Melaleuca ericifolia, also known as swamp paperbark, is a plant in the myrtle family native to south-eastern Australia. It is a tall shrub with papery bark and dark green, linear leaves. Creamy-white flowers appear in October and November, followed by woody capsules. This species is similar to Melaleuca armillaris and Melaleuca pustulata, but can be distinguished by its bark and flower heads. It grows in swampy areas and has been affected by land clearance in some regions. The plant has traditional uses for Aboriginal people, and is also popular in horticulture for its hardiness and fast growth. Its leaves contain essential oils that have been used in dental and medical preparations. The foliage has also been used for fencing and nesting sites for birds.

Synonyms Top

Scientific name	Authority	First published in
Melaleuca axillaris	hort. ex Steud.	Nomencl. Bot. , ed. 2, 2: 111 (1841)
Melaleuca gunniana	Schauer	Repert. Bot. Syst. 2: 928 (1843)
Melaleuca gunniana var. capitata	Miq.	Ned. Kruidk. Arch. 4: 120 (1856)
Melaleuca heliophila	F.Muell. ex Miq.	Ned. Kruidk. Arch. 4: 120 (1856)
Melaleuca pinifolia	hort. ex Colla	Hortus Ripul. , App. 2: 352 (1825)
Melaleuca ternifolia	F.Muell. ex Miq.	Ned. Kruidk. Arch. 4: 123 (1856)
Myrtoleucodendron ericifolium	Kuntze	Revis. Gen. Pl. 1: 241 (1891)
Cajuputi ericifolia	(Sm.) A.Lyons	Pl. Nam. : 74 (1900)

Common names Top

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Filter by language:

Language	Common/alternative name
English	swamp paperbark
Arabic	ملالوكا خلنجية الأوراق
Arabic	بلقاء خلنجية الأوراق
Japanese	ラベンダーティーツリー

Subspecies (abbr. subsp./ssp.) Top

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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

Australasia click to expand
- Australia
  - New South Wales
  - Tasmania
  - Victoria

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000239561
UNII	57NLQ49A85
USDA Plants	MEER4
Tropicos	22102195
KEW	urn:lsid:ipni.org:names:597937-1
The Plant List	kew-123631
Open Tree Of Life	81283
NCBI Taxonomy	73757
IUCN Red List	177374613
IPNI	597937-1
iNaturalist	323834
GBIF	5415723
Freebase	/m/07s38qz
EPPO	MLAER
USDA GRIN	23789
Wikipedia	Melaleuca_ericifolia

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

Heterogeneous Antibiotic Resistance Gene Removal Impedes Evaluation of Constructed Wetlands for Effective Greywater Treatment

Itzhari D, Shuai W, Hartmann EM, Ronen Z

Antibiotics (Basel)

29-Mar-2024

PMCID:	PMC11047525
doi:	10.3390/antibiotics13040315
PMID:	38666991

Exploring the Antimicrobial Properties of 99 Natural Flavour and Fragrance Raw Materials against Pathogenic Bacteria: A Comparative Study with Antibiotics

Bacińska Z, Baberowska K, Surowiak AK, Balcerzak L, Strub DJ

Plants (Basel)

06-Nov-2023

PMCID:	PMC10648197
doi:	10.3390/plants12213777
PMID:	37960133

The Legacy of Plant Invasion: Impacts on Soil Nitrification and Management Implications

Afzal MR, Naz M, Ashraf W, Du D

Plants (Basel)

18-Aug-2023

PMCID:	PMC10458916
doi:	10.3390/plants12162980
PMID:	37631191

Appendage-Bearing Sordariomycetes from Dipterocarpus alatus Leaf Litter in Thailand

Samaradiwakara NP, de Farias AR, Tennakoon DS, Aluthmuhandiram JV, Bhunjun CS, Chethana KW, Kumla J, Lumyong S

J Fungi (Basel)

29-May-2023

PMCID:	PMC10299658
doi:	10.3390/jof9060625
PMID:	37367561

Antiviral Potentialities of Chemical Characterized Essential Oils of Acacia nilotica Bark and Fruits against Hepatitis A and Herpes Simplex Viruses: In Vitro, In Silico, and Molecular Dynamics Studies

El Gendy AE, Essa AF, El-Rashedy AA, Elgamal AM, Khalaf DD, Hassan EM, Abd-ElGawad AM, Elgorban AM, Zaghloul NS, Alamery SF, Elshamy AI

Plants (Basel)

28-Oct-2022

PMCID:	PMC9656187
doi:	10.3390/plants11212889
PMID:	36365342

Diversity of Sporocadaceae (pestalotioid fungi) from Rosa in China

Peng C, Crous PW, Jiang N, Fan XL, Liang YM, Tian CM

Persoonia

13-Aug-2022

PMCID:	PMC10792223
doi:	10.3767/persoonia.2022.49.07
PMID:	38234377

In vitro efficacy of essential oils against Sarcoptes scabiei

Andriantsoanirina V, Guillot J, Ratsimbason M, Mekhloufi G, Randriamialinoro F, Ranarivelo L, Ariey F, Durand R

Sci Rep

03-May-2022

PMCID:	PMC9065015
doi:	10.1038/s41598-022-11176-x
PMID:	35504935

Microencapsulation of Essential Oils: A Review

Sousa VI, Parente JF, Marques JF, Forte MA, Tavares CJ

Polymers (Basel)

23-Apr-2022

PMCID:	PMC9099681
doi:	10.3390/polym14091730
PMID:	35566899

Cannabidiol and Terpene Formulation Reducing SARS-CoV-2 Infectivity Tackling a Therapeutic Strategy

Santos S, Barata P, Charmier A, Lehmann I, Rodrigues S, Melosini MM, Pais PJ, Sousa AP, Teixeira C, Santos I, Rocha AC, Baylina P, Fernandes R

Front Immunol

15-Feb-2022

PMCID:	PMC8886108
doi:	10.3389/fimmu.2022.841459
PMID:	35242142

In Silico Prediction of Steroids and Triterpenoids as Potential Regulators of Lipid Metabolism

Dembitsky VM

Mar Drugs

22-Nov-2021

PMCID:	PMC8618826
doi:	10.3390/md19110650
PMID:	34822521

Antifungal Activities and Mode of Action of Cymbopogon citratus, Thymus vulgraris, and Origanum heracleoticum Essential Oil Vapors against Botrytis cinerea and Their Potential Application to Control Postharvest Strawberry Gray Mold

Yan J, Wu H, Chen K, Feng J, Zhang Y

Foods

15-Oct-2021

PMCID:	PMC8536117
doi:	10.3390/foods10102451
PMID:	34681505

Description of an Australian endemic species of Trioza (Hemiptera: Triozidae) pest of the endemic tea tree, Melaleuca alternifolia (Myrtaceae)

Martoni F, Blacket MJ

PLoS One

22-Sep-2021

PMCID:	PMC8457488
doi:	10.1371/journal.pone.0257031
PMID:	34550976

Environmental suitability of bare-nosed wombat burrows for Sarcoptes scabiei

Browne E, Driessen MM, Ross R, Roach M, Carver S

Int J Parasitol Parasites Wildl

10-Aug-2021

PMCID:	PMC8374697
doi:	10.1016/j.ijppaw.2021.08.003
PMID:	34434693

Backhousia citriodora F. Muell. (Lemon Myrtle), an Unrivalled Source of Citral

Southwell I

Foods

09-Jul-2021

PMCID:	PMC8305781
doi:	10.3390/foods10071596
PMID:	34359465

Antimicrobial Activity and Chemical Composition of Essential Oils against Pathogenic Microorganisms of Freshwater Fish

Klūga A, Terentjeva M, Vukovic NL, Kačániová M

Plants (Basel)

22-Jun-2021

PMCID:	PMC8309039
doi:	10.3390/plants10071265
PMID:	34206270

Phytochemical Profile Top

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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 / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	14428084	Click to see C1=CC(=CC=C1C(=O)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O	452.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
[3,4,5-Trihydroxy-6-(4-hydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	14428083	Click to see C1=CC(=CC=C1C(=O)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O	452.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
[3,4,6-Trihydroxy-5-(4-hydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	73309950	Click to see C1=CC(=CC=C1C(=O)OC2C(C(C(OC2O)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	452.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
2-O-(4-Hydroxybenzoyl)-6-O-(galloyl)-beta-D-glucopyranose	102086065	Click to see C1=CC(=CC=C1C(=O)OC2C(C(C(OC2O)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	452.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
2,3-Bis-O-(3,4,5-trihydroxybenzoyl)hexopyranose	14213991	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)O)CO)O	484.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
2,6-di-O-galloyl-beta-glucose	14034262	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)O)O	484.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
2,6-Digalloylglucose	14034261	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)O)O	484.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
galloyl(-2)[galloyl(-3)]b-Man	163082172	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)O)CO)O	484.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-hydroperoxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol	25136231	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)OO	444.70	unknown	https://doi.org/10.1021/NP800360A
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a,9-diol	163009603	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)O	428.70	unknown	https://doi.org/10.1021/NP800360A
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	26975211	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	https://doi.org/10.1021/NP800360A
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-hydroperoxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol	25136233	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)OO	444.70	unknown	https://doi.org/10.1021/NP800360A
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a,9-diol	15838686	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)O	428.70	unknown	https://doi.org/10.1021/NP800360A
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carbaldehyde	124407318	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O	440.70	unknown	https://doi.org/10.1021/NP800360A
(1S,2R,4aS,6aS,6bR,10S,12aR,12bR,14bS)-10-Hydroxy-1,2,6a,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-carbaldehyde	14423519	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C=O	440.70	unknown	https://doi.org/10.1021/NP800360A
(1S,4R,5R,10S,13R,19S,20R)-4,5,9,9,13,20-hexamethyl-22-oxahexacyclo[17.3.2.01,18.04,17.05,14.08,13]tetracosan-10-ol	162872511	Click to see CC1COC23CCC1C2C4CCC5C6(CCC(C(C6CCC5(C4(CC3)C)C)(C)C)O)C	428.70	unknown	https://doi.org/10.1021/NP800360A
(1S,4R,5R,8R,10S,13R,14R,17R,18R,19S,20R)-4,5,9,9,13,20-hexamethyl-22-oxahexacyclo[17.3.2.01,18.04,17.05,14.08,13]tetracosan-10-ol	25136232	Click to see CC1COC23CCC1C2C4CCC5C6(CCC(C(C6CCC5(C4(CC3)C)C)(C)C)O)C	428.70	unknown	https://doi.org/10.1021/NP800360A
2,3,24-Trihydroxy-12-ursen-28-oic acid	296191	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/10.1021/NP800360A
3a-Hydroperoxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol	74392501	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)OO	444.70	unknown	https://doi.org/10.1021/NP800360A
5a,5b,8,8,11a-Pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a,9-diol	85260065	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)O	428.70	unknown	https://doi.org/10.1021/NP800360A
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carbaldehyde	317607	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O	440.70	unknown	https://doi.org/10.1021/NP800360A
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	2371	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	https://doi.org/10.1021/NP800360A
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/10.1021/NP800360A
beta-Ursolic acid	220774	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/10.1021/NP800360A
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	https://doi.org/10.1021/NP800360A
Betulinaldehyde	99615	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O	440.70	unknown	https://doi.org/10.1021/NP800360A
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	https://doi.org/10.1021/NP800360A
Lup-20(29)-ene-3beta,28-diol	221023	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	https://doi.org/10.1021/NP800360A
Oleanolic aldehyde	10321055	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C=O)C	440.70	unknown	https://doi.org/10.1021/NP800360A
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/10.1021/NP800360A
Ursolic acid acetate	6475119	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O	498.70	unknown	https://doi.org/10.1021/NP800360A
Ursolic aldehyde	14423521	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C=O	440.70	unknown	https://doi.org/10.1021/NP800360A
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(1R,3aS,5aR,5bR,7aS,9S,11aR,11bR,13aR,13bR)-1-acetyl-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	124900004	Click to see CC(=O)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	458.70	unknown	https://doi.org/10.1021/NP800360A
1-Acetyl-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	12314362	Click to see CC(=O)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	458.70	unknown	https://doi.org/10.1021/NP800360A
Platanic Acid	64980	Click to see CC(=O)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	458.70	unknown	https://doi.org/10.1021/NP800360A
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[3,4,5-Trihydroxy-6-(2-hydroxy-3-methoxy-5-prop-2-enylphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	85067005	Click to see COC1=C(C(=CC(=C1)CC=C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O	494.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
Pimentol	9917512	Click to see COC1=C(C(=CC(=C1)CC=C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O	494.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
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	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
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	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	12304323	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/10.1016/J.PHYTOCHEM.2007.03.010
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	51402820	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/10.1016/J.PHYTOCHEM.2007.03.010
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/10.1016/J.PHYTOCHEM.2007.03.010
3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one	163075144	Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C(=C5)O)O)O)CO)O)O)O)O)O	612.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	14825575	Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O	596.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	162899763	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	432.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
5,7-dihydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one	51402816	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)O	464.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
Hyperoside	5281643	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/10.1016/J.PHYTOCHEM.2007.03.010
Kaempferol-3-O-rhamnoside	5835713	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	432.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
Leucoside	44566720	Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O	580.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
Myricetin 3-rhamnoside	5352000	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)O	464.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
Myricetin3-O-beta-D-xylopyranosyl-(1-2)-beta-D-glucopyranoside	74978290	Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C(=C5)O)O)O)CO)O)O)O)O)O	612.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
O-Quercetin 3-(2-O-xylopyranosylglucopyranoside)	101138141	Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O	596.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
Quercetin 3-O-rhamnoside	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/10.1016/J.PHYTOCHEM.2007.03.010
Rustoside	74977996	Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O	580.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
> Phenylpropanoids and polyketides / Tannins
1,6-bis-O-galloyl-beta-D-glucose	440221	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)O)O)O	484.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
1,6-Digalloyl-beta-D-glucopyranose	3332212	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)O)O)O	484.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
3-O-Methylellagic acid 4-O-rhamnoside	16720461	Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)OC)O)O)O	462.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
3,3'-Di-O-methylellagic acid	5488919	Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)OC)O)O	330.24	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
6,7-Dihydroxy-14-methoxy-13-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione	73310005	Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)OC)O)O)O	462.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.03.010

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Melaleuca ericifolia

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