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Backhousia angustifolia

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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 UUID643fec4858c0a748613931
Scientific name Backhousia angustifolia
Authority F.Muell.
First published in Fragm. 1: 79 (1859)

Description Top

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Backhousia angustifolia, also known as narrow leaf myrtle, is a flowering plant that belongs to the Myrtaceae family. It is found in the regions of Queensland and northeastern New South Wales. This plant is known for its beautiful flowers and is native to Australia.

Synonyms Top

No known synonyms.

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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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

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Database ID/link to page
World Flora Online wfo-0000305762
Tropicos 100151747
KEW urn:lsid:ipni.org:names:591021-1
The Plant List kew-18712
Open Tree Of Life 807430
NCBI Taxonomy 1288326
IPNI 591021-1
iNaturalist 1113189
GBIF 3185102
EOL 5454292
USDA GRIN 6248
Wikipedia Backhousia_angustifolia
CMAUP NPO16254

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
Changes in trait covariance along an orographic moisture gradient reveal the relative importance of light‐ and moisture‐driven trade‐offs in subtropical rainforest communities Brown A, Butler DW, Radford‐Smith J, Dwyer JM New Phytol 20-Aug-2022
PMCID:PMC9804723
doi:10.1111/nph.18418
PMID:35922934
Review of the Leaf Essential Oils of the Genus Backhousia Sens. Lat. and a Report on the Leaf Essential Oils of B. gundarara and B. tetraptera Bowden BF, Brophy JJ, Jackes BR Plants (Basel) 02-May-2022
PMCID:PMC9103502
doi:10.3390/plants11091231
PMID:35567231
Physiological Forms of Backhousia angustifolia F. Muell JR Cannon, NH Corbett CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9620168
Triterpenoid constituents of Backhousia angustifolia F. Muell KT Potts, SK Roy CSIRO Publishing 01-Sep-2010
doi:10.1071/CH9650767
CXLIX.—The essential oil of Backhousia angustifolia. Part II. The isolation of naturally occurring β-diketones: angustione and dehydroangustione Charles Stanley Gibson, Arthur Ramon Penfold, John Lionel Simonsen Royal Society of Chemistry (RSC) 21-Apr-2004
doi:10.1039/JR9300001184
Angustifolenone, a ketone from Backhousia angustifolia Joseph J. Brophy, John R. Clarkson, Christopher J.R. Fookes Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80225-0

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 / Phenol ethers / Aminophenyl ethers
2,4,6-Trimethoxyaniline 84271 Click to see COC1=CC(=C(C(=C1)OC)N)OC 183.20 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Maesol 128958 Click to see CC1=C(C=C(C=C1OC)CCCCCCCCCCCCC2=CC(=C(C(=C2)OC)C)O)O 442.60 unknown https://doi.org/10.1016/0031-9422(89)80225-0
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/0031-9422(89)80225-0
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/0031-9422(89)80225-0
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1016/0031-9422(89)80225-0
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1016/0031-9422(89)80225-0
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
(2R,6R)-2-acetyl-4,4,6-trimethylcyclohexane-1,3-dione 162943040 Click to see CC1CC(C(=O)C(C1=O)C(=O)C)(C)C 196.24 unknown https://doi.org/10.1016/0031-9422(89)80225-0
https://doi.org/10.1039/JR9300001184
https://doi.org/10.1071/CH9620168
Angustione 12306809 Click to see CC1CC(C(=O)C(C1=O)C(=O)C)(C)C 196.24 unknown https://doi.org/10.1071/CH9620168
https://doi.org/10.1039/JR9300001184
https://doi.org/10.1016/0031-9422(89)80225-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Plumieride 72319 Click to see CC(C1=CC2(C=CC3C2C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)OC1=O)O 470.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,4S,8R,10S,11S,14S)-11-ethyl-12-oxo-7,9,13-trioxatetracyclo[6.5.1.01,10.04,14]tetradeca-2,5-diene-5-carboxylic acid 38348951 Click to see CCC1C2C3(C=CC4C3C(O2)OC=C4C(=O)O)OC1=O 278.26 unknown via CMAUP database
Allamandin 5281540 Click to see CC=C1C2C3(C=CC4C3C(O2)OC(C4C(=O)OC)O)OC1=O 308.28 unknown via CMAUP database
Isoplumericin 5281543 Click to see CC=C1C2C3(C=CC4C3C(O2)OC=C4C(=O)OC)OC1=O 290.27 unknown via CMAUP database
methyl (1S,4S,8R,10S,11S,14S)-11-ethyl-12-oxo-7,9,13-trioxatetracyclo[6.5.1.01,10.04,14]tetradeca-2,5-diene-5-carboxylate 95790359 Click to see CCC1C2C3(C=CC4C3C(O2)OC=C4C(=O)OC)OC1=O 292.28 unknown via CMAUP database
Plumericin 5281545 Click to see CC=C1C2C3(C=CC4C3C(O2)OC=C4C(=O)OC)OC1=O 290.27 unknown via CMAUP database
Plumeridoid C 123964288 Click to see CC(C1=CC2(C=CC3C2COC(C3C(=O)OC)O)OC1=O)O 310.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aS,6aS,6bR,8aR,10R,11R,12aR,14bS)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 11887403 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1071/CH9650767
2,3-Dihydroxyolean-12-en-28-oic acid 3694932 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1071/CH9650767
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1071/CH9650767
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
beta-Amyrin acetate 92156 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown via CMAUP database
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1071/CH9650767
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1071/CH9650767
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1071/CH9650767
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(24R)-Cycloarta-25-ene-3beta,24-diol 14313591 Click to see CC(CCC(C(=C)C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / M-benzoquinones
(2S)-2-acetyl-4,6,6-trimethylcyclohex-4-ene-1,3-dione 162997271 Click to see CC1=CC(C(=O)C(C1=O)C(=O)C)(C)C 194.23 unknown https://doi.org/10.1071/CH9620168
https://doi.org/10.1039/JR9300001184
https://doi.org/10.1016/0031-9422(89)80225-0
2-Acetyl-4,6,6-trimethylcyclohex-4-ene-1,3-dione 14283284 Click to see CC1=CC(C(=O)C(C1=O)C(=O)C)(C)C 194.23 unknown https://doi.org/10.1071/CH9620168
https://doi.org/10.1039/JR9300001184
https://doi.org/10.1016/0031-9422(89)80225-0
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(4R)-2-ethyl-4,6,6-trimethylcyclohex-2-en-1-one 162870750 Click to see CCC1=CC(CC(C1=O)(C)C)C 166.26 unknown https://doi.org/10.1016/0031-9422(89)80225-0
2-Ethyl-4,6,6-trimethylcyclohex-2-en-1-one 14283283 Click to see CCC1=CC(CC(C1=O)(C)C)C 166.26 unknown https://doi.org/10.1016/0031-9422(89)80225-0
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Paroxypropione 6271 Click to see CCC(=O)C1=CC=C(C=C1)O 150.17 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
8-Methyleugenitin 12306808 Click to see CC1=CC(=O)C2=C(O1)C(=C(C(=C2O)C)OC)C 234.25 unknown https://doi.org/10.1071/CH9620168
> Organoheterocyclic compounds / Oxanes
Eucalyptol 2758 Click to see CC1(C2CCC(O1)(CC2)C)C 154.25 unknown https://doi.org/10.1016/0031-9422(89)80225-0
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Fulvoplumierin 5281541 Click to see CC=CC=C1C=CC2=C1C(=O)OC=C2C(=O)OC 244.24 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives
Plumericidine 45101897 Click to see CC(C1=CC2(CCC3=C2C=NC=C3)OC1=O)O 231.25 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolizines
Plumerinine 14583329 Click to see CC1CCC(N2C1CC(CC2C(C)C)O)C 225.37 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2S,3R,4S,5S,6R)-2-[[(2R,3S)-3-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-5-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14757896 Click to see COC1=CC2=C(CC(C(O2)C3=CC(=C(C(=C3)OC)O)OC)O)C(=C1)OC4C(C(C(C(O4)CO)O)O)O 510.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Ayanin 5280682 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)O 344.30 unknown via CMAUP database
Pilloin 5320496 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O)O 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown https://doi.org/10.1071/CH9620168

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