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Eucalyptus perriniana

Eucalyptus perriniana - Unknown
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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 UUID64403a288638b862735964
Scientific name Eucalyptus perriniana
Authority Rodway
First published in Pap. & Proc. Roy. Soc. Tasmania 1893: 181 (1860)

Description Top

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Eucalyptus perriniana, also known as spinning gum, is a tree or mallee native to New South Wales, the Australian Capital Territory, Victoria and Tasmania. It is a sub-alpine species that can grow in areas with snow cover for several months. Its bark is smooth and copper-colored, and its leaves are lance-shaped and greyish-green. The tree produces flowers in groups of three and its fruit is small and round. It was first described in 1894 and is named after George Samuel Perrin, a former Conservator of Forests in Tasmania and Victoria. Spinning gum is found in woodland on high, cold plains and is listed as "rare" under the Tasmanian Government Threatened Species Protection Act. It is also known for its ability to produce catechin-7-O-glucoside and catechin-5-O-glucoside, which can be used for biotransformation.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English spinning gum
Russian Эвкалипт Перрина
Chinese 珀琳桉

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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Start at 4°C for 3 months, then warm to 20°C for another 3 months.
see www.angelfire.com/bc/eucalyptus/seed.html

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000955603
USDA Plants EUPE19
Tropicos 100188323
INPN 97407
KEW urn:lsid:ipni.org:names:3753-3
The Plant List kew-73614
Missouri Botanical Garden 268562
Open Tree Of Life 748051
NCBI Taxonomy 183845
IUCN Red List 133378833
IPNI 593235-1
iNaturalist 135375
GBIF 3177073
Freebase /m/02q_fhs
EPPO EUCPE
EOL 631979
USDA GRIN 15987
Wikipedia Eucalyptus_perriniana

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
Bioactive Secondary Metabolites from Fungi of the Genus Cytospora Ehrenb. (Ascomycota) Kianfé BY, Tchamgoue J, Narmani A, Teponno RB, Njouonkou AL, Stadler M, Fogue Kouam S Molecules 31-Mar-2023
PMCID:PMC10096137
doi:10.3390/molecules28073120
PMID:37049883
Free and Esterified Tocopherols, Tocotrienols and Other Extractable and Non-Extractable Tocochromanol-Related Molecules: Compendium of Knowledge, Future Perspectives and Recommendations for Chromatographic Techniques, Tools, and Approaches Used for Tocochromanol Determination Górnaś P, Baškirovs G, Siger A Molecules 04-Oct-2022
PMCID:PMC9573122
doi:10.3390/molecules27196560
PMID:36235100
In vitro strategies for the enhancement of secondary metabolite production in plants: a review Fazili MA, Bashir I, Ahmad M, Yaqoob U, Geelani SN Bull Natl Res Cent 19-Feb-2022
PMCID:PMC8857880
doi:10.1186/s42269-022-00717-z
PMID:35221660
Genome-wide association study identifies SNP markers and putative candidate genes for terpene traits important for Leptocybe invasa resistance in Eucalyptus grandis Mhoswa L, Myburg AA, Slippers B, Külheim C, Naidoo S G3 (Bethesda) 03-Feb-2022
PMCID:PMC8982386
doi:10.1093/g3journal/jkac004
PMID:35134191
Glucosylation of (±)-Menthol by Uridine-Diphosphate-Sugar Dependent Glucosyltransferases from Plants Kurze E, Ruß V, Syam N, Effenberger I, Jonczyk R, Liao J, Song C, Hoffmann T, Schwab W Molecules 10-Sep-2021
PMCID:PMC8470988
doi:10.3390/molecules26185511
PMID:34576983
Prostate Apoptotic Induction and NFκB Suppression by Dammarolic Acid: Mechanistic Insight into Onco-Therapeutic Action of an Aglycone Asiaticoside Alafnan A, Hussain T, Rizvi SM, Moin A, Alamri A Curr Issues Mol Biol 10-Aug-2021
PMCID:PMC8928952
doi:10.3390/cimb43020066
PMID:34449548
Plant in vitro Culture Technologies; A Promise Into Factories of Secondary Metabolites Against COVID-19 Khan T, Khan MA, Karam K, Ullah N, Mashwani ZU, Nadhman A Front Plant Sci 12-Mar-2021
PMCID:PMC7994895
doi:10.3389/fpls.2021.610194
PMID:33777062
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
Phytotoxicity of Essential Oils: Opportunities and Constraints for the Development of Biopesticides. A Review Werrie PY, Durenne B, Delaplace P, Fauconnier ML Foods 14-Sep-2020
PMCID:PMC7554882
doi:10.3390/foods9091291
PMID:32937933
Glycosylation of Stilbene Compounds by Cultured Plant Cells Shimoda K, Kubota N, Uesugi D, Kobayashi Y, Hamada H, Hamada H Molecules 22-Mar-2020
PMCID:PMC7145310
doi:10.3390/molecules25061437
PMID:32235774
Naturally Occurring Isocoumarins Derivatives from Endophytic Fungi: Sources, Isolation, Structural Characterization, Biosynthesis, and Biological Activities Noor AO, Almasri DM, Bagalagel AA, Abdallah HM, Mohamed SG, Mohamed GA, Ibrahim SR Molecules 17-Jan-2020
PMCID:PMC7024277
doi:10.3390/molecules25020395
PMID:31963586
Identifying genetic markers for a range of phylogenetic utility–From species to family level Choi B, Crisp MD, Cook LG, Meusemann K, Edwards RD, Toon A, Külheim C PLoS One 01-Aug-2019
PMCID:PMC6675087
doi:10.1371/journal.pone.0218995
PMID:31369563
Recent Advances in Biotransformation of Saponins He Y, Hu Z, Li A, Zhu Z, Yang N, Ying Z, He J, Wang C, Yin S, Cheng S Molecules 26-Jun-2019
PMCID:PMC6650892
doi:10.3390/molecules24132365
PMID:31248032
Optimization of Regioselective α-Glucosylation of Hesperetin Catalyzed by Cyclodextrin Glucanotransferase González-Alfonso JL, Míguez N, Padilla JD, Leemans L, Poveda A, Jiménez-Barbero J, Ballesteros AO, Sandoval G, Plou FJ Molecules 05-Nov-2018
PMCID:PMC6278433
doi:10.3390/molecules23112885
PMID:30400664
Biotransformations of Flavones and an Isoflavone (Daidzein) in Cultures of Entomopathogenic Filamentous Fungi Dymarska M, Janeczko T, Kostrzewa-Susłow E Molecules 05-Jun-2018
PMCID:PMC6100588
doi:10.3390/molecules23061356
PMID:29874813

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 / Triterpenoids
19beta-Methyl-3beta,23-dihydroxy-30-norolean-12-en-28-oic acid methyl ester 13890856 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)OC 486.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
23-Hydroxyursolic Acid 14136881 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
2beta,3beta,23-Trihydroxyolean-12-en-28-oic acid methyl ester 609112 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)OC)C 502.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Asiatic Acid 119034 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O 488.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Hederagenin methyl ester 11752118 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)OC)C 486.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Maslinic acid methyl ester 609113 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)OC)C 486.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
methyl (4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 21594188 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)OC)C 502.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
methyl (4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylate 122541 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC)C 470.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
methyl 10-hydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 13890854 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)OC 486.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Methyl 10-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 12526650 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)OC)C 486.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Methyl 2,3-dihydroxyurs-12-en-28-oate 621722 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)OC 486.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Methyl 3-hydroxyurs-12-en-28-oate 621719 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC 470.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Methyl asiatate 21672634 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)OC 502.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Methyl corosolate 14109751 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)OC 486.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Methyl maslinate 13653327 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)OC)C 486.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Methyl oleanolate 92900 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC)C 470.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Methyl ursolate 636516 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC 470.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Conanine-type alkaloids
[16-(Dimethylamino)-6,7,13-trimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-10-yl] 4-methylpent-3-enoate 12310557 Click to see CC1C2CCC3C2(CN1C)C(CC4C3CC=C5C4(CCC(C5)N(C)C)C)OC(=O)CC=C(C)C 468.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84771-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 4-aminobenzoate 21186858 Click to see C1=CC(=CC=C1C(=O)OC2C(C(C(C(O2)CO)O)O)O)N 299.28 unknown https://doi.org/10.1016/S0031-9422(97)01016-9
p-aminobenzoate-beta-D-glucopyranosyl ester 67647145 Click to see C1=CC(=CC=C1C(=O)OC2C(C(C(C(O2)CO)O)O)O)N 299.28 unknown https://doi.org/10.1016/S0031-9422(97)01016-9
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
2,4,6-Trihydroxy-3-methyl-5-(3-methylbutanoyl)benzaldehyde 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/10.1080/00021369.1990.10869881
https://doi.org/10.1271/BBB1961.54.231

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