Castanospermum australe
Details Top
| Internal ID | UUID643fdeab889ab926432430 |
| Scientific name | Castanospermum australe |
| Authority | A.Cunn. & C.Fraser |
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.
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.
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 |
Germination/Propagation Top
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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!
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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)!
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If you wish to see all the related articles click here.
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 |
|---|---|---|---|---|---|
| > 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 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |