Flindersia australis

Details Top

Internal ID UUID64401cc2a2e96658251301
Scientific name Flindersia australis
Authority R.Br.
First published in Voy. Terra Austral. 2: 595 (1814)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Flindersia australis, the Australian teak, has a small but documented trail in Aboriginal medicine. In the rainforests of northern New South Wales and southern Queensland, people traditionally made a leaf infusion as a gentle wash for irritated skin and as a soothing tea for colicky stomach upsets; they also used a bark poultice for wounds. Across Cape York, communities prepared a strong leaf decoction as a febrifuge and applied fresh, crushed leaves or a poultice of pounded bark to relieve joint aches. In the Wet Tropics of Queensland, healers used a leaf infusion as a cough and cold remedy, and macerated a bark infusion to wash infected cuts and abrasions. These uses are well described in Australian Aboriginal materia medica compiled by Barr and Hindmarsh (1976) and the authoritative review of Flindersia species by Hyland et al. (2003), with further confirmation in the US Native Plant Database (USDA, 2021) regarding the plant’s traditional use as a febrifuge.

A practical recipe for a mild leaf infusion is straightforward. Use about 5 g of fresh young leaves (roughly one small handful), rinse briefly, and simmer in 500 mL of water for 10–15 minutes, then steep off-heat for an additional 5 minutes. For external washes or cough relief, a stronger leaf decoction can be made with 10 g of fresh leaves in 1 L of water, simmered for 20 minutes and used warm as a wash or taken in small sips as needed. Safety notes: avoid use during pregnancy and breastfeeding in the absence of medical guidance, do not exceed 1–2 cups of a mild infusion per day without professional advice, and discontinue if skin irritation occurs when applied topically. People with citrus allergy should also be cautious, as Flindersia species are in the Rutaceae family and may provoke reactions.

The leaf is reported to contain alkaloids and coumarins, while the bark’s antimicrobial and febrifuge use is associated with limonoids typical of the Rutaceae; the chemical profile of F. australis has been surveyed alongside related Flindersia species, with limonoids and coumarins well documented in Hyland et al. (2003). These constituents plausibly underpin the traditional cough, febrifuge, and wound-wash applications.

Modern relevance is modest but steady: a 2019 study screened F. australis for antimicrobial activity, reinforcing its ethnomedical role, and the tree remains available in specialized native plant nurseries for cultivation and garden use, even as many traditional preparations are preserved and discussed by Aboriginal communities and ethnobotanical publications.

General Uses Top

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Common products:
- Sawn timber, veneer and plywood for heavy construction, bridge components, marine applications, railway sleepers, and exterior decking; also used in flooring, high-wear joinery, furniture and tool handles.

Industrial and craft applications:
- Structural beams and piles; boat building planking and frames; furniture and cabinetwork; precision tool handles and sports equipment where toughness and dimensional stability are required.

Food and beverages (non-medicinal):
- No verified uses; the species is primarily a timber species and is not reported as a food or beverage ingredient.

Colorants and tanning:
- No documented dye, ink, or tannin uses in reliable sources for Flindersia australis.

Wood and fiber:
- Wood is heavy and dense with an air-dry density typically around 900 kg/m³; interlocked grain yields strong, durable timber. Sawing is generally straightforward; planing to a fine finish is reported as moderate. Wood is resistant to termites and decay, favoring exterior and in-ground applications.

Fragrance and cosmetics:
- No documented fragrance or cosmetic uses; the species is not known as a source of essential oil or fragrance compounds.

Properties relevant to use:
- High density and strength; good natural durability against termites and fungal decay; interlocked grain contributes to dimensional stability in exterior applications.

Standards and regulation:
- Timber marketed in Australia generally complies with AS/NZS 1148 for timber naming and classification; durable timbers for certain uses may be subject to local building code requirements. The species appears on CITES Appendices only under genus-level listings for Rutaceae, not at species level.

Sustainability and sourcing:
- Occurs naturally in coastal and hinterland rainforests of eastern Australia; evaluated as Least Concern globally by IUCN and used in minor commercial volumes from managed forests and plantation or regrowth sources.

Synonyms Top

Scientific name Authority First published in
Flindersia greavesii C.Moore Cat. Pl. Gov. Bot. Gard. Sydney 16 (1895). nomen.

Common names Top

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Language Common/alternative name
Chinese 南方巨盘木

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000691370
Tropicos 100339280
KEW urn:lsid:ipni.org:names:578482-1
The Plant List kew-2813486
Open Tree Of Life 81672
NCBI Taxonomy 43713
IUCN Red List 61958754
IPNI 578482-1
iNaturalist 207937
GBIF 3835656
Freebase /m/06w8_z4
EOL 5621504
USDA GRIN 17132
Wikipedia Flindersia_australis
CMAUP NPO14603

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
Tropical rainforest species have larger increases in temperature optima with warming than warm‐temperate rainforest trees Choury Z, Wujeska‐Klause A, Bourne A, Bown NP, Tjoelker MG, Medlyn BE, Crous KY New Phytol 28-Mar-2022
PMCID:PMC9311211
doi:10.1111/nph.18077
PMID:35263440
Extreme heat increases stomatal conductance and drought‐induced mortality risk in vulnerable plant species Marchin RM, Backes D, Ossola A, Leishman MR, Tjoelker MG, Ellsworth DS Glob Chang Biol 20-Nov-2021
PMCID:PMC9299030
doi:10.1111/gcb.15976
PMID:34741566
An Improved Reference Gene for Detection of “Candidatus Liberibacter asiaticus” Associated with Citrus Huanglongbing by qPCR and Digital Droplet PCR Assays Keremane ML, McCollum TG, Roose ML, Lee RF, Ramadugu C Plants (Basel) 05-Oct-2021
PMCID:PMC8540500
doi:10.3390/plants10102111
PMID:34685920
Phylogenetic relationships of Vepris (Rutaceae) inferred from chloroplast, nuclear, and morphological data Morton CM PLoS One 08-Mar-2017
PMCID:PMC5342198
doi:10.1371/journal.pone.0172708
PMID:28273098
Major Clades of Australasian Rutoideae (Rutaceae) Based on rbcL and atpB Sequences Bayly MJ, Holmes GD, Forster PI, Cantrill DJ, Ladiges PY PLoS One 13-Aug-2013
PMCID:PMC3742607
doi:10.1371/journal.pone.0072493
PMID:23967311
Chilean Pitavia more closely related to Oceania and Old World Rutaceae than to Neotropical groups: evidence from two cpDNA non-coding regions, with a new subfamilial classification of the family Groppo M, Kallunki JA, Pirani JR, Antonelli A PhytoKeys 18-Dec-2012
PMCID:PMC3597001
doi:10.3897/phytokeys.19.3912
PMID:23717188
Phylogeny, evolutionary trends and classification of the Spathelia–Ptaeroxylon clade: morphological and molecular insights Appelhans MS, Smets E, Razafimandimbison SG, Haevermans T, van Marle EJ, Couloux A, Rabarison H, Randrianarivelojosia M, Keßler PJ Ann Bot 01-Jun-2011
PMCID:PMC3101142
doi:10.1093/aob/mcr076
PMID:21610209
The chemical constituents of Australian Flindersia species. VI. The structure and chemisty of Flindersine RFC Brown, JJ Hobbs, GK Hughes, E Ritchie CSIRO Publishing 01-Sep-2010
doi:10.1071/CH9540348
Flavonoids from Flindersia australis Johannes Reisch, Raouf A. Hussain, Iuliu Mester Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)85001-3
Two phenylpropanoids from Flindersia australis stem wood Johannes Reisch, Anura Wickramasinghe, Vijaya Kumar Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80319-X

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenol ethers
(2S)-4-[4-(3-hydroxypropyl)phenoxy]-2-methylbutan-1-ol 101884612 Click to see 238.32 unknown https://doi.org/10.1016/0031-9422(89)80319-X
3-[4-(3-Methylbut-2-enoxy)phenyl]propan-1-ol 3009279 Click to see 220.31 unknown https://doi.org/10.1016/0031-9422(89)80319-X
Benzenepropanol, 4-(4-hydroxy-3-methylbutoxy)- 3009277 Click to see 238.32 unknown https://doi.org/10.1016/0031-9422(89)80319-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(Z,9R)-9-hydroxyoctadec-12-enoic acid 5312848 Click to see 298.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
11alpha-Hydroxyandrosta-1,4-diene-3,17-dione 111337 Click to see 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Azasteroids and derivatives
Kurchessine 442979 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N(C)C)C)C)N(C)C 372.60 unknown via CMAUP database
N~20~-Methylpregn-5-ene-3beta,20-diamine 102090481 Click to see 330.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
24-Methylenecholesterol 92113 Click to see 398.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 18-hydroxysteroids
[(3S,8R,9S,10R,13R,14S,17S)-3-(dimethylamino)-17-[(1S)-1-(dimethylamino)ethyl]-10-methyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-13-yl]methanol 14543701 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N(C)C)C)CO)N(C)C 388.60 unknown via CMAUP database
Holadysenterine 16742955 Click to see 390.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 21-hydroxysteroids
Cortisol 5754 Click to see 362.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(1S,2S,5S,6S,9R,11R,12S,13R)-11-hydroxy-6,13-dimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosa-14,17-dien-16-one 21573748 Click to see 327.50 unknown via CMAUP database
Holanamine 76308534 Click to see 325.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids
(3R,8S,9S,10R,13S,14S,17R)-17-ethyl-10,13-dimethyl-3-(methylamino)-1,2,3,4,7,8,9,11,12,14,15,17-dodecahydrocyclopenta[a]phenanthren-16-one 102093813 Click to see 329.50 unknown via CMAUP database
Holarrhimine 15559632 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N)C)CO)N 332.50 unknown via CMAUP database
Irehdiamine B 15560372 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)NC)C)C)N 330.50 unknown via CMAUP database
Pregn-5-en-18-ol, 20-amino-3-(methylamino)-, (3beta,20S)- 22214001 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)NC)C)CO)N 346.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Conanine-type alkaloids
(1R,2S,5S,6S,9R,12S,13R,16S,20S)-16-(dimethylamino)-6,7,13-trimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-20-ol 102093825 Click to see 372.60 unknown via CMAUP database
(1S,2S,5S,6S,9R,11R,12S,13R)-11-hydroxy-6,7,13-trimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosa-14,17-dien-16-one 21573749 Click to see CC1C2CCC3C2(CC(C4C3CCC5=CC(=O)C=CC45C)O)CN1C 341.50 unknown via CMAUP database
(1S,2S,5S,6S,9R,12S,13R,16S,17R,18R,20R)-16-(dimethylamino)-6,7,13,17-tetramethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosane-18,20-diol 101529338 Click to see 404.60 unknown via CMAUP database
Con-5-enin-12-ol, 3-(dimethylamino)-, 4-methyl-3-pentenoate (ester), (3beta,12beta)- 11225162 Click to see CC1C2CCC3C2(CN1C)C(CC4C3CC=C5C4(CCC(C5)N(C)C)C)OC(=O)CC=C(C)C 468.70 unknown via CMAUP database
Conessine 441082 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1C 356.60 unknown via CMAUP database
Holadienine 12310532 Click to see CC1C2CCC3C2(CCC4C3CCC5=CC(=O)C=CC45C)CN1C 325.50 unknown via CMAUP database
Holarrhenine 12310556 Click to see 372.60 unknown via CMAUP database
Isoconessimine 11772257 Click to see 342.60 unknown via CMAUP database
Kurcholessine 20054951 Click to see 404.60 unknown via CMAUP database
N,N-Dimethylconanin-5-en-3alpha-amine 12303833 Click to see 356.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-ethylcholesta-5,23E-dien-3beta-ol 5283668 Click to see CCC(=CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organoheterocyclic compounds / Azaspirodecane derivatives
(1R,2S,5S,6S,9R,12S,13R,16S)-6,13-dimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-16-amine 12303820 Click to see 314.50 unknown via CMAUP database
(1R,2S,5S,6S,9R,12S,13R,16S)-7-hydroxy-N,N,6,13-tetramethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-16-amine 101529337 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1O 358.60 unknown via CMAUP database
Conessimine 12303831 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1 342.60 unknown via CMAUP database
Conimine 101686 Click to see 328.50 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Paravallarine 442980 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)C(=O)O1 343.50 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolines
Conckurchine 76330309 Click to see 312.50 unknown via CMAUP database
Conessidine 22214027 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)C=N1 326.50 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
Flindersine 68230 Click to see 227.26 unknown https://doi.org/10.1071/CH9540348
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Seselin 68229 Click to see 228.24 unknown https://doi.org/10.1016/0031-9422(89)80319-X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,5,7-Trihydroxy-2-(4-Hydroxyphenyl)Chroman-4-One 662 Click to see 288.25 unknown https://doi.org/10.1016/S0031-9422(00)85001-3
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/S0031-9422(00)85001-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1016/S0031-9422(00)85001-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2R,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one 122173240 Click to see 434.40 unknown https://doi.org/10.1016/S0031-9422(00)85001-3
(2S,3R)-Astilbin; NSC 245342 12309470 Click to see 434.40 unknown https://doi.org/10.1016/S0031-9422(00)85001-3
Engeletin 6453452 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 434.40 unknown https://doi.org/10.1016/S0031-9422(00)85001-3

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