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Packera clevelandii

Packera clevelandii - 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 UUID643fcd2f22e5a616246989
Scientific name Packera clevelandii
Authority (Greene) W.A.Weber & Á.Löve
First published in Phytologia 49: 46 (1981)

Description Top

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Synonyms Top

Scientific name Authority First published in
Senecio clevelandii Greene Bull. Torrey Bot. Club 10(8): 87 (1883)

Common names Top

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Language Common/alternative name
English cleveland's ragwort

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Packera clevelandii var. heterophylla (Hoover) D.W.Taylor Fl. Yosemite Sierra : 373 (2010)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000069980
USDA Plants PACL10
Tropicos 50087051
KEW urn:lsid:ipni.org:names:179978-2
The Plant List gcc-26782
Open Tree Of Life 3899439
Nature Serve 2.146652
IPNI 179978-2
iNaturalist 78318
GBIF 3113947
Freebase /m/0cmdr5c
EOL 468406
Calflora (Californian flora) 9615
USDA GRIN 452811
Wikipedia Packera_clevelandii

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
Sandaracopimarene derivatives from Senecio subrubriflorus Ferdinand Bohlmann, Christa Zdero Elsevier BV 03-Jan-2008
doi:10.1016/S0031-9422(82)85042-5
The first acetylenic monoterpene and other constituents from Senecio clevelandii Ferdinand Bohlmann, Christa Zdero, Robert M. King, Harold Robinson Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82681-3

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 / Fatty Acyls / Fatty aldehydes
14-Oxotetradeca-2,4,9-trien-6-ynyl 2-methylbut-2-enoate 162889479 Click to see CC=C(C)C(=O)OCC=CC=CC#CCC=CCCCC=O 300.40 unknown https://doi.org/10.1016/S0031-9422(00)82681-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
3-(4-methylpenta-1,3-dienyl)-2H-furan-5-one 85344447 Click to see CC(=CC=CC1=CC(=O)OC1)C 164.20 unknown https://doi.org/10.1016/S0031-9422(00)82681-3
3-[(1E)-4-methylpenta-1,3-dienyl]-2H-furan-5-one 10986587 Click to see CC(=CC=CC1=CC(=O)OC1)C 164.20 unknown https://doi.org/10.1016/S0031-9422(00)82681-3
3-[(1Z)-4-methylpenta-1,3-dienyl]-2H-furan-5-one 10953862 Click to see CC(=CC=CC1=CC(=O)OC1)C 164.20 unknown https://doi.org/10.1016/S0031-9422(00)82681-3
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Methyl 1-hydroxy-4-oxocyclohexane-1-carboxylate 53640954 Click to see COC(=O)C1(CCC(=O)CC1)O 172.18 unknown https://doi.org/10.1016/S0031-9422(00)82681-3
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
4-Methyl-2(5H)-furanone 145832 Click to see CC1=CC(=O)OC1 98.10 unknown https://doi.org/10.1016/S0031-9422(82)85042-5
Cleviolide 10888228 Click to see CC(=CC#CC1=CC(=O)OC1)C 162.18 unknown https://doi.org/10.1016/S0031-9422(00)82681-3
https://doi.org/10.1016/S0031-9422(82)85042-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
[1-Hydroxy-10-[2-[(2-hydroxy-2-methylbutanoyl)amino]pyrrolidine-1-carbonyl]-3,5-dimethoxy-9-(4-methoxyphenyl)-11-phenyl-8-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-12-yl] acetate 73657039 Click to see CCC(C)(C(=O)NC1CCCN1C(=O)C2C(C3(C(C2(OC4=C3C(=CC(=C4)OC)OC)C5=CC=C(C=C5)OC)OC(=O)C)O)C6=CC=CC=C6)O 688.80 unknown https://doi.org/10.1016/S0031-9422(00)82681-3

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