Language	Common/alternative name
English	shining gum
English	silvertop
Bulgarian	блестящ евкалипт
Galician	eucalipto nitens
Lithuanian	Žvilgusis eukaliptas
Russian	Эвкалипт блестящий
Chinese	亮果桉

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
  - Tasmania
  - Victoria

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000955429
USDA Plants	EUNI5
Tropicos	22103181
INPN	97405
KEW	urn:lsid:ipni.org:names:593164-1
The Plant List	kew-73436
Open Tree Of Life	380501
NCBI Taxonomy	87674
IUCN Red List	61914129
IPNI	593164-1
iNaturalist	401772
GBIF	3176336
Freebase	/m/04cv0wb
EPPO	EUCNT
EOL	630139
USDA GRIN	15971
Wikipedia	Eucalyptus_nitens

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

Identification of Phytophthora cinnamomi CRN effectors and their roles in manipulating cell death during Persea americana infection

Midgley KA, van den Berg N, Backer R, Swart V

BMC Genomics

02-May-2024

PMCID:	PMC11064341
doi:	10.1186/s12864-024-10358-3
PMID:	38698341

Hemicellulose pyrolysis: mechanism and kinetics of functionalized xylopyranose

Ayarde-Henríquez L, Lupi J, Dooley S

Phys Chem Chem Phys

04-Apr-2024

PMCID:	PMC11041873
doi:	10.1039/d3cp06094b
PMID:	38622974

Apple crown and collar canker and necrosis caused by Cytospora balanejica sp. nov. in Iran

Azizi R, Ghosta Y, Ahmadpour A

Sci Rep

19-Mar-2024

PMCID:	PMC10951349
doi:	10.1038/s41598-024-57235-3
PMID:	38504125

Natural selection and genetic diversity maintenance in a parasitic wasp during continuous biological control application

Li B, Duan Y, Du Z, Wang X, Liu S, Feng Z, Tian L, Song F, Yang H, Cai W, Lin Z, Li H

Nat Commun

14-Feb-2024

PMCID:	PMC10866907
doi:	10.1038/s41467-024-45631-2
PMID:	38355730

Histological, chemical and gene expression differences between western redcedar seedlings resistant and susceptible to cedar leaf blight

Aldana JA, Moa B, Mattsson J, Russell JH, Hawkins BJ

Front Plant Sci

06-Feb-2024

PMCID:	PMC10878471
doi:	10.3389/fpls.2024.1309762
PMID:	38379949

Wide Distribution of Teratosphaeria epicoccoides and T. destructans Associated with Diseased Eucalyptus Leaves in Plantations in Southern China

Chen B, Wu W, Chen S

Microorganisms

09-Jan-2024

PMCID:	PMC10819926
doi:	10.3390/microorganisms12010129
PMID:	38257956

The genus Rachicladosporium: introducing new species from sooty mould communities and excluding cold adapted species

Piątek M, Stryjak-Bogacka M, Czachura P, Owczarek-Kościelniak M

Sci Rep

21-Dec-2023

PMCID:	PMC10739867
doi:	10.1038/s41598-023-49696-9
PMID:	38129458

The Bending Properties of Hybrid Cross-Laminated Timber (CLT) Using Various Species Combinations

Altaher Omer Ahmed A, Garab J, Horváth-Szováti E, Kozelka J, Bejó L

Materials (Basel)

14-Nov-2023

PMCID:	PMC10672904
doi:	10.3390/ma16227153
PMID:	38005081

Ecophysiological adaptations shape distributions of closely related trees along a climatic moisture gradient

Smith DD, Adams MA, Salvi AM, Krieg CP, Ané C, McCulloh KA, Givnish TJ

Nat Commun

07-Nov-2023

PMCID:	PMC10630429
doi:	10.1038/s41467-023-42352-w
PMID:	37935674

Presence of the Eucalyptus snout beetle in Ecuador and potential invasion risk in South America

Crespo‐Pérez V, Soto‐Centeno JA, Pinto CM, Avilés A, Pruna W, Terán C, Barragán Á

Ecol Evol

19-Sep-2023

PMCID:	PMC10509408
doi:	10.1002/ece3.10531
PMID:	37736275

Expanding the Microcolonial Black Fungi Aeminiaceae Family: Saxispiralis lemnorum gen. et sp. nov. (Mycosphaerellales), Isolated from Deteriorated Limestone in the Lemos Pantheon, Portugal

Paiva DS, Trovão J, Fernandes L, Mesquita N, Tiago I, Portugal A

J Fungi (Basel)

10-Sep-2023

PMCID:	PMC10533162
doi:	10.3390/jof9090916
PMID:	37755024

Dewatering of Juglans mandshurica Wood Using Supercritical Carbon Dioxide

Zheng J, Zhu X, Yang L

Materials (Basel)

08-Aug-2023

PMCID:	PMC10456349
doi:	10.3390/ma16165521
PMID:	37629810

Long‐distance gene flow in Acacia senegal: Hope for disturbed and fragmented populations

Omondi SF, Githae EW, Khasa DP

Ecol Evol

12-Jul-2023

PMCID:	PMC10337015
doi:	10.1002/ece3.10292
PMID:	37449018

Hydrolyzable tannins are incorporated into the endocarp during sclerification of the water caltrop Trapa natans

Huss JC, Antreich SJ, Felhofer M, Mayer K, Eder M, Vieira Dias dos Santos AC, Ramer G, Lendl B, Gierlinger N

Plant Physiol

10-Jul-2023

PMCID:	PMC10762508
doi:	10.1093/plphys/kiad408
PMID:	37427803

Self-Assembled CNF/rGO/Tannin Composite: Study of the Physicochemical and Wound Healing Properties

Fernández K, Llanquileo A, Bustos M, Aedo V, Ruiz I, Carrasco S, Tapia M, Pereira M, Meléndrez MF, Aguayo C, Atanase LI

Polymers (Basel)

20-Jun-2023

PMCID:	PMC10304054
doi:	10.3390/polym15122752
PMID:	37376399

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 / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	https://doi.org/10.1002/PCA.548
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
3-Methylbutyl hexanoate	16617	Click to see CCCCCC(=O)OCCC(C)C	186.29	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
Ethyl isovalerate	7945	Click to see CCOC(=O)CC(C)C	130.18	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
Hexyl isovalerate	61455	Click to see CCCCCCOC(=O)CC(C)C	186.29	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
Isoamyl isovalerate	12613	Click to see CC(C)CCOC(=O)CC(C)C	172.26	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C20-gibberellins / C20-gibberellin 6-carboxylic acids
Gibberellin A19	5460209	Click to see CC1(CCCC2(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)O)C=O)C(=O)O	362.40	unknown	https://doi.org/10.1111/J.1399-3054.1994.TB08804.X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
> 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/10.1016/S0031-9422(00)94539-4
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1S,3R,5S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol	12314318	Click to see CC1(C2CC1C(=C)C(C2)O)C	152.23	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
CID 44630107	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
Fenchol	15406	Click to see CC1(C2CCC(C2)(C1O)C)C	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
Myrtenol	10582	Click to see CC1(C2CC=C(C1C2)CO)C	152.23	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
Pinocarveol	102667	Click to see CC1(C2CC1C(=C)C(C2)O)C	152.23	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
> 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/10.1016/S0031-9422(00)94539-4
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
Dihydrocarvone	24473	Click to see CC1CCC(CC1=O)C(=C)C	152.23	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)94539-4
> 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/10.1016/S0031-9422(00)94539-4
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1002/PCA.548
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11R)-10-[(15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate	101601178	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	936.60	unknown	https://doi.org/10.1002/PCA.548
1(beta)-O-Galloylpedunculagin	118701062	Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O	936.60	unknown	https://doi.org/10.1002/PCA.548
Casuarictin	73644	Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O	936.60	unknown	https://doi.org/10.1002/PCA.548
Casuarinin	442673	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	936.60	unknown	https://doi.org/10.1002/PCA.548
CID 11766372	11766372	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O	938.70	unknown	https://doi.org/10.1002/PCA.548
CID 442690	442690	Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O	786.60	unknown	https://doi.org/10.1002/PCA.548
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	https://doi.org/10.1002/PCA.548
Eugeniin	442679	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O	938.70	unknown	https://doi.org/10.1002/PCA.548
Pedunculagin	442688	Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O	784.50	unknown	https://doi.org/10.1002/PCA.548

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Eucalyptus nitens

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