Language	Common/alternative name
English	silver-leaved mountain gum
English	silverleaf mountain gum
Russian	Эвкалипт припудренный
Chinese	粉叶桉
Chinese	圆叶桉
Chinese	圓葉桉
Chinese	银叶山桉

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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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

Northern America click to expand
- Southwestern U.S.A.
  - California

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000955710
USDA Plants	EUPU
Tropicos	50133207
INPN	717757
KEW	urn:lsid:ipni.org:names:593283-1
The Plant List	kew-73720
Open Tree Of Life	278179
NCBI Taxonomy	881203
IUCN Red List	133372846
IPNI	593283-1
iNaturalist	64294
GBIF	3176788
Freebase	/m/02r3j8_
EPPO	EUCPL
EOL	301319
Calflora (Californian flora)	3536
USDA GRIN	16002
Wikipedia	Eucalyptus_pulverulenta

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

Antimicrobial, Herbicidal and pesticidal potential of Tunisian eucalyptus species: Chemoprofiling and biological evaluation

Khedhri S, Polito F, Caputo L, Khammassi M, Dhaouadi F, Amri I, Hamrouni L, Mabrouk Y, Fratianni F, Nazzaro F, De Feo V

Heliyon

24-Apr-2024

PMCID:	PMC11076916
doi:	10.1016/j.heliyon.2024.e29905
PMID:	38720723

Which horticultural activities are more effective for children’s recovery from stress and mental fatigue? A quasi-experimental study

Guo L, Xu W, Shi Y, Gao S, Xiao C, Zhang X, Liu X, Zhang Q, Zhang Y

Front Psychol

12-Apr-2024

PMCID:	PMC11050040
doi:	10.3389/fpsyg.2024.1352186
PMID:	38680274

Taxonomy, Phylogeny, Divergence Time Estimation, and Biogeography of the Family Pseudoplagiostomataceae (Ascomycota, Diaporthales)

Zhang Z, Liu X, Tao M, Liu X, Xia J, Zhang X, Meng Z

J Fungi (Basel)

05-Jan-2023

PMCID:	PMC9860658
doi:	10.3390/jof9010082
PMID:	36675903

Eucalyptus gunnii and Eucalyptus pulverulenta ‘Baby Blue’ Essential Oils as Potential Natural Herbicides

Danna C, Cornara L, Smeriglio A, Trombetta D, Amato G, Aicardi P, De Martino L, De Feo V, Caputo L

Molecules

08-Nov-2021

PMCID:	PMC8587786
doi:	10.3390/molecules26216749
PMID:	34771155

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

UPLC-PDA-Q Exactive Orbitrap-MS profiling of the lipophilic compounds product isolated from Eucalyptus viminalis plants

Ossipov V, Koivuniemi A, Mizina P, Salminen JP

Heliyon

23-Dec-2020

PMCID:	PMC7772544
doi:	10.1016/j.heliyon.2020.e05768
PMID:	33385084

Dataset of leaf inclination angles for 71 different Eucalyptus species

Pisek J, Adamson K

Data Brief

09-Oct-2020

PMCID:	PMC7569295
doi:	10.1016/j.dib.2020.106391
PMID:	33102658

Occurrence of Cryptococcus neoformans and other yeast-like fungi in environmental sources in Bonaire (Dutch Caribbean)

Gugnani HC, Hagen F, Meis JF, Chakrabarti A

Germs

01-Sep-2020

PMCID:	PMC7572204
doi:	10.18683/germs.2020.1205
PMID:	33134197

GC-MS and HS-SPME-GC×GC-TOFMS Determination of the Volatile Composition of Essential Oils and Hydrosols (By-Products) from Four Eucalyptus Species Cultivated in Tuscany

Ieri F, Cecchi L, Giannini E, Clemente C, Romani A

Molecules

09-Jan-2019

PMCID:	PMC6358850
doi:	10.3390/molecules24020226
PMID:	30634495

Antibacterial, Antioxidant, and Antiproliferative Activities of Corymbia citriodora and the Essential Oils of Eight Eucalyptus Species

Miguel MG, Gago C, Antunes MD, Lagoas S, Faleiro ML, Megías C, Cortés-Giraldo I, Vioque J, Figueiredo AC

Medicines (Basel)

21-Jun-2018

PMCID:	PMC6163473
doi:	10.3390/medicines5030061
PMID:	29933560

Advancing Eucalyptus Genomics: Cytogenomics Reveals Conservation of Eucalyptus Genomes

Ribeiro T, Barrela RM, Bergès H, Marques C, Loureiro J, Morais-Cecílio L, Paiva JA

Front Plant Sci

22-Apr-2016

PMCID:	PMC4840385
doi:	10.3389/fpls.2016.00510
PMID:	27148332

Germination Inhibitor from<i>Eucalyptus pulverulenta</i>

Matthew L. Bolte, Jenny Bowers, Wilfrid D. Crow, Dugald M. Paton, Akira Sakurai, Nobutaka Takahashi, Masami Ujiie, Shigeo Yoshida

Oxford University Press (OUP)

13-Apr-2016

doi:	10.1080/00021369.1984.10866137

The Steam Volatile Leaf Oil of<i>Eucalyptus pulverulenta</i>

Joseph Brophy, Erich Lassak, Robert Toia

Georg Thieme Verlag KG

06-Mar-2007

doi:	10.1055/S-2007-969442

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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Methyl 3,4,5-trimethoxybenzoate	15956	Click to see COC1=CC(=CC(=C1OC)OC)C(=O)OC	226.23	unknown	https://doi.org/10.1080/00021369.1984.10866137
> 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/10.1055/S-2007-969442
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1055/S-2007-969442
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral	638011	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	https://doi.org/10.1055/S-2007-969442
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1055/S-2007-969442
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1055/S-2007-969442
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1055/S-2007-969442
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1055/S-2007-969442
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1055/S-2007-969442
> 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/10.1055/S-2007-969442
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1055/S-2007-969442
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1055/S-2007-969442
Pinocarveol	102667	Click to see CC1(C2CC1C(=C)C(C2)O)C	152.23	unknown	https://doi.org/10.1055/S-2007-969442
Pinocarvone	121719	Click to see CC1(C2CC1C(=C)C(=O)C2)C	150.22	unknown	https://doi.org/10.1055/S-2007-969442
> 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/10.1055/S-2007-969442
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1055/S-2007-969442
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1055/S-2007-969442
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1055/S-2007-969442
Delta-Terpineol	81722	Click to see CC(C)(C1CCC(=C)CC1)O	154.25	unknown	https://doi.org/10.1055/S-2007-969442
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1055/S-2007-969442
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1055/S-2007-969442
> 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/10.1055/S-2007-969442
> 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/10.1055/S-2007-969442
(1aR,4R,4aR,7S,7aS,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol	162940145	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1080/00021369.1984.10866137
Globulol	101716	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1055/S-2007-969442 https://doi.org/10.1080/00021369.1984.10866137
Viridiflorol	11996452	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1055/S-2007-969442
Viridiflorol (incomplete stereochemistry)	94174	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1055/S-2007-969442
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Eudesmol	92762	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	https://doi.org/10.1055/S-2007-969442
beta-EUDESMOL	91457	Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O	222.37	unknown	https://doi.org/10.1055/S-2007-969442
gamma-EUDESMOL	6432005	Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O	222.37	unknown	https://doi.org/10.1055/S-2007-969442
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4,5,9,9,13,19,20-Heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl) acetate	73800256	Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)OC(=O)C)(C)C)C)C	496.70	unknown	https://doi.org/10.1080/00021369.1984.10866137
3-Acetoxy-11-ursen-28,13-olide	21606662	Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)OC(=O)C)(C)C)C)C	496.70	unknown	https://doi.org/10.1080/00021369.1984.10866137
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / 1,3-dicarbonyl compounds / Beta-diketones
12,14-Nonacosanedione	568008	Click to see CCCCCCCCCCCCCCCC(=O)CC(=O)CCCCCCCCCCC	436.80	unknown	https://doi.org/10.1080/00021369.1984.10866137
Hentriacontane-14,16-dione	441489	Click to see CCCCCCCCCCCCCCCC(=O)CC(=O)CCCCCCCCCCCCC	464.80	unknown	https://doi.org/10.1080/00021369.1984.10866137
Tritriacontane-16,18-dione	154874	Click to see CCCCCCCCCCCCCCCC(=O)CC(=O)CCCCCCCCCCCCCCC	492.90	unknown	https://doi.org/10.1080/00021369.1984.10866137
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Isovaleraldehyde	11552	Click to see CC(C)CC=O	86.13	unknown	https://doi.org/10.1055/S-2007-969442
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2R)-1-(2,6-dihydroxy-4-methoxy-3-methylphenyl)-2-methylbutan-1-one	162980013	Click to see CCC(C)C(=O)C1=C(C(=C(C=C1O)OC)C)O	238.28	unknown	https://doi.org/10.1080/00021369.1984.10866137
1-(2,6-Dihydroxy-4-methoxy-3-methylphenyl)-2-methyl-1-propanone	129835676	Click to see CC1=C(C=C(C(=C1O)C(=O)C(C)C)O)OC	224.25	unknown	https://doi.org/10.1080/00021369.1984.10866137
Aspidinol D	50908690	Click to see CCC(C)C(=O)C1=C(C(=C(C=C1O)OC)C)O	238.28	unknown	https://doi.org/10.1080/00021369.1984.10866137
Grandinol	11043217	Click to see CC1=C(C(=C(C(=C1O)C(=O)CC(C)C)O)C=O)O	252.26	unknown	https://doi.org/10.1080/00021369.1984.10866137

Biological Material Top

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Eucalyptus pulverulenta

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