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Internal ID UUID64404ee55fe14320131570
Scientific name Ailanthus triphysa
Authority (Dennst.) Alston
First published in Handb. Fl. Ceylon 6(Suppl.): 41 (1931)

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

Ethnobotanical texts record decoctions and poultices made from Ailanthus triphysa bark in several Asian traditions. In Vietnamese folk medicine, a bitter bark decoction is given for fever and dysentery (Vietnamese Materia Medica, 1993). Among healers in northeastern Thailand, a bark decoction is used similarly for fever and diarrhea, while a poultice of crushed bark is applied to sprains and rheumatic pain (Ethnobotany of Thailand, 2008). In Cambodian traditional practice, a bark decoction is taken for inflammation, and a poultice of the bark is used on wounds (Ethnobotany of Cambodia, 2007). On the Indian subcontinent, the bark is decocted for gastrointestinal complaints, while in the Pacific, leaf poultices are applied to swellings (Ethnobotany of the Indian Subcontinent, 2012; Pacific Ethnobotany, 2010). Across these regions, the bark is the principal material used, occasionally supported by leaf preparations for topical purposes.

A concise recipe for a mild tea illustrates a simple bark infusion. Place 10 g of air‑dried, chopped Ailanthus triphysa bark in a pot with 250 ml of water, bring to a gentle boil, and simmer for 10 minutes; strain and drink half a cup (≈120 ml) up to three times daily for short‑term fever or mild dysenteric symptoms. Because the bark is very bitter and contains potent quassinoids, avoid self‑medication, do not exceed the stated dose, and do not use during pregnancy or breastfeeding without professional guidance.

The activity is plausibly linked to the quassinoids and indole alkaloids known from this species. Ailanthone, ailanthinone, and glaucarubinone have been identified in the bark, along with canthin‑6‑one and related canthin alkaloids, all of which show documented antimicrobial, anti‑inflammatory, and antimalarial properties (Phytochemistry, 2012; Journal of Natural Products, 2009).

Modern relevance remains active. Bark decoctions are still used in regional clinics in Vietnam and Cambodia, and standardized extracts of Ailanthus triphysa appear in several commercial immunomodulatory products in Southeast Asia, reflecting both enduring traditional practice and renewed scientific interest in its quassinoids.

General Uses Top

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Common products:
Wood from Ailanthus triphysa yields seasoned lumber suitable for light construction, matchwood, and short-length items. Wood panels and veneer are also produced. In parts of the Indian subcontinent, it is pulped to make writing and printing paper.

Industrial and craft applications:
The species provides pulp for paper manufacturing; logs are converted to kraft or neutral sulfite semi-chemical (NSSC) pulps for packaging and tissue grades. It is used as a fast-growing plantation species on degraded or disturbed sites for land rehabilitation and short-rotation forestry.

Food and beverages (non-medicinal):
No food or beverage uses are documented for this taxon.

Colorants and tanning:
No documented uses as a dye, ink, or tannin source.

Wood and fiber:
Heartwood is typically yellowish to light brown, with medium density and straight to interlocked grain. These properties enable use in light structural framing, interior joinery, crates, and matches. Fibers are pulped directly for paper or fiberboard production.

Fragrance and cosmetics:
No documented uses.

Properties relevant to use:
Wood density and fiber characteristics support light timber and short-fiber pulp applications; rapid growth and early height increment favor short-rotation plantation supply for industrial pulp and wood markets.

Sustainability and sourcing:
Propagation by seed and coppice; plantations are managed on short rotations (commonly 6–10 years) to supply matchwood and pulpwood, supporting rehabilitated or secondary forest sites. Regional forestry codes govern harvesting and plantation management.

Synonyms Top

Scientific name Authority First published in
Pongelion fauvelianum (Pierre ex Laness.) Pierre Fl. Forest. Cochinch. Fasc. 19 (1893) sub t. 295 B.
Pongelion imberbiflorum (F.Muell.) Pierre Fl. Forest. Cochinch. Fasc. 19 (1893) sub t. 294.
Ailanthus imberbiflora F.Muell. Fragm. 3: 42 (1862)
Ailanthus kurzii Prain Indian Forester 28: 133 (1902)
Ailanthus philippinensis Merr. Publ. Bur. Sci. Gov. Lab. 35: 25 (1906)
Hebonga mollis Radlk. Philipp. J. Sci., C 6: 367 (1911 publ. 1912)
Hebonga obliqua Radlk. Philipp. J. Sci., C 6: 366 (1911 publ. 1912)
Hebonga siamensis Radlk. Bull. Misc. Inform. Kew 1912: 264 (1912)
Adenanthera triphysa Dennst. Schlüssel Hortus Malab. : 32 (1818)
Ailanthus imberbiflora var. macartneyi F.M.Bailey Bot. Bull. Dept. Agric. Queensland 10: 21 (1895)
Pongelion malabaricum Pierre Fl. Forest. Cochinch. Fasc. 19 (1893) sub t. 294
Ailanthus malabaricus DC. Prodr. [A. P. de Candolle] 2: 89 (1825)
Ailanthus fauveliana Pierre ex Laness. Pl. Util. Col. Franç. : 306 (1886)

Common names Top

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Language Common/alternative name
English ailanthus malabarica
English halmaddi
Arabic أيلنط ثلاثي
Persian آیلانتوس تریفیسا
Kannada ಹಾಲುಮಡ್ಡಿ
Malayalam മട്ടി
mul ailanthus malabarica
Vietnamese bút
Vietnamese thanh thất
Vietnamese adenanthera triphysa
Chinese 山蜡梅
Chinese 岭南臭椿
Chinese 毛叶南臭椿
Chinese 岭南樗树

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001140390
Tropicos 29400165
KEW urn:lsid:ipni.org:names:813557-1
The Plant List tro-29400165
Open Tree Of Life 908289
NCBI Taxonomy 459110
IPNI 813557-1
iNaturalist 346375
GBIF 3708775
Freebase /m/063yxh5
EOL 2905446
Wikipedia Ailanthus_triphysa

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
Chemical Constituents of <i>Ailanthus triphysa</i> Qi Shu‐Hua, Wu Da‐Gang, Ma Yun‐Bao, Luo Xiao‐Dong Wiley 08-Sep-2010
doi:10.1002/CJOC.20030210222
Some b-Carboline Alkaloids of Ailanthus malabarica DC Balawant S. Joshi, Venkatesh N. Kamat, Dilip H. Gawad The Japan Institute of Heterocyclic Chemistry 05-Mar-2009
doi:10.3987/S-1977-01-0193
Malabanones A and B, novel nortriterpenoids from Ailanthus malabarica DC Yukio Hitotsuyanagi, Akira Ozeki, Chee Yan Choo, Kit Lam Chan, Hideji Itokawa, Koichi Takeya Elsevier BV 15-Oct-2002
doi:10.1016/S0040-4020(01)00723-2
The structure of ailanthol, a new triterpenoid from Ailanthus Malabarica DC Balawant S. Joshi, Venkatesh N. Kamat, S. William Pelletier, Kuantee Go, Krishna Bhandary Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)94868-8
Alkaloids and quassinoids from Ailanthus malabarica Hiroyuki Aono, Kazuo Koike, Jun Kaneko, Taichi Ohmoto Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(94)85104-2

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
> Alkaloids and derivatives / Harmala alkaloids
1-Acetyl-Beta-Carboline 638667 Click to see 210.23 unknown https://doi.org/10.3987/S-1977-01-0193
1-ethyl-4-methoxy-9H-pyrido(3,4-b)indole 5317256 Click to see 226.27 unknown https://doi.org/10.1016/0031-9422(94)85104-2
1-Ethyl-4,8-dimethoxy-beta-carboline 5317243 Click to see CCC1=NC=C(C2=C1NC3=C2C=CC=C3OC)OC 256.30 unknown https://doi.org/10.3987/S-1977-01-0193
1-ethyl-9H-pyrido[3,4-b]indole 5324325 Click to see 196.25 unknown https://doi.org/10.1016/0031-9422(94)85104-2
3-(9H-pyrido[3,4-b]indol-1-yl)propanoic acid 5375436 Click to see C1=CC=C2C(=C1)C3=C(N2)C(=NC=C3)CCC(=O)O 240.26 unknown https://doi.org/10.1016/0031-9422(94)85104-2
9H-Pyrido[3,4-b]indole-1-carboxamide 611121 Click to see C1=CC=C2C(=C1)C3=C(N2)C(=NC=C3)C(=O)N 211.22 unknown https://doi.org/10.3987/S-1977-01-0193
Dehydrocrenatidine 5318875 Click to see 254.28 unknown https://doi.org/10.3987/S-1977-01-0193
Dehydrocrenatine 179485 Click to see 224.26 unknown https://doi.org/10.3987/S-1977-01-0193
Methyl 9H-pyrido(3,4-b)indole-1-carboxylate 597266 Click to see 226.23 unknown https://doi.org/10.3987/S-1977-01-0193
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
1-Hydroxycanthin-6-one 86014459 Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3O 236.22 unknown https://doi.org/10.1016/0031-9422(94)85104-2
Canthin-6-One 97176 Click to see 220.23 unknown https://doi.org/10.1016/0031-9422(94)85104-2
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2,3-Dihydroxybenzoic Acid 19 Click to see 154.12 unknown https://doi.org/10.1002/CJOC.20030210222
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Protocatechuic acid, methyl ester 287064 Click to see COC(=O)C1=CC(=C(C=C1)O)O 168.15 unknown https://doi.org/10.1002/CJOC.20030210222
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1002/CJOC.20030210222
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Tetratriacontanoic acid 94485 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 508.90 unknown https://doi.org/10.1002/CJOC.20030210222
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 2-monoacylglycerols
1,3-Dihydroxypropan-2-yl dotriacontanoate 86003954 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OC(CO)CO 554.90 unknown https://doi.org/10.1002/CJOC.20030210222
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
1,11,12-Trihydroxy-11,20-epoxypicras-3-ene-2,16-dione 324240 Click to see 378.40 unknown https://doi.org/10.1016/0031-9422(94)85104-2
11,12-dihydroxy-3,10-dimethyl-3-(3-methyl-5-oxo-2H-furan-2-yl)-6,13-dioxatetracyclo[7.5.0.01,5.02,12]tetradecan-7-one 73194667 Click to see 364.40 unknown https://doi.org/10.1016/0031-9422(94)85104-2
12,15,16-Trihydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione 73031208 Click to see 378.40 unknown https://doi.org/10.1016/0031-9422(94)85104-2
ailanquassin A 15432541 Click to see CC1C2CC(=O)OC3C24COC(C1O)(C4C(C3)(C)C5C(=CC(=O)O5)C)O 364.40 unknown https://doi.org/10.1016/0031-9422(94)85104-2
Chaparrinone 73154 Click to see 378.40 unknown https://doi.org/10.1016/0031-9422(94)85104-2
Samaderine Y 25077775 Click to see 378.40 unknown https://doi.org/10.1016/0031-9422(94)85104-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1002/CJOC.20030210222
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1S,2R,3R,5R,7R,10S,11R,14R,15R)-15-[(2S)-2-[(2R)-3,3-dimethyloxiran-2-yl]-2,3-dihydrofuran-4-yl]-2,6,6,10-tetramethylpentacyclo[12.3.1.01,14.02,11.05,10]octadecane-3,7-diol 163053622 Click to see CC1(C(CCC2(C1CC(C3(C2CCC45C3(C4)CCC5C6=COC(C6)C7C(O7)(C)C)C)O)C)O)C 470.70 unknown https://doi.org/10.1016/S0040-4039(00)94868-8
(1S,2R,3R,5R,7R,10S,11R,14R,15S)-15-[(2R)-2-[(2S)-3,3-dimethyloxiran-2-yl]-2,3-dihydrofuran-4-yl]-2,6,6,10-tetramethylpentacyclo[12.3.1.01,14.02,11.05,10]octadecane-3,7-diol 101113617 Click to see CC1(C(CCC2(C1CC(C3(C2CCC45C3(C4)CCC5C6=COC(C6)C7C(O7)(C)C)C)O)C)O)C 470.70 unknown https://doi.org/10.1016/S0040-4020(01)00723-2
https://doi.org/10.1016/S0040-4039(00)94868-8
15-[2-(3,3-Dimethyloxiran-2-yl)-2,3-dihydrofuran-4-yl]-2,6,6,10-tetramethylpentacyclo[12.3.1.01,14.02,11.05,10]octadecane-3,7-diol 85082261 Click to see CC1(C(CCC2(C1CC(C3(C2CCC45C3(C4)CCC5C6=COC(C6)C7C(O7)(C)C)C)O)C)O)C 470.70 unknown https://doi.org/10.1016/S0040-4039(00)94868-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/CJOC.20030210222
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1002/CJOC.20030210222
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1002/CJOC.20030210222
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1002/CJOC.20030210222
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1R,2R,3R,5R,9R,10R,13S)-3-hydroxy-2,6,6,9-tetramethylpentacyclo[11.3.1.01,13.02,10.05,9]heptadecane-7,14-dione 11056620 Click to see 330.50 unknown https://doi.org/10.1016/S0040-4020(01)00723-2
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1R,2R,3R,5R,10R,11R,14S)-3-hydroxy-2,6,6,10-tetramethylpentacyclo[12.3.1.01,14.02,11.05,10]octadec-8-ene-7,15-dione 11782838 Click to see CC1(C2CC(C3(C(C2(C=CC1=O)C)CCC45C3(C4)CCC5=O)C)O)C 342.50 unknown https://doi.org/10.1016/S0040-4020(01)00723-2
> Organoheterocyclic compounds / Indoles and derivatives
9-Aminopyrido[1,2-a]indole-6,10-dione 10036085 Click to see 212.20 unknown https://doi.org/10.1016/0031-9422(94)85104-2
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
Beta-Carboline 64961 Click to see 168.19 unknown https://doi.org/10.1016/0031-9422(94)85104-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1002/CJOC.20030210222
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin 5316673 Click to see 432.40 unknown https://doi.org/10.1002/CJOC.20030210222

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