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Internal ID UUID643fc961808d0376254673
Scientific name Centaurea deflexa
Authority Wagenitz
First published in Notes Roy. Bot. Gard. Edinburgh 33(2): 229, nom. nov. (1974)

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Synonyms Top

Scientific name Authority First published in
Phaeopappus declinatus Boiss. Fl. Orient. 3: 595 (1875)
Centaurea nivea var. declinata (Boiss.) Wagenitz Bot. Jahrb. Syst. 82: 172. 1963 (1963)
Cheirolepis declinata (Boiss.) Czerep. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 20: 471 (1960)

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000029939
Tropicos 50323951
KEW urn:lsid:ipni.org:names:190340-1
The Plant List gcc-128939
Open Tree Of Life 202734
NCBI Taxonomy 363423
IPNI 190340-1
GBIF 3127854
EOL 6216090

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
Sesquiterpene Lactones as Promising Candidates for Cancer Therapy: Focus on Pancreatic Cancer Laurella LC, Mirakian NT, Garcia MN, Grasso DH, Sülsen VP, Papademetrio DL Molecules 29-May-2022
PMCID:PMC9182036
doi:10.3390/molecules27113492
PMID:35684434
Anti-proliferative activity of aguerin B and a new rare nor-guaianolide lactone isolated from the aerial parts of Centaurea deflexa. Chicca A, Tebano M, Adinolfi B, Ertugrul K, Flamini G, Nieri P Eur J Med Chem 01-Jul-2011
doi:10.1016/J.EJMECH.2011.03.011
PMID:21458113
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

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Arctigenin 64981 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
l-Arctigenin 230232 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
> Lignans, neolignans and related compounds / Lignan glycosides
Arctii;NSC 315527;Arctigenin-4-glucoside 3660596 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 534.60 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
Arctiin 100528 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 534.60 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(8-Hydroxy-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 13996678 Click to see CC(=C)C(=O)OC1CC(=C)C2CC(C(=C)C2C3C1C(=C)C(=O)O3)O 330.40 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
Aguerin B 155102 Click to see CC(=C)C(=O)OC1CC(=C)C2CC(C(=C)C2C3C1C(=C)C(=O)O3)O 330.40 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
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/10.1016/J.EJMECH.2011.03.011
Deacylcynaropicrin 3084544 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)O 262.30 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
Desacylcynaropicrin 13943205 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)O 262.30 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
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/J.EJMECH.2011.03.011
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 348159 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
Isochlorogensaure 12310829 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 323959 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
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/10.1016/J.EJMECH.2011.03.011
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
15-Nor-guaianolide 53328018 Click to see CC1C2C(CC(=C)C3CC(=O)CC3C2OC1=O)O 250.29 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
Kaempferide 5281666 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
Quercetin 7,3',4'-trimethyl ether 5748558 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)O)OC 344.30 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Luteolin 4'-glucoside 12304737 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
Luteolin-4'-o-glucoside 5319116 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Chrysoeriol-7-O-beta-D-glucoside 13871877 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
Thermopsoside 11294177 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown https://doi.org/10.1016/J.EJMECH.2011.03.011

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