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Senecio selloi

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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 UUID643fccf4e00bc823188770
Scientific name Senecio selloi
Authority DC.
First published in Prodr. 6: 419 (1838)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cineraria selloi Spreng. Syst. Veg. 3: 541 (1826)

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
  • Southern America
    • Brazil
      • Brazil South
    • Southern South America
      • Argentina Northeast
      • Uruguay

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000067789
Tropicos 2708090
KEW urn:lsid:ipni.org:names:247541-1
The Plant List gcc-24651
Open Tree Of Life 42140
NCBI Taxonomy 462559
IPNI 247541-1
iNaturalist 790303
GBIF 3108638

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
Plants causing poisoning outbreaks of livestock in South America: A review Riet-Correa F, Machado M, Micheloud JF Toxicon X 21-Jan-2023
PMCID:PMC9898795
doi:10.1016/j.toxcx.2023.100150
PMID:36747993
Antiprotozoal and Antitumor Activity of Natural Polycyclic Endoperoxides: Origin, Structures and Biological Activity Dembitsky VM, Ermolenko E, Savidov N, Gloriozova TA, Poroikov VV Molecules 28-Jan-2021
PMCID:PMC7865715
doi:10.3390/molecules26030686
PMID:33525706
A triterpene ozonide from Senecio selloi. Rücker G, Manns D, Schenkel EP, Hartmann R, Heinzmann BM Arch Pharm (Weinheim) 01-Jul-2003
doi:10.1002/ARDP.200300740
PMID:12916053
Pyrrolizidine alkaloid composition in six brazilian Senecio species Hans Chr. Krebs, Torsten Carl, Gerhard G. Habermehl Elsevier BV 04-Apr-2003
doi:10.1016/S0031-9422(96)00445-1
Triterpenes with a new 9-epi-cucurbitan skeleton from Senecio selloi Gerhard Rücker, Detlef Manns, Eloir P Schenkel, Rudolf Hartmann, Berta M Heinzmann Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00276-9
Sesquiterpene peroxides from Senecio selloi and Eupatorium rufescens. Rücker G, Schenkel EP, Manns D, Mayer R, Heiden K, Heinzmann BM Planta Med 01-Dec-1996
doi:10.1055/S-2006-957974
PMID:17252501
Livestock poisoning in South America by species of the Senecio plant. Habermehl GG, Martz W, Tokarnia CH, Döbereiner J, Mendez MC Toxicon 01-Jan-1988
doi:10.1016/0041-0101(88)90218-8
PMID:3394160

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,2S,5R,6R,9S,10S,13R,15R)-2,5,9,14,14-pentamethyl-6-[(2R)-6-methylhept-5-en-2-yl]-18-oxapentacyclo[13.2.1.01,13.02,10.05,9]octadecane 163005814 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3(C2CCC4C35CCC(C4(C)C)O5)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(99)00276-9
(1S,2S,5R,6R,9S,10S,13R,15R)-2,5,9,14,14-pentamethyl-6-[(2S)-6-methylhept-5-en-2-yl]-18-oxapentacyclo[13.2.1.01,13.02,10.05,9]octadecane 163005813 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3(C2CCC4C35CCC(C4(C)C)O5)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(99)00276-9
(1S,2S,5R,6R,9S,10S,13R,15R)-6-[(2S)-4-[(3R)-5,5-dimethyl-1,2,4-trioxolan-3-yl]butan-2-yl]-2,5,9,14,14-pentamethyl-18-oxapentacyclo[13.2.1.01,13.02,10.05,9]octadecane 162875610 Click to see CC(CCC1OC(OO1)(C)C)C2CCC3(C2(CCC4(C3CCC5C46CCC(C5(C)C)O6)C)C)C 474.70 unknown https://doi.org/10.1002/ARDP.200300740
2,5,9,14,14-Pentamethyl-6-(6-methylhept-5-en-2-yl)-18-oxapentacyclo[13.2.1.01,13.02,10.05,9]octadecane 163005812 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3(C2CCC4C35CCC(C4(C)C)O5)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(99)00276-9
6-[4-(5,5-Dimethyl-1,2,4-trioxolan-3-yl)butan-2-yl]-2,5,9,14,14-pentamethyl-18-oxapentacyclo[13.2.1.01,13.02,10.05,9]octadecane 85123088 Click to see CC(CCC1OC(OO1)(C)C)C2CCC3(C2(CCC4(C3CCC5C46CCC(C5(C)C)O6)C)C)C 474.70 unknown https://doi.org/10.1002/ARDP.200300740
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
(1R,4S,7S)-5-methyl-7-[(2R)-6-methylhept-5-en-2-yl]-2,3-dioxabicyclo[2.2.2]oct-5-ene 162897431 Click to see CC1=CC2C(CC1OO2)C(C)CCC=C(C)C 236.35 unknown https://doi.org/10.1055/S-2006-957974
> Phenylpropanoids and polyketides / Macrolides and analogues
(1R,4R,6R,7S,17R)-4-[(1S)-1-chloroethyl]-4,7-dihydroxy-7-(hydroxymethyl)-6-methyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 162877177 Click to see CC1CC(C(=O)OC2CCN3C2C(=CC3)COC(=O)C1(CO)O)(C(C)Cl)O 403.90 unknown https://doi.org/10.1016/S0031-9422(96)00445-1
(1R,6R,7S,17S)-4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6-methyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 126968828 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CO)O)C 351.40 unknown https://doi.org/10.1016/0041-0101(88)90218-8
4-(1-Chloroethyl)-4,7-dihydroxy-7-(hydroxymethyl)-6-methyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 152771922 Click to see CC1CC(C(=O)OC2CCN3C2C(=CC3)COC(=O)C1(CO)O)(C(C)Cl)O 403.90 unknown https://doi.org/10.1016/S0031-9422(96)00445-1
4-Ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 254855 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1016/S0031-9422(96)00445-1
Integerrimine 5281733 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1016/S0031-9422(99)00276-9
Retrorsine 5281743 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CO)O)C 351.40 unknown https://doi.org/10.1016/S0031-9422(99)00276-9
Senecionine 5280906 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1016/S0031-9422(96)00445-1
https://doi.org/10.1016/S0031-9422(99)00276-9
https://doi.org/10.1016/0041-0101(88)90218-8
Senecivernine 442764 Click to see CC1C(C(C(=O)OCC2=CCN3C2C(CC3)OC(=O)C1=C)(C)O)C 335.40 unknown https://doi.org/10.1016/S0031-9422(96)00445-1
Usaramine 5281756 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CO)O)C 351.40 unknown https://doi.org/10.1016/S0031-9422(99)00276-9

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