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Packera glabella

Packera glabella - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fcfde34b29461040429
Scientific name Packera glabella
Authority (Poir.) C.Jeffrey
First published in Kew Bull. 47(1): 101. 1992 [28 Feb 1992]

Description Top

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Synonyms Top

Scientific name Authority First published in
Senecio lyratus Michx. Fl. Bor.-Amer. 2: 120 (1803)
Senecio lobatus Pers. Syn. Pl. 2(2): 436 (1807)
Senecio glabellus Poir. Encycl. [J. Lamarck & al.] 7: 102. 1806 [6 Jul 1806]
Senecio mississipianus DC. Prodr. 6: 427 (1838)
Senecio carolinianus Spreng. Syst. Veg. 3: 559 (1826)
Senecio densiflorus M.Martens Bull. Acad. Roy. Sci. Bruxelles 8(1): 66 (1841)

Common names Top

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Language Common/alternative name
English butterweed

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000094239
Florida Plant Atlas 839
Flora of Alabama 941
Canadensys 3327
USDA Plants PAGL17
Tropicos 50113144
KEW urn:lsid:ipni.org:names:963667-1
The Plant List gcc-50443
Open Tree Of Life 538440
NCBI Taxonomy 34220
Nature Serve 2.133695
IPNI 1063375-2
iNaturalist 54921
GBIF 3113939
Freebase /m/02r0_br
EOL 477669
USDA GRIN 452816
Wikipedia Packera_glabella

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
Compositae‐ParaLoss‐1272: A complementary sunflower‐specific probe set reduces paralogs in phylogenomic analyses of complex systems Moore‐Pollard ER, Jones DS, Mandel JR Appl Plant Sci 27-Jan-2024
PMCID:PMC10873820
doi:10.1002/aps3.11568
PMID:38369976
An initial industrial flora: A framework for botanical research in cooperation with industry for biodiversity conservation Lucardi RD, Cunard CE, Hughes SC, Burgess KS, Reed JN, Whitehurst LE, Worthy SJ, Marsico TD PLoS One 01-Apr-2020
PMCID:PMC7112212
doi:10.1371/journal.pone.0230729
PMID:32236107
Pest categorisation of Nemorimyza maculosa Bragard C, Dehnen‐Schmutz K, Di Serio F, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Czwienczek E, Streissl F, MacLeod A EFSA J 05-Mar-2020
PMCID:PMC7448062
doi:10.2903/j.efsa.2020.6036
PMID:32874252
Pyrrolizidine Alkaloids of <i>Senecio Glabellus</i> Govind J. Kapadia 2, Anthony Ramdass, Funso Bada Informa UK Limited 25-Nov-2007
doi:10.3109/13880209009082780
Usaramoensine, the Alkaloid in Crotalaria usaramoensis E. G. Baker. Integerrimine from Crotalaria incana Linn and Senecionine from Senecio glabellus D. C. Stereochemical Relationships Roger Adams, Benjamin L. Van Duuren American Chemical Society (ACS) 19-Mar-2005
doi:10.1021/JA01115A001
Pyrrolizidine alkaloids from Senecio longilobus and Senecio glabellus Allen C. Ray, Howard J. Williams, John C. Reagor Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84745-7
The in vitro anti-fungal and anti-bacterial activities of beta-sitosterol from Senecio lyratus (Asteraceae). Kiprono PC, Kaberia F, Keriko JM, Karanja JN Z Naturforsch C J Biosci 01-May-2000
doi:10.1515/ZNC-2000-5-629
PMID:10928565
Comparison of the toxicities of Senecio jacobaea, Senecio vulgaris and Senecio glabellus in rats. Goeger DE, Cheeke PR, Ramsdell HS, Nicholson SS, Buhler DR Toxicol Lett 01-Jan-1983
doi:10.1016/0378-4274(83)90163-7
PMID:6836586

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
(1R,4E,6R,7R,14R,17R)-4-ethylidene-7-hydroxy-6,7-dimethyl-14-oxido-2,9-dioxa-14-azoniatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 163194492 Click to see CC=C1CC(C(C(=O)OCC2=CC[N+]3(C2C(CC3)OC1=O)[O-])(C)O)C 351.40 unknown https://doi.org/10.1016/S0031-9422(00)84745-7
Integerrimine N-oxide 6437374 Click to see CC=C1CC(C(C(=O)OCC2=CC[N+]3(C2C(CC3)OC1=O)[O-])(C)O)C 351.40 unknown https://doi.org/10.1016/S0031-9422(00)84745-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1515/ZNC-2000-5-629
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1515/ZNC-2000-5-629
> Organoheterocyclic compounds / Azaspirodecane derivatives
Florosenine (neutral) 6441404 Click to see CC1CC2(C(O2)C)C(=O)OC3CCN(CC=C(C3=O)COC(=O)C1(C)OC(=O)C)C 423.50 unknown https://doi.org/10.3109/13880209009082780
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/10.3109/13880209009082780
Otosenine 12-acetate 122362136 Click to see CC1CC2(C(O2)C)C(=O)OC3CCN(CC=C(C3=O)COC(=O)C1(C)OC(=O)C)C 423.50 unknown https://doi.org/10.3109/13880209009082780
> Phenylpropanoids and polyketides / Macrolides and analogues
(1R,4E,6S,7S,17R)-4-ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 162932518 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(00)84745-7
(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/10.3109/13880209009082780
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(00)84745-7
Aurein 12299899 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(00)84745-7
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(00)84745-7
Renardine (neutral) (VAN) 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/10.3109/13880209009082780
Senecionine 5280906 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1016/0378-4274(83)90163-7
https://doi.org/10.3109/13880209009082780
https://doi.org/10.1021/JA01115A001
Senkirkine 5281752 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/10.3109/13880209009082780

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