C)C(=O)OC1CC(=C)C2C1C(=C)CC(C3C2OC(=O)C3=C)O	332.40	unknown	https://doi.org/10.1016/0031-9422(93)80027-P
[(3aR,4S,6aR,8R,9S,9aR,9bR)-8-hydroxy-3,6-dimethylidene-2-oxospiro[3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-9,2'-oxirane]-4-yl] (2S)-2-methyloxirane-2-carboxylate	91567	Click to see CC1(CO1)C(=O)OC2CC(=C)C3CC(C4(C3C5C2C(=C)C(=O)O5)CO4)O	362.40	unknown	https://doi.org/10.5586/ASBP.1993.006 https://doi.org/10.1007/BF02277519
[(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-methyloxirane-2-carboxylate	102058099	Click to see CC1(CO1)C(=O)OC2CC(=C)C3CC(C(=C)C3C4C2C(=C)C(=O)O4)O	346.40	unknown	https://doi.org/10.5586/ASBP.1993.006 https://doi.org/10.1007/BF02277519
[(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] (E)-4-hydroxy-2-methylbut-2-enoate	101705723	Click to see CC(=CCO)C(=O)OC1CC(=C)C2CC(C(=C)C2C3C1C(=C)C(=O)O3)O	360.40	unknown	https://doi.org/10.5586/ASBP.1993.006 https://doi.org/10.1007/BF02277519
[(3aR,4S,6aR,8S,9S,9aS,9bR)-9-(chloromethyl)-8,9-dihydroxy-3,6-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] 2-methylprop-2-enoate	163000650	Click to see CC(=C)C(=O)OC1CC(=C)C2CC(C(C2C3C1C(=C)C(=O)O3)(CCl)O)O	382.80	unknown	https://doi.org/10.1016/0031-9422(93)80027-P
[(3aR,4S,6aR,8S,9S,9aS,9bS)-8-hydroxy-3,6-dimethylidene-2-oxospiro[3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-9,2'-oxirane]-4-yl] 2-methyloxirane-2-carboxylate	5320928	Click to see CC1(CO1)C(=O)OC2CC(=C)C3CC(C4(C3C5C2C(=C)C(=O)O5)CO4)O	362.40	unknown	https://doi.org/10.5586/ASBP.1993.006 https://doi.org/10.1007/BF02277519
[(3aR,4S,6aS,8S,9R,9aR,9bS)-6a,8-dihydroxy-3,6-dimethylidene-2-oxospiro[4,5,7,8,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-9,2'-oxirane]-4-yl] 2-methylprop-2-enoate	102057347	Click to see CC(=C)C(=O)OC1CC(=C)C2(CC(C3(C2C4C1C(=C)C(=O)O4)CO3)O)O	362.40	unknown	https://doi.org/10.5586/ASBP.1993.006 https://doi.org/10.1007/BF02277519 https://doi.org/10.1016/0031-9422(92)83281-3
[(3aS,6aR,7R,8R,9aR,9bS)-8-hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-7-yl] 2-methylpropanoate	163027188	Click to see CC(C)C(=O)OC1C2C(C3C(CCC2=C)C(=C)C(=O)O3)C(=C)C1O	332.40	unknown	https://doi.org/10.1016/0031-9422(93)80027-P
[(4S,8R,9S,9bS)-9-(chloromethyl)-8,9-dihydroxy-3,6-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] (2S)-3-chloro-2-hydroxy-2-methylpropanoate	118701337	Click to see CC(CCl)(C(=O)OC1CC(=C)C2CC(C(C2C3C1C(=C)C(=O)O3)(CCl)O)O)O	435.30	unknown	https://doi.org/10.5586/ASBP.1993.006 https://doi.org/10.1007/BF02277519
19-Deoxy-15-chlorojanerin	327915	Click to see CC(=C)C(=O)OC1CC(=C)C2CC(C(C2C3C1C(=C)C(=O)O3)(CCl)O)O	382.80	unknown	https://doi.org/10.1016/0031-9422(93)80027-P
Acroptilin	442140	Click to see CC(CCl)(C(=O)OC1CC(=C)C2CC(C3(C2C4C1C(=C)C(=O)O4)CO3)O)O	398.80	unknown	https://doi.org/10.1007/BF02277519 https://doi.org/10.5586/ASBP.1993.006
Cebellin D	6442949	Click to see CC(=CCO)C(=O)OC1CC(=C)C2CC(C(C2C3C1C(=C)C(=O)O3)(CCl)O)O	412.90	unknown	https://doi.org/10.1007/BF02277519 https://doi.org/10.5586/ASBP.1993.006
Cebellin J	44559228	Click to see CC(CO)(C(=O)OC1CC(=C)C2CC(C(C2C3C1C(=C)C(=O)O3)(CCl)O)O)O	416.80	unknown	https://doi.org/10.5586/ASBP.1989.008 https://doi.org/10.5586/ASBP.1993.006 https://doi.org/10.1007/BF02277519 https://doi.org/10.1016/0031-9422(92)83281-3
Chlorojanerin	182408	Click to see C=C1CC(C2C(C3C1CC(C3(CCl)O)O)OC(=O)C2=C)OC(=O)C(=C)CO	398.80	unknown	https://doi.org/10.1007/BF02277519 https://doi.org/10.5586/ASBP.1993.006
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/10.1007/BF02277519 https://doi.org/10.1016/0031-9422(93)80027-P https://doi.org/10.5586/ASBP.1993.006 https://doi.org/10.1016/0031-9422(92)80134-Z
Janerin	14021480	Click to see C=C1CC(C2C(C3C1CC(C34CO4)O)OC(=O)C2=C)OC(=O)C(=C)CO	362.40	unknown	https://doi.org/10.1007/BF02277519 https://doi.org/10.5586/ASBP.1993.006
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(93)80027-P
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eleutheroside B	5316860	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	https://doi.org/10.5586/ASBP.2003.013

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Psephellus bellus

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