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Eucalyptus macrocarpa

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64403a186d82a028573309
Scientific name Eucalyptus macrocarpa
Authority Hook.
First published in Hooker's Icon. Pl. 5: t. 405 (1842)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English mottlecah
Chinese 红蕊大果桉

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Eucalyptus macrocarpa subsp. elachantha Brooker & Hopper Nuytsia 9: 37 (1993)
Eucalyptus macrocarpa subsp. macrocarpa Hook. Nuytsia 9(1) 1-68. 1993

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000955298
USDA Plants EUMA21
Tropicos 50183449
KEW urn:lsid:ipni.org:names:593088-1
The Plant List kew-73306
Open Tree Of Life 3936165
NCBI Taxonomy 1711389
IUCN Red List 133380853
IPNI 593088-1
iNaturalist 131659
GBIF 3176430
Freebase /m/027v61r
EOL 635316
USDA GRIN 15949
Wikipedia Eucalyptus_macrocarpa

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
Breathing Fresh Air in the City: Implementing Avenue Trees as a Sustainable Solution to Reduce Particulate Pollution in Urban Agglomerations Mandal M, Popek R, Przybysz A, Roy A, Das S, Sarkar A Plants (Basel) 03-Apr-2023
PMCID:PMC10097214
doi:10.3390/plants12071545
PMID:37050171
Co-developing an international TLS network for the 3D ecological understanding of global trees: System architecture, remote sensing models, and functional prospects Lin Y, Filin S, Billen R, Mizoue N Environ Sci Ecotechnol 21-Feb-2023
PMCID:PMC10024182
doi:10.1016/j.ese.2023.100257
PMID:36941885
Metal-based nanoparticles, sensors, and their multifaceted application in food packaging Kumar A, Choudhary A, Kaur H, Mehta S, Husen A J Nanobiotechnology 26-Aug-2021
PMCID:PMC8393480
doi:10.1186/s12951-021-00996-0
PMID:34446005
Green Synthesis of Metallic Nanoparticles and Their Potential Applications to Treat Cancer Zhang D, Ma XL, Gu Y, Huang H, Zhang GW Front Chem 29-Oct-2020
PMCID:PMC7658653
doi:10.3389/fchem.2020.00799
PMID:33195027
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
Nanoparticles: Synthesis, Morphophysiological Effects, and Proteomic Responses of Crop Plants Hossain Z, Yasmeen F, Komatsu S Int J Mol Sci 26-Apr-2020
PMCID:PMC7246787
doi:10.3390/ijms21093056
PMID:32357514
Extinction pulse at Eocene–Oligocene boundary drives diversification dynamics of two Australian temperate floras Nge FJ, Biffin E, Thiele KR, Waycott M Proc Biol Sci 22-Jan-2020
PMCID:PMC7015341
doi:10.1098/rspb.2019.2546
PMID:31964242
Elemental Silver Nanoparticles: Biosynthesis and Bio Applications Mikhailov OV, Mikhailova EO Materials (Basel) 27-Sep-2019
PMCID:PMC6803994
doi:10.3390/ma12193177
PMID:31569794
Green Nanotechnology: Advancement in Phytoformulation Research Verma A, Gautam SP, Bansal KK, Prabhakar N, Rosenholm JM Medicines (Basel) 14-Mar-2019
PMCID:PMC6473607
doi:10.3390/medicines6010039
PMID:30875823
Plant Surfaces: Structures and Functions for Biomimetic Innovations Barthlott W, Mail M, Bhushan B, Koch K Nanomicro Lett 04-Jan-2017
PMCID:PMC6223843
doi:10.1007/s40820-016-0125-1
PMID:30464998
Green Synthesis of Metallic Nanoparticles via Biological Entities Shah M, Fawcett D, Sharma S, Tripathy SK, Poinern GE Materials (Basel) 29-Oct-2015
PMCID:PMC5458933
doi:10.3390/ma8115377
PMID:28793638
Superhydrophobic nature of nanostructures on an indigenous Australian eucalyptus plant and its potential application Poinern GE, Le XT, Fawcett D Nanotechnol Sci Appl 20-Oct-2011
PMCID:PMC3781715
doi:10.2147/NSA.S24834
PMID:24198490
Macrocarpal A, a novel antibacterial compound from Eucalyptus macrocarpa. Masatsune MURATA, Youko YAMAKOSHI, Seiichi HOMMA, Koh AIDA, Kayako HORI, Yuji OHASHI Oxford University Press (OUP) 13-Jul-2011
doi:10.1271/BBB1961.54.3221
Superhydrophobicity in perfection: the outstanding properties of the lotus leaf Ensikat HJ, Ditsche-Kuru P, Neinhuis C, Barthlott W Beilstein J Nanotechnol 10-Mar-2011
PMCID:PMC3148040
doi:10.3762/bjnano.2.19
PMID:21977427
Isolation and characterization of macrocarpals B--G antibacterial compounds from Eucalyptus macrocarpa. Yamakoshi Y, Murata M, Shimizu A, Homma S Biosci Biotechnol Biochem 01-Oct-1992
doi:10.1271/BBB.56.1570
PMID:1369057

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Macrocarpal D; Macrocarpal-d 44566862 Click to see 472.60 unknown https://doi.org/10.1271/BBB.56.1570
Macrocarpal D 454460 Click to see 472.60 unknown https://doi.org/10.1271/BBB.56.1570
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
5-[(1R)-1-[(1aR,4aR,7S,7aR,7bR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-yl]-3-methylbutyl]-2,4,6-trihydroxybenzene-1,3-dicarbaldehyde 10095499 Click to see CC(C)CC(C1=C(C(=C(C(=C1O)C=O)O)C=O)O)C2(CCC3C2C4C(C4(C)C)CCC3=C)C 454.60 unknown https://doi.org/10.1271/BBB.56.1570
5-[(1S)-1-[(1aS,4aR,7R,7aS,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-yl]-3-methylbutyl]-2,4,6-trihydroxybenzene-1,3-dicarbaldehyde 162995875 Click to see CC(C)CC(C1=C(C(=C(C(=C1O)C=O)O)C=O)O)C2(CCC3C2C4C(C4(C)C)CCC3=C)C 454.60 unknown https://doi.org/10.1271/BBB.56.1570
5-[(1S)-1-[(1aS,4R,4aR,7R,7aR,7bS)-4-hydroxy-1,1,4,7-tetramethyl-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-yl]-3-methylbutyl]-2,4,6-trihydroxybenzene-1,3-dicarbaldehyde 162941668 Click to see 472.60 unknown https://doi.org/10.1271/BBB.56.1570
Macrocarpal A 454457 Click to see 472.60 unknown https://doi.org/10.1271/BBB1961.54.3221
https://doi.org/10.1271/BBB.56.1570
Macrocarpal B 454458 Click to see 472.60 unknown https://doi.org/10.1271/BBB.56.1570
Macrocarpal C 454459 Click to see CC(C)CC(C1=C(C(=C(C(=C1O)C=O)O)C=O)O)C2(CCC3C2C4C(C4(C)C)CCC3=C)C 454.60 unknown https://doi.org/10.1271/BBB.56.1570
rel-5-[1-[(1aR,4R,4aR,7R,7aR,7bS)-Decahydro-4-hydroxy-1,1,4,7-tetramethyl-1H-cycloprop[e]azulen-7-yl]-3-methylbutyl]-2,4,6-trihydroxy-1,3-benzenedicarboxaldehyde 14807364 Click to see 472.60 unknown https://doi.org/10.1271/BBB.56.1570
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2,4,6-trihydroxy-5-[1-[5-(2-hydroxypropan-2-yl)-2,8-dimethyl-4,4a,5,6,7,8-hexahydro-3H-naphthalen-2-yl]-3-methylbutyl]benzene-1,3-dicarbaldehyde 58120335 Click to see 472.60 unknown https://doi.org/10.1271/BBB.56.1570
5-[(1S)-1-[(2S,4aR,5S,8R)-5-(2-hydroxypropan-2-yl)-2,8-dimethyl-4,4a,5,6,7,8-hexahydro-3H-naphthalen-2-yl]-3-methylbutyl]-2,4,6-trihydroxybenzene-1,3-dicarbaldehyde 162931043 Click to see CC1CCC(C2C1=CC(CC2)(C)C(CC(C)C)C3=C(C(=C(C(=C3O)C=O)O)C=O)O)C(C)(C)O 472.60 unknown https://doi.org/10.1271/BBB.56.1570
Macrocarpal E 454461 Click to see 472.60 unknown https://doi.org/10.1271/BBB.56.1570

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