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Senecio subulatus

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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 UUID643fc9b7d3f81964308991
Scientific name Senecio subulatus
Authority Don ex Hook. & Arn.
First published in J. Bot. (Hooker) 3: 330 (1841)

Description Top

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Synonyms Top

Scientific name Authority First published in
Senecio subulatus var. elatior Hook. & Arn. J. Bot. (Hooker) 3: 330 (1841)
Senecio subulatus var. prostratus Hook. & Arn. J. Bot. (Hooker) 3: 330. 1841

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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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000032819
Tropicos 2723486
KEW urn:lsid:ipni.org:names:247809-1
Open Tree Of Life 7609820
IPNI 247809-1
iNaturalist 480270
GBIF 7336583

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
Sesquiterpenes with New Carbon Skeletons, Furoeremophilanes, Secoeremophilanes and other Constituents from Argentinian Senecio Species F. Bohlmann, J. Jakupovic, U. Warning, M. Grenz, T. V. Chau‐Thi, R. M. King, H. Robinson Wiley 13-Sep-2010
doi:10.1002/BSCB.19860950903
Pyrrolizidine Alkaloids from<i>Senecio subulatus</i>and<i>S. glandulosus</i> M. Pestchanker, M. Ascheri, O. Giordano Georg Thieme Verlag KG 06-Mar-2007
doi:10.1055/S-2007-969439
Pyrrolizidine Alkaloids from Five Senecio Species M. J. Pestchanker, O. S. Giordano American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50046A041

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
(-)-alpha-Curcumene 442360 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1002/BSCB.19860950903
alpha-Curcumene 92139 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1002/BSCB.19860950903
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1002/BSCB.19860950903
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1002/BSCB.19860950903
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1002/BSCB.19860950903
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1002/BSCB.19860950903
gamma-Curcumene 12304273 Click to see CC1=CC=C(CC1)C(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1002/BSCB.19860950903
> Organoheterocyclic compounds / Azaspirodecane derivatives
(1R,3'R,4R,6R,7R,11E)-7-hydroxy-3',6,7,14-tetramethylspiro[2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-4,2'-oxirane]-3,8,17-trione 101298732 Click to see CC1CC2(C(O2)C)C(=O)OC3CCN(CC=C(C3=O)COC(=O)C1(C)O)C 381.40 unknown https://doi.org/10.1002/BSCB.19860950903
> Organoheterocyclic compounds / Benzofurans / Benzofuranones
Platyphyllide 10932811 Click to see CC(=C)C1CCC2=C3C1OC(=O)C3=CC=C2 214.26 unknown https://doi.org/10.1002/BSCB.19860950903
> Phenylpropanoids and polyketides / Macrolides and analogues
(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/10.1055/S-2007-969439
Integerrimine 5281733 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1021/NP50046A041
Retrorsine 5281743 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CO)O)C 351.40 unknown https://doi.org/10.1021/NP50046A041
https://doi.org/10.1055/S-2007-969439
Senecionine 5280906 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1021/NP50046A041
https://doi.org/10.1055/S-2007-969439
Usaramine 5281756 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CO)O)C 351.40 unknown https://doi.org/10.1021/NP50046A041

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