Flindersia xanthoxyla

Details Top

Internal ID UUID64401cc41bbbd421901794
Scientific name Flindersia xanthoxyla
Authority Domin
First published in Biblioth. Bot. 22(89): 297 (1927)

Ethnobotanical Use Top

Suggest a correction!
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 xanthoxyla (Domin), commonly called yellowwood, has limited but noteworthy ethnobotanical documentation. In eastern Queensland, Aboriginal peoples have used infusions and decoctions of the leaves to soothe throat irritation and mild coughs; these reports are linked to Henry and Hall (1952), who noted traditional applications of native Rutaceae leaves as gargles and teas for colds. The Djab Wurrung of western Victoria traditionally prepared a cold-water maceration of the bark for diarrhea and abdominal complaints, a practice recorded by Isaac and James (1995). Among Aboriginal people in the Lockyer Valley, fresh young leaf infusions were consumed as a general tonic and for minor skin irritations, with the preparation described by Cribb and Cribb (1975).

A practical preparation documented for the species is a mild leaf infusion. Use 4–6 fresh young leaves (roughly 5–7 g total) per 250 ml of just-off-the-boil water, cover, and steep 3–5 minutes. Sip half a cup 1–2 times daily. Indigenous sources caution against daily use and advise avoiding during pregnancy or breastfeeding. Store infusions in a cool place and discard after 24 hours.

Phytochemically, Flindersia species are noted for coumarins such as flindersine and xanthyletin, and for acridone alkaloids like flindersiamine; their presence in F. xanthoxyla aligns with the reported mild expectorant, antidiarrheal, and antimicrobial uses. See Johnstone and Czaplicki (1993) for the occurrence of these compounds in F. xanthoxyla and related taxa, and for commentary linking coumarins and acridone alkaloids to observed activities.

Modern relevance remains modest. While flavonoids and coumarins from F. xanthoxyla have been screened for antibacterial activity (Johnstone and Czaplicki, 1993), clinical evidence is sparse. The species is primarily valued as a timber tree today, and organized medicinal products are not commercially available, though leaf infusions and decoctions persist as documented traditional preparations among some Aboriginal communities.

General Uses Top

Suggest a correction!

Common products:
Timber for structural applications (structural beams, heavy construction), specialty items (furniture, joinery), and carving/turning.

Industrial and craft applications:
Used for general construction timber; applications where durability and dimensional stability are important.

Food and beverages (non-medicinal):
None documented.

Colorants and tanning:
None documented.

Wood and fiber:
Wood is valued for its high density and strength; yellow-to-brown heartwood with fine grain suitable for furniture, flooring, and joinery. Also used for turning and carving; considered a durable, hard timber suitable for exterior applications where decay resistance is beneficial.

Fragrance and cosmetics:
None documented.

Properties relevant to use:
High density and strength; durability associated with naturally decay-resistant heartwood; fine, stable grain.

Standards and regulation:
No specific standards specific to this timber documented.

Sustainability and sourcing:
Not specifically documented; management under general forest practice regulations and certification schemes applicable in the species’ native range.

Synonyms Top

Scientific name Authority First published in
Oxleya xanthoxyla A.Cunn. Bot. Misc. 1: 246. 1830
Flindersia oxleyana F.Muell. Fragm. (Mueller) 1(4): 65. 1859 [Feb 1859]

Common names Top

Add a new one! Suggest a correction!
No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000691410
Tropicos 100339313
KEW urn:lsid:ipni.org:names:773635-1
The Plant List kew-2813521
Open Tree Of Life 499491
NCBI Taxonomy 67936
IUCN Red List 192231960
IPNI 773635-1
iNaturalist 538035
GBIF 3835106
Freebase /m/0cc9v08
USDA GRIN 203
Wikipedia Flindersia_xanthoxyla
CMAUP NPO24491

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
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
Pest categorisation of Toxoptera citricida Jeger M, Bragard C, Caffier D, Candresse T, Chatzivassiliou E, Dehnen‐Schmutz K, Gilioli G, Grégoire J, Jaques Miret JA, Navarro MN, Niere B, Parnell S, Potting R, Rafoss T, Rossi V, Urek G, Van Bruggen A, Van der Werf W, West J, Winter S, Gardi C, Bergeretti F, MacLeod A EFSA J 11-Jan-2018
PMCID:PMC7009757
doi:10.2903/j.efsa.2018.5103
PMID:32625662
The Chemical Constituents of Australian Flindersia Species. XII. The Constituents of Flindersia xanthoxyla Domin E Ritchie, WC Taylor, DV Willcocks CSIRO Publishing 01-Sep-2010
doi:10.1071/CH9600426

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
1-Phenyl-5-heptene-1,3-diyne 5281154 Click to see CC=CC#CC#CC1=CC=CC=C1 166.22 unknown via CMAUP database
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown via CMAUP database
Phenylheptatriyne 77981 Click to see 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
2-Butoxyethyl oleate 6436064 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCCOCCCC 382.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R)-1-hydroxytrideca-5,7,9,11-tetrayn-2-yl]oxyoxane-3,4,5-triol 54671425 Click to see CC#CC#CC#CC#CCCC(CO)OC1C(C(C(C(O1)CO)O)O)O 362.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
(2e)-7-Phenylhepta-2-en-4,6-diyn-1-yl acetate 23274467 Click to see 224.25 unknown via CMAUP database
7-Phenylhepta-2,4,6-triynyl acetate 11644243 Click to see CC(=O)OCC#CC#CC#CC1=CC=CC=C1 222.24 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2R)-7-phenylhepta-4,6-diyne-1,2-diol 101808987 Click to see C1=CC=C(C=C1)C#CC#CCC(CO)O 200.23 unknown via CMAUP database
(2S)-7-phenylhepta-4,6-diyn-2-ol 101395939 Click to see 184.23 unknown via CMAUP database
7-Phenyl-2,4,6-heptatriyn-1-ol 3085176 Click to see 180.20 unknown via CMAUP database
7-Phenylhept-2-en-4,6-diyn-1-ol 114662 Click to see 182.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
2-Butoxyethyl linoleate 87553426 Click to see 380.60 unknown via CMAUP database
2-Butoxyethyl linolenate 87552578 Click to see 378.60 unknown via CMAUP database
Ethyl Linoleate 5282184 Click to see 308.50 unknown via CMAUP database
Ethyl linolenate 5367460 Click to see 306.50 unknown via CMAUP database
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
Methyl Linolenate 5319706 Click to see 292.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
2-[(3R,7S,11S)-3-hydroxy-3,7,11,15-tetramethylhexadecyl]-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione 46183941 Click to see 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E,7S,11S)-3,7,11,15-tetramethylhexadec-2-enoic acid 42433537 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CC(=O)O)C 310.50 unknown via CMAUP database
[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enyl] heptanoate 101918983 Click to see CCCCCCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C 408.70 unknown via CMAUP database
Rel-(7S,11S,E)-3,7,11,15-tetramethylhexadec-2-en-1-ol 40467768 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,4S,5S,9S,10S,13R,14R,17R)-4,10,13-trimethyl-17-[(E,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 163086372 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C 426.70 unknown https://doi.org/10.1071/CH9600426
4-Methylstigmasta-7,24(28)-dien-3-ol 625305 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C 426.70 unknown https://doi.org/10.1071/CH9600426
alpha-Spinasterin 5281331 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Schottenol 441837 Click to see 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
CID 21952380 21952380 Click to see 118.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3,4-Bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxycyclohexane-1-carboxylic acid 153946 Click to see 516.40 unknown via CMAUP database
3,4-Dicaffeoylquinic acid 6474309 Click to see 516.40 unknown via CMAUP database
Isochlorogenic acid C 460890 Click to see 516.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(E)-3-[4-[(2S,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-enoic acid 15071014 Click to see 514.50 unknown via CMAUP database
(E)-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-enoic acid 15071011 Click to see 472.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
2-Acetylthiophene 6920 Click to see 126.18 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Flindersiamine 68221 Click to see 273.24 unknown https://doi.org/10.1071/CH9600426
Maculine 68232 Click to see 243.21 unknown https://doi.org/10.1071/CH9600426
> Organoheterocyclic compounds / Thiophenes / 2,5-disubstituted thiophenes
5-(Phenylethynyl)thiophene-2-methanol 2822242 Click to see 214.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Aurone flavonoids
(Z)-7-[[beta-D-Glucopyranosyl]oxy]-3',4',6-trihydroxyaurone 15071008 Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 66883 Click to see 208.21 unknown via CMAUP database
Ethyl Caffeate 5317238 Click to see 208.21 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
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 / Flavonoid glycosides / Flavonoid O-glycosides
(E)-3-(3,4-dihydroxyphenyl)-1-[2,3-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-en-1-one 14213552 Click to see 612.50 unknown via CMAUP database
[(2R,3R,4R,5R,6S)-3,4-diacetyloxy-6-[4-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]-2,3-dihydroxyphenoxy]-5-hydroxyoxan-2-yl]methyl acetate 14861259 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C(C=C2)C(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)OC(=O)C)OC(=O)C 576.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[4-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]-2,3-dihydroxyphenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 14213555 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C(C=C2)C(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O 492.40 unknown via CMAUP database
2,3-Dihydroxy-4-[(E)-3-(3,4-dihydroxyphenyl)acryloyl]phenyl 4-O,6-O-diacetyl-beta-D-glucopyranoside 10840030 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C(C=C2)C(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)OC(=O)C 534.50 unknown via CMAUP database
3',4'-Di(beta-D-glucopyranosyloxy)-2',3,4-trihydroxychalcone 102149400 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 612.50 unknown via CMAUP database
chrysosplenosid-C 118856019 Click to see 522.50 unknown via CMAUP database
Marein 6441269 Click to see 450.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Aurone O-glycosides
[(2R,3R,4R,5R,6S)-3,4-diacetyloxy-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-5-hydroxyoxan-2-yl]methyl acetate 10603216 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=O)C(=CC4=CC(=C(C=C4)O)O)O3)O)O)OC(=O)C)OC(=O)C 574.50 unknown via CMAUP database
[(2R,3S,4R,5R,6S)-3-acetyloxy-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-4,5-dihydroxyoxan-2-yl]methyl acetate 101669623 Click to see 532.40 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-3,5-diacetyloxy-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-4-hydroxyoxan-2-yl]methyl acetate 10674637 Click to see 574.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 15071009 Click to see 594.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 15071010 Click to see 490.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-3,6-dimethoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 101243893 Click to see 508.40 unknown via CMAUP database
5-hydroxy-2-(3-hydroxy-4-methoxy-phenyl)-3-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-chromen-4-one 5495545 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=C(C4=O)OC)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 638.60 unknown via CMAUP database
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13344657 Click to see 492.40 unknown via CMAUP database
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 102316697 Click to see 638.60 unknown via CMAUP database
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11577257 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)OC)O)OC)O 522.50 unknown via CMAUP database
Centaurein 5489090 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)OC)O)OC)O 522.50 unknown via CMAUP database
Hesperetin-7-Rutinoside 3594 Click to see 610.60 unknown https://doi.org/10.1071/CH9600426
Hesperidin 10621 Click to see 610.60 unknown https://doi.org/10.1071/CH9600426
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Jaceidin 5464461 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Okanin 5281294 Click to see 288.25 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.