Eucalyptus viminalis, also known as the manna gum, white gum, or ribbon gum, is a tree species native to south-eastern Australia. It can grow up to 50 meters tall and has smooth, white to pale brown bark that sheds in long ribbons. The leaves are lance-shaped and the flowers are white. There are several subspecies of Eucalyptus viminalis, each with unique characteristics and distributions. Indigenous Australians used the wood of this tree to make shields and bowls, and the bark produces a sweet, white substance known as manna. The exact source of this substance is still debated among scientists.

Synonyms Top

No known synonyms.

Common names Top

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Filter by language:

Language	Common/alternative name
English	manna gum
English	white gum
English	ribbon gum
Azerbaijani	Çubuqvari evkalipt
Welsh	ewcalyptws gwialennog
German	rutenförmiger eukalyptus
Galician	eucalipto do maná
Hebrew	אקליפטוס המוט
Japanese	ビミナリスユーカリ
Japanese	リボンガム
Lithuanian	vytelinis eukaliptas
Dutch	suikereucalyptus
Russian	Эвкалипт прутовидный
Ukrainian	Евкаліпт прутовидний
Chinese	多枝桉
Chinese	多枝桉樹

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Eucalyptus viminalis subsp. hentyensis	Brooker & Slee	J. Adelaide Bot. Gard. 21: 92 (2007)
Eucalyptus viminalis subsp. pryoriana	(L.A.S.Johnson) Brooker & Slee	Muelleria 9: 80 (1996)
Eucalyptus viminalis subsp. siliceana	Rule	Muelleria 29: 5 (2011)
Eucalyptus viminalis subsp. viminalis	Labill.	-

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
- Middle Atlantic Ocean
  - Saint Helena

Asia-temperate click to expand
- Caucasus
  - Transcaucasus

Australasia click to expand
- Australia
  - New South Wales
  - Queensland
  - South Australia
  - Tasmania
  - Victoria
- New Zealand
  - New Zealand North
  - New Zealand South

Europe click to expand
- Southeastern Europe
  - Italy
  - Sicilia
- Southwestern Europe
  - France
  - Portugal
  - Spain

Northern America click to expand
- Southwestern U.S.A.
  - California

Pacific click to expand
- North-central Pacific
  - Hawaii

Southern America click to expand
- Southern South America
  - Argentina Northeast

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000956115
UNII	UQI6S3HZ8R
USDA Plants	EUVI
Tropicos	22103168
INPN	97411
KEW	urn:lsid:ipni.org:names:593454-1
The Plant List	kew-74103
Open Tree Of Life	566581
Observations.org	149927
NCBI Taxonomy	155764
NBN Atlas	NHMSYS0000458622
Nature Serve	2.135438
IUCN Red List	133377586
IPNI	593454-1
iNaturalist	77093
GBIF	3177112
Freebase	/m/084knk
EPPO	EUCVI
EOL	245551
Elurikkus	209744
Calflora (Californian flora)	3539
USDA GRIN	16104
Wikipedia	Eucalyptus_viminalis
CMAUP	NPO28778
PaleoBotany	51655

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
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_014182385.1	ASM1418238v1	Chromosome	Australian National University	2020-08-14	29.0x	532.82 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

Eucalypt Extracts Prepared by a No-Waste Method and Their 3D-Printed Dosage Forms Show Antimicrobial and Anti-Inflammatory Activity

Koshovyi O, Komisarenko M, Osolodchenko T, Komissarenko A, Mändar R, Kõljalg S, Heinämäki J, Raal A

Plants (Basel)

07-Mar-2024

PMCID:	PMC10976152
doi:	10.3390/plants13060754
PMID:	38592748

Gut Microbiome Profiling of the Endangered Southern Greater Glider (Petauroides volans) after the 2019–2020 Australian Megafire

Clough J, Schwab S, Mikac K

Animals (Basel)

20-Nov-2023

PMCID:	PMC10668662
doi:	10.3390/ani13223583
PMID:	38003202

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

Climate, host and geography shape insect and fungal communities of trees

Franić I, Allan E, Prospero S, Adamson K, Attorre F, Auger-Rozenberg MA, Augustin S, Avtzis D, Baert W, Barta M, Bauters K, Bellahirech A, Boroń P, Bragança H, Brestovanská T, Brurberg MB, Burgess T, Burokienė D, Cleary M, Corley J, Coyle DR, Csóka G, Černý K, Davydenko K, de Groot M, Diez JJ, Doğmuş Lehtijärvi HT, Drenkhan R, Edwards J, Elsafy M, Eötvös CB, Falko R, Fan J, Feddern N, Fürjes-Mikó Á, Gossner MM, Grad B, Hartmann M, Havrdova L, Kádasi Horáková M, Hrabětová M, Justesen MJ, Kacprzyk M, Kenis M, Kirichenko N, Kovač M, Kramarets V, Lacković N, Lantschner MV, Lazarević J, Leskiv M, Li H, Madsen CL, Malumphy C, Matošević D, Matsiakh I, May TW, Meffert J, Migliorini D, Nikolov C, O’Hanlon R, Oskay F, Paap T, Parpan T, Piškur B, Ravn HP, Richard J, Ronse A, Roques A, Ruffner B, Santini A, Sivickis K, Soliani C, Talgø V, Tomoshevich M, Uimari A, Ulyshen M, Vettraino AM, Villari C, Wang Y, Witzell J, Zlatković M, Eschen R

Sci Rep

18-Jul-2023

PMCID:	PMC10354058
doi:	10.1038/s41598-023-36795-w
PMID:	37463904

From the Bush to the Brain: Preclinical Stages of Ethnobotanical Anti-Inflammatory and Neuroprotective Drug Discovery—An Australian Example

Kumar P, Mathew S, Gamage R, Bodkin F, Doyle K, Rossetti I, Wagnon I, Zhou X, Raju R, Gyengesi E, Münch G

Int J Mol Sci

04-Jul-2023

PMCID:	PMC10342267
doi:	10.3390/ijms241311086
PMID:	37446262

Using conservation genetics to prioritise management options for an endangered songbird

Alves F, Banks SC, Edworthy M, Stojanovic D, Langmore NE, Heinsohn R

Heredity (Edinb)

05-Apr-2023

PMCID:	PMC10162965
doi:	10.1038/s41437-023-00609-6
PMID:	37016134

Growth-stimulating and antioxidant effects of vanillic acid on healthy broiler chickens

Duskaev G, Kurilkina M, Zavyalov O

Vet World

21-Mar-2023

PMCID:	PMC10082733
doi:	10.14202/vetworld.2023.518-525
PMID:	37041822

The koala gut microbiome is largely unaffected by host translocation but rather influences host diet

Blyton MD, Pascoe J, Hynes E, Soo RM, Hugenholtz P, Moore BD

Front Microbiol

02-Mar-2023

PMCID:	PMC10018171
doi:	10.3389/fmicb.2023.1085090
PMID:	36937253

Thermal Profiles of Chainsaw Hollows and Natural Hollows during Extreme Heat Events

Callan MN, Krix D, McLean CM, Murray BR, Webb JK

Biology (Basel)

24-Feb-2023

PMCID:	PMC10045291
doi:	10.3390/biology12030361
PMID:	36979053

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

Deadly acceleration in dehydration of Eucalyptus viminalis leaves coincides with high-order vein cavitation

Tonet V, Carins-Murphy M, Deans R, Brodribb TJ

Plant Physiol

24-Jan-2023

PMCID:	PMC10022613
doi:	10.1093/plphys/kiad016
PMID:	36690460

Individuality and stability of the koala (Phascolarctos cinereus) faecal microbiota through time

Eisenhofer R, Brice KL, Blyton MD, Bevins SE, Leigh K, Singh BK, Helgen KM, Hough I, Daniels CB, Speight N, Moore BD

PeerJ

23-Jan-2023

PMCID:	PMC9879153
doi:	10.7717/peerj.14598
PMID:	36710873

Effect of feeding bioactive compounds identified from plant extracts (4-hexylresorcinol, 7-hydroxycoumarin, and gamma-octalactone) on the productivity and quality of broiler meat

Zavyalov O, Galimzhan D, Marina K

Vet World

30-Dec-2022

PMCID:	PMC9880825
doi:	10.14202/vetworld.2022.2986-2996
PMID:	36718328

Chemical Composition, Phytotoxic and Antibiofilm Activity of Seven Eucalyptus Species from Tunisia

Khedhri S, Polito F, Caputo L, Manna F, Khammassi M, Hamrouni L, Amri I, Nazzaro F, De Feo V, Fratianni F

Molecules

25-Nov-2022

PMCID:	PMC9738237
doi:	10.3390/molecules27238227
PMID:	36500316

Exploring Contact Toxicity of Essential Oils against Sitophilus zeamais through a Meta-Analysis Approach

Achimón F, Peschiutta ML, Brito VD, Beato M, Pizzolitto RP, Zygadlo JA, Zunino MP

Plants (Basel)

13-Nov-2022

PMCID:	PMC9696113
doi:	10.3390/plants11223070
PMID:	36432799

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Undecane	14257	Click to see CCCCCCCCCCC	156.31	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid	445639	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,4bR,7R,9R,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-9-ol	13966170	Click to see CC1(CCC2C(=C1)C(CC3C2(CCCC3(C)CO)C)O)C=C	304.50	unknown	via CMAUP database
(1R,4aS,4bS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	11870275	Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C	302.50	unknown	via CMAUP database
18-Nordehydroabiet-4(19)-ene	44268166	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(=C)C3CC2)C	254.40	unknown	via CMAUP database
7-Dehydroabietanone	11289118	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)C)C	284.40	unknown	via CMAUP database
7-Oxodehydroabietinol	15715176	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)CO)C	300.40	unknown	via CMAUP database
Abieta-8,11,13-trien-15-ol	101586702	Click to see CC1(CCCC2(C1CCC3=C2C=CC(=C3)C(C)(C)O)C)C	286.50	unknown	via CMAUP database
Abieta-8,11,13-trien-7alpha-ol	21764434	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C)C	286.50	unknown	via CMAUP database
Abietatriene	6432211	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C)C	270.50	unknown	via CMAUP database
Anticopalic acid	11808890	Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C)C	304.50	unknown	via CMAUP database
Anticopalic acid methyl ester	11290126	Click to see CC(=CC(=O)OC)CCC1C(=C)CCC2C1(CCCC2(C)C)C	318.50	unknown	via CMAUP database
Ethyl abietate	61182	Click to see CCOC(=O)C1(CCCC2(C1CC=C3C2CCC(=C3)C(C)C)C)C	330.50	unknown	via CMAUP database
Isopimara-7,15-diene	13969536	Click to see CC1(CCCC2(C1CC=C3C2CCC(C3)(C)C=C)C)C	272.50	unknown	via CMAUP database
Pimarol	12314285	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C	288.50	unknown	via CMAUP database
Sandaracopimaradiene	443469	Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C=C)C)C	272.50	unknown	via CMAUP database
Sandaracopimarinol	12314286	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C	288.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	via CMAUP database
(+)-3-Carene	443156	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	via CMAUP database
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
Borneol, (-)-	1201518	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene	443161	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	via CMAUP database
(+)-beta-Phellandrene	442484	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	via CMAUP database
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene	1796220	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	via CMAUP database
delta-Cadinol	3084311	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
5-[(1S)-1-[(1aR,4R,4aR,7R,7aR,7bR)-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	101619916	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)O)C	472.60	unknown	https://doi.org/10.1007/BF00629928
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(24S)-Lanosta-9(11)-ene-3beta,24,25-triol	101121169	Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C	460.70	unknown	via CMAUP database
16-Oxo-21-episerratenediol	101280208	Click to see CC1(C2CCC3(CC4=CC(=O)C5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C	456.70	unknown	via CMAUP database
2,3-Dihydroxyolean-12-en-28-oic acid	3694932	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/10.1007/BF00579992
21-Episerratenediol	12309682	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C	442.70	unknown	via CMAUP database
21-Episerratenediol 3-methyl ether	101280203	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)O)(C)C)C)C	456.70	unknown	via CMAUP database
3beta-Methoxy-21-oxoserratene	14830066	Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1OC)C)C)(C)C)C)C	454.70	unknown	via CMAUP database
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/10.1007/BF00579992
Serratenediol 3-methyl ether	21672660	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)O)(C)C)C)C	456.70	unknown	via CMAUP database
Serratenediol dimethyl ether	101280202	Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1OC)C)C)OC)(C)C)C)C	470.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesta-4,6-dien-3-one	3034666	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2C=CC4=CC(=O)CCC34C)C	382.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one	12943207	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C=CC4=CC(=O)CCC34C)C)C(C)C	410.70	unknown	via CMAUP database
Stigmast-4-en-3-one	5484202	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	via CMAUP database
Stigmasta-3,5-dien-7-one	12444466	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC=C4)C)C)C(C)C	410.70	unknown	via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Alpha-keto acids and derivatives
2-(4-Methoxycyclohexa-1,3-dien-1-yl)-2-oxoacetic acid	29927927	Click to see COC1=CC=C(CC1)C(=O)C(=O)O	182.17	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D-Galactose	6036	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	via CMAUP database
D-Glucose	5793	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
(2S,3R,4R)-2,3,4,5-tetrahydroxypentanal	66308	Click to see C(C(C(C(C=O)O)O)O)O	150.13	unknown	via CMAUP database
L-ribopyranose	11008084	Click to see C1C(C(C(C(O1)O)O)O)O	150.13	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Benzofuranones
Catalpalactone	3014018	Click to see CC1(CC=C(C(=O)O1)C2C3=CC=CC=C3C(=O)O2)C	258.27	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
13-Vinyl-16,17-dinor-14-oxaabietane	102594798	Click to see CC1(CCCC2(C1CCC3C2CCC(O3)(C)C=C)C)C	276.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin	323	Click to see C1=CC=C2C(=C1)C=CC(=O)O2	146.14	unknown	https://doi.org/10.1007/S10600-009-9388-9
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-Methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	346340	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	354.31	unknown	https://doi.org/10.1007/S10600-009-9388-9
7-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	320361	Click to see C1=CC(=CC2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	324.28	unknown	https://doi.org/10.1007/S10600-009-9388-9
Scopolin	439514	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	354.31	unknown	https://doi.org/10.1007/S10600-009-9388-9
Skimmin	99693	Click to see C1=CC(=CC2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	324.28	unknown	https://doi.org/10.1007/S10600-009-9388-9
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
6-Hydroxy-7-methoxy-3-(2-oxochromen-7-yl)oxychromen-2-one	162890509	Click to see COC1=C(C=C2C=C(C(=O)OC2=C1)OC3=CC4=C(C=C3)C=CC(=O)O4)O	352.30	unknown	https://doi.org/10.1007/S10600-009-9388-9
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	https://doi.org/10.1007/S10600-009-9388-9
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	https://doi.org/10.1007/S10600-009-9388-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-Dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone	6453244	Click to see CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3	270.28	unknown	via CMAUP database
Strobopinin	442520	Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin	5281607	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	254.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one	5353915	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1007/BF00565364
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	54579866	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1007/BF00565364
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-chromen-4-one	15939939	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1007/BF00565364
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5378597	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1007/BF00565364
Isoquercitin	10813969	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1007/BF00565364
Vitamin P	5293655	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1007/BF00565364
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin	5281954	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Pinosylvin methyl ether	5281719	Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2	226.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate	4628122	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O	332.26	unknown	https://doi.org/10.1016/S0367-326X(00)00252-5
1,2,3,6-Tetragalloyl-beta-D-glucopyranose	5153644	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(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)O	788.60	unknown	https://doi.org/10.1016/S0367-326X(00)00252-5
1,2,4,6-Tetragalloyl-beta-D-glucopyranose	14464350	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O	788.60	unknown	https://doi.org/10.1016/S0367-326X(00)00252-5
1,2,4,6-Tetragalloylglucose	11297287	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O	788.60	unknown	https://doi.org/10.1016/S0367-326X(00)00252-5
2,3,4,6-Tetragalloyl-D-glucopyranose	13888121	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(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(=C5)O)O)O	788.60	unknown	https://doi.org/10.1016/S0367-326X(00)00252-5
2,3,4,6-Tetragalloylglucose	13888120	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(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(=C5)O)O)O	788.60	unknown	https://doi.org/10.1016/S0367-326X(00)00252-5
beta-Glucogallin	124021	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O	332.26	unknown	https://doi.org/10.1016/S0367-326X(00)00252-5
NP-003686	73178	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(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)O	788.60	unknown	https://doi.org/10.1016/S0367-326X(00)00252-5
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(1S,11R,12S,13S,14R)-4,5,12,13,14-pentahydroxy-2,9,15-trioxatricyclo[9.3.1.13,7]hexadeca-3(16),4,6-trien-8-one	162861374	Click to see C1C2C(C(C(C(O2)OC3=CC(=CC(=C3O)O)C(=O)O1)O)O)O	314.24	unknown	https://doi.org/10.1016/S0367-326X(00)00252-5
(3,4,5,11,13,21,22,23-Octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl) 3,4,5-trihydroxybenzoate	323958	Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1016/S0367-326X(00)00252-5
[(10S,11S,12R,13S,15R)-3,4,5,11,13,21,22,23-octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 3,4,5-trihydroxybenzoate	10461724	Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1016/S0367-326X(00)00252-5
[(11R,12S,14R,15R,37R,38R,40R,57R,58S,64S)-4,5,6,12,20,21,22,25,26,30,31,32,38,46,47,48,51,52-octadecahydroxy-9,17,35,43,55,61-hexaoxo-64-(3,4,5-trihydroxybenzoyl)oxy-2,10,13,16,28,36,39,42,56,62-decaoxaundecacyclo[35.15.6.514,27.111,15.03,8.018,23.029,34.040,57.044,49.050,54.024,60]tetrahexaconta-1(52),3,5,7,18,20,22,24,26,29,31,33,44,46,48,50,53,59-octadecaen-58-yl] 3,4,5-trihydroxybenzoate	16135666	Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC7C(C(C(C(O7)O)OC(=O)C8=CC(=C(C(=C8OC9=C(C(=C(C(=C9)C(=O)O3)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C16)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O	1569.10	unknown	https://doi.org/10.1016/S0367-326X(00)00252-5
[(1S,2R)-1-[(11R)-3,4,5,11,17,18,19-heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-3-oxo-1-(3,4,5-trihydroxybenzoyl)oxypropan-2-yl] 3,4,5-trihydroxybenzoate	50990002	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)C(C(C=O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O	786.60	unknown	via CMAUP database
[(1S,2S,19R,20S,22R)-7,8,9,12,13,14,28,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-20-yl] 3,4,5-trihydroxybenzoate	50990634	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	via CMAUP database
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 2-[[3,4,5,12,22,23-hexahydroxy-8,18-dioxo-11,13-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]-3,4,5-trihydroxybenzoate	16174339	Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C(C(C(O6)OC(=O)C7=CC(=C(C(=C7)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C95)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1571.10	unknown	https://doi.org/10.1016/S0367-326X(00)00252-5
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-12-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate	5153915	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/10.1016/S0367-326X(00)00252-5
1-Desgalloyleugeniin	9918701	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/10.1016/S0367-326X(00)00252-5
4,5,12,13,14-Pentahydroxy-2,9,15-trioxatricyclo[9.3.1.13,7]hexadeca-3(16),4,6-trien-8-one	162861373	Click to see C1C2C(C(C(C(O2)OC3=CC(=CC(=C3O)O)C(=O)O1)O)O)O	314.24	unknown	https://doi.org/10.1016/S0367-326X(00)00252-5
7,8,9,12,13,14,20,28,29,30,33,34,35-Tridecahydroxy-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaene-4,17,25,38-tetrone	492391	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/10.1016/S0367-326X(00)00252-5
alpha-Pedunculagin	13834142	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/10.1016/S0367-326X(00)00252-5
Casuariin	14035442	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)O	784.50	unknown	via CMAUP database
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/10.1016/S0367-326X(00)00252-5
CID 13834145	13834145	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	via CMAUP database
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/10.1016/S0367-326X(00)00252-5
Oenothein B	16129800	Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC7C(C(C(C(O7)O)OC(=O)C8=CC(=C(C(=C8OC9=C(C(=C(C(=C9)C(=O)O3)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C16)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O	1569.10	unknown	https://doi.org/10.1016/S0367-326X(00)00252-5
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/10.1016/S0367-326X(00)00252-5
Tellimagrandin I	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/10.1016/S0367-326X(00)00252-5
Tellimagrandin II	151590	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/10.1016/S0367-326X(00)00252-5

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Eucalyptus viminalis

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