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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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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

Australasia click to expand
- Australia
  - New South Wales
  - Tasmania
  - Victoria

Links to other databases Top

Suggest others/fix!

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

Scent Detection Threshold of Trained Dogs to Eucalyptus Hydrolat

Turunen S, Paavilainen S, Vepsäläinen J, Hielm-Björkman A

Animals (Basel)

03-Apr-2024

PMCID:	PMC11010826
doi:	10.3390/ani14071083
PMID:	38612322

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

Efficacy of a Non-Pharmacological Intervention in Seasonal Allergic Rhinitis Symptoms

Caimmi D, Clark E, Fogel P, Heddebaut N, Aubier M, Demoly P

Int Arch Allergy Immunol

03-Nov-2023

PMCID:	PMC10836848
doi:	10.1159/000533271
PMID:	37926078

In Vitro and In Silico Activities of E. radiata and E. cinerea as an Enhancer of Antibacterial, Antioxidant, and Anti-Inflammatory Agents

Elkolli H, Elkolli M, Ataya FS, Salem-Bekhit MM, Zahrani SA, Abdelmageed MW, Ernst B, Benguerba Y

Molecules

18-Oct-2023

PMCID:	PMC10609132
doi:	10.3390/molecules28207153
PMID:	37894631

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

Phytochemical Profile Top

Add a new one!

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 / 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
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
Delta-Terpineol	81722	Click to see CC(C)(C1CCC(=C)CC1)O	154.25	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
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
Salicyloyltremuloidin	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
> 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

Biological Material Top

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Eucalyptus radiata

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top