Packera anonyma - Unknown
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Internal ID UUID643fd264325f6656380025
Scientific name Packera anonyma
Authority (Wood) W.A.Weber & Á.Löve
First published in Phytologia 49: 45 (1981)

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Synonyms Top

Scientific name Authority First published in
Senecio earlei Small Bull. Torrey Bot. Club 25(3): 147 (1898)
Senecio smallii Britton ex Small & Vail Mem. Torrey Bot. Club iv. (1893) 132, et v. (1894)
Senecio smallii Britton Mem. Torrey Bot. Club 4: 132. 1894
Senecio anonymus Alph.Wood Class-book Bot. (ed. 1861). : 464 (1861)
Senecio aureus var. angustifolius Britton Mem. Torrey Bot. Club 2: 39 (1890)

Common names Top

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Language Common/alternative name
English small's ragwort

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Northeastern U.S.A.
      • New York
      • Ohio
      • Pennsylvania
      • West Virginia
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • District Of Columbia
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000123235
Florida Plant Atlas 549
Flora of Alabama 938
USDA Plants PAAN6
Tropicos 50087046
KEW urn:lsid:ipni.org:names:179969-2
The Plant List gcc-84382
Open Tree Of Life 597460
NCBI Taxonomy 942057
Nature Serve 2.146382
IPNI 179969-2
iNaturalist 67825
GBIF 3113928
Freebase /m/04g26gf
EPPO SENAA
EOL 392769
USDA GRIN 455545
Wikipedia Packera_anonyma

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
Jacaranone Derivatives with Antiproliferative Activity from Crepis pulchra and Relevance of This Group of Plant Metabolites Dávid CZ, Kúsz N, Pinke G, Kulmány Á, Zupkó I, Hohmann J, Vasas A Plants (Basel) 16-Mar-2022
PMCID:PMC8955310
doi:10.3390/plants11060782
PMID:35336664
A multivariate test of disease risk reveals conditions leading to disease amplification Halliday FW, Heckman RW, Wilfahrt PA, Mitchell CE Proc Biol Sci 18-Oct-2017
PMCID:PMC5666094
doi:10.1098/rspb.2017.1340
PMID:29046374
Acetylanonamine, a new secopyrrolizidine alkaloid from Senecio anonymus. Asibal CF, Zalkow LH, Gelbaum LT J Nat Prod 01-Sep-1991
doi:10.1021/NP50077A035
PMID:1800641
Anonamine, C19H27NO7, neosenkirkine, C19H27NO6, and hydroxysenkirkine, C19H27NO7.CH3OH. Macrocyclic secopyrrolizidine alkaloids from Senecio anonymus Wood. Glinski JA, Asibal CF, Van Derveer D, Zalkow LH Acta Crystallogr C 15-Sep-1988
doi:10.1107/S0108270188004214
PMID:3271098
Macrocyclic pyrrolizidine alkaloids from Senecio anonymus. Separation of a complex alkaloid extract using droplet counter-current chromatography. Zalkow LH, Asibal CF, Glinski JA, Bonetti SJ, Gelbaum LT, VanDerveer D, Powis G J Nat Prod 01-Jul-1988
doi:10.1021/NP50058A005
PMID:3210016
Cytotoxic agent from Senecio anonymus wood. Gelbaum LT, Zalkow LH, Hamilton D J Nat Prod 01-May-1982
doi:10.1021/NP50021A024
PMID:7119810

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
> Alkaloids and derivatives
Anonamine 6441178 Click to see CC1CC(=CCO)C(=O)OC2CC[N+]3(C2(C(=CC3)COC(=O)C1(C)O)O)C 382.40 unknown https://doi.org/10.1107/S0108270188004214
Hydroxysenkirkine 76957522 Click to see CC=C1CC(C(C(=O)OCC2=CC[N+]3(C2(C(CC3)OC1=O)O)C)(CO)O)C 382.40 unknown https://doi.org/10.1021/NP50058A005
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl Oleate 5363269 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC 310.50 unknown https://doi.org/10.1021/NP50021A024
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(2E)-2-[(1R,6S,7R,11Z)-7-hydroxy-6,7,14-trimethyl-3,8,17-trioxo-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-en-4-ylidene]ethyl] acetate 134714983 Click to see CC1CC(=CCOC(=O)C)C(=O)OC2CCN(CC=C(C2=O)COC(=O)C1(C)O)C 423.50 unknown https://doi.org/10.1021/NP50077A035
> Organoheterocyclic compounds / Azaspirodecane derivatives
Otosenine 6438142 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/10.1021/NP50058A005
https://doi.org/10.1021/NP50077A035
> Phenylpropanoids and polyketides / Macrolides and analogues
(1R,4E,6S,7R,11Z)-4-ethylidene-7-hydroxy-6,7,14-trimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione 134714985 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)O)C 365.40 unknown https://doi.org/10.1021/NP50077A035
https://doi.org/10.1021/NP50058A005
(1R,4Z,6S,7R,11Z)-4-ethylidene-7-hydroxy-6,7,14-trimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione 102004936 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)O)C 365.40 unknown https://doi.org/10.1021/NP50077A035
https://doi.org/10.1021/NP50058A005
(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/10.1021/NP50058A005
https://doi.org/10.1021/NP50077A035
(1S,4Z,7S,17S)-4-ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 133562009 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1021/NP50058A005
https://doi.org/10.1021/NP50077A035
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/NP50077A035
https://doi.org/10.1021/NP50058A005
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/NP50058A005
https://doi.org/10.1021/NP50077A035

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