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Eucalyptus sideroxylon

Eucalyptus sideroxylon - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Eucalyptus sideroxylon - 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 UUID64403a398b69b392970646
Scientific name Eucalyptus sideroxylon
Authority A.Cunn. ex Woolls
First published in Proc. Linn. Soc. New South Wales , ser. 2, 1: 859 (1886)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English red ironbark
English mugga ironbark
Spanish mugga
German mugga-eukalyptus
Hebrew אקליפטוס כהה-קליפה
Hebrew אקליפטוס כהה קליפה
Russian Эвкалипт железнодревесный
Swedish småblommig blåeukalyptus
Chinese 红铁木桉

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Eucalyptus sideroxylon subsp. improcera A.R.Bean Austrobaileya 8: 139 (2010)
Eucalyptus sideroxylon subsp. sideroxylon Woolls -

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Macaronesia
      • Canary Islands
    • Northern Africa
      • Algeria
      • Morocco
      • Tunisia
    • Southern Africa
      • Free State
    • West Tropical Africa
      • Gambia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000955894
USDA Plants EUSI2
Tropicos 22102086
INPN 453244
Flora of Italy 9478
KEW urn:lsid:ipni.org:names:593359-1
The Plant List kew-73898
Open Tree Of Life 3935808
NCBI Taxonomy 1541731
Nature Serve 2.144663
IUCN Red List 133377043
IPNI 593359-1
iNaturalist 77092
GBIF 3177189
Freebase /m/0977cp
EPPO EUCSD
EOL 632020
Calflora (Californian flora) 3537
USDA GRIN 16030
Wikipedia Eucalyptus_sideroxylon

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_014182405.2 ASM1418240v2 Chromosome Australian National University 2024-03-20 72.0x 564.69 Mb

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
Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants Kirker GT, Hassan B, Mankowski ME, Eller FJ Insects 18-Jan-2024
PMCID:PMC10816604
doi:10.3390/insects15010069
PMID:38249075
Salt Stress—Regulation of Root Water Uptake in a Whole-Plant and Diurnal Context Lu Y, Fricke W Int J Mol Sci 29-Apr-2023
PMCID:PMC10179082
doi:10.3390/ijms24098070
PMID:37175779
The Effect of Surrounding Vegetation on Basal Stem Measurements Acquired Using Low-Cost Depth Sensors in Urban and Native Forest Environments McGlade J, Wallace L, Hally B, Reinke K, Jones S Sensors (Basel) 12-Apr-2023
PMCID:PMC10143225
doi:10.3390/s23083933
PMID:37112278
Essential Oils and Biological Activities of Eucalyptus falcata, E. sideroxylon and E. citriodora Growing in Tunisia Amri I, Khammassi M, Ben Ayed R, Khedhri S, Mansour MB, Kochti O, Pieracci Y, Flamini G, Mabrouk Y, Gargouri S, Hanana M, Hamrouni L Plants (Basel) 11-Feb-2023
PMCID:PMC9965493
doi:10.3390/plants12040816
PMID:36840164
Cost-conscious generation of multiplexed short-read DNA libraries for whole-genome sequencing Jones A, Stanley D, Ferguson S, Schwessinger B, Borevitz J, Warthmann N PLoS One 27-Jan-2023
PMCID:PMC9882895
doi:10.1371/journal.pone.0280004
PMID:36706059
An Insight into Current Treatment Strategies, Their Limitations, and Ongoing Developments in Vaccine Technologies against Herpes Simplex Infections Sharma D, Sharma S, Akojwar N, Dondulkar A, Yenorkar N, Pandita D, Prasad SK, Dhobi M Vaccines (Basel) 17-Jan-2023
PMCID:PMC9966607
doi:10.3390/vaccines11020206
PMID:36851084
Irrigated urban trees exhibit greater functional trait plasticity compared to natural stands Ibsen PC, Santiago LS, Shiflett SA, Chandler M, Jenerette GD Biol Lett 04-Jan-2023
PMCID:PMC9810417
doi:10.1098/rsbl.2022.0448
PMID:36596464
Canopy dieback and recovery in Australian native forests following extreme drought Losso A, Challis A, Gauthey A, Nolan RH, Hislop S, Roff A, Boer MM, Jiang M, Medlyn BE, Choat B Sci Rep 14-Dec-2022
PMCID:PMC9751299
doi:10.1038/s41598-022-24833-y
PMID:36517498
Insights into Antiviral Properties and Molecular Mechanisms of Non-Flavonoid Polyphenols against Human Herpesviruses Hassan ST, Šudomová M, Mazurakova A, Kubatka P Int J Mol Sci 11-Nov-2022
PMCID:PMC9693824
doi:10.3390/ijms232213891
PMID:36430369
Unlocking Drought-Induced Tree Mortality: Physiological Mechanisms to Modeling Li X, Xi B, Wu X, Choat B, Feng J, Jiang M, Tissue D Front Plant Sci 04-Apr-2022
PMCID:PMC9015645
doi:10.3389/fpls.2022.835921
PMID:35444681
Antiviral Activities of Eucalyptus Essential Oils: Their Effectiveness as Therapeutic Targets against Human Viruses Mieres-Castro D, Ahmar S, Shabbir R, Mora-Poblete F Pharmaceuticals (Basel) 23-Nov-2021
PMCID:PMC8706319
doi:10.3390/ph14121210
PMID:34959612
Plant-Based Natural Products and Extracts: Potential Source to Develop New Antiviral Drug Candidates Thomas E, Stewart LE, Darley BA, Pham AM, Esteban I, Panda SS Molecules 14-Oct-2021
PMCID:PMC8537559
doi:10.3390/molecules26206197
PMID:34684782
Can Eucalyptol Replace Antibiotics? Mączka W, Duda-Madej A, Górny A, Grabarczyk M, Wińska K Molecules 14-Aug-2021
PMCID:PMC8398027
doi:10.3390/molecules26164933
PMID:34443521
HPLC-PDA-ESI-MS/MS Profiling and Anti-Biofilm Potential of Eucalyptus sideroxylon Flowers Okba MM, El-Shiekh RA, Abu-Elghait M, Sobeh M, Ashour RM Antibiotics (Basel) 23-Jun-2021
PMCID:PMC8300825
doi:10.3390/antibiotics10070761
PMID:34201471
A meta-analysis of the combined effects of elevated carbon dioxide and chronic warming on plant %N, protein content and N-uptake rate Jayawardena DM, Heckathorn SA, Boldt JK AoB Plants 25-May-2021
PMCID:PMC8286714
doi:10.1093/aobpla/plab031
PMID:34285792

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 / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown https://doi.org/10.1080/10412905.1991.9697921
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-CITRONELLOL, (+/-)- 8842 Click to see CC(CCC=C(C)C)CCO 156.26 unknown https://doi.org/10.1080/10412905.1991.9697921
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.1991.9697921
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Cuminaldehyde 326 Click to see CC(C)C1=CC=C(C=C1)C=O 148.20 unknown https://doi.org/10.1080/10412905.1991.9697921
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene 6451618 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1992.9698059
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697921
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1992.9698059
Pinocarveol 102667 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1080/10412905.1991.9697921
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.4324/9780203219430_CHAPTER_13
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1992.9698059
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1080/10412905.1992.9698059
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
gamma-Bisabolene, (Z)- 3033866 Click to see CC1=CCC(=C(C)CCC=C(C)C)CC1 204.35 unknown https://doi.org/10.4324/9780203219430_CHAPTER_13
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698059
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.4324/9780203219430_CHAPTER_13
Macrocarpal A 454457 Click to see CC(C)CC(C1=C(C(=C(C(=C1O)C=O)O)C=O)O)C2(CCC3C2C4C(C4(C)C)CCC3(C)O)C 472.60 unknown https://doi.org/10.1246/CL.1992.1917
Macrocarpal B 454458 Click to see CC(C)CC(C1=C(C(=C(C(=C1O)C=O)O)C=O)O)C2(CCC3C2C4C(C4(C)C)CCC3(C)O)C 472.60 unknown https://doi.org/10.1246/CL.1992.1917
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698059
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
sideroxylonal A 10391273 Click to see CC(C)CC1C(C(OC2=C(C(=C(C(=C12)O)C=O)O)C=O)C3=C(C(=C(C(=C3O)C=O)O)C=O)O)C(C)C 500.50 unknown https://doi.org/10.1246/CL.1992.1917
sideroxylonal B 9848832 Click to see CC(C)CC1C(C(OC2=C(C(=C(C(=C12)O)C=O)O)C=O)C3=C(C(=C(C(=C3O)C=O)O)C=O)O)C(C)C 500.50 unknown https://doi.org/10.1246/CL.1992.1917
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Sideroxylin 3083788 Click to see CC1=C(C2=C(C(=C1OC)C)OC(=CC2=O)C3=CC=C(C=C3)O)O 312.30 unknown https://doi.org/10.1016/S0031-9422(00)86214-7
> Phenylpropanoids and polyketides / Stilbenes
4-[2-(3,5-Dihydroxyphenyl)ethenyl]benzene-1,2-diol 4813 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown https://doi.org/10.1016/S0031-9422(00)86214-7
Piceatannol 667639 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown https://doi.org/10.1016/S0031-9422(00)86214-7
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(2R,3R,4S,5S,6R)-2-[3-hydroxy-5-[(E)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 11968900 Click to see COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 420.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1243587/
(e)-resveratrol 3-O-alpha-d-glucopyranoside 11968839 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 390.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1243587/
2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 5062 Click to see COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 420.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1243587/
2-[3-Hydroxy-5-[2-(4-hydroxyphenyl)vinyl]phenoxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol 393787 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 390.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1243587/

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