Genista corsica - Unknown
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Internal ID UUID643fdf112436c589132347
Scientific name Genista corsica
Authority (Loisel.) DC.
First published in J.B.A.M.de Lamarck & A.P.de Candolle, Fl. Franç., éd. 3, 6: 548 (1815)

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Synonyms Top

Scientific name Authority First published in
Cytisanthus corsicus (Loisel.) P.Fourn. Quatre Fl. France: 535 (1936)
Spartium corsicum Loisel. Fl. Gall.: 440 (1807)
Argelasia corsica (Loisel.) Fourr. Ann. Soc. Linn. Lyon, n.s., 16: 357 (1868)
Corniola corsica (Loisel.) C.Presl Abh. Königl. Böhm. Ges. Wiss., ser. 5, 3: 567 (1845)

Common names Top

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Language Common/alternative name
French genêt de corse

Subspecies (abbr. subsp./ssp.) Top

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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-0000213730
Tropicos 13019272
INPN 99736
Flora of Italy 2288
KEW urn:lsid:ipni.org:names:495970-1
The Plant List ild-8797
Open Tree Of Life 561954
Observations.org 118181
NCBI Taxonomy 319660
IUCN Red List 83756047
IPNI 495970-1
iNaturalist 333701
GBIF 5347832
Freebase /m/0w4v3bx
EPPO GENCO
EOL 703913
Elurikkus 523864
USDA GRIN 406254
Wikipedia Genista_corsica

Genomes (via NCBI) Top

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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
Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2022 Gibin D, Pasinato L, Delbianco A EFSA J 13-Jun-2023
PMCID:PMC10262070
doi:10.2903/j.efsa.2023.8061
PMID:37325259
Integrative Taxonomy of Armeria Taxa (Plumbaginaceae) Endemic to Sardinia and Corsica Tiburtini M, Bacchetta G, Sarigu M, Cambria S, Caputo P, De Luca D, Domina G, Turini A, Peruzzi L Plants (Basel) 05-Jun-2023
PMCID:PMC10255103
doi:10.3390/plants12112229
PMID:37299208
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2022 Delbianco A, Gibin D, Pasinato L, Boscia D, Morelli M EFSA J 09-Jan-2023
PMCID:PMC9827234
doi:10.2903/j.efsa.2023.7726
PMID:36628332
Xylella fastidiosa in Europe: From the Introduction to the Current Status Trkulja V, Tomić A, Iličić R, Nožinić M, Milovanović TP Plant Pathol J 01-Dec-2022
PMCID:PMC9742796
doi:10.5423/PPJ.RW.09.2022.0127
PMID:36503185
Ethnopharmacobotany and Diversity of Mediterranean Endemic Plants in Marmilla Subregion, Sardinia, Italy Cocco E, Maccioni D, Sanjust E, Falconieri D, Farris E, Maxia A Plants (Basel) 18-Nov-2022
PMCID:PMC9695302
doi:10.3390/plants11223165
PMID:36432894
Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2021 Delbianco A, Gibin D, Pasinato L, Boscia D, Morelli M EFSA J 15-Jun-2022
PMCID:PMC9198695
doi:10.2903/j.efsa.2022.7356
PMID:35734284
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2021 Delbianco A, Gibin D, Pasinato L, Morelli M EFSA J 12-Jan-2022
PMCID:PMC8753584
doi:10.2903/j.efsa.2022.7039
PMID:35035582
Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2020 Delbianco A, Gibin D, Pasinato L, Morelli M EFSA J 23-Jun-2021
PMCID:PMC8220458
doi:10.2903/j.efsa.2021.6674
PMID:34188716
So Uncommon and so Singular, but Underexplored: An Updated Overview on Ethnobotanical Uses, Biological Properties and Phytoconstituents of Sardinian Endemic Plants Sanna C, Maxia A, Fenu G, Loi MC Plants (Basel) 29-Jul-2020
PMCID:PMC7465485
doi:10.3390/plants9080958
PMID:32751394
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2019 N/A EFSA J 28-Apr-2020
PMCID:PMC7448098
doi:10.2903/j.efsa.2020.6114
PMID:32874307
Antitumor Potential and Phytochemical Profile of Plants from Sardinia (Italy), a Hotspot for Biodiversity in the Mediterranean Basin Cappadone C, Mandrone M, Chiocchio I, Sanna C, Malucelli E, Bassi V, Picone G, Poli F Plants (Basel) 24-Dec-2019
PMCID:PMC7020228
doi:10.3390/plants9010026
PMID:31878127
Update of the Xylella spp. host plant database N/A EFSA J 10-Sep-2018
PMCID:PMC7009760
doi:10.2903/j.efsa.2018.5408
PMID:32626043
Updated pest categorisation of Xylella fastidiosa Jeger M, Caffier D, Candresse T, Chatzivassiliou E, Dehnen‐Schmutz K, Gilioli G, Grégoire J, Jaques Miret JA, MacLeod A, Navajas Navarro M, Niere B, Parnell S, Potting R, Rafoss T, Rossi V, Urek G, Van Bruggen A, Van der Werf W, West J, Winter S, Almeida R, Bosco D, Jacques M, Landa B, Purcell A, Saponari M, Czwienczek E, Delbianco A, Stancanelli G, Bragard C EFSA J 23-Jul-2018
PMCID:PMC7009507
doi:10.2903/j.efsa.2018.5357
PMID:32625990
Rapid Identification of Antioxidant Compounds of Genista saharae Coss. & Dur. by Combination of DPPH Scavenging Assay and HPTLC-MS Meriane D, Genta-Jouve G, Kaabeche M, Michel S, Boutefnouchet S Molecules 09-Apr-2014
PMCID:PMC6271480
doi:10.3390/molecules19044369
PMID:24722590
Characterization of Botanical and Geographical Origin of Corsican “Spring” Honeys by Melissopalynological and Volatile Analysis Yang Y, Battesti MJ, Costa J, Paolini J Foods 27-Jan-2014
PMCID:PMC5302302
doi:10.3390/foods3010128
PMID:28234308

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
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Lariciresinol dimethyl ether 14237703 Click to see COC1=C(C=C(C=C1)CC2COC(C2CO)C3=CC(=C(C=C3)OC)OC)OC 388.50 unknown https://doi.org/10.1021/NP990282K
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
8,9,12-Trihydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.02,11.05,10]hexadec-6-ene-3,15-dione 73880589 Click to see CC1C2C(C3C4(C(CC(=O)C3(C1C(=O)O2)C)C(=CC(C4O)O)C)C)O 350.40 unknown https://doi.org/10.1021/NP990282K
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
6-Methoxycyclohexane-1,2,3,4,5-pentol 230881 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1021/NP990282K
D-Pinitol 164619 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1016/J.BSE.2004.10.015
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Hex-2-ulofuranosyl hexopyranoside 1115 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1021/NP990282K
Ido(b1-2b)D-Sorf 93091914 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1021/NP990282K
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1021/NP990282K
https://doi.org/10.1016/J.BSE.2004.10.015
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/NP990282K
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/NP990282K
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/J.BSE.2004.10.015
https://doi.org/10.1021/NP990282K
> 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.BSE.2004.10.015
https://doi.org/10.1021/NP990282K
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
5,7-dihydroxy-2-[3-hydroxy-4-[(2S,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 51521836 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/10.1021/NP990282K
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/10.1021/NP990282K
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/10.1021/NP990282K
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-galactoside 5291488 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP990282K
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP990282K
https://doi.org/10.1016/J.BSE.2004.10.015
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
(2S)-2-(3,4-dihydroxyphenyl)-7-hydroxy-5-methoxy-2,3-dihydrochromen-4-one 162937038 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC(=C(C=C3)O)O)O 302.28 unknown https://doi.org/10.1021/NP990282K
2-(3,4-Dihydroxyphenyl)-7-hydroxy-5-methoxy-2,3-dihydrochromen-4-one 17841897 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC(=C(C=C3)O)O)O 302.28 unknown https://doi.org/10.1021/NP990282K
5-O-Methyldihydroquercetin 637323 Click to see COC1=CC(=CC2=C1C(=O)C(C(O2)C3=CC(=C(C=C3)O)O)O)O 318.28 unknown https://doi.org/10.1021/NP990282K
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
5-O-Methylgenistein 5748551 Click to see COC1=CC(=CC2=C1C(=O)C(=CO2)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1016/J.BSE.2004.10.015
https://doi.org/10.1021/NP990282K
Daidzein 5281708 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O 254.24 unknown https://doi.org/10.1021/NP990282K
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
3-(3,4-Dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-5,7-dihydroxychromen-4-one 163002758 Click to see CC1(C(C(C2=C(O1)C=CC(=C2)C3=COC4=CC(=CC(=C4C3=O)O)O)O)O)C 370.40 unknown https://doi.org/10.1021/NP990282K
5,7-Dihydroxy-3-(3-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)chromen-4-one 21591962 Click to see CC1(C(CC2=C(O1)C=CC(=C2)C3=COC4=CC(=CC(=C4C3=O)O)O)O)C 354.40 unknown https://doi.org/10.1021/NP990282K
Dihydroisoderrondiol 10832934 Click to see CC1(C(C(C2=C(O1)C=CC(=C2)C3=COC4=CC(=CC(=C4C3=O)O)O)O)O)C 370.40 unknown https://doi.org/10.1021/NP990282K
Ficuisoflavone 10546044 Click to see CC1(C(CC2=C(O1)C=CC(=C2)C3=COC4=CC(=CC(=C4C3=O)O)O)O)C 354.40 unknown https://doi.org/10.1021/NP990282K
https://doi.org/10.1016/J.BSE.2004.10.015
Isoderrone 14237660 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C3=COC4=CC(=CC(=C4C3=O)O)O)C 336.30 unknown https://doi.org/10.1016/J.BSE.2004.10.015
https://doi.org/10.1021/NP990282K

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