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Cassinia aculeata

Cassinia aculeata - 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 UUID643fca21dcf76795666942
Scientific name Cassinia aculeata
Authority (Labill.) R.Br.
First published in Observations on the Natural Family of Plants called Compositae 1817 = Transactions of the Linnean Society of London 12 (25 Feb. 1818) 127

Description Top

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Synonyms Top

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Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Cassinia aculeata subsp. nova-anglica Orchard Austral. Syst. Bot. 22(5): 353 (349; fig. 2B-K) (2009)

Varieties (abbr. var.) Top

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Name Authority First published in
Cassinia aculeata var. aculeata (Labill.) R.Br. Fl. Austral. (1867)

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

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-0000035898
Tropicos 2731715
The Plant List gcc-134719
Open Tree Of Life 281712
NCBI Taxonomy 1284849
IPNI 167123-3
iNaturalist 323103
GBIF 5390402
Freebase /m/09gprv0
EOL 6265398
USDA GRIN 9428
Wikipedia Cassinia_aculeata

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
Assessing the diet and seed dispersal ability of non‐native sambar deer (Rusa unicolor) in native ecosystems of south‐eastern Australia Quin MJ, Morgan JW, Murphy NP Ecol Evol 27-Nov-2023
PMCID:PMC10682569
doi:10.1002/ece3.10711
PMID:38034333
Temporal patterns of forest seedling emergence across different disturbance histories Bowd EJ, McBurney L, Blair DP, Lindenmayer DB Ecol Evol 26-Jun-2021
PMCID:PMC8293764
doi:10.1002/ece3.7568
PMID:34306621
Biophysical Mechanistic Modelling Quantifies the Effects of Plant Traits on Fire Severity: Species, Not Surface Fuel Loads, Determine Flame Dimensions in Eucalypt Forests Zylstra P, Bradstock RA, Bedward M, Penman TD, Doherty MD, Weber RO, Gill AM, Cary GJ PLoS One 16-Aug-2016
PMCID:PMC4986950
doi:10.1371/journal.pone.0160715
PMID:27529789
An overview of Australia’s Phytophthora species assemblage in natural ecosystems recovered from a survey in Victoria Dunstan WA, Howard K, StJ. Hardy GE, Burgess TI IMA Fungus 02-Mar-2016
PMCID:PMC4941687
doi:10.5598/imafungus.2016.07.01.04
PMID:27433440
Eudesmane derivatives other constituents fromApalochlamys spectabilis Cassinia species C. Zdero, F. Bohlmann, R.M. King Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)80185-J

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
Tridecapentaynene 129689980 Click to see CC=CC#CC#CC#CC#CC#C 162.19 unknown https://doi.org/10.1016/0031-9422(90)80185-J
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(1R,4S,5R,9S,10R,12S)-5,9-dimethyl-13-methylidenetetracyclo[10.2.2.01,10.04,9]hexadecane-5-carboxylic acid 101607225 Click to see CC12CCCC(C1CCC34C2CC(CC3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/0031-9422(90)80185-J
(5,9-Dimethyl-13-methylidene-5-tetracyclo[10.2.2.01,10.04,9]hexadecanyl)methyl acetate 14707082 Click to see CC(=O)OCC1(CCCC2(C1CCC34C2CC(CC3)C(=C)C4)C)C 330.50 unknown https://doi.org/10.1016/0031-9422(90)80185-J
[(1R,4S,5R,9S,10R,12S)-5,9-dimethyl-13-methylidene-5-tetracyclo[10.2.2.01,10.04,9]hexadecanyl]methyl acetate 101589318 Click to see CC(=O)OCC1(CCCC2(C1CCC34C2CC(CC3)C(=C)C4)C)C 330.50 unknown https://doi.org/10.1016/0031-9422(90)80185-J
5,9-Dimethyl-13-methylidenetetracyclo[10.2.2.01,10.04,9]hexadecane-5-carboxylic acid 14707085 Click to see CC12CCCC(C1CCC34C2CC(CC3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/0031-9422(90)80185-J
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/0031-9422(90)80185-J
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/0031-9422(90)80185-J
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)80185-J
Bicyclogermacrene 5315347 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)80185-J
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-(4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl)prop-2-enoic acid 14706940 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C(=O)O)C 234.33 unknown https://doi.org/10.1016/0031-9422(90)80185-J
2-[(2R,4aR,8aR)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid 168796 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C(=O)O)C 234.33 unknown https://doi.org/10.1016/0031-9422(90)80185-J
2-[(2R,4aR,8aR)-8-(hydroxymethyl)-4a-methyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid 14191238 Click to see CC12CCC=C(C1CC(CC2)C(=C)C(=O)O)CO 250.33 unknown https://doi.org/10.1016/0031-9422(90)80185-J
2-[8-(hydroxymethyl)-4a-methyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]prop-2-enoic acid 14191237 Click to see CC12CCC=C(C1CC(CC2)C(=C)C(=O)O)CO 250.33 unknown https://doi.org/10.1016/0031-9422(90)80185-J
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(6,10-Dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl) acetate 97215 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(90)80185-J
[(3aR,4R,6Z,10Z,11aR)-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] acetate 92043108 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(90)80185-J
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(90)80185-J
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(90)80185-J
> Lipids and lipid-like molecules / Saccharolipids
3-Hydroxy-4-oxo-4-[(3,4,5,6-tetrahydroxyoxan-2-yl)methoxy]butanoic acid 72761399 Click to see C(C1C(C(C(C(O1)O)O)O)O)OC(=O)C(CC(=O)O)O 296.23 unknown https://doi.org/10.1016/0031-9422(90)80185-J

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