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Eremophila deserti

Eremophila deserti - 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 UUID64401a1dbf790346352666
Scientific name Eremophila deserti
Authority (A.Cunn. ex Benth.) Chinnock
First published in Fl. S. Austral. 3: 1338 (1986)

Description Top

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Synonyms Top

Scientific name Authority First published in
Myoporum dulce Benth. J. Exped. Trop. Australia : 384 (1848)
Myoporum deserti A.Cunn. ex Benth. Enum. Pl. Hügel : 78 (1837)
Myoporum myoporoides (F.Muell.) Druce Rep. Bot. Soc. Exch. Club Brit. Isles 1916: 637 (1917)
Myoporum laxiflorum Benth. Fl. Austral. 5: 6 (1870)
Myoporum rugulosum F.Muell. Linnaea 25: 427 (1853)
Myoporum strictum A.Cunn. ex A.DC. Prodr. 11: 708 (1847)
Eremophila myoporoides F.Muell. Fragm. 5: 23 (1865)

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
  • Australasia
    • Australia
      • New South Wales
      • Queensland
      • South Australia
      • Victoria
      • Western Australia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000670976
Tropicos 100331671
KEW urn:lsid:ipni.org:names:943500-1
The Plant List kew-2792224
Open Tree Of Life 5144572
NCBI Taxonomy 2652521
IPNI 943500-1
iNaturalist 953190
GBIF 5565700
Freebase /m/0411d8w
USDA GRIN 410520
Wikipedia Eremophila_deserti

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
Fundamental Chemistry of Essential Oils and Volatile Organic Compounds, Methods of Analysis and Authentication Sadgrove NJ, Padilla-González GF, Phumthum M Plants (Basel) 16-Mar-2022
PMCID:PMC8955314
doi:10.3390/plants11060789
PMID:35336671
Navigating through chemical space and evolutionary time across the Australian continent in plant genus Eremophila Gericke O, Fowler RM, Heskes AM, Bayly MJ, Semple SJ, Ndi CP, Stærk D, Løland CJ, Murphy DJ, Buirchell BJ, Møller BL Plant J 16-Sep-2021
PMCID:PMC9292440
doi:10.1111/tpj.15448
PMID:34324744
The Diversity of Volatile Compounds in Australia’s Semi-Desert Genus Eremophila (Scrophulariaceae) Sadgrove NJ, Padilla-González GF, Green A, Langat MK, Mas-Claret E, Lyddiard D, Klepp J, Legendre SV, Greatrex BW, Jones GL, Ramli IM, Leuner O, Fernandez-Cusimamani E Plants (Basel) 16-Apr-2021
PMCID:PMC8073941
doi:10.3390/plants10040785
PMID:33923613
Plant and Fungal Hepatotoxicities of Cattle in Australia, with a Focus on Minimally Understood Toxins Manthorpe EM, Jerrett IV, Rawlin GT, Woolford L Toxins (Basel) 08-Nov-2020
PMCID:PMC7695254
doi:10.3390/toxins12110707
PMID:33171661
Revision of Poliaspis (Hemiptera, Coccoidea, Diaspididae), with descriptions of 8 new species from Australia Hardy N, Henderson RC Zookeys 14-Oct-2011
PMCID:PMC3260887
doi:10.3897/zookeys.137.1786
PMID:22259303
Terpenoid Chemistry. XXVIII. Furanosesquiterpene β-Ketols From Myoporum betcheanum, M. deserti, M. montanum and Other Myoporaceae MD Sutherland, JL Rodwell CSIRO Publishing 03-Sep-2010
doi:10.1071/CH9891995
Terpenoid Chemistry. XXVII. Further Iridoid Constituents, (1R)- and (1S)-1-Acetoxymyodesert-3-ene, from Myoporum deserti (Myoporaceae). HG Grant, CA Russell-Maynard, M.D. Sutherland CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9850325
Terpenoid chemistry. XXI. ( - )-Epingaione, ( - )-Dehydrongaione, ( - )-Dehydroepingaione, and ( - )-Deisopropylngaione, toxic furanoid sesquiterpenoid ketones from Myoporum deserti WD Hamilton, RJ Park, GJ Perry, MD Sutherland CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9730375
Terpenoid chemistry. XXIV. (1R)-1-Methoxymyodesert-3-ene, an Iridoid Constitutent of Myoporum deserti (Myoporaceae) HG Grant, PJ O'Regan, RJ Park, MD Sutherland CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9800853
Terpenoid chemistry. XVIII. Myodesmone and isomyodesmone, toxic furanoid ketones from myoporum deserti and m. acuminatum ID Blackburne, RJ Park, MD Sutherland CSIRO Publishing 01-Sep-2010
doi:10.1071/CH9710995
Terpenoid chemistry. XX. Myoporone and dehydromyoporone, toxic furanoid ketones from Myoporum and Eremophila species ID Blackburne, RJ Park, MD Sutherland CSIRO Publishing 22-Nov-2006
doi:10.1071/CH9721787
Terpenoid chemistry. XIX. Dehydro- and Dehydroiso-myodesmone, toxic furanoid sesquiterpene ketones from Myoporum deserti ID Blackburne, MD Sutherland CSIRO Publishing 22-Nov-2006
doi:10.1071/CH9721779

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1071/CH9850325
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
1-[(1S,5S)-2-(furan-3-yl)-5-methylcyclopent-2-en-1-yl]-3-methylbut-2-en-1-one 101306815 Click to see CC1CC=C(C1C(=O)C=C(C)C)C2=COC=C2 230.30 unknown https://doi.org/10.1071/CH9721787
https://doi.org/10.1071/CH9721779
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(4,7-Dimethyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-1-yl) acetate 72951935 Click to see CC1CCC2C1C(OC=C2C)OC(=O)C 210.27 unknown https://doi.org/10.1071/CH9850325
(4aS,7R,7aR)-1-Methoxy-4,7-dimethyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran 71356025 Click to see CC1CCC2C1C(OC=C2C)OC 182.26 unknown https://doi.org/10.1071/CH9800853
[(1R,4aS,7S,7aR)-4,7-dimethyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-1-yl] acetate 163086955 Click to see CC1CCC2C1C(OC=C2C)OC(=O)C 210.27 unknown https://doi.org/10.1071/CH9800853
[(1S,4aS,7R,7aR)-4,7-dimethyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-1-yl] acetate 163086956 Click to see CC1CCC2C1C(OC=C2C)OC(=O)C 210.27 unknown https://doi.org/10.1071/CH9850325
1-Methoxy-4,7-dimethyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran 78062349 Click to see CC1CCC2C1C(OC=C2C)OC 182.26 unknown https://doi.org/10.1071/CH9800853
3-Myodeserten-1-ol acetate 101415775 Click to see CC1CCC2C1C(OC=C2C)OC(=O)C 210.27 unknown https://doi.org/10.1071/CH9850325
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
(1S,2R,5R)-2-methyl-5-[(2S)-1-oxopropan-2-yl]cyclopentane-1-carbaldehyde 162883530 Click to see CC1CCC(C1C=O)C(C)C=O 168.23 unknown https://doi.org/10.1071/CH9850325
Iridodial 222140 Click to see CC1CCC(C1C=O)C(C)C=O 168.23 unknown https://doi.org/10.1071/CH9850325
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclopentanols
1-[(1R,2R,5S)-2-(furan-3-yl)-2-hydroxy-5-methylcyclopentyl]-3-methylbutan-1-one 163010989 Click to see CC1CCC(C1C(=O)CC(C)C)(C2=COC=C2)O 250.33 unknown https://doi.org/10.1071/CH9891995
1-[(1R,2S,5S)-2-(furan-3-yl)-2-hydroxy-5-methylcyclopentyl]-3-methylbutan-1-one 14486230 Click to see CC1CCC(C1C(=O)CC(C)C)(C2=COC=C2)O 250.33 unknown https://doi.org/10.1071/CH9891995
1-[(1S,2R,5S)-2-(furan-3-yl)-2-hydroxy-5-methylcyclopentyl]-3-methylbutan-1-one 163010988 Click to see CC1CCC(C1C(=O)CC(C)C)(C2=COC=C2)O 250.33 unknown https://doi.org/10.1071/CH9891995
Jackson ketol, TMS 14486228 Click to see CC1CCC(C1C(=O)CC(C)C)(C2=COC=C2)O 250.33 unknown https://doi.org/10.1071/CH9891995
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
(4R)-1-(furan-3-yl)-4,8-dimethylnonane-1,6-dione 11010382 Click to see CC(C)CC(=O)CC(C)CCC(=O)C1=COC=C1 250.33 unknown https://doi.org/10.1071/CH9891995
1-(Furan-3-yl)-4,8-dimethylnonane-1,6-dione 12313048 Click to see CC(C)CC(=O)CC(C)CCC(=O)C1=COC=C1 250.33 unknown https://doi.org/10.1071/CH9721787
https://doi.org/10.1071/CH9891995
Myoporone 29632 Click to see CC(C)CC(=O)CC(C)CCC(=O)C1=COC=C1 250.33 unknown https://doi.org/10.1071/CH9721787
> Organoheterocyclic compounds / Heteroaromatic compounds
1-[(1S,5S)-2-(furan-3-yl)-5-methylcyclopent-2-en-1-yl]-3-methylbutan-1-one 101316970 Click to see CC1CC=C(C1C(=O)CC(C)C)C2=COC=C2 232.32 unknown https://doi.org/10.1071/CH9710995
1-[(2R,5R)-5-(furan-3-yl)-2-methyloxolan-2-yl]propan-2-one 101566922 Click to see CC(=O)CC1(CCC(O1)C2=COC=C2)C 208.25 unknown https://doi.org/10.1071/CH9730375
1-[(5S)-2-(furan-3-yl)-5-methylcyclopenten-1-yl]-3-methylbutan-1-one 90471514 Click to see CC1CCC(=C1C(=O)CC(C)C)C2=COC=C2 232.32 unknown https://doi.org/10.1071/CH9800853
Deisopropylngaione 162446 Click to see CC(=O)CC1(CCC(O1)C2=COC=C2)C 208.25 unknown https://doi.org/10.1071/CH9730375
Ipomoeamarone 442379 Click to see CC(C)CC(=O)CC1(CCC(O1)C2=COC=C2)C 250.33 unknown https://doi.org/10.1071/CH9800853
Ngaione 120744 Click to see CC(C)CC(=O)CC1(CCC(O1)C2=COC=C2)C 250.33 unknown https://doi.org/10.1071/CH9800853

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