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Bedfordia arborescens

Bedfordia arborescens - 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 UUID643fca4db8615248256917
Scientific name Bedfordia arborescens
Authority Hochr.
First published in Candollea v. 332 (1934).

Description Top

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Synonyms Top

Scientific name Authority First published in
Senecio bedfordii F.Muell. Cat. Hort. Melb. 1858: 26.

Common names Top

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Language Common/alternative name
Spanish bedfordia salicina
Japanese ブランケットリーフ

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000037257
KEW urn:lsid:ipni.org:names:184329-1
The Plant List gcc-13603
Open Tree Of Life 754455
NCBI Taxonomy 196008
IPNI 184329-1
iNaturalist 59927
GBIF 5386071
Freebase /m/06ztcg4
EOL 6264370
Wikipedia Bedfordia_arborescens

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
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
Plant traits linked to field-scale flammability metrics in prescribed burns in Eucalyptus forest Tumino BJ, Duff TJ, Goodger JQ, Cawson JG PLoS One 26-Aug-2019
PMCID:PMC6709903
doi:10.1371/journal.pone.0221403
PMID:31449564
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
Disturbance regimes, gap‐demanding trees and seed mass related to tree height in warm temperate rain forests worldwide Grubb PJ, Bellingham PJ, Kohyama TS, Piper FI, Valido A Biol Rev Camb Philos Soc 19-Mar-2013
PMCID:PMC7161821
doi:10.1111/brv.12029
PMID:23506298
Sesquiterpene lactones from Bedfordia arborescens C. Zdero, F. Bohlmann, R.M. King, H. Robinson Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82383-3

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 / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(E)-5-[(1S,2R,4aR,8aR)-1,2,4a-trimethyl-5-methylidene-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]-3-methylpent-2-en-1-ol 162888209 Click to see CC1CCC2(C(C1(C)CCC(=CCO)C)CCCC2=C)C 290.50 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
5-(1,2,4a-trimethyl-5-methylidene-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl)-3-methylpent-2-en-1-ol 74996907 Click to see CC1CCC2(C(C1(C)CCC(=CCO)C)CCCC2=C)C 290.50 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(5R,9S,13S)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 49775756 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
5,9-Dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 433869 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
Kaurenoic acid 73062 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(E)-beta-farnesene 10407 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
beta Farnesene 15228937 Click to see CCC(=C)CCC=C(C)CCC=C(C)C 206.37 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4aR,5S,9aS)-9a-hydroxy-3,4a,5-trimethyl-5,6,7,8-tetrahydro-4H-benzo[f][1]benzofuran-2-one 12989517 Click to see CC1CCCC2=CC3(C(=C(C(=O)O3)C)CC12C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
(4R)-4-[[(1R,2S,5S)-2-hydroxy-2-methyl-5-prop-1-en-2-ylcyclopentyl]methyl]-3-methylideneoxolan-2-one 162879213 Click to see CC(=C)C1CCC(C1CC2COC(=O)C2=C)(C)O 250.33 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
4-[(2-Hydroxy-2-methyl-5-prop-1-en-2-ylcyclopentyl)methyl]-3-methylideneoxolan-2-one 162879212 Click to see CC(=C)C1CCC(C1CC2COC(=O)C2=C)(C)O 250.33 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
9a-hydroxy-3,4a,5-trimethyl-5,6,7,8-tetrahydro-4H-benzo[f][1]benzofuran-2-one 163040123 Click to see CC1CCCC2=CC3(C(=C(C(=O)O3)C)CC12C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
(1S,3aR,5R,5aS,8aS,9aS)-1-hydroxy-1,5,8a-trimethyl-3a,4,5,5a,6,7,9,9a-octahydroazuleno[6,7-b]furan-2,8-dione 163001980 Click to see CC1CC2C(CC3(C1CCC3=O)C)C(C(=O)O2)(C)O 266.33 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
1-Hydroxy-1,5,8a-trimethyl-3a,4,5,5a,6,7,9,9a-octahydroazuleno[6,7-b]furan-2,8-dione 163001979 Click to see CC1CC2C(CC3(C1CCC3=O)C)C(C(=O)O2)(C)O 266.33 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
Azuleno[6,5-b]furan-2,5-dione, decahydro-4a,8-dimethyl-3-methylene-, [3aR-(3aalpha,4abeta,7aalpha,8beta,9aalpha)]- 619106 Click to see CC1CC2C(CC3(C1CCC3=O)C)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
Graveolide 11043090 Click to see CC1CC2C(CC3(C1CCC3=O)C)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3aR,5aS,8S,8aR,9aR)-8-hydroxy-8-methyl-1,5-dimethylidene-3a,4,5a,6,7,8a,9,9a-octahydroazuleno[6,5-b]furan-2-one 57398175 Click to see CC1(CCC2C1CC3C(CC2=C)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
8-Epiinuviscolide 13817985 Click to see CC1(CCC2C1CC3C(CC2=C)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
8-Hydroxy-8-methyl-1,5-dimethylidene-3a,4,5a,6,7,8a,9,9a-octahydroazuleno[6,5-b]furan-2-one 13817983 Click to see CC1(CCC2C1CC3C(CC2=C)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
Inuviscolide 176489 Click to see CC1(CCC2C1CC3C(CC2=C)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
8-hydroxy-5,8-dimethyl-1-methylidene-4,6,7,8a,9,9a-hexahydro-3aH-azuleno[6,5-b]furan-2-one 5042278 Click to see CC1=C2CCC(C2CC3C(C1)OC(=O)C3=C)(C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)82383-3
Pseudoivalin 257279 Click to see CC1=C2CCC(C2CC3C(C1)OC(=O)C3=C)(C)O 248.32 unknown https://doi.org/10.1016/S0031-9422(00)82383-3

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