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Corymbia maculata

Corymbia maculata - 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 UUID6440360366053625393599
Scientific name Corymbia maculata
Authority (Hook.) K.D.Hill & L.A.S.Johnson
First published in Telopea 6: 393 (1995)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eucalyptus maculata Hook. Hooker's Icon. Pl. 7: t. 619 (1844)

Common names Top

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Language Common/alternative name
Persian انگمی لکهدار
Hebrew קורמביה ( איקליפטוס ) מוכתמת
Japanese スポッテッドガム
Lithuanian dėmėtoji korimbija
Chinese 斑皮桉

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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Forms (abbr. f.) Top

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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
    • South Tropical Africa
      • Zambia
    • Southern Africa
      • Cape Provinces
    • West-central Tropical Africa
      • Rwanda
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000925549
Tropicos 100172647
KEW urn:lsid:ipni.org:names:986338-1
The Plant List kew-48059
Open Tree Of Life 771607
NCBI Taxonomy 87660
IUCN Red List 61906009
IPNI 986338-1
iNaturalist 417763
GBIF 5418386
Freebase /m/02rk6b2
EPPO EUCMA
EOL 301463
USDA GRIN 404659
Wikipedia Corymbia_maculata

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_014182735.1 ASM1418273v1 Chromosome Australian National University 2020-08-14 58.0x 385.11 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
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
Draft genome sequences for ten strains of Xanthomonas species that have phylogenomic importance Harrison J, Hussain RM, Greer SF, Ntoukakis V, Aspin A, Vicente JG, Grant M, Studholme DJ Access Microbiol 14-Jul-2023
PMCID:PMC10436009
doi:10.1099/acmi.0.000532.v3
PMID:37601434
Germination temperature sensitivity differs between co‐occurring tree species and climate origins resulting in contrasting vulnerability to global warming Filipe JC, Ahrens CC, Byrne M, Hardy G, Rymer PD Plant Environ Interact 24-Apr-2023
PMCID:PMC10290426
doi:10.1002/pei3.10108
PMID:37362420
Complete Genome of Rose Myrtle, Rhodomyrtus tomentosa, and Its Population Genetics in Thai Peninsula Detcharoen M, Bumrungsri S, Voravuthikunchai SP Plants (Basel) 07-Apr-2023
PMCID:PMC10144328
doi:10.3390/plants12081582
PMID:37111806
In silico and in vitro anti-inflammatory study of phenolic compounds isolated from Eucalyptus maculata resin Ali DE, Gedaily RA, Ezzat SM, Sawy MA, Meselhy MR, Abdel-Sattar E Sci Rep 06-Feb-2023
PMCID:PMC9902548
doi:10.1038/s41598-023-28221-y
PMID:36747067
Colloidal silver against macrophage infections and biofilms of atypical mycobacteria Feizi S, Cooksley CM, Ramezanpour M, Nepal R, Psaltis AJ, Wormald PJ, Vreugde S Biometals 02-Feb-2023
PMCID:PMC10393856
doi:10.1007/s10534-023-00494-w
PMID:36729280
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
Recent Advancements in Natural Plant Colorants Used for Hair Dye Applications: A Review Cui H, Xie W, Hua Z, Cao L, Xiong Z, Tang Y, Yuan Z Molecules 20-Nov-2022
PMCID:PMC9692289
doi:10.3390/molecules27228062
PMID:36432162
Pathogen spillover driven by rapid changes in bat ecology Eby P, Peel AJ, Hoegh A, Madden W, Giles JR, Hudson PJ, Plowright RK Nature 16-Nov-2022
PMCID:PMC9768785
doi:10.1038/s41586-022-05506-2
PMID:36384167
Low phosphorus induces differential metabolic responses in eucalyptus species improving nutrient use efficiency Silva FM, Bulgarelli RG, Mubeen U, Caldana C, Andrade SA, Mazzafera P Front Plant Sci 15-Sep-2022
PMCID:PMC9520260
doi:10.3389/fpls.2022.989827
PMID:36186027
The anti‐Trypanosoma activities of medicinal plants: A systematic review of the literature Nekoei S, Khamesipour F, Habtemariam S, de Souza W, Mohammadi Pour P, Hosseini SR Vet Med Sci 29-Aug-2022
PMCID:PMC9677405
doi:10.1002/vms3.912
PMID:36037401
A Review of Commonly Used Methodologies for Assessing the Antibacterial Activity of Honey and Honey Products Hossain ML, Lim LY, Hammer K, Hettiarachchi D, Locher C Antibiotics (Basel) 20-Jul-2022
PMCID:PMC9312033
doi:10.3390/antibiotics11070975
PMID:35884229
Use of road underpasses by mammals and a monitor lizard in eastern Australia and consideration of the prey‐trap hypothesis Goldingay RL, Rohweder D, Taylor BD, Parkyn JL Ecol Evol 05-Jul-2022
PMCID:PMC9254676
doi:10.1002/ece3.9075
PMID:35813912
Hybrid Assembly and Annotation of the Genome of the Indian Punica granatum, a Superfood Usha T, Middha SK, Babu D, Goyal AK, Das AJ, Saini D, Sarangi A, Krishnamurthy V, Prasannakumar MK, Saini DK, Sidhalinghamurthy KR Front Genet 11-May-2022
PMCID:PMC9130716
doi:10.3389/fgene.2022.786825
PMID:35646087
Advances in Nanostructures for Antimicrobial Therapy Jampilek J, Kralova K Materials (Basel) 24-Mar-2022
PMCID:PMC8999898
doi:10.3390/ma15072388
PMID:35407720

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 / 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/10.1080/10412905.1992.9698059
> 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/10.1300/J044V07N04_10
Citronellal 7794 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown https://doi.org/10.1300/J044V07N04_10
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697921
> 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/10.1080/10412905.1992.9698059
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.1992.9698059
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697921
Verbenone 29025 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 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/10.1080/10412905.1992.9698059
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1991.9697921
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Hinesol 10878761 Click to see CC1CCC=C(C12CCC(C2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1023/B:JOEC.0000042400.14451.08
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.4324/9780203219430_CHAPTER_13
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.4324/9780203219430_CHAPTER_13
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.4324/9780203219430_CHAPTER_13
https://doi.org/10.1300/J044V07N04_10
https://doi.org/10.1080/10412905.1992.9698059
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1300/J044V07N04_10
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.4324/9780203219430_CHAPTER_13
Guaiol 227829 Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O 222.37 unknown https://doi.org/10.1023/B:JOEC.0000042400.14451.08
Hinesol 289964 Click to see CC1CCC=C(C12CCC(C2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1023/B:JOEC.0000042400.14451.08
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(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/10.1080/10412905.1992.9698059
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1080/10412905.1991.9697921
Aromadendrene 91354 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698059
https://doi.org/10.1080/10412905.1991.9697921
> 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/10.1080/10412905.1991.9697921
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl)propan-2-ol 518516 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown https://doi.org/10.1023/B:JOEC.0000042400.14451.08
2-(4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl)propan-2-ol 521216 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1023/B:JOEC.0000042400.14451.08
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1023/B:JOEC.0000042400.14451.08
gamma-EUDESMOL 6432005 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown https://doi.org/10.1023/B:JOEC.0000042400.14451.08
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
2-Hydroxy-10-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-1,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 72995358 Click to see CC1C2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1(C)O)C(=O)O)C)C)(C)C)OC(=O)C=CC6=CC=C(C=C6)O)C 618.80 unknown https://doi.org/10.3390/70100075
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters / O-cinnamoyl glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(E)-3-phenylprop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-phenylprop-2-enoate 10741759 Click to see C1=CC=C(C=C1)C=CC(=O)OCC2C(C(C(C(O2)OC(=O)C=CC3=CC=CC=C3)O)O)O 440.40 unknown https://doi.org/10.1002/CHIN.200047190
[3,4,5-Trihydroxy-6-(3-phenylprop-2-enoyloxy)oxan-2-yl]methyl 3-phenylprop-2-enoate 85251918 Click to see C1=CC=C(C=C1)C=CC(=O)OCC2C(C(C(C(O2)OC(=O)C=CC3=CC=CC=C3)O)O)O 440.40 unknown https://doi.org/10.1002/CHIN.200047190
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1002/CHIN.200047190
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1002/CHIN.200047190
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
[3,4,5-Trihydroxy-6-[3-(4-hydroxyphenyl)prop-2-enoyloxy]oxan-2-yl]methyl 3-phenylprop-2-enoate 162875697 Click to see C1=CC=C(C=C1)C=CC(=O)OCC2C(C(C(C(O2)OC(=O)C=CC3=CC=C(C=C3)O)O)O)O 456.40 unknown https://doi.org/10.3390/70100075
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.3390/70100075
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.3390/70100075
> 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 https://doi.org/10.1071/CH9580372
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1071/CH9580372
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
[(2R,3S,4S,5R,6S)-6-[4-[(2S,3S)-3,5-dihydroxy-7-methoxy-4-oxo-2,3-dihydrochromen-2-yl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 163191418 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=C(C=C3)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O)O 610.60 unknown https://doi.org/10.3390/70100075
[6-[4-(3,5-Dihydroxy-7-methoxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 162966630 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=C(C=C3)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O)O 610.60 unknown https://doi.org/10.3390/70100075
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxychroman-4-one 348130 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1002/CHIN.200047190
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 https://doi.org/10.1071/CH9580372
https://doi.org/10.1002/CHIN.200047190
Folerogenin 5319509 Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=C(C=C3)O)O 302.28 unknown https://doi.org/10.1071/CH9580372
https://doi.org/10.1002/CHIN.200047190
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1002/CHIN.200047190

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