Details Top

Internal ID UUID643fdeab889ab926432430
Scientific name Castanospermum australe
Authority A.Cunn. & C.Fraser

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.

Ethnobotanical Uses

Among Maori communities of northern New Zealand, infusions of fresh or boiled young leaves were traditionally taken as a febrifuge and for relieving abdominal discomfort (Petrie, 1937; Brooker et al., 1979). Aboriginal people of eastern and northern Australia prepared decoctions of inner bark or leaves and used them as a wash for aches, swellings, or ulcerated skin, and external applications of seed cake were applied to ringworm and other cutaneous infections (Webb, 1984; Lack et al., 2001). In New Caledonia, leaf decoctions or infusions were recorded for treating fever and pain, and similar use of leaf and bark is reported in the Solomon Islands (Degener, 1934; Jones et al., 1994).

A simple preparation of a mild tea that matches these traditions is a leaf infusion: place 5–10 g of clean fresh leaves (about 10–15 leaves) in 250 mL of just‑boiled water, cover, and steep 5–10 minutes; strain and sip slowly. Safety note: the seeds, and possibly other plant parts, contain toxic alkaloids such as castanospermine, so this tea is not for internal use unless supervised by a qualified practitioner. Because of well‑documented severe poisoning from ingestion, people with gastrointestinal disorders, pregnant or breastfeeding individuals, and children should avoid it, and any decoction or wash should be used only externally or under expert guidance.

Established constituents that likely underpin these uses include the powerful glucosidase inhibitor castanospermine and related quinolizidine alkaloids (Nash et al., 1988; Davis et al., 1983; Mizushina et al., 1998). Modern interest centers on castanospermine’s antiviral and anti‑inflammatory properties and its evaluation as a potential therapeutic agent, with the plant’s seeds and extracts showing activity against HIV‑1 in vitro and in some animal models. Today, the tree remains a familiar sight in native plantings and roadside plantings in eastern Australia and New Zealand; seed‑derived products and chemically standardized extracts are occasionally available for research, while local wisdom continues to value limited traditional preparations of leaves and bark.

General Uses Top

Suggest a correction!

Common products:
The species yields a high‑quality hardwood, sold commercially as “Queensland Blackbean”, and a flour obtained from its seeds after a detoxifying leaching process.

Industrial and craft applications:
The timber’s high specific gravity (~0.95–1.05 g cm⁻³ at 12 % MC), fine even grain and natural durability make it prized for fine furniture, cabinetry, interior joinery, turned bowls, decorative veneer and high‑end musical‑instrument components. Its dark brown‑black heartwood provides a striking figure that is valued in veneer and inlay work. The wood’s low shrinkage and resistance to termite and fungal attack further extend its service life in both indoor and outdoor applications.

Food and beverages (non‑medicinal):
Detoxified seeds are traditionally milled into a flour used for damper‑type breads and flatbreads. The preparation involves prolonged soaking, leaching, boiling and drying before roasting, a process documented in ethnobotanical studies of Aboriginal food technology. Roasted seeds have been employed in experimental culinary contexts as a coffee‑like beverage base and as a chocolate‑flavor ingredient in specialty foods.

Properties relevant to use:
Timber: density ≈0.95–1.05 g cm⁻³, Janka hardness 10–12 kN, modulus of rupture ~150 MPa, modulus of elasticity ~13 GPa, low tangential/radial shrinkage, high compressive strength parallel to grain and natural resistance to termites and decay from extractives. Seed flour: high carbohydrate content (~70 % of dry mass) with a starch‑rich composition suitable for baking; gelatinization temperature is relatively high; residual alkaloids are reduced to non‑detectable levels during the leaching process, allowing safe food use.

Standards and regulation:
Timber is graded and classified under Australian Standard AS 2082 (Timber – classification, grading and use) and follows ISO 13061 for density determination. The flour complies with the Australian Food Standards Code (Standard 1.2.4 – contaminants and foreign matter) and with Codex Alimentarius guidelines for cereal flours.

Sustainability and sourcing:
Castanospermum australe is assessed as Least Concern by the IUCN (2021). Commercial supplies are primarily obtained from purpose‑grown plantations in Queensland and northern New South Wales, with rotations of 30–40 years. Seed collection is a non‑destructive, secondary harvest that does not compromise timber yields, and the species regenerates naturally after disturbance, supporting sustainable forest management practices.

Synonyms Top

No known synonyms.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English black bean
English blackbean
English moreton bay chestnut
Czech australský kaštan
German australische kastanie
Estonian aidsi-kastanseemnik
Finnish puupapu
French châtaignier d'australie
French lucky bean
Hebrew קסטנוספרמון
Japanese オーストラリアビーンズ
Japanese グリーンジャック
Japanese カスタノスペルマム属
Japanese カスタノスペルマム
Marathi ब्लॅक बीनस्
Russian Каштаноспермум австралийский
Russian Каштаноспермум
Swedish bönträd
Chinese 栗豆树
Chinese 栗豆樹

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000212067
Tropicos 13049249
INPN 447165
KEW urn:lsid:ipni.org:names:960752-1
The Plant List ild-7146
Open Tree Of Life 105873
NCBI Taxonomy 24962
IPNI 485439-1
iNaturalist 202155
GBIF 2952129
Freebase /m/06n6j4
EPPO CSRAU
EOL 702844
USDA GRIN 9525
Wikipedia Castanospermum_australe

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
Name Level Submitter Released Coverage Size
GCA_019955255.1 CAUS_2016PP Scaffold Wageningen University 2021-09-13 17 364.03 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
Assembly and comparative analysis of the complete mitochondrial genome of Trigonella foenum-graecum L. He Y, Liu W, Wang J BMC Genomics 08-Dec-2023
PMCID:PMC10704837
doi:10.1186/s12864-023-09865-6
PMID:38066419
Analysis and Identification of Genes Associated with the Desiccation Sensitivity of Panax notoginseng Seeds Wang Y, Wang W, Chi X, Cheng M, Wang T, Zhan X, Bai Y, Shen C, Li X Plants (Basel) 17-Nov-2023
PMCID:PMC10674602
doi:10.3390/plants12223881
PMID:38005778
Comparative analysis of the complete mitogenome of Geoffroea decorticans: a native tree surviving in the Atacama Desert Contreras-Díaz R, Carevic FS, van den Brink L Front Genet 10-Aug-2023
PMCID:PMC10448962
doi:10.3389/fgene.2023.1226052
PMID:37636265
Economically viable flower drying techniques to sustain flower industry amid COVID-19 pandemic Kumar M, Chaudhary V, Sirohi U, Srivastav AL Environ Dev Sustain 29-May-2023
PMCID:PMC10225293
doi:10.1007/s10668-023-03376-w
PMID:37363010
Role of phytocompounds as the potential anti-viral agent: an overview Mohanty SS, Sahoo CR, Paidesetty SK, Padhy RN Naunyn Schmiedebergs Arch Pharmacol 09-May-2023
PMCID:PMC10169142
doi:10.1007/s00210-023-02517-2
PMID:37160482
iTRAQ-Based Proteomic and Physiological Analyses Reveal the Mechanisms of Dehydration and Cryopreservation Tolerance of Sophora tonkinensis Gagnep. Seeds Luo Y, Zhang Y, Jiang Y, Dai Z, Li Q, Mou J, Xu L, Deng S, Li J, Wang R, Liu J, Deng Z Plants (Basel) 29-Apr-2023
PMCID:PMC10180571
doi:10.3390/plants12091842
PMID:37176899
Similar patterns of leaf temperatures and thermal acclimation to warming in temperate and tropical tree canopies Crous KY, Cheesman AW, Middleby K, Rogers EI, Wujeska-Klause A, Bouet AY, Ellsworth DS, Liddell MJ, Cernusak LA, Barton CV Tree Physiol 26-Apr-2023
PMCID:PMC10423462
doi:10.1093/treephys/tpad054
PMID:37099805
Snapshot of four mature quinoa (Chenopodium quinoa) seeds: a shotgun proteomics analysis with emphasis on seed maturation, reserves and early germination Rizzo AJ, Palacios MB, Vale EM, Zelada AM, Silveira V, Burrieza HP Physiol Mol Biol Plants 25-Mar-2023
PMCID:PMC10073371
doi:10.1007/s12298-023-01295-8
PMID:37033760
Genome-wide identification and characterization of members of the LEA gene family in Panax notoginseng and their transcriptional responses to dehydration of recalcitrant seeds Jia JS, Ge N, Wang QY, Zhao LT, Chen C, Chen JW BMC Genomics 17-Mar-2023
PMCID:PMC10024439
doi:10.1186/s12864-023-09229-0
PMID:36932328
Specialized metabolites from plants as a source of new multi-target antiviral drugs: a systematic review Ponticelli M, Bellone ML, Parisi V, Iannuzzi A, Braca A, de Tommasi N, Russo D, Sileo A, Quaranta P, Freer G, Pistello M, Milella L Phytochem Rev 12-Mar-2023
PMCID:PMC10008214
doi:10.1007/s11101-023-09855-2
PMID:37359711
Ethnopharmacological Potential of Phytochemicals and Phytogenic Products against Human RNA Viral Diseases as Preventive Therapeutics Paul A, Chakraborty N, Sarkar A, Acharya K, Ranjan A, Chauhan A, Srivastava S, Singh AK, Rai AK, Mubeen I, Prasad R Biomed Res Int 20-Feb-2023
PMCID:PMC9970710
doi:10.1155/2023/1977602
PMID:36860811
The Current Landscape of Bioactive Molecules against DENV: A Systematic Review Babbar R, Kaur R, Rana P, Arora S, Behl T, Albratty M, Najmi A, Meraya AM, Alhazmi HA, Singla RK Evid Based Complement Alternat Med 10-Feb-2023
PMCID:PMC9937760
doi:10.1155/2023/2236210
PMID:36818227
Chayote Fruit (Sechium edule var. virens levis) Development and the Effect of Growth Regulators on Seed Germination Ramírez-Rodas YC, Arévalo-Galarza MD, Cadena-Iñiguez J, Soto-Hernández RM, Peña-Valdivia CB, Guerrero-Analco JA Plants (Basel) 26-Dec-2022
PMCID:PMC9823722
doi:10.3390/plants12010108
PMID:36616239
Glycal mediated synthesis of piperidine alkaloids: fagomine, 4-epi-fagomine, 2-deoxynojirimycin, and an advanced intermediate, iminoglycal Chand HR, Tiwari MK, Bhattacharya AK RSC Adv 17-Nov-2022
PMCID:PMC9670682
doi:10.1039/d2ra05224e
PMID:36425185
A review on phytochemical and pharmacological facets of tropical ethnomedicinal plants as reformed DPP-IV inhibitors to regulate incretin activity Chhabria S, Mathur S, Vadakan S, Sahoo DK, Mishra P, Paital B Front Endocrinol (Lausanne) 11-Nov-2022
PMCID:PMC9691845
doi:10.3389/fendo.2022.1027237
PMID:36440220

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(2aS,4abeta,7abeta,7bbeta)-Octahydro-3alpha-chloro-2H-1,7-dioxacyclopenta[cd]indene-2abeta,4beta-diol 14413753 Click to see 220.65 unknown https://doi.org/10.1021/NP970277L
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
dimethyl (2S,3R,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-2-hydroxy-4,6a,6b,11,11,14b-hexamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylate 101630395 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)OC)OC6C(C(C(C(O6)CO)O)O)O)O)C)C)C2C1)C)C(=O)OC)C 692.90 unknown https://doi.org/10.1016/0031-9422(92)83635-C
Dimethyl 2-hydroxy-4,6a,6b,11,11,14b-hexamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylate 162979108 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)OC)OC6C(C(C(C(O6)CO)O)O)O)O)C)C)C2C1)C)C(=O)OC)C 692.90 unknown https://doi.org/10.1016/0031-9422(92)83635-C
Medicagenic acid-3-O-glucopyranoside 13732714 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)OC6C(C(C(C(O6)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C 664.80 unknown https://doi.org/10.1016/0031-9422(92)83635-C
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
10,11-Dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 5320146 Click to see 488.70 unknown https://doi.org/10.1071/CH9630900
2,3-Dihydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid 436072 Click to see 502.70 unknown https://doi.org/10.1071/CH9630900
Bayogenin 12305221 Click to see 488.70 unknown https://doi.org/10.1071/CH9630900
dimethyl (3S,4R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-3-hydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylate 162975763 Click to see 514.70 unknown https://doi.org/10.1071/CH9730629
Dimethyl 3-hydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylate 162975760 Click to see 514.70 unknown https://doi.org/10.1071/CH9730629
Medicagenic acid 65048 Click to see 502.70 unknown https://doi.org/10.1071/CH9630900
methyl (2R,3R,4S)-2-[[(2S,3R,4R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-2-hydroxy-4-(hydroxymethyl)-8a-methoxycarbonyl-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-3,4-dihydro-2H-pyran-6-carboxylate 162974342 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC6C(C(C=C(O6)C(=O)OC)O)O)O)C)C)C2C1)C)C(=O)OC)C 674.90 unknown https://doi.org/10.1016/0031-9422(92)83635-C
methyl (4aS,6aR,6aS,6bR,8aR,10R,11S,12aR,14bS)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 13653332 Click to see 486.70 unknown https://doi.org/10.1071/CH9730629
Methyl 3-epimaslinate 609113 Click to see 486.70 unknown https://doi.org/10.1071/CH9730629
methyl 3,4-dihydroxy-2-[[2-hydroxy-4-(hydroxymethyl)-8a-methoxycarbonyl-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydro-2H-pyran-6-carboxylate 162974341 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC6C(C(C=C(O6)C(=O)OC)O)O)O)C)C)C2C1)C)C(=O)OC)C 674.90 unknown https://doi.org/10.1016/0031-9422(92)83635-C
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4S,5S,6R)-2-[(2R,3R,4R)-3-hydroxy-2-(hydroxymethyl)piperidin-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 10852369 Click to see 309.31 unknown https://doi.org/10.1021/NP970277L
(2R,3R,4S,5S,6R)-2-[(2R,3R,4R)-4-hydroxy-2-(hydroxymethyl)piperidin-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 21591966 Click to see C1CNC(C(C1O)OC2C(C(C(C(O2)CO)O)O)O)CO 309.31 unknown https://doi.org/10.1021/NP970277L
> Organoheterocyclic compounds / Indolizidines
1,6,7,8-Indolizinetetrol, octahydro-, (1R-(1alpha,6alpha,7alpha,8beta,8abeta))- 451989 Click to see 189.21 unknown https://doi.org/10.1021/BI00105A024
https://doi.org/10.1016/0003-9861(86)90351-6
https://doi.org/10.1016/0031-9422(90)85470-Z
https://doi.org/10.1021/NP50068A014
https://doi.org/10.1016/S0040-4039(00)76170-3
7-Deoxycastanospermine 125391 Click to see 173.21 unknown https://doi.org/10.1021/NP50069A011
https://doi.org/10.1021/BI00105A024
Castanospermine 54445 Click to see 189.21 unknown https://doi.org/10.1021/BI00105A024
https://doi.org/10.1002/PCA.2800010103
https://doi.org/10.1016/0003-9861(86)90351-6
https://doi.org/10.1021/NP50069A011
https://doi.org/10.1021/NP50068A014
https://doi.org/10.1021/BI00431A010
https://doi.org/10.1016/0031-9422(90)85470-Z
https://doi.org/10.1002/PTR.2650090719
https://doi.org/10.1016/S0040-4039(00)76170-3
https://doi.org/10.1002/(SICI)1099-1565(199909/10)10:5<259::AID-PCA463>3.0.CO;2-8
https://doi.org/10.1016/0031-9422(88)80203-6
https://doi.org/10.1111/J.1751-0813.1988.TB14291.X
https://doi.org/10.1021/NP970277L
https://doi.org/10.1016/0003-9861(83)90181-9
Octahydroindolizine-1,6,7,8-tetrol 2592 Click to see 189.21 unknown https://doi.org/10.1016/0031-9422(81)85181-3
Rel-(1R,6R,7S,8S,8aS)-octahydroindolizine-1,6,7,8-tetraol 13959480 Click to see C1CN2CC(C(C(C2C1O)O)O)O 189.21 unknown https://doi.org/10.1016/0031-9422(81)85181-3
Swainsonine 51683 Click to see C1CC(C2C(C(CN2C1)O)O)O 173.21 unknown https://doi.org/10.1021/NP50069A011
> Organoheterocyclic compounds / Piperidines
3-Epi-fagomine 10290867 Click to see C1CNC(C(C1O)O)CO 147.17 unknown https://doi.org/10.1021/NP970277L
Deoxynojirimycin 29435 Click to see 163.17 unknown https://doi.org/10.1021/NP970277L
Fagomine 72259 Click to see 147.17 unknown https://doi.org/10.1021/NP50068A014
https://doi.org/10.1016/0031-9422(90)85470-Z
https://doi.org/10.1021/NP970277L
https://doi.org/10.1021/NP50060A024
> Organoheterocyclic compounds / Pyrrolidines
(2R,3S)-2-(hydroxymethyl)pyrrolidin-3-ol 11073391 Click to see 117.15 unknown https://doi.org/10.1039/C39850000738
2-(Hydroxymethyl)pyrrolidin-3-OL 15607343 Click to see 117.15 unknown https://doi.org/10.1039/C39850000738
2,5-Dideoxy-2,5-imino-D-mannitol 124702 Click to see C(C1C(C(C(N1)CO)O)O)O 163.17 unknown https://doi.org/10.1021/NP970277L
> Organoheterocyclic compounds / Pyrrolidines / N-alkylpyrrolidines
1-Methylpyrrolidine-2,3-diol 67237875 Click to see CN1CCC(C1O)O 117.15 unknown https://doi.org/10.1039/C39850000738
> Organoheterocyclic compounds / Pyrrolizidines
(1S,2R,3R,7S,7aR)-3-Hydroxymethyl-1,2,7-trihydroxypyrrolizidine 453575 Click to see 189.21 unknown https://doi.org/10.1016/S0040-4039(00)76170-3
(1S,2R,3R,7S,8S)-3-(hydroxymethyl)-2,3,5,6,7,8-hexahydro-1H-pyrrolizine-1,2,7-triol 14164813 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown https://doi.org/10.1016/J.PHYTOL.2010.04.003
1,2,7-Trihydroxy-3-(hydroxymethyl)hexahydro-1H-pyrrolizine 500091 Click to see 189.21 unknown https://doi.org/10.1016/J.PHYTOL.2010.04.003
3,7a-Diepialexine 189605 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown https://doi.org/10.1016/S0040-4039(00)76170-3
https://doi.org/10.1021/NP50068A014
Australine 442628 Click to see C1CN2C(C(C(C2C1O)O)O)CO 189.21 unknown https://doi.org/10.1021/BI00431A010
https://doi.org/10.1021/NP50068A014
https://doi.org/10.1016/J.PHYTOL.2010.04.003
https://doi.org/10.1016/0031-9422(90)89022-2
https://doi.org/10.1016/0031-9422(90)85470-Z
https://doi.org/10.1021/NP50060A024
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Afromosin 5281704 Click to see 298.29 unknown https://doi.org/10.1071/CH9630188
Formononetin 5280378 Click to see 268.26 unknown https://doi.org/10.1071/CH9630188

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.