Eucalyptus radiata - Unknown
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Internal ID UUID64403a300e269481765515
Scientific name Eucalyptus radiata
Authority Sieber ex DC.
First published in Prodr. 3: 218 (1828)

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Synonyms Top

Scientific name Authority First published in
Eucalyptus amygdalina var. radiata (DC.) Benth. Fl. Austral. 3: 203 (1867)

Common names Top

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Language Common/alternative name
English narrow-leaf peppermint gum
Bulgarian лъчист евкалипт
German pfefferminz-eukalyptus
Japanese ユーカリプタス・ラディアータ
Russian Эвкалипт лучистый
Swedish pepparmintseukalyptus
Chinese 澳洲辐状桉
Chinese 辐射桉
Chinese 辐状桉

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Eucalyptus radiata subsp. radiata DC. -
Eucalyptus radiata subsp. robertsonii (Blakely) L.A.S.Johnson & Blaxell Contr. New South Wales Natl. Herb. 4: 380 (1973)
Eucalyptus radiata subsp. sejuncta L.A.S.Johnson & K.D.Hill Telopea 4: 98 (1990)

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-0000955747
UNII I4HY0IFO7T
USDA Plants EURA8
Tropicos 50291527
INPN 621620
KEW urn:lsid:ipni.org:names:593296-1
The Plant List kew-73756
Open Tree Of Life 248689
NCBI Taxonomy 87679
IUCN Red List 133374163
IPNI 593296-1
iNaturalist 639221
GBIF 3176655
Freebase /m/02qkbg7
EOL 301326
USDA GRIN 16007
Wikipedia Eucalyptus_radiata
CMAUP NPO1715

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
Essential oil-containing solutions (mouthwashes) preserve dental enamel with releasing low Ca and P concentrations without morphology alterations: an in vitro study Mutran SC, de Carvalho-Filho PR, Ribeiro ME, Faial KD, Lima RR, D’Almeida Couto RS Front Chem 28-Feb-2024
PMCID:PMC10933047
doi:10.3389/fchem.2024.1341769
PMID:38482175
Study of the antimicrobial activity of zinc oxide nanostructures mediated by two morphological structures of leaf extracts of Eucalyptus radiata Droepenu EK, Amenyogbe E, Boatemaa MA, Opoku E Heliyon 07-Feb-2024
PMCID:PMC10869787
doi:10.1016/j.heliyon.2024.e25590
PMID:38370246
In Vitro Effect of Eucalyptus Essential Oils and Antiseptics (Chlorhexidine Gluconate and Povidone-Iodine) against Bacterial Isolates from Equine Wounds Pimenta J, Dias C, Cotovio M, Saavedra MJ Vet Sci 26-Dec-2023
PMCID:PMC10819342
doi:10.3390/vetsci11010012
PMID:38250918
Egyptian mandarin peel oil's anti-scabies potential via downregulation-of-inflammatory/immune-cross-talk: GC–MS and PPI network studies Elmaidomy AH, Abdel-Maqsoud NM, Tammam OY, Abdel-Rahman IM, Elrehany MA, Bakhsh HT, Altemani FH, Algehainy NA, Alzubaidi MA, Alsenani F, Sayed AM, Abdelmohsen UR, Zahran EM Sci Rep 30-Aug-2023
PMCID:PMC10469216
doi:10.1038/s41598-023-38390-5
PMID:37648727
Climate, host and geography shape insect and fungal communities of trees Franić I, Allan E, Prospero S, Adamson K, Attorre F, Auger-Rozenberg MA, Augustin S, Avtzis D, Baert W, Barta M, Bauters K, Bellahirech A, Boroń P, Bragança H, Brestovanská T, Brurberg MB, Burgess T, Burokienė D, Cleary M, Corley J, Coyle DR, Csóka G, Černý K, Davydenko K, de Groot M, Diez JJ, Doğmuş Lehtijärvi HT, Drenkhan R, Edwards J, Elsafy M, Eötvös CB, Falko R, Fan J, Feddern N, Fürjes-Mikó Á, Gossner MM, Grad B, Hartmann M, Havrdova L, Kádasi Horáková M, Hrabětová M, Justesen MJ, Kacprzyk M, Kenis M, Kirichenko N, Kovač M, Kramarets V, Lacković N, Lantschner MV, Lazarević J, Leskiv M, Li H, Madsen CL, Malumphy C, Matošević D, Matsiakh I, May TW, Meffert J, Migliorini D, Nikolov C, O’Hanlon R, Oskay F, Paap T, Parpan T, Piškur B, Ravn HP, Richard J, Ronse A, Roques A, Ruffner B, Santini A, Sivickis K, Soliani C, Talgø V, Tomoshevich M, Uimari A, Ulyshen M, Vettraino AM, Villari C, Wang Y, Witzell J, Zlatković M, Eschen R Sci Rep 18-Jul-2023
PMCID:PMC10354058
doi:10.1038/s41598-023-36795-w
PMID:37463904
Short communication: Antibacterial effects of essential oils from Cinnamomum cassia bark and Eucalyptus globulus leaves–The involvements of major constituents Nguyen HT, Miyamoto A, Nguyen HT, Pham HT, Hoang HT, Tong NT, Truong LT, Nguyen HT PLoS One 14-Jul-2023
PMCID:PMC10348583
doi:10.1371/journal.pone.0288787
PMID:37450504
Polymeric nanoparticles for enhanced delivery and improved bioactivity of essential oils Adeyemi SB, Akere AM, Orege JI, Ejeromeghene O, Orege OB, Akolade JO Heliyon 02-Jun-2023
PMCID:PMC10360594
doi:10.1016/j.heliyon.2023.e16543
PMID:37484246
Chemical Variability and Chemotype Concept of Essential Oils from Algerian Wild Plants Benomari FZ, Sarazin M, Chaib D, Pichette A, Boumghar H, Boumghar Y, Djabou N Molecules 30-May-2023
PMCID:PMC10254628
doi:10.3390/molecules28114439
PMID:37298915
A Comprehensive Review on Significance and Advancements of Antimicrobial Agents in Biodegradable Food Packaging Bose I, Roy S, Pandey VK, Singh R Antibiotics (Basel) 26-May-2023
PMCID:PMC10295204
doi:10.3390/antibiotics12060968
PMID:37370286
Effectiveness of aroma-Tea Tree Oil and Eucalyptus oil in alleviating COVID-19 vaccine discomfort side effects Lee KW, Chang YY, Wu XF, Wang YC, Shen MH, Yeh C, Zheng ZF, Wang JJ Explore (NY) 01-Apr-2023
PMCID:PMC10066580
doi:10.1016/j.explore.2023.03.008
PMID:37024404
Essential oil of Cymbopogon martini, source of geraniol, as a potential antibacterial agent against Bacillus subtilis, a pathogen of the bakery industry Santamarta S, Aldavero AC, Rojo MA F1000Res 24-Mar-2023
PMCID:PMC9936101
doi:10.12688/f1000research.54196.1
PMID:36817513
The koala gut microbiome is largely unaffected by host translocation but rather influences host diet Blyton MD, Pascoe J, Hynes E, Soo RM, Hugenholtz P, Moore BD Front Microbiol 02-Mar-2023
PMCID:PMC10018171
doi:10.3389/fmicb.2023.1085090
PMID:36937253
Essential Oils against Sarcoptes scabiei Nardoni S, Mancianti F Molecules 19-Dec-2022
PMCID:PMC9788335
doi:10.3390/molecules27249067
PMID:36558200
Treatment with Glyphosate Induces Tolerance of Citrus Pathogens to Glyphosate and Fungicides but Not to 1,8-Cineole Tahiri NE, Saghrouchni H, Hamamouch N, Khomsi ME, Alzahrani A, Salamatullah AM, Badiaa L, Lrhorfi LA Molecules 28-Nov-2022
PMCID:PMC9737398
doi:10.3390/molecules27238300
PMID:36500391
Plant as an Alternative Source of Antifungals against Aspergillus Infections: A Review Tan LF, Yap VL, Rajagopal M, Wiart C, Selvaraja M, Leong MY, Tan PL Plants (Basel) 08-Nov-2022
PMCID:PMC9697101
doi:10.3390/plants11223009
PMID:36432738

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Coniferyl p-hydroxybenzoate 14352617 Click to see COC1=C(C=CC(=C1)C=CCOC(=O)C2=CC=C(C=C2)O)O 300.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol 14529 Click to see CC1=CC=C(C=C1)C(C)(C)O 150.22 unknown https://doi.org/10.1080/10412905.1994.9699365
> Benzenoids / Phenols / Benzenediols / Catechols
Catechol 289 Click to see C1=CC=C(C(=C1)O)O 110.11 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
4-Hydroxy-3-methoxycinnamaldehyde 5280536 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9699365
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2E)-3-phenyl-2-propen-1-yl-6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside 10072035 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC=CC3=CC=CC=C3)O)O)O)O)O)O 442.50 unknown via CMAUP database
[(2R,3S,4R,5R,6R)-4,5-dihydroxy-6-[(E)-3-phenylprop-2-enoxy]-2-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] benzoate 10098958 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC=CC3=CC=CC=C3)O)O)OC(=O)C4=CC=CC=C4)O)O)O 546.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9699365
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.1994.9699365
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9699365
> 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/10.1080/10412905.1994.9699365
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1080/10412905.1994.9699365
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9699365
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9699365
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1080/10412905.1994.9699365
> 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/10.1080/10412905.1994.9699365
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9699365
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1080/10412905.1994.9699365
alpha,alpha-Dimethyl-4-methylenecyclohexanemethanol 81722 Click to see CC(C)(C1CCC(=C)CC1)O 154.25 unknown https://doi.org/10.1080/10412905.1994.9699365
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1080/10412905.1994.9699365
Carvone, (+/-)- 7439 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1080/10412905.1994.9699365
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9699365
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1080/10412905.1994.9699365
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699365
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9699365
Globulol 101716 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9699365
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9699365
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9699365
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-[[(1S)-1-hydroxy-6-oxocyclohex-2-ene-1-carbonyl]oxymethyl]phenoxy]oxan-3-yl] benzoate 92212918 Click to see C1CC(=O)C(C=C1)(C(=O)OCC2=CC=CC=C2OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=CC=C4)O 528.50 unknown via CMAUP database
[2-[(2S,3R,4S,5S,6R)-3-benzoyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-hydroxybenzoate 21578031 Click to see C1=CC=C(C=C1)C(=O)OC2C(C(C(OC2OC3=CC=CC=C3COC(=O)C4=CC=CC=C4O)CO)O)O 510.50 unknown via CMAUP database
Populin 92735 Click to see C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC3=CC=CC=C3CO)O)O)O 390.40 unknown via CMAUP database
Salicin 439503 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O 286.28 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
4-Isopropyl-2-cyclohexenone 92780 Click to see CC(C)C1CCC(=O)C=C1 138.21 unknown https://doi.org/10.1080/10412905.1994.9699365
> Phenylpropanoids and polyketides / Cinnamaldehydes
p-Coumaraldehyde 641301 Click to see C1=CC(=CC=C1C=CC=O)O 148.16 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 / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Rhamnetin 5281691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O 316.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Aromadendrin 7-methyl ether 181132 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=C(C=C3)O)O 302.28 unknown via CMAUP database

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