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Hakea trifurcata

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64401f9db6c25823987045
Scientific name Hakea trifurcata
Authority R.Br.
First published in Trans. Linn. Soc. London 10: 183 (1810)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Industrial and craft applications:
Food and beverages (non-medicinal):
Colorants and tanning:
Wood and fiber:
Fragrance and cosmetics:
Properties relevant to use:
Standards and regulation:
Sustainability and sourcing:

Synonyms Top

Scientific name Authority First published in
Conchium trifurcatum Sm. Rees' Cyclopaedia 9 1807
Hakea boucheana Kunth Index Seminum (B, Berolinensis) 1844: 9 (1844)
Hakea mixta Lindl. Sketch Veg. Swan R. : 36 (1840)
Hakea tricruris Lindl. Sketch Veg. Swan R. : 36 (1840)
Hakea trifurcata var. sericantha Meisn. Pl. Preiss. 1: 559 (1845)

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-0000714501
KEW urn:lsid:ipni.org:names:704353-1
The Plant List kew-2837894
Open Tree Of Life 481564
NCBI Taxonomy 1136213
IUCN Red List 118136520
IPNI 704353-1
iNaturalist 532691
GBIF 7287520
Freebase /m/07s5v21
Wikipedia Hakea_trifurcata
CMAUP NPO28314

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
Temporally stacked bee forage species distribution modeling for flower abundance mapping Patel V, Boruff B, Biggs E, Pauli N, Dixon DJ MethodsX 17-Aug-2023
PMCID:PMC10477801
doi:10.1016/j.mex.2023.102327
PMID:37674866
Data representing climate-induced changes in the spatial distribution of key bee forage species for southwest Western Australia Patel V, Boruff B, Biggs E, Pauli N Data Brief 25-Nov-2022
PMCID:PMC9730158
doi:10.1016/j.dib.2022.108783
PMID:36506799
Vulnerability to xylem cavitation of Hakea species (Proteaceae) from a range of biomes and life histories predicted by climatic niche Oyanoghafo OO, O’ Brien C, Choat B, Tissue D, Rymer PD Ann Bot 19-Feb-2021
PMCID:PMC8225280
doi:10.1093/aob/mcab020
PMID:33606015
Phosphorus Nutrition of Proteaceae in Severely Phosphorus-Impoverished Soils: Are There Lessons To Be Learned for Future Crops? Lambers H, Finnegan PM, Laliberté E, Pearse SJ, Ryan MH, Shane MW, Veneklaas EJ Plant Physiol 15-Apr-2011
PMCID:PMC3135942
doi:10.1104/pp.111.174318
PMID:21498583
5-Alkylresorcinols from Hakea trifurcata, that cleave DNA. William Lytollis, Ralph T. Scannell, Haoyun An, V. S. Murty, K. Sambi Reddy, John R. Barr, Sidney M. Hecht American Chemical Society (ACS) 18-Mar-2005
doi:10.1021/JA00156A004
5-Alkylresorcinols from Hakea amplexicaulis that cleave DNA. Barr JR, Murty VS, Yamaguchi K, Singh S, Smith DH, Hecht SM Chem Res Toxicol 01-Jul-1988
doi:10.1021/TX00004A003
PMID:2980968

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenols / Benzenediols / Resorcinols
5-[(Z)-14-(3,5-dihydroxyphenyl)tetradec-8-enyl]benzene-1,3-diol 10525745 Click to see C1=C(C=C(C=C1O)O)CCCCCCCC=CCCCCCC2=CC(=CC(=C2)O)O 412.60 unknown https://doi.org/10.1021/JA00156A004
https://doi.org/10.1021/TX00004A003
5-[(Z)-16-(3,5-dihydroxyphenyl)hexadec-8-enyl]benzene-1,3-diol 10741793 Click to see 440.60 unknown https://doi.org/10.1021/JA00156A004
5-[14-(3,5-Dihydroxyphenyl)tetradec-8-enyl]benzene-1,3-diol 156602790 Click to see C1=C(C=C(C=C1O)O)CCCCCCCC=CCCCCCC2=CC(=CC(=C2)O)O 412.60 unknown https://doi.org/10.1021/JA00156A004
https://doi.org/10.1021/TX00004A003
5-[16-(3,5-Dihydroxyphenyl)hexadec-8-enyl]benzene-1,3-diol 85129102 Click to see 440.60 unknown https://doi.org/10.1021/JA00156A004
5-Pentadec-8-enylbenzene-1,3-diol 5462454 Click to see CCCCCCC=CCCCCCCCC1=CC(=CC(=C1)O)O 318.50 unknown https://doi.org/10.1021/JA00156A004
https://doi.org/10.1021/TX00004A003
Bilobol 5281852 Click to see CCCCCCC=CCCCCCCCC1=CC(=CC(=C1)O)O 318.50 unknown https://doi.org/10.1021/TX00004A003
https://doi.org/10.1021/JA00156A004
Bisnorstriatol 10431955 Click to see C1=C(C=C(C=C1O)O)CCCCCCCCCCCCCCC2=CC(=CC(=C2)O)O 414.60 unknown https://doi.org/10.1021/JA00156A004
Grevillol 174862 Click to see CCCCCCCCCCCCCC1=CC(=CC(=C1)O)O 292.50 unknown https://doi.org/10.1021/TX00004A003
https://doi.org/10.1021/JA00156A004
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Pentyl hentriacontanoate 21775821 Click to see 537.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Amino fatty acids
3-Aminopentanedioic acid 73064 Click to see C(C(CC(=O)O)N)C(=O)O 147.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,4R,5S,6S,9R)-9-bromo-4-[[(1R,4R)-4-bromo-1-hydroxy-3,3-dimethylcyclohexyl]methyl]-6-methyl-11-oxatricyclo[4.3.2.01,5]undecan-10-one 46703590 Click to see CC1(CC(CCC1Br)(CC2CCC34C2C(CCC3Br)(OC4=O)C)O)C 478.30 unknown via CMAUP database
[(1R,4R)-4-bromo-1-[[(1R,4R,5S,6S,9R)-9-bromo-6-methyl-10-oxo-11-oxatricyclo[4.3.2.01,5]undecan-4-yl]methyl]-3,3-dimethylcyclohexyl] acetate 46703591 Click to see CC(=O)OC1(CCC(C(C1)(C)C)Br)CC2CCC34C2C(CCC3Br)(OC4=O)C 520.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2R)-2-[(2S,5S)-5-[(2R,4aS,6R,8aR)-2-[(2S,5R)-5-bromo-2,6,6-trimethyloxan-2-yl]-4a-methyl-3,4,6,7,8,8a-hexahydro-2H-pyrano[3,2-b]pyran-6-yl]-5-methyloxolan-2-yl]-6-methylhept-5-en-2-ol 101519535 Click to see 571.60 unknown via CMAUP database
(6R,7S,10R,11S,14R)-2,6,10-Trimethyl-14-[(S)-1-hydroxy-1-methyl-3-(3beta-hydroxy-3,7,7-trimethyl-6beta-bromohexahydrooxepin-2beta-yl)propyl]-2,7:6,11:10,14-triepoxy-3-tetradecene 102432674 Click to see CC1(C=CCC2(C(O1)CCC3(C(O2)CCC(O3)C(C)(CCC4C(CCC(C(O4)(C)C)Br)(C)O)O)C)C)C 587.60 unknown via CMAUP database
(E,6R)-6-[(2S,5S)-5-[(2R,4aS,6R,8aR)-2-[(2S,5R)-5-bromo-2,6,6-trimethyloxan-2-yl]-4a-methyl-3,4,6,7,8,8a-hexahydro-2H-pyrano[3,2-b]pyran-6-yl]-5-methyloxolan-2-yl]-2-methylhept-3-ene-2,6-diol 46703589 Click to see 587.60 unknown via CMAUP database
Aplysiol E 101519536 Click to see CC1(C(CCC(O1)(C)C2CCC3(C(O2)CCC(O3)C4(CCC(O4)C(C)(CC(C5C(O5)(C)C)Cl)O)C)C)Br)C 622.10 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
gamma-Ureidonorvaline 6992098 Click to see 175.19 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
D-Aspartic Acid 83887 Click to see 133.10 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Kainoids
alpha-Kainic acid 10255 Click to see 213.23 unknown via CMAUP database
CID 17753955 17753955 Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O 311.33 unknown via CMAUP database
Domoic Acid 5282253 Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O 311.33 unknown via CMAUP database
Isodomoic acid A 6442601 Click to see CC(=CCC=C(C)C(=O)O)C1CNC(C1CC(=O)O)C(=O)O 311.33 unknown via CMAUP database
isodomoic acid B 6442550 Click to see 311.33 unknown via CMAUP database
isodomoic acid C 11301378 Click to see CC(=CCCC(=C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O 311.33 unknown via CMAUP database
isodomoic acid D 6442551 Click to see 311.33 unknown via CMAUP database
Isodomoic acid F 101790920 Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O 311.33 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
CID 21952380 21952380 Click to see 118.09 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Purinones / Hypoxanthines
CID 790 790 Click to see 136.11 unknown via CMAUP database

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