Senecio speciosus - Unknown
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Internal ID UUID643fd19f7875b045509797
Scientific name Senecio speciosus
Authority Willd.
First published in Sp. Pl., ed. 4 , 3: 1991 (1803)

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Synonyms Top

Scientific name Authority First published in
Senecio concolor DC. Prodr. 6: 407 (1838)
Senecio concolor Harv. Fl. Cap. 3: 362 (1865)

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • South Tropical Africa
      • Mozambique
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Northern Provinces
      • Swaziland

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000116843
Tropicos 2721177
KEW urn:lsid:ipni.org:names:247677-1
The Plant List gcc-78226
Open Tree Of Life 7609793
NCBI Taxonomy 2962187
IPNI 247677-1
iNaturalist 569624
GBIF 3107637
CMAUP NPO22522

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
Effect of fuchsin fixation of pollen on DNA barcode recovery Streicher MB, Johnson SD, Willows‐Munro S Ecol Evol 31-Aug-2023
PMCID:PMC10468989
doi:10.1002/ece3.10475
PMID:37664513
The evaluation of biological indices to assess the condition of hillslope seep wetlands in the Tsitsa River Catchment, South Africa Libala N, Palmer CG, Odume ON PLoS One 18-May-2021
PMCID:PMC8130940
doi:10.1371/journal.pone.0251370
PMID:34003835
Using a trait‐based approach for assessing the vulnerability and resilience of hillslope seep wetland vegetation cover to disturbances in the Tsitsa River catchment, Eastern Cape, South Africa Libala N, Palmer CG, Odume ON Ecol Evol 11-Dec-2019
PMCID:PMC6972813
doi:10.1002/ece3.5893
PMID:31988728
Diversity of use and local knowledge of wild and cultivated plants in the Eastern Cape province, South Africa Maroyi A J Ethnobiol Ethnomed 08-Aug-2017
PMCID:PMC5549312
doi:10.1186/s13002-017-0173-8
PMID:28789692
Ethnopharmacological Survey of Plants Used in the Traditional Treatment of Gastrointestinal Pain, Inflammation and Diarrhea in Africa: Future Perspectives for Integration into Modern Medicine Stark TD, Mtui DJ, Balemba OB Animals (Basel) 04-Mar-2013
PMCID:PMC4495512
doi:10.3390/ani3010158
PMID:26487315
Neuartige ester von eremophilen-derivaten aus südafrikanischen Senecio-arten Ferdinand Bolhmann, Albert Suwita, Christa Zdero Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)88690-2
Eremophilane derivatives and other constituents from Senecio species F Bohlmann Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81111-5

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 / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(5-Hydroxy-1,8a-dimethyl-6-oxo-7-prop-1-en-2-yl-1,2,3,4,4a,5,7,8-octahydronaphthalen-2-yl) 5-(2-methylbut-2-enoyloxy)hex-2-enoate 162940600 Click to see CC=C(C)C(=O)OC(C)CC=CC(=O)OC1CCC2C(C(=O)C(CC2(C1C)C)C(=C)C)O 446.60 unknown https://doi.org/10.1016/S0031-9422(00)88690-2
(5-hydroxy-1,8a-dimethyl-6-oxo-7-propan-2-ylidene-2,3,4,4a,5,8-hexahydro-1H-naphthalen-2-yl) 4-(2-methylbut-2-enoyloxy)hex-2-enoate 163070957 Click to see CCC(C=CC(=O)OC1CCC2C(C(=O)C(=C(C)C)CC2(C1C)C)O)OC(=O)C(=CC)C 446.60 unknown https://doi.org/10.1016/S0031-9422(00)88690-2
(5-hydroxy-1,8a-dimethyl-6-oxo-7-propan-2-ylidene-2,3,4,4a,5,8-hexahydro-1H-naphthalen-2-yl) 5-(2-methylbut-2-enoyloxy)hex-2-enoate 163038339 Click to see CC=C(C)C(=O)OC(C)CC=CC(=O)OC1CCC2C(C(=O)C(=C(C)C)CC2(C1C)C)O 446.60 unknown https://doi.org/10.1016/S0031-9422(00)88690-2
(5,6-dihydroxy-1,8a-dimethyl-7-prop-1-en-2-yl-2,3,4,4a,5,6,7,8-octahydro-1H-naphthalen-2-yl) 5-(2-methylbut-2-enoyloxy)hex-2-enoate 163084959 Click to see CC=C(C)C(=O)OC(C)CC=CC(=O)OC1CCC2C(C(C(CC2(C1C)C)C(=C)C)O)O 448.60 unknown https://doi.org/10.1016/S0031-9422(00)88690-2
(6-Hydroxy-1,8a-dimethyl-5-oxo-7-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalen-2-yl) 5-methyldodeca-2,4,6-trienoate 162991231 Click to see CCCCCC=CC(=CC=CC(=O)OC1CCC2C(=O)C(C(CC2(C1C)C)C(=C)C)O)C 442.60 unknown https://doi.org/10.1016/S0031-9422(00)88690-2
[(1R,2R,4aS,5R,6S,7R,8aR)-5,6-dihydroxy-1,8a-dimethyl-7-prop-1-en-2-yl-2,3,4,4a,5,6,7,8-octahydro-1H-naphthalen-2-yl] (Z,5R)-5-[(Z)-2-methylbut-2-enoyl]oxyhex-2-enoate 163084960 Click to see CC=C(C)C(=O)OC(C)CC=CC(=O)OC1CCC2C(C(C(CC2(C1C)C)C(=C)C)O)O 448.60 unknown https://doi.org/10.1016/S0031-9422(00)88690-2
[(1R,2R,4aS,5R,7R,8aR)-5-hydroxy-1,8a-dimethyl-6-oxo-7-prop-1-en-2-yl-1,2,3,4,4a,5,7,8-octahydronaphthalen-2-yl] (Z,5R)-5-[(Z)-2-methylbut-2-enoyl]oxyhex-2-enoate 162940601 Click to see CC=C(C)C(=O)OC(C)CC=CC(=O)OC1CCC2C(C(=O)C(CC2(C1C)C)C(=C)C)O 446.60 unknown https://doi.org/10.1016/S0031-9422(00)88690-2
[(1R,2R,4aS,5R,8aR)-5-hydroxy-1,8a-dimethyl-6-oxo-7-propan-2-ylidene-2,3,4,4a,5,8-hexahydro-1H-naphthalen-2-yl] (Z,4R)-4-[(Z)-2-methylbut-2-enoyl]oxyhex-2-enoate 163070958 Click to see CCC(C=CC(=O)OC1CCC2C(C(=O)C(=C(C)C)CC2(C1C)C)O)OC(=O)C(=CC)C 446.60 unknown https://doi.org/10.1016/S0031-9422(00)88690-2
[(1R,2R,4aS,5R,8aR)-5-hydroxy-1,8a-dimethyl-6-oxo-7-propan-2-ylidene-2,3,4,4a,5,8-hexahydro-1H-naphthalen-2-yl] (Z,5R)-5-[(Z)-2-methylbut-2-enoyl]oxyhex-2-enoate 163038340 Click to see CC=C(C)C(=O)OC(C)CC=CC(=O)OC1CCC2C(C(=O)C(=C(C)C)CC2(C1C)C)O 446.60 unknown https://doi.org/10.1016/S0031-9422(00)88690-2
[(1R,2R,4aS,6S,7R,8aR)-6-hydroxy-1,8a-dimethyl-5-oxo-7-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalen-2-yl] (2E,4E,6E)-5-methyldodeca-2,4,6-trienoate 162991232 Click to see CCCCCC=CC(=CC=CC(=O)OC1CCC2C(=O)C(C(CC2(C1C)C)C(=C)C)O)C 442.60 unknown https://doi.org/10.1016/S0031-9422(00)88690-2
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Capparin B 24813533 Click to see COC1=CC2=C(C=C1)C(=C(N2)SC)C=O 221.28 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
6-Methoxyindoline-2,3-dione 10374972 Click to see COC1=CC2=C(C=C1)C(=O)C(=O)N2 177.16 unknown via CMAUP database
Capparin A 101457836 Click to see COC1=CC2=C(C=C1)C3(CN=C(S3)SC)C(=O)N2 280.40 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
(9-Hydroxy-9a-methoxy-4a,5-dimethyl-3-methylidene-3a,4,5,6,7,8,8a,9-octahydrobenzo[f][1]benzofuran-6-yl) 5-methyldodeca-2,4,6-trienoate 162931610 Click to see CCCCCC=CC(=CC=CC(=O)OC1CCC2C(C3(C(CC2(C1C)C)C(=C)CO3)OC)O)C 472.70 unknown https://doi.org/10.1016/S0031-9422(00)81111-5
[(3aS,4aR,5R,6R,8aR,9S,9aS)-9-hydroxy-9a-methoxy-4a,5-dimethyl-3-methylidene-3a,4,5,6,7,8,8a,9-octahydrobenzo[f][1]benzofuran-6-yl] (2E,4E,6E)-5-methyldodeca-2,4,6-trienoate 162931611 Click to see CCCCCC=CC(=CC=CC(=O)OC1CCC2C(C3(C(CC2(C1C)C)C(=C)CO3)OC)O)C 472.70 unknown https://doi.org/10.1016/S0031-9422(00)81111-5
> 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 via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Oroxylin A 5320315 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=CC=C3)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Wogonin 5281703 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)O 284.26 unknown via CMAUP database

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