Rhodanthe floribunda - Unknown
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Internal ID UUID643fc9142e9f7451243903
Scientific name Rhodanthe floribunda
Authority (DC.) Paul G.Wilson
First published in Nuytsia 8(3) 1992

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Rhodanthe floribunda, also known as the common white sunray, is a herbaceous plant native to arid and semi-arid regions of Australia. It is an annual plant that can reach a height of 30 cm and blooms in the spring. Its name, floribunda, refers to its abundance of flowers. This plant was first described by Swiss botanist Augustin Pyramus de Candolle in 1838 as Helipterum floribundum. It belongs to the daisy family and is commonly found in scientific literature.

Synonyms Top

Scientific name Authority First published in
Helichrysum floribundum A.Cunn. ex DC. Prodr. 6: 217 (1838)
Helipterum cirratum Morrison J. Bot. 50: 168 (1912)
Roccardia floribunda (DC.) Voss Vilm. Blumengärtn. ed. 3 1: 531, in obs. (1894)

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Distribution (via POWO/KEW) Top

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Database ID/link to page
World Flora Online wfo-0000027543
Tropicos 50293139
KEW urn:lsid:ipni.org:names:969126-1
The Plant List gcc-12662
Open Tree Of Life 7051429
NCBI Taxonomy 2529049
NBN Atlas NBNSYS0200003007
IPNI 169239-3
iNaturalist 604603
GBIF 3137629
Wikipedia Rhodanthe_floribunda

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Spatio-Temporal Variation in Landscape Composition May Speed Resistance Evolution of Pests to Bt Crops Ives AR, Paull C, Hulthen A, Downes S, Andow DA, Haygood R, Zalucki MP, Schellhorn NA PLoS One 03-Jan-2017
PMCID:PMC5207666
doi:10.1371/journal.pone.0169167
PMID:28046073
Sesquiterpene lactones and other constituents from Australian Helipterum species C. Zdero, F. Bohlmann, R.M. King, H. Robinson Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80045-7

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4S,5S,9S,10R,13S)-5,9,13-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-5-carboxylic acid 162989720 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)C=C2)(C)C(=O)O)C 302.50 unknown https://doi.org/10.1016/0031-9422(89)80045-7
(8R,13S)-13-Methyl-17-norkaur-15-en-18-ol 500043 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)C=C2)(C)CO)C 288.50 unknown https://doi.org/10.1016/0031-9422(89)80045-7
[(1R,4S,5S,9S,10R,13S)-5,9,13-trimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl]methanol 163065096 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)C=C2)(C)CO)C 288.50 unknown https://doi.org/10.1016/0031-9422(89)80045-7
3-Oxo-3-[(5,9,13-trimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl)methoxy]propanoic acid 13820239 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)C=C2)(C)COC(=O)CC(=O)O)C 374.50 unknown https://doi.org/10.1016/0031-9422(89)80045-7
3-oxo-3-[[(1R,4S,5S,9S,10R,13S)-5,9,13-trimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl]methoxy]propanoic acid 162926840 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)C=C2)(C)COC(=O)CC(=O)O)C 374.50 unknown https://doi.org/10.1016/0031-9422(89)80045-7
4-[(2-Hydroxy-5,9,13-trimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl)methoxy]-4-oxobutanoic acid 14262517 Click to see CC12CCC3C4(CCCC(C4CC(C3(C1)C=C2)O)(C)COC(=O)CCC(=O)O)C 404.50 unknown https://doi.org/10.1016/0031-9422(89)80045-7
4-[[(1S,2S,4S,5S,9R,10R,13S)-2-hydroxy-5,9,13-trimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl]methoxy]-4-oxobutanoic acid 162975903 Click to see CC12CCC3C4(CCCC(C4CC(C3(C1)C=C2)O)(C)COC(=O)CCC(=O)O)C 404.50 unknown https://doi.org/10.1016/0031-9422(89)80045-7
4-Oxo-4-[(5,9,13-trimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl)methoxy]butanoic acid 14262514 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)C=C2)(C)COC(=O)CCC(=O)O)C 388.50 unknown https://doi.org/10.1016/0031-9422(89)80045-7
4-oxo-4-[[(1R,4S,5S,9S,10R,13S)-5,9,13-trimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl]methoxy]butanoic acid 163063240 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)C=C2)(C)COC(=O)CCC(=O)O)C 388.50 unknown https://doi.org/10.1016/0031-9422(89)80045-7
5,9,13-Trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-5-carboxylic acid 13820232 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)C=C2)(C)C(=O)O)C 302.50 unknown https://doi.org/10.1016/0031-9422(89)80045-7
Beyer-15-en-18-oic acid 149083 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)C=C2)(C)C(=O)O)C 302.50 unknown https://doi.org/10.1016/0031-9422(89)80045-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-(4a-Methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enyl 3-methylbutanoate 14262537 Click to see CC(C)CC(=O)OCC(=C)C1CCC2(CCCC(=C)C2C1)C 304.50 unknown https://doi.org/10.1016/0031-9422(89)80045-7
2-(4a-Methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enyl acetate 14262535 Click to see CC(=O)OCC(=C)C1CCC2(CCCC(=C)C2C1)C 262.40 unknown https://doi.org/10.1016/0031-9422(89)80045-7
2-[(2S,4aS,8aR)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enyl 3-methylbutanoate 162851672 Click to see CC(C)CC(=O)OCC(=C)C1CCC2(CCCC(=C)C2C1)C 304.50 unknown https://doi.org/10.1016/0031-9422(89)80045-7
2-[(2S,4aS,8aR)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enyl acetate 162916145 Click to see CC(=O)OCC(=C)C1CCC2(CCCC(=C)C2C1)C 262.40 unknown https://doi.org/10.1016/0031-9422(89)80045-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
4-Hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 98949 Click to see CC1=CC2C(C(CC(=CCC1)C)O)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/0031-9422(89)80045-7
Eupatolide 5281460 Click to see CC1=CC2C(C(CC(=CCC1)C)O)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/0031-9422(89)80045-7
Tulipinolide 5281504 Click to see CC1=CC2C(C(CC(=CCC1)C)OC(=O)C)C(=C)C(=O)O2 290.40 unknown https://doi.org/10.1016/0031-9422(89)80045-7

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