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Genista lydia

Genista lydia - Unknown
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Author: Public Domain - WikiMedia
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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 UUID643fdf12b3594676614727
Scientific name Genista lydia
Authority Boiss.
First published in Diagn. Pl. Orient.2: 8 (1843)

Description Top

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Synonyms Top

Scientific name Authority First published in
Genista lydia var. antiochia (Boiss.) P.E.Gibbs P.H.Davis (ed.), Fl. Turkey3: 26 (1970)
Genista antiochia Boiss. Diagn. Pl. Orient.9: 4 (1849)
Genista lydia var. lydia Boiss.
Genista rumelica Velen. Sitzungsber. Königl. Böhm. Ges. Wiss., Math.-Naturwiss. Cl.1890(2): 43 (1890)
Corniola pontica (Spach) K.Koch Hort. Dendrol.: 247 (1853)
Genista caespitosa K.Koch Linnaea19: 60 (1847)
Genista leptophylla Spach Ann. Sci. Nat., Bot., sér. 2, 6: 127 (1836)
Genista transsilvanica Schur Enum. Pl. Transsilv.: 144 (1866)
Genista lydia var. rumelica (Velen.) Bornm. Mitth. Thüring. Bot. Vereins, n.f., 23: 31 (1908)
Genista patula var. antiochia (Boiss.) Boiss. Fl. Orient.2: 44 (1872)
Genista lamprophylla Spach Ann. Sci. Nat., Bot., sér. 3, 3: 126 (1845)
Genista lydia subsp. antiochia (Boiss.) Ponert Feddes Repert.83: 619 (1972 publ. 1973)
Genista januensis subsp. lydia (Boiss.) Kit Tan & Ziel. Ann. Bot. Fenn.41: 456 (2004)
Genista lydia subsp. antalayaensis Ponert Feddes Repert.83: 619 (1972 publ. 1973)
Genista lydia subsp. rumelica (Velen.) Ponert Feddes Repert.83: 619 (1972 publ. 1973)
Genista pontica Spach Ann. Sci. Nat., Bot., sér. 3, 3: 127 (1845)

Common names Top

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Language Common/alternative name
Arabic جينيستا ليدية
Bulgarian теснолистна жълтуга
Czech kručinka lydijská
Chinese 矮丛小金雀
Chinese 矮丛染料木

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
  • Europe
    • Southeastern Europe
      • Bulgaria
      • Greece
      • Turkey-in-Europe
      • Yugoslavia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000213748
Cornell Woody Plants 319
Tropicos 13019404
INPN 99778
KEW urn:lsid:ipni.org:names:496158-1
The Plant List ild-8813
Open Tree Of Life 1045883
Observations.org 132782
NCBI Taxonomy 529822
NBN Atlas NBNSYS0500000388
IPNI 496158-1
GBIF 5347712
EPPO GENLY
EOL 703263
Elurikkus 523817
USDA GRIN 17317
Wikipedia Genista_lydia
CMAUP NPO24576

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
Streptococcosis a Re-Emerging Disease in Aquaculture: Significance and Phytotherapy Van Doan H, Soltani M, Leitão A, Shafiei S, Asadi S, Lymbery AJ, Ringø E Animals (Basel) 16-Sep-2022
PMCID:PMC9495100
doi:10.3390/ani12182443
PMID:36139303
Enantiomeric Natural Products: Occurrence and Biogenesis Finefield JM, Sherman DH, Kreitman M, Williams RM Angew Chem Int Ed Engl 03-May-2012
PMCID:PMC3498912
doi:10.1002/anie.201107204
PMID:22555867
Ulceroprotective activity of the flavonoids of <i>Genista rumelica</i> Vel L. Rainova, N. Nakov, S. Bogdanova, E. Minkov, D. Staneva‐Stoytcheva Wiley 18-Oct-2006
doi:10.1002/PTR.2650020307
Alkaloid profile of Bulgarian species from genus Senecio L. Christov V, Evstatieva L Z Naturforsch C J Biosci 01-Mar-2003
doi:10.1515/ZNC-2003-3-427
PMID:12710745
Alkaloids of Genista lydia var. lydia and var. antiochia. Tosun A, Tanker M, Tosun F, Ozden T Planta Med 01-Oct-1988
doi:10.1055/S-2006-962506
PMID:17265322
Alkaloids from the flowers of Genista lydia. Ulubelen A, Doguç T Planta Med 01-Dec-1974
doi:10.1055/S-0028-1099397
PMID:4465816

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
(1S,9S,10R,12S)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 131676079 Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown https://doi.org/10.1055/S-2006-962506
(1S,9S,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 171283 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1055/S-0028-1099397
Thermopsine 92768 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1055/S-0028-1099397
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(1R)-1,2,3,4,5,6-Hexahydro-1,5-methano-8H-pyrido[1,2-a][1,5]diazocin-8-one 1278189 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1055/S-0028-1099397
N-Methylcytisine 234566 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1055/S-0028-1099397
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(+)-Retamine 76972451 Click to see C1CCN2CC3CC(C2C1)CN4C3C(CCC4)O 250.38 unknown https://doi.org/10.1055/S-0028-1099397
(2S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-8-one 139031726 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3CCCC4 248.36 unknown https://doi.org/10.1515/ZNC-2003-3-427
13alpha-Hydroxyspartein-2-one 5459919 Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)O 264.36 unknown https://doi.org/10.1515/ZNC-2003-3-427
6-Phosphogluconic acid tri(cyclohexylammonium) salt, Grade V 16212687 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1515/ZNC-2003-3-427
alpha-Isolupanine 119201 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1055/S-0028-1099397
Lupanine 91471 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1055/S-0028-1099397
Retamine 197754 Click to see C1CCN2CC3CC(C2C1)CN4C3C(CCC4)O 250.38 unknown https://doi.org/10.1055/S-0028-1099397
Sparteine 644020 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1515/ZNC-2003-3-427
> Benzenoids / Phenols / 4-alkoxyphenols
(E)-1-(4-Hydroxyphenoxy)-4-icosene-3-one 15458654 Click to see CCCCCCCCCCCCCCCC=CC(=O)CCOC1=CC=C(C=C1)O 402.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
(E)-1-Methoxy-4-icosene-3-one 15458653 Click to see CCCCCCCCCCCCCCCC=CC(=O)CCOC 324.50 unknown via CMAUP database
> 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/10.1002/PTR.2650020307
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3-Hydroxy-5,7-dimethoxy-2-(4-methoxyphenyl)chromen-4-one 624831 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)O 328.30 unknown via CMAUP database
3,7-Dihydroxy-5,3',4'-trimethoxyflavone 14234929 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)O)O)OC 344.30 unknown via CMAUP database
3,7-Dihydroxy-5,4'-dimethoxyflavone 44259527 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)O)O 314.29 unknown via CMAUP database
Ombuin 5320287 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)O)O 330.29 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
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/10.1002/PTR.2650020307
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Ayanin 5280682 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)O 344.30 unknown via CMAUP database
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown via CMAUP database
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 via CMAUP database
Quercetin pentamethyl ether 97332 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC)OC 372.40 unknown via CMAUP database
Retusin 5352005 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC 358.30 unknown via CMAUP database
Tetramethylkaempferol 631095 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC 342.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
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/10.1002/PTR.2650020307

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