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Genista ephedroides

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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 UUID643fdf1192464802419863
Scientific name Genista ephedroides
Authority DC.
First published in Mém. Légum.: 210 (1826)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cytisanthus ephedroides (DC.) Gams G.Hegi, Ill. Fl. Mitt.-Eur.4: 1193 (1923)
Spartium gymnopterum Viv. Fl. Cors. Prodr., App.: 6 (1825)
Spartium ephedroides Spreng. Syst. Veg. ed. 16, 4(2): 266 (1827)

Common names Top

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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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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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000213735
Tropicos 13019310
INPN 99748
Flora of Italy 2301
KEW urn:lsid:ipni.org:names:496029-1
The Plant List ild-8800
Open Tree Of Life 104029
Observations.org 124395
NCBI Taxonomy 123905
IPNI 496029-1
iNaturalist 486582
iNaturalist 486581
GBIF 5347647
EPPO GENEP
EOL 703916
Elurikkus 523790
USDA GRIN 17308

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
Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023 Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A EFSA J 15-Dec-2023
PMCID:PMC10722330
doi:10.2903/j.efsa.2023.8477
PMID:38107375
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
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
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
Specialized Metabolites from the Allelopathic Plant Retama raetam as Potential Biopesticides Soriano G, Petrillo C, Masi M, Bouafiane M, Khelil A, Tuzi A, Isticato R, Fernández-Aparicio M, Cimmino A Toxins (Basel) 28-Apr-2022
PMCID:PMC9146260
doi:10.3390/toxins14050311
PMID:35622558
The Endemic Vascular Flora of Sardinia: A Dynamic Checklist with an Overview of Biogeography and Conservation Status Fois M, Farris E, Calvia G, Campus G, Fenu G, Porceddu M, Bacchetta G Plants (Basel) 23-Feb-2022
PMCID:PMC8912449
doi:10.3390/plants11050601
PMID:35270071
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
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
Licoflavone C attenuates the genotoxicity of cancer drugs in human peripheral lymphocytes. Scarpato R, Paganucci L, Bertoli A, Fiore L, Pistelli L, Federico G Phytother Res 01-Dec-2008
doi:10.1002/PTR.2546
PMID:18979523

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
> Alkaloids and derivatives / Lupin alkaloids / Anagyrine-type alkaloids
Anagyrin 71056954 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/S0305-1978(00)00046-6
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(1R,2R,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 92143189 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/S0305-1978(00)00046-6
(2S,3S,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-3-ol 139031197 Click to see C1CCN2CC3CC(C2C1)CN4C3C(CCC4)O 250.38 unknown https://doi.org/10.1016/S0305-1978(00)00046-6
alpha-Isolupanine 119201 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/S0305-1978(00)00046-6
Spartein-5-ol 442962 Click to see C1CCN2CC3CC(C2C1)CN4C3C(CCC4)O 250.38 unknown https://doi.org/10.1016/S0305-1978(00)00046-6
> 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/NP980112S
> 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/NP980112S
> 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/NP980112S
D-Pinitol 164619 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1021/NP980112S
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1021/NP980112S
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
5,7-dihydroxy-8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-2-(4-hydroxyphenyl)chromen-4-one 163036003 Click to see CC(=C)C(CC1=C2C(=C(C=C1O)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)O 354.40 unknown https://doi.org/10.1021/NP980112S
Ephedroidin 11792417 Click to see CC(=C)C(CC1=C2C(=C(C=C1O)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)O 354.40 unknown https://doi.org/10.1021/NP980112S
Licoflavone C 10246505 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C 338.40 unknown https://doi.org/10.1002/PTR.2327
https://doi.org/10.1002/PTR.2546
https://doi.org/10.1021/NP980112S
> 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/NP980112S
> 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/10.1021/NP980112S
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown https://doi.org/10.1021/NP980112S
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(2R)-5-hydroxy-2-(hydroxymethyl)-7-(4-hydroxyphenyl)-2-methylpyrano[3,2-g]chromen-6-one 92446139 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)CO 352.30 unknown https://doi.org/10.1021/NP980112S
(2S)-5-hydroxy-2-(hydroxymethyl)-7-(4-hydroxyphenyl)-2-methylpyrano[3,2-g]chromen-6-one 92446140 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)CO 352.30 unknown https://doi.org/10.1021/NP980112S
5,7-Dihydroxy-6-(2-hydroxy-3-methylbut-3-enyl)-3-(4-hydroxyphenyl)chromen-4-one 15237156 Click to see CC(=C)C(CC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O)O 354.40 unknown https://doi.org/10.1021/NP980112S
5,7-dihydroxy-6-[(2S)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)chromen-4-one 26250192 Click to see CC(=C)C(CC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O)O 354.40 unknown https://doi.org/10.1021/NP980112S
Alpinumisoflavone 5490139 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C 336.30 unknown https://doi.org/10.1021/NP980112S
Erysubin B 10760434 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)CO 352.30 unknown https://doi.org/10.1021/NP980112S
Wighteone 5281814 Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O)C 338.40 unknown https://doi.org/10.1021/NP980112S
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid C-glycosides
3-Genistein-8-C-glucoside 5472471 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O)O 432.40 unknown https://doi.org/10.1021/NP980112S
5,7-dihydroxy-3-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 154496626 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O)O 432.40 unknown https://doi.org/10.1021/NP980112S
Genistein 8-C-glucoside 5281757 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O)O 432.40 unknown https://doi.org/10.1021/NP980112S
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
5-hydroxy-3-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 10791517 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)C 500.50 unknown https://doi.org/10.1021/NP980112S
5-hydroxy-3-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-7-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162976814 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)C 500.50 unknown https://doi.org/10.1021/NP980112S
5-Hydroxy-3-(4-hydroxyphenyl)-6-(3-methylbut-2-enyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162976813 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)C 500.50 unknown https://doi.org/10.1021/NP980112S
5-hydroxy-3-(4-hydroxyphenyl)-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 12310089 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1021/NP980112S
5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 154496625 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1021/NP980112S
Genistin 5281377 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1021/NP980112S
Genistoside 5284639 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1021/NP980112S

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