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Senecio lividus

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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 UUID643fd24468891104611028
Scientific name Senecio lividus
Authority L.
First published in Sp. Pl. : 867 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Senecio litardierei (Rouy) P.Fourn. P. Fourn.. 1939. 987 1939
Senecio foeniculaceus Ten. Fl. Napol. Prodr. p. xlix (1811)
Senecio sonchoides Lojac. Fl. Sicul. (Lojacono) 2(1): 66. 1903
Senecio lividus var. pinguis Ball
Senecio lividus subsp. lividus L.
Senecio lividus var. major Gren. & Godr.
Senecio lividus var. biennis Humbert
Senecio lividus subsp. foeniculaceus (Ten.) Braun-Blanq. & Maire

Common names Top

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Language Common/alternative name
Finnish korvavillakko

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
  • Europe
    • Southeastern Europe
      • Greece
      • Italy
      • Sicilia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000122180
Tropicos 2743832
INPN 122656
Flora of Italy 5796
KEW urn:lsid:ipni.org:names:246100-1
The Plant List gcc-83361
Open Tree Of Life 962482
Observations.org 132311
NCBI Taxonomy 121549
IPNI 246100-1
iNaturalist 341158
GBIF 3107156
EPPO SENLV

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
Eremophilane-, bisabolane- and shikimic acid-derivatives from Portugese Senecio species J.M. Cardoso, J. Jakupovic, F. Bohlmann Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84711-1
An Improved Three Step Synthesis of (-)-3β-Hydroxycarvone from (-)-Carvone dos Santos RB, Brocksom TJ, Zanotto PR, Brocksom U Molecules 28-Feb-2002
PMCID:PMC6146741
doi:10.3390/70200129

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
[(1S,3S,4S,6S)-4-[(3R)-3-acetyloxy-6-methylhepta-1,5-dien-2-yl]-1-methyl-2-oxo-7-oxabicyclo[4.1.0]heptan-3-yl] 3-methylbut-2-enoate 162900383 Click to see CC(=CCC(C(=C)C1CC2C(O2)(C(=O)C1OC(=O)C=C(C)C)C)OC(=O)C)C 390.50 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
[(1S,3S,4S,6S)-4-[(3S)-3-acetyloxy-6-methylhepta-1,5-dien-2-yl]-1-methyl-2-oxo-7-oxabicyclo[4.1.0]heptan-3-yl] (Z)-2-methylbut-2-enoate 162862459 Click to see CC=C(C)C(=O)OC1C(CC2C(C1=O)(O2)C)C(=C)C(CC=C(C)C)OC(=O)C 390.50 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
[4-(3-Acetyloxy-6-methylhepta-1,5-dien-2-yl)-1-methyl-2-oxo-7-oxabicyclo[4.1.0]heptan-3-yl] 2-methylbut-2-enoate 162862458 Click to see CC=C(C)C(=O)OC1C(CC2C(C1=O)(O2)C)C(=C)C(CC=C(C)C)OC(=O)C 390.50 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
[4-(3-Acetyloxy-6-methylhepta-1,5-dien-2-yl)-1-methyl-2-oxo-7-oxabicyclo[4.1.0]heptan-3-yl] 3-methylbut-2-enoate 162900382 Click to see CC(=CCC(C(=C)C1CC2C(O2)(C(=O)C1OC(=O)C=C(C)C)C)OC(=O)C)C 390.50 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(5-hydroxy-1,8a-dimethyl-6-oxo-7-propan-2-ylidene-2,3,4,4a,5,8-hexahydro-1H-naphthalen-2-yl) 2-methyl-4-(2-methylbut-2-enoyloxy)but-2-enoate 163030309 Click to see CC=C(C)C(=O)OCC=C(C)C(=O)OC1CCC2C(C(=O)C(=C(C)C)CC2(C1C)C)O 432.50 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
(5-hydroxy-1,8a-dimethyl-6-oxo-7-propan-2-ylidene-2,3,4,4a,5,8-hexahydro-1H-naphthalen-2-yl) 3-methyl-4-(2-methylbut-2-enoyloxy)but-2-enoate 163003741 Click to see CC=C(C)C(=O)OCC(=CC(=O)OC1CCC2C(C(=O)C(=C(C)C)CC2(C1C)C)O)C 432.50 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
(5-hydroxy-1,8a-dimethyl-6-oxo-7-propan-2-ylidene-2,3,4,8-tetrahydro-1H-naphthalen-2-yl) 2-methyl-4-(2-methylbut-2-enoyloxy)but-2-enoate 163024182 Click to see CC=C(C)C(=O)OCC=C(C)C(=O)OC1CCC2=C(C(=O)C(=C(C)C)CC2(C1C)C)O 430.50 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
(5-hydroxy-1,8a-dimethyl-6-oxo-7-propan-2-ylidene-2,3,4,8-tetrahydro-1H-naphthalen-2-yl) 3-methyl-4-(2-methylbut-2-enoyloxy)but-2-enoate 162957935 Click to see CC=C(C)C(=O)OCC(=CC(=O)OC1CCC2=C(C(=O)C(=C(C)C)CC2(C1C)C)O)C 430.50 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
[(1R,2R,4aR,5S,8aR)-5-hydroxy-1,8a-dimethyl-6-oxo-7-propan-2-ylidene-2,3,4,4a,5,8-hexahydro-1H-naphthalen-2-yl] (Z)-2-methyl-4-[(Z)-2-methylbut-2-enoyl]oxybut-2-enoate 13855824 Click to see CC=C(C)C(=O)OCC=C(C)C(=O)OC1CCC2C(C(=O)C(=C(C)C)CC2(C1C)C)O 432.50 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
[(1R,2R,4aR,5S,8aR)-5-hydroxy-1,8a-dimethyl-6-oxo-7-propan-2-ylidene-2,3,4,4a,5,8-hexahydro-1H-naphthalen-2-yl] (Z)-3-methyl-4-[(Z)-2-methylbut-2-enoyl]oxybut-2-enoate 163195122 Click to see CC=C(C)C(=O)OCC(=CC(=O)OC1CCC2C(C(=O)C(=C(C)C)CC2(C1C)C)O)C 432.50 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
[(1R,2R,8aR)-5-hydroxy-1,8a-dimethyl-6-oxo-7-propan-2-ylidene-2,3,4,8-tetrahydro-1H-naphthalen-2-yl] (Z)-2-methyl-4-[(Z)-2-methylbut-2-enoyl]oxybut-2-enoate 13855832 Click to see CC=C(C)C(=O)OCC=C(C)C(=O)OC1CCC2=C(C(=O)C(=C(C)C)CC2(C1C)C)O 430.50 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
[(1R,2R,8aR)-5-hydroxy-1,8a-dimethyl-6-oxo-7-propan-2-ylidene-2,3,4,8-tetrahydro-1H-naphthalen-2-yl] (Z)-3-methyl-4-[(Z)-2-methylbut-2-enoyl]oxybut-2-enoate 162957936 Click to see CC=C(C)C(=O)OCC(=CC(=O)OC1CCC2=C(C(=O)C(=C(C)C)CC2(C1C)C)O)C 430.50 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
methyl (3R,4S,5R)-3,5-bis[[(2R)-2-methylbutanoyl]oxy]-4-octanoyloxycyclohexene-1-carboxylate 162908699 Click to see CCCCCCCC(=O)OC1C(CC(=CC1OC(=O)C(C)CC)C(=O)OC)OC(=O)C(C)CC 482.60 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
methyl (3R,4S,5R)-4-decanoyloxy-3-[(2R)-2-methylbutanoyl]oxy-5-(2-methylpropanoyloxy)cyclohexene-1-carboxylate 163040503 Click to see CCCCCCCCCC(=O)OC1C(CC(=CC1OC(=O)C(C)CC)C(=O)OC)OC(=O)C(C)C 496.60 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
methyl (3R,4S,5R)-4-decanoyloxy-3,5-bis(2-methylpropanoyloxy)cyclohexene-1-carboxylate 13855850 Click to see CCCCCCCCCC(=O)OC1C(CC(=CC1OC(=O)C(C)C)C(=O)OC)OC(=O)C(C)C 482.60 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
methyl (3R,4S,5R)-4-decanoyloxy-3,5-bis[[(2R)-2-methylbutanoyl]oxy]cyclohexene-1-carboxylate 163035895 Click to see CCCCCCCCCC(=O)OC1C(CC(=CC1OC(=O)C(C)CC)C(=O)OC)OC(=O)C(C)CC 510.70 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
Methyl 3,5-bis(2-methylbutanoyloxy)-4-octanoyloxycyclohexene-1-carboxylate 13855837 Click to see CCCCCCCC(=O)OC1C(CC(=CC1OC(=O)C(C)CC)C(=O)OC)OC(=O)C(C)CC 482.60 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
Methyl 4-decanoyloxy-3-(2-methylbutanoyloxy)-5-(2-methylpropanoyloxy)cyclohexene-1-carboxylate 13855839 Click to see CCCCCCCCCC(=O)OC1C(CC(=CC1OC(=O)C(C)CC)C(=O)OC)OC(=O)C(C)C 496.60 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
Methyl 4-decanoyloxy-3,5-bis(2-methylbutanoyloxy)cyclohexene-1-carboxylate 13855835 Click to see CCCCCCCCCC(=O)OC1C(CC(=CC1OC(=O)C(C)CC)C(=O)OC)OC(=O)C(C)CC 510.70 unknown https://doi.org/10.1016/S0031-9422(00)84711-1
Methyl 4-decanoyloxy-3,5-bis(2-methylpropanoyloxy)cyclohexene-1-carboxylate 13855849 Click to see CCCCCCCCCC(=O)OC1C(CC(=CC1OC(=O)C(C)C)C(=O)OC)OC(=O)C(C)C 482.60 unknown https://doi.org/10.1016/S0031-9422(00)84711-1

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