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Senecio rosmarinus

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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 UUID643fc6475c5a2414286798
Scientific name Senecio rosmarinus
Authority Phil.
First published in Anales Mus. Nac. Santiago de Chile Bot. 1891: 41 (1891)

Description Top

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Synonyms Top

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Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Senecio rosmarinus var. ascotanensis (Phil.) Cabrera Lilloa 15: 261 (1949)

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
  • Southern America
    • Southern South America
      • Argentina Northwest
      • Chile North
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000003901
Tropicos 2708064
KEW urn:lsid:ipni.org:names:233913-2
The Plant List gcc-103764
Open Tree Of Life 5739103
IPNI 233913-2
GBIF 3107970

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)!
Title Authors Publication Released IDs
An eremophilanolide from Senecio rosmarinus Morales B. Glauco, Bórquez R. Jorge, Mancilla P. Arlett, Pedreros T. Samuel, A.Loyola M. Luis Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81708-2

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 / Terpene lactones
(4aR,5S,8aR,9aS)-3,4a,5-trimethyl-5,6,7,8a,9,9a-hexahydro-4H-benzo[f][1]benzofuran-2,8-dione 162955206 Click to see CC1CCC(=O)C2C1(CC3=C(C(=O)OC3C2)C)C 248.32 unknown https://doi.org/10.1016/S0031-9422(00)81708-2
(4aR,5S,8aS,9aR)-3,4a,5-trimethyl-5,6,7,8a,9,9a-hexahydro-4H-benzo[f][1]benzofuran-2,8-dione 145957091 Click to see CC1CCC(=O)C2C1(CC3=C(C(=O)OC3C2)C)C 248.32 unknown https://doi.org/10.1016/S0031-9422(00)81708-2
(4aS,5R,8aR,9aS)-9a-Hydroxy-3,4a,5-trimethyl-2,4,4a,5,6,7,8,8a,9,9a-decahydronaphtho[2,3-b]furan-2,8-dione 145949896 Click to see CC1CCC(=O)C2C1(CC3=C(C(=O)OC3(C2)O)C)C 264.32 unknown https://doi.org/10.1016/S0031-9422(00)81708-2
Ent-8a-Hydroxy-1-oxo-7(11)-eremophilen-12,8-olide 12304519 Click to see CC1CCC(=O)C2C1(CC3=C(C(=O)OC3(C2)O)C)C 264.32 unknown https://doi.org/10.1016/S0031-9422(00)81708-2
Istanbulin A 3082428 Click to see CC1CCC(=O)C2C1(CC3=C(C(=O)OC3(C2)O)C)C 264.32 unknown https://doi.org/10.1016/S0031-9422(00)81708-2
Istanbulin B 131751897 Click to see CC1CCC(=O)C2C1(CC3=C(C(=O)OC3C2)C)C 248.32 unknown https://doi.org/10.1016/S0031-9422(00)81708-2
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetovanillone 2214 Click to see CC(=O)C1=CC(=C(C=C1)O)OC 166.17 unknown https://doi.org/10.1016/S0031-9422(00)81708-2

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Collections Top

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