Eucalyptus resinifera, also known as red mahogany or red messmate, is a tall tree native to coastal areas of eastern Australia. It has rough, stringy bark, lance-shaped leaves, white flowers, and woody fruit. The tree is highly valued for its high-quality timber, which is used in various applications such as flooring, construction, and boat building. It is also a food source for koalas. The species has been exported to other countries for use in plantations. There are two recognized subspecies, differing in the length of the operculum. Red mahogany is found in coastal areas from New South Wales to Queensland, with some populations further north.

Synonyms Top

Scientific name	Authority	First published in
Melaleuca gummifera	Steud.	Nomencl. Bot. : 515 (1821)
Eucalyptus hemilampra	F.Muell.	J. Proc. Linn. Soc., Bot. 3: 85 (1858)
Eucalyptus resinifera var. grandiflora	Benth.	Fl. Austral. 3: 246 (1867)
Eucalyptus resinifera subsp. hemilampra	(F.Muell.) L.A.S.Johnson & K.D.Hill	Telopea 4: 46 (1990)
Eucalyptus resinifera var. hemilampra	(F.Muell.) Domin	Biblioth. Bot. 22(89): 468 (1928)

Common names Top

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Filter by language:

Language	Common/alternative name
English	red mahogany
English	redmahogany
Bulgarian	Червено махагоново дърво
Chinese	树胶桉

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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 click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
  - Uganda
- Northeast Tropical Africa
  - Eritrea
  - Ethiopia
- South Tropical Africa
  - Zimbabwe

Asia-tropical click to expand
- Indo-China
  - Andaman Islands
  - Nicobar Nicobar

Australasia click to expand
- Australia
  - New South Wales
  - Queensland

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

Pacific click to expand
- North-central Pacific
  - Hawaii

Southern America click to expand
- Caribbean
  - Cuba
  - Puerto Rico
  - Trinidad-Tobago

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000955779
USDA Plants	EURE2
Tropicos	22103328
INPN	97408
Flora of Italy	11858
KEW	urn:lsid:ipni.org:names:593305-1
The Plant List	kew-73786
Open Tree Of Life	3935754
NCBI Taxonomy	1711506
Nature Serve	2.140464
IUCN Red List	61915737
IPNI	593305-1
iNaturalist	162760
GBIF	3176649
Freebase	/m/07kdff9
EOL	633032
USDA GRIN	16011
Wikipedia	Eucalyptus_resinifera
CMAUP	NPO7418

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

Advances in Natural Product Extraction Techniques, Electrospun Fiber Fabrication, and the Integration of Experimental Design: A Comprehensive Review

Ponphaiboon J, Krongrawa W, Aung WW, Chinatangkul N, Limmatvapirat S, Limmatvapirat C

Molecules

02-Jul-2023

PMCID:	PMC10343563
doi:	10.3390/molecules28135163
PMID:	37446825

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

TRPV1 in dorsal root ganglion contributed to bone cancer pain

Chen W, Li H, Hao X, Liu C

Front Pain Res (Lausanne)

09-Nov-2022

PMCID:	PMC9682177
doi:	10.3389/fpain.2022.1022022
PMID:	36438444

Aboriginal medicinal plants of Queensland: ethnopharmacological uses, species diversity, and biodiscovery pathways

Turpin G, Ritmejerytė E, Jamie J, Crayn D, Wangchuk P

J Ethnobiol Ethnomed

10-Aug-2022

PMCID:	PMC9364609
doi:	10.1186/s13002-022-00552-6
PMID:	35948982

Evolutionary processes in an undescribed eucalypt: implications for the translocation of a critically endangered species

Rutherford S, Wilson TC, Yap JY, Lee E, Errington G, Rossetto M

Ann Bot

08-Jul-2022

PMCID:	PMC9510949
doi:	10.1093/aob/mcac091
PMID:	35802354

Fungal Planet description sheets: 1284–1382

Crous PW, Osieck ER, Jurjević Ž, Boers J, van Iperen AL, Starink-Willemse M, Dima B, Balashov S, Bulgakov TS, Johnston PR, Morozova OV, Pinruan U, Sommai S, Alvarado P, Decock CA, Lebel T, McMullan-Fisher S, Moreno G, Shivas RG, Zhao L, Abdollahzadeh J, Abrinbana M, Ageev DV, Akhmetova G, Alexandrova AV, Altés A, Amaral AG, Angelini C, Antonín V, Arenas F, Asselman P, Badali F, Baghela A, Bañares A, Barreto RW, Baseia IG, Bellanger JM, Berraf-Tebbal A, Biketova AY, Bukharova NV, Burgess TI, Cabero J, Câmara MP, Cano-Lira JF, Ceryngier P, Chávez R, Cowan DA, de Lima AF, Oliveira RL, Denman S, Dang QN, Dovana F, Duarte IG, Eichmeier A, Erhard A, Esteve-Raventós F, Fellin A, Ferisin G, Ferreira RJ, Ferrer A, Finy P, Gaya E, Geering AD, Gil-Durán C, Glässnerová K, Glushakova AM, Gramaje D, Guard FE, Guarnizo AL, Haelewaters D, Halling RE, Hill R, Hirooka Y, Hubka V, Iliushin VA, Ivanova DD, Ivanushkina NE, Jangsantear P, Justo A, Kachalkin AV, Kato S, Khamsuntorn P, Kirtsideli IY, Knapp DG, Kochkina GA, Koukol O, Kovács GM, Kruse J, Kumar TK, Kušan I, Læssøe T, Larsson E, Lebeuf R, Levicán G, Loizides M, Marinho P, Luangsa-ard JJ, Lukina EG, Magaña-Dueñas V, Maggs-Kölling G, Malysheva EF, Malysheva VF, Martín B, Martín MP, Matočec N, McTaggart AR, Mehrabi-Koushki M, Mešić A, Miller AN, Mironova P, Moreau PA, Morte A, Müller K, Nagy LG, Nanu S, Navarro-Ródenas A, Nel WJ, Nguyen TH, Nóbrega TF, Noordeloos ME, Olariaga I, Overton BE, Ozerskaya SM, Palani P, Pancorbo F, Papp V, Pawłowska J, Pham TQ, Phosri C, Popov ES, Portugal A, Pošta A, Reschke K, Reul M, Ricci GM, Rodríguez A, Romanowski J, Ruchikachorn N, Saar I, Safi A, Sakolrak B, Salzmann F, Sandoval-Denis M, Sangwichein E, Sanhueza L, Sato T, Sastoque A, Senn-Irlet B, Shibata A, Siepe K, Somrithipol S, Spetik M, Sridhar P, Stchigel AM, Stuskova K, Suwannasai N, Tan YP, Thangavel R, Tiago I, Tiwari S, Tkalčec Z, Tomashevskaya MA, Tonegawa C, Tran HX, Tran NT, Trovão J, Trubitsyn VE, Van Wyk J, Vieira WA, Vila J, Visagie CM, Vizzini A, Volobuev SV, Vu DT, Wangsawat N, Yaguchi T, Ercole E, Ferreira BW, de Souza AP, Vieira BS, Groenewald JZ

Persoonia

24-Dec-2021

PMCID:	PMC10784667
doi:	10.3767/persoonia.2023.47.06
PMID:	38352974

Fungal Planet description sheets: 1284–1382

Persoonia

24-Dec-2021

PMCID:	PMC10486635
doi:	10.3767/persoonia.2021.47.06
PMID:	37693795

Can Eucalyptol Replace Antibiotics?

Mączka W, Duda-Madej A, Górny A, Grabarczyk M, Wińska K

Molecules

14-Aug-2021

PMCID:	PMC8398027
doi:	10.3390/molecules26164933
PMID:	34443521

The Eucalyptus Cuticular Waxes Contribute in Preformed Defense Against Austropuccinia psidii

dos Santos IB, Lopes MD, Bini AP, Tschoeke BA, Verssani BA, Figueredo EF, Cataldi TR, Marques JP, Silva LD, Labate CA, Quecine MC

Front Plant Sci

09-Jan-2019

PMCID:	PMC6334236
doi:	10.3389/fpls.2018.01978
PMID:	30687371

Allelochaeta (Sporocadaceae): pigmentation lost and gained

Crous PW, Liu F, Cai L, Barber PA, Thangavel R, Summerell BA, Wingfield MJ, Edwards J, Carnegie AJ, Groenewald JZ

Fungal Syst Evol

10-Sep-2018

PMCID:	PMC7225576
doi:	10.3114/fuse.2018.02.08
PMID:	32467891

Targeting nociceptive transient receptor potential channels to treat chronic pain: current state of the field

Moran MM, Szallasi A

Br J Pharmacol

06-Nov-2017

PMCID:	PMC5980611
doi:	10.1111/bph.14044
PMID:	28924972

The relationship between climate change and the endangered rainforest shrub Triunia robusta (Proteaceae) endemic to southeast Queensland, Australia

Shimizu-Kimura Y, Accad A, Shapcott A

Sci Rep

19-Apr-2017

PMCID:	PMC5395822
doi:	10.1038/srep46399
PMID:	28422136

Medicinal Plants of the Australian Aboriginal Dharawal People Exhibiting Anti-Inflammatory Activity

Akhtar MA, Raju R, Beattie KD, Bodkin F, Münch G

Evid Based Complement Alternat Med

27-Dec-2016

PMCID:	PMC5223016
doi:	10.1155/2016/2935403
PMID:	28115968

Sensitivity of jarrah (Eucalyptus marginata) to phosphate, phosphite, and arsenate pulses as influenced by fungal symbiotic associations

Kariman K, Barker SJ, Jost R, Finnegan PM, Tibbett M

Mycorrhiza

26-Jan-2016

PMCID:	PMC4909810
doi:	10.1007/s00572-015-0674-z
PMID:	26810895

Long term repeated fire disturbance alters soil bacterial diversity but not the abundance in an Australian wet sclerophyll forest

Shen JP, Chen CR, Lewis T

Sci Rep

20-Jan-2016

PMCID:	PMC4726133
doi:	10.1038/srep19639
PMID:	26787458

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives
N-Formyl-4-hydroxybenzamide	71370414	Click to see C1=CC(=CC=C1C(=O)NC=O)O	165.15	unknown	via CMAUP database
N-Formylbenzamide	151196	Click to see C1=CC=C(C=C1)C(=O)NC=O	149.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
4-Hydroxybenzamide	65052	Click to see C1=CC(=CC=C1C(=O)N)O	137.14	unknown	via CMAUP database
Benzamide, N-[(2S)-2-hydroxy-2-phenylethyl]-	6542363	Click to see C1=CC=C(C=C1)C(CNC(=O)C2=CC=CC=C2)O	241.28	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Cyclobutane lignans
[(1R,2R,3S,4S)-2-(2,4-dihydroxybenzoyl)-3,4-diphenylcyclobutyl]-(2,4-dihydroxyphenyl)methanone	102228233	Click to see C1=CC=C(C=C1)C2C(C(C2C(=O)C3=C(C=C(C=C3)O)O)C(=O)C4=C(C=C(C=C4)O)O)C5=CC=CC=C5	480.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R,22R)-10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-ene-11,22-diol	44253988	Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6O)C)C)C)C)(C)CO)O	472.70	unknown	via CMAUP database
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R,22R)-10-(hydroxymethyl)-22-methoxy-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-11-ol	44253989	Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6OC)C)C)C)C)(C)CO)O	486.70	unknown	via CMAUP database
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R)-11-hydroxy-10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-22-one	102482971	Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6=O)C)C)C)C)(C)CO)O	470.70	unknown	via CMAUP database
(2R,4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bR)-10-hydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylic acid	21594159	Click to see CC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)(C)C(=O)O	472.70	unknown	via CMAUP database
(2R,4aS,6aR,6aS,6bR,8aR,9S,12aR,14bR)-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-2-carboxylic acid	44253990	Click to see CC12CCC(CC1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)CO)C)(C)C(=O)O	470.70	unknown	via CMAUP database
(3S,4S,4aR,6aR,6bS,8aR,9R,11R,12aS,14aR,14bR)-4,11-bis(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,9-diol	14335966	Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC(CC5O)(C)CO)C)C)C)(C)CO)O	474.70	unknown	via CMAUP database
24-Hydroxy-beta-amyrin	14167253	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C)C	442.70	unknown	via CMAUP database
Melilotigenin B	91895471	Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)C)C	454.70	unknown	via CMAUP database
Melilotigenin C	10551785	Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)C)C	456.70	unknown	via CMAUP database
Soyasapogenol B	115012	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C	458.70	unknown	via CMAUP database
Soyasapogenol E	13632872	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)O)C)C	456.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans
Oxytropisoflavan B	46918734	Click to see COC1=C(C(=C(C=C1)C2CC3(CCC(=O)C=C3OC2)O)O)OC	320.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Benzoylindoles
(3-Hydroxyindol-1-yl)-(3-hydroxyphenyl)methanone	46850207	Click to see C1=CC=C2C(=C1)C(=CN2C(=O)C3=CC(=CC=C3)O)O	253.25	unknown	via CMAUP database
(3-Hydroxyindol-1-yl)-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]methanone	46850206	Click to see CC(=CCC1=C(C=CC(=C1)C(=O)N2C=C(C3=CC=CC=C32)O)O)C	321.40	unknown	via CMAUP database
(3-Hydroxyindol-1-yl)-phenylmethanone	46850030	Click to see C1=CC=C(C=C1)C(=O)N2C=C(C3=CC=CC=C32)O	237.25	unknown	via CMAUP database
(4-Hydroxy-3-methoxyindol-1-yl)-(4-hydroxyphenyl)methanone	46850205	Click to see COC1=CN(C2=C1C(=CC=C2)O)C(=O)C3=CC=C(C=C3)O	283.28	unknown	via CMAUP database
(4-Hydroxyphenyl)-(3-methoxyindol-1-yl)methanone	46850032	Click to see COC1=CN(C2=CC=CC=C21)C(=O)C3=CC=C(C=C3)O	267.28	unknown	via CMAUP database
Oxytrofalcatin B	46850031	Click to see C1=CC=C2C(=C1)C(=CN2C(=O)C3=CC=C(C=C3)O)O	253.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone	688857	Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3	240.25	unknown	via CMAUP database
Liquiritigenin	114829	Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O	256.25	unknown	via CMAUP database
Pinocembrin	68071	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
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
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin	5281654	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	316.26	unknown	via CMAUP database
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	via CMAUP database
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (4R)-4-(2-hydroxypropan-2-yl)cyclohexene-1-carboxylate	162849270	Click to see CC(C)(C1CCC(=CC1)C(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O	614.60	unknown	https://doi.org/10.1271/BBB.56.138
[(2R,3R,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 4-(2-hydroxypropan-2-yl)cyclohexene-1-carboxylate	101618995	Click to see CC(C)(C1CCC(=CC1)C(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O	614.60	unknown	https://doi.org/10.1271/BBB.56.138
[(2R,3S,4R,5S,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (4R)-4-(2-hydroxypropan-2-yl)cyclohexene-1-carboxylate	154497787	Click to see CC(C)(C1CCC(=CC1)C(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O	614.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.004
[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (4R)-4-(2-hydroxypropan-2-yl)cyclohexene-1-carboxylate	162849268	Click to see CC(C)(C1CCC(=CC1)C(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O	614.60	unknown	https://doi.org/10.1271/BBB.56.138
[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 4-(2-hydroxypropan-2-yl)cyclohexene-1-carboxylate	15172373	Click to see CC(C)(C1CCC(=CC1)C(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O	614.60	unknown	https://doi.org/10.1271/BBB.56.138
[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 4-(2-hydroxypropan-2-yl)cyclohexene-1-carboxylate	162849266	Click to see CC(C)(C1CCC(=CC1)C(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O	614.60	unknown	https://doi.org/10.1271/BBB.56.138
3-[(2S,3R,4S,5R,6R)-4,5-Dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one	10919701	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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O	740.70	unknown	via CMAUP database
3-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one	60200223	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)O)O)O)O)O	608.50	unknown	via CMAUP database
3-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one	10865825	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)COC6C(C(C(C(O6)C)O)OC7C(C(C(CO7)O)O)O)O)O)O)O)O)O	872.80	unknown	via CMAUP database
3-[6-O-(3-O-beta-D-Xylopyranosyl-alpha-L-rhamnopyranosyl)-beta-D-galactopyranosyloxy]-4',5,7-trihydroxyflavone	21668680	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)OC6C(C(C(CO6)O)O)O)O	726.60	unknown	via CMAUP database
Biorobin	15944778	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	594.50	unknown	via CMAUP database
Oxytroflavoside A	60200065	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)COC(=O)CC(C)(CC(=O)O)O)O)O)O)O)O	752.70	unknown	via CMAUP database
Oxytroflavoside B	60200066	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)O)OC(=O)CC(C)(CC(=O)O)O)O)O)O	752.70	unknown	via CMAUP database
Oxytroflavoside C	60200220	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)OC(=O)CC(C)(CC(=O)O)O)O)O)O)O	752.70	unknown	via CMAUP database
Oxytroflavoside D	60200221	Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC)C4=CC=C(C=C4)O)O)O)O)O	606.50	unknown	via CMAUP database
Oxytroflavoside E	60200222	Click to see CC(CC(=O)O)(CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC)C4=CC=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O	768.70	unknown	via CMAUP database
Oxytroflavoside G	60200370	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O	754.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 3-O-[alpha-L-rhamnopyranosyl(1->2)-beta-D-galactopyranosyl]-7-O-alpha-L-rhamnopyranoside	57397583	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)CO)O)O)O)O)O	740.70	unknown	via CMAUP database
Robinin	5281693	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)C)O)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O	740.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-2-(4-hydroxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one	14157884	Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=C(C=C3)O	270.28	unknown	via CMAUP database
(R,S)-7-Methoxy-2-phenyl-chroman-4-one	688883	Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=CC=C3	254.28	unknown	via CMAUP database
5-Hydroxy-7-methoxy-2-phenylchroman-4-one	73201	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O	270.28	unknown	via CMAUP database
Sakuranetin	73571	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O	286.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one	26088035	Click to see C1C(C(=O)C2=C(O1)C=C(C=C2)O)CC3=CC=C(C=C3)O	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(6aR)-9,10-Dimethoxy-6aalpha,11aalpha-dihydro-6H-benzofuro[3,2-c][1]benzopyran-3,8-diol	46918735	Click to see COC1=C(C=C2C3COC4=C(C3OC2=C1OC)C=CC(=C4)O)O	316.30	unknown	via CMAUP database
(l)-Edunol	182148	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=CC5=C(C=C34)OCO5)C	352.40	unknown	via CMAUP database
Maackiain	91510	Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein	5281708	Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O	254.24	unknown	via CMAUP database
Pseudobaptigenin	5281805	Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)O	282.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavanquinones
5-[(3R)-7-hydroxy-3,4-dihydro-2H-chromen-3-yl]-2,3-dimethoxycyclohexa-2,5-diene-1,4-dione	10403457	Click to see COC1=C(C(=O)C(=CC1=O)C2CC3=C(C=C(C=C3)O)OC2)OC	316.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Daidzein-4'-glucoside	49862229	Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)OC4C(C(C(C(O4)CO)O)O)O	416.40	unknown	via CMAUP database
Sophoricoside	5321398	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)OC4C(C(C(C(O4)CO)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-Methoxydaidzein	5319422	Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(R)-Isomucronulatol	10380176	Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O)OC	302.32	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
(3R)-2',3',7-trihydroxy-4'-methoxyisoflavan	15939757	Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O)O	288.29	unknown	via CMAUP database
2H-1-Benzopyran-7-ol, 3,4-dihydro-3-(3-hydroxy-2,4-dimethoxyphenyl)-, (3R)-	13873811	Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)OC)O	302.32	unknown	via CMAUP database
Calycosin	5280448	Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2'-Hydroxybiochanin A	5282075	Click to see COC1=CC(=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O	300.26	unknown	via CMAUP database
Formononetin	5280378	Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Isoformononetin	3764	Click to see COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=C(C=C3)O	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',4'-Dihydroxydihydrochalcone	586491	Click to see C1=CC=C(C=C1)CCC(=O)C2=C(C=C(C=C2)O)O	242.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2-Hydroxy-4-methoxyphenyl)-3-phenylprop-2-en-1-one	265720	Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=CC=C2)O	254.28	unknown	via CMAUP database
1-(2,4-Dihydroxyphenyl)-3-phenylprop-2-en-1-one	344530	Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O	240.25	unknown	via CMAUP database
2-Propen-1-one, 1-(2-hydroxy-4-methoxyphenyl)-3-(4-hydroxyphenyl)-	592216	Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O	270.28	unknown	via CMAUP database
2',4'-Dihydroxychalcone	5376979	Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O	240.25	unknown	via CMAUP database
Acrylophenone, 2',4'-dihydroxy-3-(p-methoxyphenyl)-	166795	Click to see COC1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O	270.28	unknown	via CMAUP database
GU17;ISL;Isoliquiritigen	425	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O	256.25	unknown	via CMAUP database
Trihydroxychalcone	638278	Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O	256.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
2',4',4-Trihydroxy-3'-prenylchalcone	193568	Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C	324.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
1-(4-Hydroxy-2-methoxyphenyl)-3-phenylprop-2-en-1-one	71442332	Click to see COC1=C(C=CC(=C1)O)C(=O)C=CC2=CC=CC=C2	254.28	unknown	via CMAUP database

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Eucalyptus resinifera

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