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Onoseris albicans

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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 UUID643fd28299b77362680442
Scientific name Onoseris albicans
Authority (D.Don) Ferreyra
First published in J. Arnold Arbor. 25: 389 (1944)

Description Top

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Synonyms Top

Scientific name Authority First published in
Seris integrifolia Kuntze Revis. Gen. Pl. 1: 364 (1891)
Onoseris integrifolia Less. Linnaea 5: 343 (1830)
Onoseris reflexa Less. Syn. Gen. Compos. : 119 (1832)
Centroclinium appressum Hook.
Centroclinium adpressum Hook. Bot. Mag. 58: t. 3115 (1831)
Seris adpressa Kuntze Revis. Gen. Pl. 1: 364 (1891)
Seris reflexa Kuntze Revis. Gen. Pl. 1: 364 (1891)
Centroclinium albicans D.Don Trans. Linn. Soc. London 16(2): 254 (1830)
Centroclinium reflexum Hook. Bot. Mag. 58: t. 3115 (1831)

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

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-0000124283
Tropicos 2701080
KEW urn:lsid:ipni.org:names:174420-2
The Plant List gcc-85390
Open Tree Of Life 7624326
IPNI 174420-2
iNaturalist 709803
GBIF 3143173
USDA GRIN 25768

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
Pyrrolizidine Alkaloids from Ligularia sibirica Cass. and Tephroseris integrifolia L. Helmut Wiedenfeld, S. Narantuya, M. Dumaa, A. Monhbaatar MDPI AG 03-May-2019
doi:10.3797/SCIPHARM.AUT-03-14
Onoseriolid, ein neues sesquiterpenlacton aus Onoseris albicans Ferdinand Bohlmann, Christa Zdero, Robert M. King, Harold Robinson Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)87042-7

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
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
1-Tridecene-3,5,7,9,11-pentayne 441552 Click to see CC#CC#CC#CC#CC#CC=C 162.19 unknown https://doi.org/10.1016/0031-9422(80)87042-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-one 323075 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(80)87042-7
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/0031-9422(80)87042-7
> Organoheterocyclic compounds / Naphthofurans
(1S,9R,10R,12S)-4-(hydroxymethyl)-9-methyl-13-methylidene-6-oxatetracyclo[7.4.0.03,7.010,12]trideca-3,7-dien-5-one 154497131 Click to see CC12C=C3C(=C(C(=O)O3)CO)CC1C(=C)C4C2C4 244.28 unknown https://doi.org/10.1016/0031-9422(80)87042-7
(1S,9S,10S,12R)-4-(hydroxymethyl)-9-methyl-13-methylidene-6-oxatetracyclo[7.4.0.03,7.010,12]trideca-3,7-dien-5-one 162859736 Click to see CC12C=C3C(=C(C(=O)O3)CO)CC1C(=C)C4C2C4 244.28 unknown https://doi.org/10.1016/0031-9422(80)87042-7
4-(Hydroxymethyl)-9-methyl-13-methylidene-6-oxatetracyclo[7.4.0.03,7.010,12]trideca-3,7-dien-5-one 162859735 Click to see CC12C=C3C(=C(C(=O)O3)CO)CC1C(=C)C4C2C4 244.28 unknown https://doi.org/10.1016/0031-9422(80)87042-7
> Phenylpropanoids and polyketides / Coumarins and derivatives
5-Methyl-4-(methylsulfanyl)-2H-1-benzopyran-2-one 14804142 Click to see CC1=C2C(=CC=C1)OC(=O)C=C2SC 206.26 unknown https://doi.org/10.1016/0031-9422(80)87042-7
> Phenylpropanoids and polyketides / Macrolides and analogues
4-Ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione 85433052 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(CO)O)C 381.40 unknown https://doi.org/10.3797/SCIPHARM.AUT-03-14

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