Castanopsis hystrix
Details Top
| Internal ID | UUID6440554b371d1173457730 |
| Scientific name | Castanopsis hystrix |
| Authority | A.DC. |
| First published in | J. Bot. 1: 182. 1863 [Jun ? 1863] |
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.
An infusion of Cassia angustifolia leaves is a classic digestive remedy in the Unani tradition of the Middle East and North Africa, prepared by steeping 1–2 g of dried leaflets in 150 mL of near‑boiling water for 10–15 minutes; the dose of this “tea” is typically taken before breakfast and at bedtime, and the Unani pharmacopoeia advises limiting use to a short course due to cathartic effects. In West Africa, particularly Nigeria and Ghana, a decoction of the dried leaflets or pods in water is taken daily as a “bitter” tonic to promote regularity; Odugbemi and Akinsulire (2008) document this preparation and emphasize careful dosing to avoid griping. Across the Horn of Africa and the Arabian Peninsula, herbal practitioners likewise report short courses of strong leaf or pod infusions for occasional constipation, with the WHO monographs noting these aqueous preparations as standard practice. In both Unani and contemporary domestic settings, the leaves are most commonly used for infusions, while the mature pods are preferred for longer‑simmered decoctions.
A practical leaf tea can be made by pouring 200 mL of just‑boiled water over 1–2 g of dried Cassia angustifolia leaflets, covering and steeping 10–15 minutes, then straining. For a decoction, simmer 2 g of dried leaflets or crushed pods in 250 mL of water for 10 minutes, cool briefly, and take warm. For a tincture, a 1:5 ethanolic extract (45% alcohol) can be prepared at a common ratio such as 100 g dried leaves macerated in 500 mL solvent for two weeks with daily shaking; typical short‑course oral use is 1–2 mL once or twice daily for mild constipation. Safety notes are widely consistent: avoid continuous use beyond 7–10 days and do not use in intestinal obstruction, inflammatory bowel disease, or during pregnancy; children and those with gallstones should use under professional guidance. While tincture usage is documented in modern herbal practice, most classic and contemporary sources emphasize the infusions and decoctions.
The anthraquinone glycosides sennosides A and B, which are the principal laxative constituents in the leaves and pods, are well‑documented, and senna is recognized by WHO and the British Herbal Medicine Association for short‑term constipation relief. Other constituents, including flavonoids and mucilage, are also present and contribute to the plant’s bitterness and soothing qualities. The modern relevance is clear: senna tea remains widely available globally as a registered herbal medicinal product and dietary supplement, with ongoing research on standardization and pharmacokinetics, yet in practice, cautious short‑term use of the infusions remains common for occasional constipation.
General Uses Top
Suggest a correction!Common products:
Edible nuts are roasted or milled into flour; tannin extracts are produced from bark and wood chips; timber yields sawnwood, plywood, and veneer; charcoal and fuelwood are produced locally.
Industrial and craft applications:
Tannin extracts are used in leather tanning and as binding agents in plywood adhesives; silica-rich bark and sapwood generate fine charcoal for metalworking and drawing. Timbers produce veneers and plywood for furniture, flooring, and joinery; sawnwood is used in construction and carpentry.
Food and beverages (non-medicinal):
Nuts are eaten roasted or as flour for noodles, confections, and baking; they are not described as staples but occasionally used as snacks. No fermented beverages are documented for this species.
Colorants and tanning:
Bark and wood yield brown tannin extracts widely used for leather tanning; tannins are of the hydrolyzable class typical of Castanopsis. Extracts produce natural brown dyes suitable for protein fibers and mordanted cellulose fibers.
Wood and fiber:
Timber is dense and strong with fine to medium texture; species-specific grading and marking for furniture-grade veneers, joinery, and interior millwork are recognized in regional trade. Fiber is used for charcoal; pulp and paper usage is not documented for the species.
Fragrance and cosmetics:
Fragrance or cosmetic uses are not documented for this species.
Properties relevant to use:
High tannin content provides reactivity and UV stability in tanning and adhesives; hydrolyzable tannins are relatively soluble and metal-ion reactive. Wood density is high and species-specific timber grading systems recognize it for furniture applications; ring-porous wood contributes to strength but higher shrinkage.
Standards and regulation:
Regional timber grading and export standards apply to furniture-grade and veneer timbers; national regulations govern processed tannin products used in leather; compliance with timber legality and chain-of-custody systems is common in international trade. Food uses are subject to local food safety and labeling rules where applicable.
Sustainability and sourcing:
Castanopsis hystrix has a wide East and Southeast Asian distribution and is commonly harvested from natural forests and secondary stands for tannin extracts, nuts, and timber; local management practices aim to maintain viable populations through selection cutting and regeneration measures.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Castanopsis brunnea | (H.Lév.) A.Camus | Les Chataigniers 482 1929 |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | patle katus |
| Nepali | पातले कटुस |
| Chinese | 锥丝栗 |
| Chinese | 一种维管植物 |
| Chinese | 紅錐 |
| Chinese | 鉤栗 |
| Chinese | 火燒柯 |
| Chinese | 锥栗 |
| Chinese | 刺锥栗 |
| Chinese | 红㰀 |
| Chinese | 红锥栗 |
| Chinese | 椆栗 |
| Chinese | 红锥 |
| Chinese | 红椽木子 |
| Chinese | 栲树 |
| Chinese | 刺栲 |
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-0001240111 |
| KEW | urn:lsid:ipni.org:names:60450806-2 |
| The Plant List | tro-50106202 |
| PaleoBotany | 93849 |
| Open Tree Of Life | 129485 |
| NCBI Taxonomy | 167390 |
| IPNI | 295396-1 |
| iNaturalist | 544430 |
| GBIF | 5333131 |
| Freebase | /m/0271hkk |
| EOL | 1251942 |
| USDA GRIN | 9512 |
| Wikipedia | Castanopsis_hystrix |
| CMAUP | NPO10093 |
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)!
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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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Acylaminobenzoic acid and derivatives | |||||
| 4-[(2-amino-4-oxo-1H-pteridin-6-yl)methyl-formylamino]benzoic acid | 97575 | Click to see | 340.29 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives | |||||
| Abscisic Acid | 5280896 | Click to see | 264.32 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids | |||||
| (5S,6S,8S,9S,10S,11R,13S,14S)-6,11-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one | 92835934 | Click to see | 306.40 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives | |||||
| (3beta,5alpha,7alpha)-3,7-Dihydroxyandrostan-17-one | 9815044 | Click to see CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O | 306.40 | unknown | via CMAUP database |
| (3R,5R,7S,8R,9S,10S,13S,14S)-3,7-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one | 57386710 | Click to see CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O | 306.40 | unknown | via CMAUP database |
| (3R,5R,8R,9S,10S,13S,14S,17S)-3,17-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one | 69924431 | Click to see CC12CCC3C(C1CCC2O)C(=O)CC4C3(CCC(C4)O)C | 306.40 | unknown | via CMAUP database |
| (3R,5R,8R,9S,10S,13S,14S)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthrene-7,17-dione | 57386713 | Click to see CC12CCC(CC1CC(=O)C3C2CCC4(C3CCC4=O)C)O | 304.40 | unknown | via CMAUP database |
| (3R,5S,6S,8R,9S,10R,13S,14S)-3,6-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one | 69766330 | Click to see CC12CCC(CC1C(CC3C2CCC4(C3CCC4=O)C)O)O | 306.40 | unknown | via CMAUP database |
| (3S,5R,7R,8S,9S,10S,13R,14S,16S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,7,16-triol | 99574281 | Click to see | 308.50 | unknown | via CMAUP database |
| (3S,5R,7S,8S,9S,10S,13S,14S,16S)-3,7,16-trihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one | 99572894 | Click to see | 322.40 | unknown | via CMAUP database |
| (3S,5R,8S,9S,10S,13R,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one | 99573267 | Click to see CC12CCC3C(C1CC(C2)O)C(=O)CC4C3(CCC(C4)O)C | 306.40 | unknown | via CMAUP database |
| (3S,5R,8S,9S,10S,13R,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one | 99573266 | Click to see | 306.40 | unknown | via CMAUP database |
| (3S,5S,6S,8S,9S,10R,13R,14S,16R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,6,16-triol | 99574278 | Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(C4)O)C)O | 308.50 | unknown | via CMAUP database |
| (3S,5S,8S,9S,10R,13R,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one | 99571962 | Click to see | 306.40 | unknown | via CMAUP database |
| (3S,5S,8S,9S,10R,13R,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one | 99571961 | Click to see CC12CCC3C(C1CC(C2)O)CC(=O)C4C3(CCC(C4)O)C | 306.40 | unknown | via CMAUP database |
| (3S,5S,8S,9S,10S,11R,13S,14S,16S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,11,16-triol | 100922640 | Click to see CC12CCC(CC1CCC3C2C(CC4(C3CC(C4)O)C)O)O | 308.50 | unknown | via CMAUP database |
| (3S,5S,8S,9S,10S,13S,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one | 99601533 | Click to see | 306.40 | unknown | via CMAUP database |
| (3S,5S,8S,9S,10S,13S,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one | 99575783 | Click to see | 306.40 | unknown | via CMAUP database |
| (5R,8S,9S,10R,13S,14S,17S)-5,17-dihydroxy-10,13-dimethyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one | 10979706 | Click to see | 306.40 | unknown | via CMAUP database |
| (5R,8S,9S,10S,13R,14S,16S)-16-hydroxy-10,13-dimethyl-2,4,5,6,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,7-dione | 99571971 | Click to see | 304.40 | unknown | via CMAUP database |
| (5S,6R,8S,9S,10R,13R,14S,16S)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one | 99573707 | Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(=O)C4)C)O | 306.40 | unknown | via CMAUP database |
| (5S,6S,8S,9S,10R,13R,14S,16R)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one | 99573706 | Click to see | 306.40 | unknown | via CMAUP database |
| (5S,6S,8S,9S,10R,13R,14S,16S)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one | 99573705 | Click to see | 306.40 | unknown | via CMAUP database |
| (5S,6S,8S,9S,10S,11R,13S,14S)-6,11-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one | 99574441 | Click to see | 306.40 | unknown | via CMAUP database |
| (5S,8S,9R,10S,13S,14S,16R)-9,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,11-dione | 99571360 | Click to see | 320.40 | unknown | via CMAUP database |
| (5S,8S,9R,10S,13S,14S,16S)-9,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,11-dione | 99571358 | Click to see CC12CCC(=O)CC1CCC3C2(C(=O)CC4(C3CC(C4)O)C)O | 320.40 | unknown | via CMAUP database |
| (5S,8S,9S,10S,11R,13S,14S,16R)-11,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one | 100922644 | Click to see | 306.40 | unknown | via CMAUP database |
| (5S,8S,9S,10S,13S,14S,16R)-16-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,11-dione | 99574177 | Click to see | 304.40 | unknown | via CMAUP database |
| (5S,8S,9S,10S,13S,14S,16S)-16-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,11-dione | 99574175 | Click to see CC12CCC(=O)CC1CCC3C2C(=O)CC4(C3CC(C4)O)C | 304.40 | unknown | via CMAUP database |
| 11-Hydroxyandrosterone | 21139727 | Click to see CC12CCC(CC1CCC3C2C(CC4(C3CCC4=O)C)O)O | 306.40 | unknown | via CMAUP database |
| 11alpha-Hydroxy-5alpha-androstane-3,17-dione | 101709630 | Click to see CC12CCC(=O)CC1CCC3C2C(CC4(C3CCC4=O)C)O | 304.40 | unknown | via CMAUP database |
| 3beta-Hydroxy-5alpha-androstane-7,17-dione | 11954160 | Click to see CC12CCC(CC1CC(=O)C3C2CCC4(C3CCC4=O)C)O | 304.40 | unknown | via CMAUP database |
| 5alpha-Androstan-11-one, 3alpha,17beta-dihydroxy- | 10125601 | Click to see | 306.40 | unknown | via CMAUP database |
| 5alpha-Androstan-3-one, 11alpha,17beta-dihydroxy- | 22796602 | Click to see | 306.40 | unknown | via CMAUP database |
| 5alpha-Androstan-3beta,17beta-diol-7-one | 11868973 | Click to see CC12CCC3C(C1CCC2O)C(=O)CC4C3(CCC(C4)O)C | 306.40 | unknown | via CMAUP database |
| 5alpha-Androstan-6-one, 3beta,17beta-dihydroxy- | 11551286 | Click to see CC12CCC3C(C1CCC2O)CC(=O)C4C3(CCC(C4)O)C | 306.40 | unknown | via CMAUP database |
| 5alpha-Androstane-3,7,17-trione | 11266632 | Click to see CC12CCC(=O)CC1CC(=O)C3C2CCC4(C3CCC4=O)C | 302.40 | unknown | via CMAUP database |
| 7-beta-Hydroxyepiandrosterone | 9836181 | Click to see | 306.40 | unknown | via CMAUP database |
| Androstan-3-one, 6,17-dihydroxy-, (5alpha,6alpha,17beta)- | 15838416 | Click to see | 306.40 | unknown | via CMAUP database |
| Androstan-6-one, 3,17-dihydroxy-, (3alpha,5alpha,17beta)- | 15929496 | Click to see | 306.40 | unknown | via CMAUP database |
| Androstane-3,11,17-triol | 57396177 | Click to see | 308.50 | unknown | via CMAUP database |
| Androstane-3,17-dione, 6-hydroxy-, (5alpha,6alpha)- | 22296022 | Click to see | 304.40 | unknown | via CMAUP database |
| Androstane-3,6,17-triol | 170796 | Click to see CC12CCC3C(C1CCC2O)CC(C4C3(CCC(C4)O)C)O | 308.50 | unknown | via CMAUP database |
| Androstane-3,7,17-triol, (3beta,5alpha,7beta,17beta)- | 68995028 | Click to see | 308.50 | unknown | via CMAUP database |
| Exemestane Impurity 30 | 15917986 | Click to see | 306.40 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters | |||||
| 10-Hydroxy-3-oxoestr-4-en-17-yl acetate | 91691749 | Click to see CC(=O)OC1CCC2C1(CCC3C2CCC4=CC(=O)CCC34O)C | 332.40 | unknown | via CMAUP database |
| > Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives | |||||
| (E)-but-2-enedioate;hydron | 21883788 | Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-] | 116.07 | unknown | via CMAUP database |
| CID 21952380 | 21952380 | Click to see | 118.09 | unknown | via CMAUP database |
| Glutaric acid | 743 | Click to see C(CC(=O)O)CC(=O)O | 132.11 | unknown | via CMAUP database |
| > Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives | |||||
| 2-Oxonioacetate | 3698251 | Click to see C(C(=O)[O-])[OH2+] | 76.05 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Quinolines and derivatives / Quinoline carboxylic acids | |||||
| Quininic acid | 345824 | Click to see | 203.19 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins | |||||
| (2R,3S,10S)-2,10-bis(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4,9,10-tetrahydro-2H-pyrano[2,3-f]chromen-8-one | 10366587 | Click to see | 452.40 | unknown | https://doi.org/10.1016/0031-9422(93)85419-R |
| (4R,8R,9S)-4,8-bis(3,4-dihydroxyphenyl)-5,9-dihydroxy-4,8,9,10-tetrahydro-3H-pyrano[2,3-h]chromen-2-one | 100978387 | Click to see | 452.40 | unknown | https://doi.org/10.1016/0031-9422(93)85419-R |
| 4,8-bis(3,4-dihydroxyphenyl)-5,9-dihydroxy-4,8,9,10-tetrahydro-3H-pyrano[2,3-h]chromen-2-one | 73822599 | Click to see C1C(C(OC2=C1C3=C(C(CC(=O)O3)C4=CC(=C(C=C4)O)O)C(=C2)O)C5=CC(=C(C=C5)O)O)O | 452.40 | unknown | https://doi.org/10.1016/0031-9422(93)85419-R |
| 9,10-Dihydro-10-(3,4-dihydroxyphenyl)-pyrano(2,3-h)catechin-8-one | 10343836 | Click to see | 452.40 | unknown | https://doi.org/10.1016/0031-9422(93)85419-R |
| Epicatechin | 72276 | Click to see | 290.27 | unknown | https://doi.org/10.1016/0031-9422(93)85419-R |
Collections Top
| In private collections | 0 |
| In public collections | 0 |