Melaleuca alternifolia

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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	UUID643fe30fe5846247327719
Scientific name	Melaleuca alternifolia
Authority	Cheel
First published in	J. Proc. Roy. Soc. New S. Wales 58: 195 (1924)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Melaleuca linariifolia var. alternifolia	Maiden & Betche	Proc. Linn. Soc. New South Wales 29: 742 (1904 publ. 1905)

Common names Top

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Filter by language:

Language	Common/alternative name
Spanish	Árbol del te
Spanish	Árbol del té
Spanish	arbol del té
Spanish	arbol del te
Spanish	Árbol de té
Spanish	arbol de te
Spanish	aceite árbol del té
Spanish	aceite árbol del te
Spanish	aceite arbol del té
Spanish	aceite arbol del te
Spanish	aceite de melaleuca
Arabic	بلقاء متبادلة الأوراق
Catalan	arbre del te
Czech	tea tree
Czech	kajeput střídavolistý
Czech	Čajový strom
Czech	Čajovníkový strom
Czech	Čajovník australský
German	teebaum
German	australischer teebaum
French	arbre a the
French	arbre À thé
French	tea tree
French	tea-tree
French	arbre à thé
Galician	Árbore do té
Hungarian	ausztrál teafa
Japanese	ティートゥリーオイル
Japanese	ティーツリー
Japanese	ティートリー
Japanese	ティートゥリー
Japanese	ティーツリーオイル
Korean	티트리
Malay	gelam wangi
oc	arbre de tè
Polish	melaleuka skrętolistna
Portuguese	árvore do chá australiana
Slovenian	Čajevec
Chinese	澳洲茶樹
Chinese	澳洲茶树
Chinese	互叶白千层
Chinese	互葉白千層

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
  - Queensland

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000239396
UNII	976KV4FXYF
Tropicos	50234332
KEW	urn:lsid:ipni.org:names:597833-1
The Plant List	kew-123479
Open Tree Of Life	782651
Observations.org	345389
NCBI Taxonomy	164405
IPNI	597833-1
iNaturalist	427159
GBIF	5416091
Freebase	/m/025t6vc
EOL	2944002
Elurikkus	535445
USDA GRIN	402629
Wikipedia	Melaleuca_alternifolia

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_019926035.1	SCU_Malt_1	Scaffold	Southern Cross University	2021-09-10	350.0x	345.26 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

Safety and efficacy of a feed additive consisting of an essential oil derived from fresh leaves of Melaleuca cajuputi Maton & Sm. ex R. Powell and Melaleuca leucadendra (L.) L. (cajuput oil) for use in all animal species (FEFANA asbl)

Bampidis V, Azimonti G, Bastos MD, Christensen H, Durjava M, Kouba M, López‐Alonso M, Puente SL, Marcon F, Mayo B, Pechová A, Petkova M, Ramos F, Villa RE, Woutersen R, Chesson A, Schlatter J, Westendorf J, Dirven Y, Manini P, Dusemund B

EFSA J

10-Apr-2024

PMCID:	PMC11004901
doi:	10.2903/j.efsa.2024.8732
PMID:	38601874

A review on antimicrobial strategies in mitigating biofilm-associated infections on medical implants

Kadirvelu L, Sivaramalingam SS, Jothivel D, Chithiraiselvan DD, Karaiyagowder Govindarajan D, Kandaswamy K

Curr Res Microb Sci

07-Mar-2024

PMCID:	PMC10951465
doi:	10.1016/j.crmicr.2024.100231
PMID:	38510214

Antimicrobial Activities of Pistacia lentiscus Essential Oils Nanoencapsulated into Hydroxypropyl-beta-cyclodextrins

Alabrahim OA, Azzazy HM

ACS Omega

04-Mar-2024

PMCID:	PMC10955754
doi:	10.1021/acsomega.3c07413
PMID:	38524461

1,8-Cineol Attenuates Checkpoint Molecule PDL-1 and Adhesion Molecule CX3CR1 in Circulating Monocytes in Otitis Media Patients

Leichtle A, Jeschke S, Plötze-Martin K, Idel C, Bruchhage KL, Pries R

J Pers Med

01-Mar-2024

PMCID:	PMC10971202
doi:	10.3390/jpm14030279
PMID:	38541021

Treatment Options for Onychomycosis: Efficacy, Side Effects, Adherence, Financial Considerations, and Ethics

Yousefian F, Smythe C, Han H, Elewski BE, Nestor M

J Clin Aesthet Dermatol

01-Mar-2024

PMCID:	PMC10941855
PMID:	38495549

Pathogenesis, Prophylaxis, and Treatment of Candida auris

Preda M, Chivu RD, Ditu LM, Popescu O, Manolescu LS

Biomedicines

01-Mar-2024

PMCID:	PMC10968176
doi:	10.3390/biomedicines12030561
PMID:	38540174

Essential oil-containing solutions (mouthwashes) preserve dental enamel with releasing low Ca and P concentrations without morphology alterations: an in vitro study

Mutran SC, de Carvalho-Filho PR, Ribeiro ME, Faial KD, Lima RR, D’Almeida Couto RS

Front Chem

28-Feb-2024

PMCID:	PMC10933047
doi:	10.3389/fchem.2024.1341769
PMID:	38482175

Confronting the complexities of antimicrobial management for Staphylococcus aureus causing bovine mastitis: an innovative paradigm

Saeed SI, Kamaruzzaman NF, Gahamanyi N, Nguyen TT, Hossain D, Kahwa I

Ir Vet J

28-Feb-2024

PMCID:	PMC10900600
doi:	10.1186/s13620-024-00264-1
PMID:	38418988

Calocedrus formosana Essential Oils Induce ROS-Mediated Autophagy and Apoptosis by Targeting SIRT1 in Colon Cancer Cells

Islam A, Chang YC, Tsao NW, Wang SY, Chueh PJ

Antioxidants (Basel)

26-Feb-2024

PMCID:	PMC10967316
doi:	10.3390/antiox13030284
PMID:	38539819

Bacillus Species: Excellent Biocontrol Agents against Tomato Diseases

Karačić V, Miljaković D, Marinković J, Ignjatov M, Milošević D, Tamindžić G, Ivanović M

Microorganisms

24-Feb-2024

PMCID:	PMC10972177
doi:	10.3390/microorganisms12030457
PMID:	38543508

Plant-Based Films and Hydrogels for Wound Healing

Lopes AI, Pintado MM, Tavaria FK

Microorganisms

21-Feb-2024

PMCID:	PMC10972459
doi:	10.3390/microorganisms12030438
PMID:	38543489

Plant-Origin Components: New Players to Combat Antibiotic Resistance in Klebsiella pneumoniae

Luna-Pineda VM, Rodríguez-Martínez G, Salazar-García M, Romo-Castillo M

Int J Mol Sci

10-Feb-2024

PMCID:	PMC10888558
doi:	10.3390/ijms25042134
PMID:	38396811

Chitosan-Based Nanoencapsulated Essential Oils: Potential Leads against Breast Cancer Cells in Preclinical Studies

Tan WN, Samling BA, Tong WY, Chear NJ, Yusof SR, Lim JW, Tchamgoue J, Leong CR, Ramanathan S

Polymers (Basel)

08-Feb-2024

PMCID:	PMC10891598
doi:	10.3390/polym16040478
PMID:	38399856

Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species

Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E

Antibiotics (Basel)

07-Feb-2024

PMCID:	PMC10885947
doi:	10.3390/antibiotics13020163
PMID:	38391549

Plant Monoterpenes and Essential Oils as Potential Anti-Ageing Agents: Insights from Preclinical Data

Zuzarte M, Sousa C, Alves-Silva J, Salgueiro L

Biomedicines

04-Feb-2024

PMCID:	PMC10886757
doi:	10.3390/biomedicines12020365
PMID:	38397967

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 / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol	7127	Click to see COC1=C(C=C(C=C1)CC=C)OC	178.23	unknown	https://doi.org/10.1021/JF00034A020
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol	14529	Click to see CC1=CC=C(C=C1)C(C)(C)O	150.22	unknown	https://doi.org/10.1021/JF00034A020
> Benzenoids / Phenols / Methoxyphenols
Maesol	128958	Click to see CC1=C(C=C(C=C1OC)CCCCCCCCCCCCC2=CC(=C(C(=C2)OC)C)O)O	442.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1360273/
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1016/0300-483X(95)03242-8 https://doi.org/10.1016/S0031-9422(02)00038-9 https://doi.org/10.1021/JF035377D https://doi.org/10.1016/S0944-7113(98)80048-2 https://doi.org/10.1021/JF00098A007 https://doi.org/10.1021/JF00034A020 https://doi.org/10.1002/JSFA.2740580109 https://doi.org/10.1080/10412905.1997.9700780 https://doi.org/10.1016/0305-1978(94)90033-7 https://doi.org/10.1080/10412905.1995.9700519 https://doi.org/10.1080/10412905.1995.9700515 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1360273/ https://doi.org/10.3390/60100092 https://doi.org/10.1080/10412905.1992.9698086
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1021/JF00098A007 https://doi.org/10.1021/JF00034A020
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1995.9700519 https://doi.org/10.1021/JF00098A007 https://doi.org/10.1021/JF00034A020 https://doi.org/10.1002/JSFA.2740580109 https://doi.org/10.1016/S0944-7113(98)80048-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1080/10412905.1995.9700519 https://doi.org/10.1080/10412905.1995.9700515 https://doi.org/10.1016/0031-9422(90)85269-L https://doi.org/10.1016/0305-1978(94)90033-7 https://doi.org/10.1021/JF00098A007 https://doi.org/10.1021/JF00034A020 https://doi.org/10.1016/0300-483X(95)03242-8 https://doi.org/10.1002/JSFA.2740580109 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1360273/ https://doi.org/10.3390/60100092 https://doi.org/10.1080/10412905.1997.9700780 https://doi.org/10.1016/S0944-7113(98)80048-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene	440968	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(02)00038-9 https://doi.org/10.1021/JF00034A020
(-)-beta-Pinene	440967	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(02)00038-9
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1021/JF00034A020
(1R,4S,5R)-4-Thujanol	12315154	Click to see CC(C)C12CCC(C1C2)(C)O	154.25	unknown	https://doi.org/10.1021/JF00034A020
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene	6451618	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1021/JF00034A020 https://doi.org/10.1080/10412905.1995.9700519 https://doi.org/10.1016/S0944-7113(98)80048-2 https://doi.org/10.1021/JF00098A007
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane	6429260	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1021/JF00098A007
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1995.9700519 https://doi.org/10.1021/JF035377D https://doi.org/10.1016/0305-1978(94)90033-7 https://doi.org/10.1021/JF00098A007 https://doi.org/10.1016/0300-483X(95)03242-8 https://doi.org/10.1002/JSFA.2740580109 https://doi.org/10.1016/S0031-9422(02)00038-9 https://doi.org/10.3390/60100092 https://doi.org/10.1080/10412905.1997.9700780 https://doi.org/10.1016/S0944-7113(98)80048-2
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1080/10412905.1995.9700519 https://doi.org/10.1021/JF00098A007 https://doi.org/10.1002/JSFA.2740580109 https://doi.org/10.1016/S0031-9422(02)00038-9 https://doi.org/10.1016/S0944-7113(98)80048-2
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)-	17868	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1992.9698086 https://doi.org/10.1080/10412905.1995.9700519 https://doi.org/10.1016/S0944-7113(98)80048-2 https://doi.org/10.1021/JF00098A007
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1016/S0944-7113(98)80048-2
cis-Sabinene hydrate	11744854	Click to see CC(C)C12CCC(C1C2)(C)O	154.25	unknown	https://doi.org/10.1016/S0031-9422(02)00038-9
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1021/JF00098A007 https://doi.org/10.1080/10412905.1992.9698086
Thujone	261491	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1016/0031-9422(90)85269-L
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol	443162	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1021/JF00034A020
(-)-Terpinen-4-ol	5325830	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1021/JF00034A020
(+)-alpha-Phellandrene	443160	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1021/JF00034A020
(+)-alpha-Terpineol	442501	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1021/JF00034A020
(+)-Terpinen-4-ol	2724161	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1016/S0031-9422(02)00038-9 https://doi.org/10.1021/JF00034A020
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1016/0300-483X(95)03242-8 https://doi.org/10.1016/S0944-7113(98)80048-2 https://doi.org/10.1021/JF0004356 https://doi.org/10.1021/JF00098A007 https://doi.org/10.1002/JSFA.2740580109 https://doi.org/10.1080/10412905.1997.9700780 https://doi.org/10.1016/0305-1978(94)90033-7 https://doi.org/10.1080/10412905.1995.9700519 https://doi.org/10.1080/10412905.1995.9700515 https://doi.org/10.1002/(SICI)1099-1026(199607)11:4<219::AID-FFJ571>3.0.CO;2-I https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1360273/ https://doi.org/10.3390/60100092 https://doi.org/10.1016/S0305-1978(99)00071-X
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1016/S0944-7113(98)80048-2 https://doi.org/10.1080/10412905.1992.9698086
alpha-PHELLANDRENE, (-)-	442482	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1021/JF00034A020
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1016/0300-483X(95)03242-8 https://doi.org/10.1021/JF035377D https://doi.org/10.1016/S0944-7113(98)80048-2 https://doi.org/10.1021/JF00098A007 https://doi.org/10.1021/JF00034A020 https://doi.org/10.1002/JSFA.2740580109 https://doi.org/10.1080/10412905.1997.9700780 https://doi.org/10.1016/0305-1978(94)90033-7 https://doi.org/10.1080/10412905.1995.9700519 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1360273/ https://doi.org/10.1016/0031-9422(90)85269-L https://doi.org/10.3390/60100092 https://doi.org/10.1080/10412905.1992.9698086
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1080/10412905.1995.9700519 https://doi.org/10.1080/10412905.1995.9700515 https://doi.org/10.1016/0305-1978(94)90033-7 https://doi.org/10.1021/JF00098A007 https://doi.org/10.1016/0300-483X(95)03242-8 https://doi.org/10.1002/JSFA.2740580109 https://doi.org/10.3390/60100092 https://doi.org/10.1080/10412905.1997.9700780 https://doi.org/10.1016/S0944-7113(98)80048-2 https://doi.org/10.1080/10412905.1992.9698086
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1021/JF00098A007 https://doi.org/10.1021/JF00034A020 https://doi.org/10.1016/0031-9422(90)85269-L https://doi.org/10.1080/10412905.1992.9698086
Limonene, (-)-	439250	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1021/JF00034A020
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1021/JF00034A020
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1995.9700519 https://doi.org/10.1016/0031-9422(90)85269-L https://doi.org/10.1021/JF00098A007 https://doi.org/10.1002/JSFA.2740580109 https://doi.org/10.1080/10412905.1997.9700780 https://doi.org/10.1016/S0944-7113(98)80048-2 https://doi.org/10.1080/10412905.1992.9698086
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1016/0300-483X(95)03242-8 https://doi.org/10.1016/S0031-9422(02)00038-9 https://doi.org/10.1021/JF035377D https://doi.org/10.1016/S0944-7113(98)80048-2 https://doi.org/10.1021/JF00098A007 https://doi.org/10.1021/JF00034A020 https://doi.org/10.1002/JSFA.2740580109 https://doi.org/10.1080/10412905.1997.9700780 https://doi.org/10.1016/0305-1978(94)90033-7 https://doi.org/10.1080/10412905.1995.9700515 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1360273/ https://doi.org/10.1016/0031-9422(90)85269-L https://doi.org/10.3390/60100092 https://doi.org/10.1016/S0305-1978(99)00071-X https://doi.org/10.1080/10412905.1992.9698086
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1016/S0944-7113(98)80048-2 https://doi.org/10.1021/JF00098A007 https://doi.org/10.1021/JF00034A020 https://doi.org/10.1016/0031-9422(90)85269-L
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	92042749	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1021/JF00034A020
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene	134779875	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1021/JF00034A020
1-Ethenyl-1,2-dimethyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane	5317024	Click to see CC(=C1CCC(C(C1)(C)C(=C)C)(C)C=C)C	218.38	unknown	https://doi.org/10.1021/JF00098A007
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane	6432312	Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C	204.35	unknown	https://doi.org/10.1021/JF00098A007
alpha-Muurolene	12306047	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1021/JF00034A020
beta-Cubebene	93081	Click to see CC1CCC(C2C13C2C(=C)CC3)C(C)C	204.35	unknown	https://doi.org/10.1021/JF00098A007
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1016/S0944-7113(98)80048-2 https://doi.org/10.1021/JF00098A007
Calamenene	6429077	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1021/JF00034A020
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1021/JF00098A007 https://doi.org/10.1021/JF00034A020
Cubenol	11770062	Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C	222.37	unknown	https://doi.org/10.1002/1099-1026(200009/10)15:5<352::AID-FFJ925>3.0.CO;2-R https://doi.org/10.1021/JF00034A020
delta-Guaiene	94275	Click to see CC1CCC2=C(CCC(CC12)C(=C)C)C	204.35	unknown	https://doi.org/10.1021/JF00034A020
gamma-Gurjunene	90805	Click to see CC1CCC(C=C2C1CCC2C)C(=C)C	204.35	unknown	https://doi.org/10.1021/JF00034A020
trans-Muurola-4(14),5-diene	91747125	Click to see CC1CCC(C2=CC(=C)CCC12)C(C)C	204.35	unknown	https://doi.org/10.1021/JF00034A020
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol	91746597	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1016/0031-9422(90)85269-L https://doi.org/10.1021/JF00034A020
(1aR,4S,4aR,7aS,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol	137704583	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1021/JF00034A020
(1aR,7S,7aS,7bS)-1,1,4,7-tetramethyl-1a,2,3,5,6,7,7a,7b-octahydrocyclopropa[e]azulene	154496877	Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C	204.35	unknown	https://doi.org/10.1021/JF60217A031
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene	91746456	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1021/JF00034A020 https://doi.org/10.1016/S0944-7113(98)80048-2
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	97032059	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1021/JF00034A020
1,1,4,7-Tetramethyl-1a,2,3,5,6,7,7a,7b-octahydrocyclopropa[e]azulene	89532	Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C	204.35	unknown	https://doi.org/10.1021/JF60217A031
Alloaromadendren	91746537	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1021/JF00098A007 https://doi.org/10.1021/JF00034A020
alpha-Gurjunene	15560276	Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C	204.35	unknown	https://doi.org/10.1021/JF00034A020
Aromadendrene	91354	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1016/S0944-7113(98)80048-2
beta-Gurjunene	6450812	Click to see CC1CCC2C(C2(C)C)C3C1CCC3=C	204.35	unknown	https://doi.org/10.1021/JF00034A020
Palustrol	110745	Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O	222.37	unknown	https://doi.org/10.1021/JF00034A020
Viridiflorene	10910653	Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C	204.35	unknown	https://doi.org/10.1021/JF60217A031 https://doi.org/10.1016/0031-9422(90)85269-L https://doi.org/10.1016/S0944-7113(98)80048-2 https://doi.org/10.1021/JF00034A020
Viridiflorol	11996452	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1021/JF00034A020
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene	44583886	Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C	204.35	unknown	https://doi.org/10.1021/JF00034A020
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1aR,3aS,7bS)-1,1,3a,7-Tetramethyl-1a,2,3,3a,4,5,6,7b-octahydro-1H-cyclopropa[a]naphthalene	101596917	Click to see CC1=C2C3C(C3(C)C)CCC2(CCC1)C	204.35	unknown	https://doi.org/10.1021/JF00034A020
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol	53436347	Click to see C12C3C4C1C5(C2C3=C45)O	118.13	unknown	https://doi.org/10.1002/1099-1026(200009/10)15:5<352::AID-FFJ925>3.0.CO;2-R
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Cyclohexanone	7967	Click to see C1CCC(=O)CC1	98.14	unknown	https://doi.org/10.1021/JF00098A007

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Melaleuca alternifolia

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