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Eremophila mitchellii

Eremophila mitchellii - 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 UUID64401a230b80d011731614
Scientific name Eremophila mitchellii
Authority Benth.
First published in J. Exped. Trop. Australia : 31 (1848)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pholidia mitchellii (Benth.) Baill. Nat. Pflanzenfam. 4(3b): 359 (1895)
Bondtia mitchellii (Benth.) Kuntze Revis. Gen. Pl. 2: 501 (1891)

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000671061
Tropicos 100331775
KEW urn:lsid:ipni.org:names:585196-1
The Plant List kew-2792306
Open Tree Of Life 5144581
NCBI Taxonomy 2652576
IUCN Red List 192234025
IPNI 585196-1
iNaturalist 370034
GBIF 5565707
Freebase /m/02ryysg
EPPO EMHMI
EOL 5652951
Elurikkus 545719
USDA GRIN 15363
Wikipedia Eremophila_mitchellii
CMAUP NPO1610

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
Trees in trees a report from remote Australia Pye J Plant Signal Behav 07-Dec-2023
PMCID:PMC10761035
doi:10.1080/15592324.2023.2286392
PMID:38059450
Four New Highly Oxygenated Eremophilane Sesquiterpenes from an Endophytic Fungus Boeremia exigua Isolated from Fritillaria hupehensis Ai HL, Lv X, Ye K, Wang MX, Huang R, Shi BB, Li ZH J Fungi (Basel) 08-May-2022
PMCID:PMC9146970
doi:10.3390/jof8050492
PMID:35628748
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
Chemical Composition and Immunomodulatory Activity of Essential Oils from Rhododendron albiflorum Schepetkin IA, Özek G, Özek T, Kirpotina LN, Khlebnikov AI, Quinn MT Molecules 15-Jun-2021
PMCID:PMC8232766
doi:10.3390/molecules26123652
PMID:34203809
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
Nurse plant effects on plant species richness in drylands: the role of grazing, rainfall and species specificity Soliveres S, Eldridge DJ, Hemmings F, Maestre FT 20-Dec-2012
PMCID:PMC4407966
doi:10.1016/j.ppees.2012.09.003
PMID:25914602
Microhabitat amelioration and reduced competition among understorey plants as drivers of facilitation across environmental gradients: towards a unifying framework Soliveres S, Eldridge DJ, Maestre FT, Bowker MA, Tighe M, Escudero A 20-Nov-2011
PMCID:PMC4407968
doi:10.1016/j.ppees.2011.06.001
PMID:25914601
Mitchellenes A-E, cyclic sesquiterpenes from the Australian plant Eremophila mitchellii. Barnes EC, Carroll AR, Davis RA J Nat Prod 23-Sep-2011
doi:10.1021/NP2003676
PMID:21877688
Chemical composition and cytotoxicity of oils and eremophilanes derived from various parts of Eremophila mitchellii Benth. (Myoporaceae). Beattie KD, Waterman PG, Forster PI, Thompson DR, Leach DN Phytochemistry 01-Apr-2011
doi:10.1016/J.PHYTOCHEM.2010.12.011
PMID:21227474

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
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
Tetradehydropodophyllotoxin 5316463 Click to see COC1=CC(=CC(=C1OC)OC)C2=C3C(=C(C4=CC5=C(C=C42)OCO5)O)COC3=O 410.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
alpha-Peltatin 92129 Click to see COC1=CC(=CC(=C1O)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)O)COC3=O 400.40 unknown via CMAUP database
beta-Peltatin 92122 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)O)COC3=O 414.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones / Podophyllotoxins
Podofilox 10607 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O 414.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2S)-2-[(1R,4R,4aR,8aR)-7-(hydroxymethyl)-4-methyl-1,2,3,4,4a,5,6,8a-octahydronaphthalen-1-yl]propanoic acid 163013126 Click to see CC1CCC(C2C1CCC(=C2)CO)C(C)C(=O)O 252.35 unknown https://doi.org/10.1021/NP2003676
(4aR,5R,8R,8aR)-8-[(1S)-1-carboxyethyl]-5-methyl-3,4,4a,5,6,7,8,8a-octahydronaphthalene-2-carboxylic acid 163007664 Click to see CC1CCC(C2C1CCC(=C2)C(=O)O)C(C)C(=O)O 266.33 unknown https://doi.org/10.1021/NP2003676
14-Hydroxy-6,12-muuroloadien-15-oic acid 70698100 Click to see CC1CCC(C2C1CCC(=C2)C(=O)O)C(=C)CO 250.33 unknown https://doi.org/10.1021/NP2003676
8-(3-Hydroxyprop-1-en-2-yl)-5-methyl-3,4,4a,5,6,7,8,8a-octahydronaphthalene-2-carboxylic acid 14526673 Click to see CC1CCC(C2C1CCC(=C2)C(=O)O)C(=C)CO 250.33 unknown https://doi.org/10.1021/NP2003676
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(2R,3R,4aR,5S,8aS)-2-Hydroxy-4a,5-dimethyl-3-(prop-1-en-2-yl)octahydronaphthalen-1(2H)-one 75953512 Click to see CC1CCCC2C1(CC(C(C2=O)O)C(=C)C)C 236.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.011
(2R,3R,4aR,5S,8aS)-2-hydroxy-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-one 58587153 Click to see CC1CCCC2C1(CC(C(C2=O)O)C(=C)C)C 236.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.011
(2R,3R,4aR,5S,8aS)-2-hydroxy-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,8a-hexahydronaphthalen-1-one 11608347 Click to see CC1CC=CC2C1(CC(C(C2=O)O)C(=C)C)C 234.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.011
(2R,3R,4aR,5S)-2-hydroxy-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7-hexahydronaphthalen-1-one 163048903 Click to see CC1CCC=C2C1(CC(C(C2=O)O)C(=C)C)C 234.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.011
(4aR,5S)-1-Hydroxy-4a,5-dimethyl-3-(propan-2-ylidene)-4,4a,5,6,7,8-hexahydronaphthalen-2(3H)-one 75953513 Click to see CC1CCCC2=C(C(=O)C(=C(C)C)CC12C)O 234.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.011
(4aR,5S)-1-hydroxy-4a,5-dimethyl-3-propan-2-ylidene-5,6-dihydro-4H-naphthalen-2-one 58587141 Click to see CC1CC=CC2=C(C(=O)C(=C(C)C)CC12C)O 232.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.011
(4aR,5S)-1-hydroxy-4a,5-dimethyl-3-propan-2-ylidene-5,6,7,8-tetrahydro-4H-naphthalen-2-one 52917992 Click to see CC1CCCC2=C(C(=O)C(=C(C)C)CC12C)O 234.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.011
1(2H)-Naphthalenone, 3,4,4a,5,6,7-hexahydro-2-hydroxy-4a,5-dimethyl-3-(1-methylethenyl)-, (2R,3R,4aR,5S)- 91699532 Click to see CC1CCC=C2C1(CC(C(C2=O)O)C(=C)C)C 234.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.011
1(2H)-Naphthalenone, 3,4,4a,5,6,7-hexahydro-4a,5-dimethyl-3-(1-methylethenyl)-, [3S-(3alpha,4aalpha,5alpha)]- 12309746 Click to see CC1CCC=C2C1(CC(CC2=O)C(=C)C)C 218.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.011
1(2H)-Naphthalenone, 3,4,4a,5,6,8a-hexahydro-2-hydroxy-4a,5-dimethyl-3-(1-methylethenyl)-, (2R,3R,4aR,5S,8aS)- 73028135 Click to see CC1CC=CC2C1(CC(C(C2=O)O)C(=C)C)C 234.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.011
Eremophilone 21591457 Click to see CC1CCC=C2C1(CC(CC2=O)C(=C)C)C 218.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.011
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(1R,2R,5R,8S)-2,6,6,8-tetramethyltricyclo[6.2.1.01,5]undecan-7-one 21576985 Click to see CC1CCC2C13CCC(C3)(C(=O)C2(C)C)C 220.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.011
Eremophila ketone 73802832 Click to see CC1CCC2C13CCC(C3)(C(=O)C2(C)C)C 220.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.011
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S,7S,8S,11R,12R,13S,14S)-8-hydroxy-8,14-dimethyl-2-oxatetracyclo[9.2.1.04,13.07,12]tetradec-4-en-3-one 162928346 Click to see CC1C2CCC(C3C2C4C1OC(=O)C4=CC3)(C)O 248.32 unknown https://doi.org/10.1021/NP2003676
Mitchellene B 54671720 Click to see CC1CCC2C(C3C4C2C1CC=C4C(=O)O3)C 232.32 unknown https://doi.org/10.1021/NP2003676
Mitchellene C 54671803 Click to see CC1CCC2C(C3C4C2C1C=CC4(C(=O)O3)O)C 248.32 unknown https://doi.org/10.1021/NP2003676
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 2-prenylated flavones
Podoverine A 13911680 Click to see CC(=CCC1=C(C=CC(=C1O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)C 384.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Centaureidin 5315773 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown https://doi.org/10.1021/NP2003676
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown https://doi.org/10.1021/NP2003676

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