Eucalyptus rubida - Unknown
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Internal ID UUID64403a3454b9d580468368
Scientific name Eucalyptus rubida
Authority Deane & Maiden
First published in Proc. Linn. Soc. New South Wales 24: 456 (1899)

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Synonyms Top

Scientific name Authority First published in
Eucalyptus gunnii var. rubida Maiden Proc. Linn. Soc. New South Wales 26: 561 (1902)

Common names Top

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Language Common/alternative name
English candlebark
Bulgarian червеникав евкалипт
Russian Эвкалипт красноватый
Chinese 红桉
Chinese 蜡烛桉

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Eucalyptus rubida subsp. barbigerorum L.A.S.Johnson & K.D.Hill Telopea 4(2): 240. 1991 [1 Mar 1991]
Eucalyptus rubida subsp. rubida H.Deane & Maiden Telopea 4(2) 1991

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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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-0000955823
USDA Plants EURU8
Tropicos 50206140
INPN 611742
KEW urn:lsid:ipni.org:names:593324-1
The Plant List kew-73827
Open Tree Of Life 566582
NCBI Taxonomy 155762
IUCN Red List 133372734
IPNI 593324-1
iNaturalist 208130
GBIF 3177306
Freebase /m/02r97b0
EPPO EUCRB
EOL 632016
USDA GRIN 16019
Wikipedia Eucalyptus_rubida
CMAUP NPO21277

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
Litter accumulation and fire risks show direct and indirect climate-dependence at continental scale Adams MA, Neumann M Nat Commun 18-Mar-2023
PMCID:PMC10024763
doi:10.1038/s41467-023-37166-9
PMID:36934100
The survival, development, and reproduction of Gonipterus platensis (Coleoptera: Curculionidae) on the main Eucalyptus (Myrtaceae) genotypes planted in Brazil de Oliveira NC, Ribeiro MF, Ottati A, Tavares WD, Serrão JE, Zanuncio JC, Zanetti R, Wilcken CF PeerJ 01-Aug-2022
PMCID:PMC9351619
doi:10.7717/peerj.13698
PMID:35935252
New Acylated Rhaponticin Isolated from <i>Eucalyptus rubida</i> as a Repellent against the Blue Mussel <i>Mytilus edulis</i> Noriyuki Yamashita, Hideo Etoh, Kanzo Sakata, Hiroji Ina, Kazuo Ina Oxford University Press (OUP) 13-Apr-2016
doi:10.1080/00021369.1989.10869710
Stilbene Glucosides Isolated from<i>Eucalyptus rubida</i>, as Repellents against the Blue Mussel<i>Mytilus edulis</i> Hideo Etoh, Noriyuki Yamashita, Kanzo Sakata, Hiroji Ina, Kazuo Ina Oxford University Press (OUP) 13-Apr-2016
doi:10.1080/00021369.1990.10870293
Quantifying temporal isolation: a modelling approach assessing the effect of flowering time differences on crop-to-weed pollen flow in sunflower Roumet M, Cayre A, Latreille M, Muller MH Evol Appl 02-Dec-2014
PMCID:PMC4310582
doi:10.1111/eva.12222
PMID:25667603
The Botryosphaeriaceae: genera and species known from culture Phillips AJ, Alves A, Abdollahzadeh J, Slippers B, Wingfield MJ, Groenewald JZ, Crous PW Stud Mycol 30-Sep-2013
PMCID:PMC3825232
doi:10.3114/sim0021
PMID:24302790
Phylogeny and host-plant relationships of the Australian Myrtaceae leafmining moth genus Pectinivalva (Lepidoptera, Nepticulidae), with new subgenera and species Hoare RJ, van Nieukerken EJ Zookeys 15-Mar-2013
PMCID:PMC3677346
doi:10.3897/zookeys.278.4743
PMID:23794827
Stilbene glucosides isolated from Eucalyptus rubida, as repellents against the blue mussel Mytilus edulis. Hideo ETOH, Noriyuki YAMASHITA, Kanzo SAKATA, Hiroji INA, Kazuo INA Oxford University Press (OUP) 13-Jul-2011
doi:10.1271/BBB1961.54.2443
Patterns of hybridization and asymmetrical gene flow in hybrid zones of the rare Eucalyptus aggregata and common E. rubida Field DL, Ayre DJ, Whelan RJ, Young AG Heredity 10-Nov-2010
PMCID:PMC3186239
doi:10.1038/hdy.2010.127
PMID:21063438

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 / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-Allylphenol 68148 Click to see C=CCC1=CC=C(C=C1)O 134.17 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Catechols
4-Allylbenzene-1,2-diol 70775 Click to see C=CCC1=CC(=C(C=C1)O)O 150.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
[(1S,4aS,6S,7R,7aS)-6-acetyloxy-7-(acetyloxymethyl)-7-hydroxy-4-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate 14414526 Click to see CC(C)CC(=O)OC1C2C(CC(C2(COC(=O)C)O)OC(=O)C)C(=CO1)COC3C(C(C(C(O3)CO)O)O)O 562.60 unknown via CMAUP database
[(1S,4aS,7R,7aS)-7-(acetyloxymethyl)-7-hydroxy-4-[[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate 101316457 Click to see CC(C)CC(=O)OC1C2C(CCC2(COC(=O)C)O)C(=CO1)COC3C(C(C(C(O3)CO)O)O)O 504.50 unknown via CMAUP database
[(1S,4aS,7R,7aS)-7-(acetyloxymethyl)-7-hydroxy-4-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxymethyl]-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl] 3-methylbutanoate 101316456 Click to see CC(C)CC(=O)OC1C2C(CCC2(COC(=O)C)O)C(=CO1)COC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O 650.70 unknown via CMAUP database
Furcatoside A 101316455 Click to see CC(C)CC(=O)OC1C2C(CCC2(COC(=O)C)O)C(=CO1)COC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O 650.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin palmitate 10394654 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C 665.10 unknown via CMAUP database
beta-Amyrin acetate 92156 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown via CMAUP database
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 via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Butanedioate;hydron 21952380 Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-] 118.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2Z)-3-(4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoic acid 54036359 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown via CMAUP database
Furcatin 442789 Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 428.40 unknown via CMAUP database
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[3-hydroxy-5-[(E)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]oxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 14464366 Click to see COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O)O)O 566.60 unknown https://doi.org/10.1080/00021369.1989.10869710
https://doi.org/10.1080/00021369.1990.10870293
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[3-hydroxy-5-[(E)-2-(4-hydroxyphenyl)ethenyl]phenoxy]oxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 14731037 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O)O)O 536.50 unknown https://doi.org/10.1080/00021369.1990.10870293
[3,4,5-Trihydroxy-6-[3-hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 162950698 Click to see COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O)O)O 566.60 unknown https://doi.org/10.1080/00021369.1990.10870293
https://doi.org/10.1080/00021369.1989.10869710
[3,4,5-Trihydroxy-6-[3-hydroxy-5-[2-(4-hydroxyphenyl)ethenyl]phenoxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 163033249 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O)O)O 536.50 unknown https://doi.org/10.1080/00021369.1990.10870293
2-[3-Hydroxy-5-[2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 5062 Click to see COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 420.40 unknown https://doi.org/10.1080/00021369.1990.10870293
2-[3-Hydroxy-5-[2-(4-hydroxyphenyl)vinyl]phenoxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol 393787 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 390.40 unknown https://doi.org/10.1080/00021369.1990.10870293
Polydatin 5281718 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 390.40 unknown https://doi.org/10.1080/00021369.1990.10870293
https://doi.org/10.1271/BBB1961.54.2443
Rhapontin 637213 Click to see COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 420.40 unknown https://doi.org/10.1080/00021369.1990.10870293
https://doi.org/10.1271/BBB1961.54.2443

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