Details Top

Internal ID UUID643ffbc6b7503817443856
Scientific name Zanthoxylum rhetsa
Authority (Roxb.) DC.
First published in Prodr. 1: 728 (1824)

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.

In parts of southern India and Sri Lanka, Zanthoxylum rhetsa is best known as a gentle carminative for the upper gut and for easing wind in infants. Preparations are usually simple teas or infusions made from the leaves and tender twigs. Among Malayali communities of the southern hills, a hot infusion of fresh leaves and shoots is drunk for stomachache and indigestion (Trivedi, 2012). In Tamil Nadu and Karnataka, “karuvellam” tea—made from leaves or leaf powder infused with hot water—is given to newborns and young children to calm colic (Singhal & Ratra, 2020). In Sri Lanka’s dry-zone villages, a weaker leaf infusion is taken to relieve flatulence, especially in children (Senanayake, 1986). Seeds are sometimes chewed as a spice after meals, but the documented ethnomedicinal forms are infusions of leaves/twigs and topical pastes.

A practical preparation is the mild karuvellam leaf tea. Add one to two heaped tablespoons of fresh, clean leaves or leaf powder to 200 ml of just-boiled water, cover, and steep 5–7 minutes. Strain, and drink a small cup warm. For external use, crush a tablespoon of seeds with a pinch of water to form a paste and apply to the skin. These small infusions are generally considered safe in culinary contexts. As with many essentials, do not use during pregnancy or give large doses to infants without professional guidance, and discontinue if irritation occurs.

The activity is supported by well-established constituents found in the species. Seeds and pericarp are rich in aromatic monoterpenes—linalool, citronellal, limonene, and α-pinene—that are documented for Zanthoxylum rhetsa and known to relax smooth muscle and reduce gas (Rastogi & Singh, 1990; Rao, 1972). Fresh leaf and shoot oils are similarly dominated by these volatiles (Naidu et al., 1995), explaining the use of leaf infusions for colic and flatulence.

Zanthoxylum rhetsa remains a minor spice in Indian and Sri Lankan markets, and Indian ayurvedic dispensaries still list it for “anaha” (flatulence). Research on the species has focused on its essential oils, which show antimicrobial activity and other biological effects consistent with traditional use.

General Uses Top

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Common products:
The species is used as a spice or condiment, commonly as the dried pericarp (“triphalā” in South Asian trade practice), and sometimes as a whole or ground spice added to curries, pickles, and spice mixes. Its seeds are occasionally used as a condiment.

Industrial and craft applications:
The green parts yield essential oil on hydrodistillation; the oil is used in flavor and fragrance applications. No established industrial processing standards are reported for the oil or other materials from this species.

Food and beverages (non-medicinal):
The dried pericarp and seeds are used as flavoring ingredients in culinary products such as curry powders and pickles. They are not reported as a major source of starch, flour, seed oils, or fats for food processing.

Colorants and tanning:
No documented use of bark or pericarp as natural dyes or for tannin extraction is reported for this species.

Wood and fiber:
No documented timber or fiber uses are reported for this species.

Fragrance and cosmetics:
Essential oil from green parts is used in flavor and fragrance applications; quantitative compositional ranges vary in reports and are not standardized for commercial fragrance compounding.

Properties relevant to use:
Chemical markers reported for the species include linalool and possibly related monoterpenes in the essential oil. No standardized specifications for fragrance use (e.g., ISO/ASTM standards) are documented.

Sustainability and sourcing:
No established sustainability or regulatory frameworks are documented for this species in commercial supply chains.

Synonyms Top

Scientific name Authority First published in
Zanthoxylum parviflorum Benth. Fl. Austral. 1: 363 (1863)
Zanthoxylum budrunga DC. Prodr. 1: 728 (1824)
Zanthoxylum limonella (Dennst.) Alston Handb. Fl. Ceylon 6(Suppl.): 37 (1931)
Tipalia limonella Dennst. Schlüssel Hortus Malab. : 31 (1818)
Fagara budrunga Roxb. Fl. Ind. 1: 437 (1820)
Fagara parviflora Engl. Nat. Pflanzenfam. 3(4): 119 (1896)
Fagara rhetsa Roxb. Fl. Ind. 1: 438 (1820)
Zanthoxylum rhetsum St.-Lag. Ann. Soc. Bot. Lyon vii. (1880) 137.
Zanthoxylum crenatum Wall. Numer. List [Wallich] n. 1216. 1829
Zanthoxylum oblongum Wall. Numer. List [Wallich] n. 1218. 1829
Lacuris illicioides Buch.-Ham. Numer. List [Wallich] n. 7119. 1832

Common names Top

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Language Common/alternative name
ban panggal buaya
Estonian india koldpuu
Kannada ಕವಟೆಕಾಯ್ಮರ
mad kaju tana
Malayalam മുള്ളിലവ്
Marathi तिरफळ
Malay hantu duri
Telugu రాచమాను
Vietnamese mắc khén

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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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

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Database ID/link to page
World Flora Online wfo-0000429347
UNII N86XJX3N15
Tropicos 28101723
KEW urn:lsid:ipni.org:names:775986-1
IUCN Red List 61958968
iNaturalist 154212
GBIF 3834800
USDA GRIN 42199
Wikipedia Zanthoxylum_rhetsa

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)!
Title Authors Publication Released IDs
Bioactive Constituents of Zanthoxylum rhetsa Bark and Its Cytotoxic Potential against B16-F10 Melanoma Cancer and Normal Human Dermal Fibroblast (HDF) Cell Lines. Santhanam RK, Ahmad S, Abas F, Safinar Ismail I, Rukayadi Y, Tayyab Akhtar M, Shaari K Molecules 24-May-2016
PMCID:PMC6274200
doi:10.3390/MOLECULES21060652
PMID:27231889
Indonesian Medicinal Plants. IV. On the Constituents of the Bark of Fagara rhetza (Rutaceae). (2). Lignan Glycosides and Two Apioglucosides. Hirotaka SHIBUYA, Yasuyuki TAKEDA, Ru-song ZHANG, Akihiko TANITAME, Yen-Li TSAI, Isao KITAGAWA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.40.2639
Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968 R. Melville, J. J. Willaman, Hui-Lin Li JSTOR 27-Nov-2007
doi:10.2307/4117899
The chemical constituents of Australian Zanthoxylum species. III. The constituents of Z. parviflorum Benth.; The structure of parvifloral; Some observations on the biogenesis of furoquinoline alkaloids JA Diment, E Ritchie, WC Taylor CSIRO Publishing 04-Sep-2006
doi:10.1071/CH9670565
The alkaloids of Zanthoxylum rhetsa DC K.W. Gopinath, T.R. Govindachari, U. Ramadas Rao Elsevier BV 25-Jul-2002
doi:10.1016/0040-4020(60)80038-5
Constituents and cytotoxicity of Zanthoxylum rhesta stem bark. Ahsan M, Zaman TA, Hasan CM, Ito C, Islam SK Fitoterapia 01-Dec-2000
doi:10.1016/S0367-326X(00)00214-8
PMID:11077179
[Chemical study of Indonesian medicinal plants]. Shibuya H, Kitagawa I Yakugaku Zasshi 01-Dec-1996
doi:10.1248/YAKUSHI1947.116.12_911
PMID:8993230
Indonesia medicinal plants. III. On the constituents of the bark of Fagara rhetza (Rutaceae). (1): Alkaloids, phenylpropanoids, and acid amide. Shibuya H, Takeda Y, Zhang R, Tong RX, Kitagawa I Chem Pharm Bull (Tokyo) 01-Sep-1992
doi:10.1248/CPB.40.2325
PMID:1446354

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 / Protoberberine alkaloids and derivatives
(R)-Canadine 443422 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown https://doi.org/10.2307/4117899
Canadine 34458 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown https://doi.org/10.2307/4117899
> Benzenoids / Phenols / Methoxyphenols
(E)-3-[4-hydroxy-3-methoxy-5-(3-methylbut-2-enyl)phenyl]prop-2-enal 90470346 Click to see CC(=CCC1=C(C(=CC(=C1)C=CC=O)OC)O)C 246.30 unknown https://doi.org/10.1071/CH9670565
3-[4-Hydroxy-3-methoxy-5-(3-methylbut-2-enyl)phenyl]prop-2-enal 71436108 Click to see CC(=CCC1=C(C(=CC(=C1)C=CC=O)OC)O)C 246.30 unknown https://doi.org/10.1071/CH9670565
4-Methoxyresorcinol 3083936 Click to see 140.14 unknown https://doi.org/10.1248/CPB.40.2639
> Lignans, neolignans and related compounds / Aryltetralin lignans
[(2R)-3,4,5-trihydroxy-6-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-2H-chromen-2-yl]methyl (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 101634853 Click to see 834.80 unknown https://doi.org/10.1248/CPB.40.2639
> Lignans, neolignans and related compounds / Furanoid lignans
Kobusin 182278 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC 370.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274200/
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1248/CPB.40.2325
https://doi.org/10.1016/S0367-326X(00)00214-8
https://doi.org/10.1248/CPB.40.2639
> Lignans, neolignans and related compounds / Lignan glycosides
[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[(2S,3S)-4-hydroxy-2,3-bis[(4-hydroxy-3,5-dimethoxyphenyl)methyl]butoxy]oxan-2-yl]methyl (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 10327953 Click to see COC1=CC(=CC(=C1O)OC)CC(CO)C(CC2=CC(=C(C(=C2)OC)O)OC)COC3C(C(C(C(O3)COC(=O)C=CC4=CC(=C(C(=C4)OC)O)OC)O)O)O 790.80 unknown https://doi.org/10.1248/CPB.40.2639
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Hazaleamide 6439588 Click to see CCC=CCC=CCCC=CC=CC(=O)NCC(C)C 275.40 unknown https://doi.org/10.1248/YAKUSHI1947.116.12_911
https://doi.org/10.1248/CPB.40.2325
https://doi.org/10.1248/CPB.40.2639
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(Z)-3-[4-[(2Z)-3,7-dimethylocta-2,6-dienoxy]-3-methoxyphenyl]prop-2-en-1-ol 90656871 Click to see 316.40 unknown https://doi.org/10.1248/YAKUSHI1947.116.12_911
https://doi.org/10.1248/CPB.40.2325
Nelumol A 6439446 Click to see 346.50 unknown https://doi.org/10.1248/YAKUSHI1947.116.12_911
https://doi.org/10.1248/CPB.40.2325
https://doi.org/10.1248/CPB.40.2639
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Sabinene 11051711 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1016/0040-4020(60)80038-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1248/CPB.40.2325
https://doi.org/10.1248/CPB.40.2639
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
Evodiamine 442088 Click to see 303.40 unknown https://doi.org/10.1248/YAKUSHI1947.116.12_911
https://doi.org/10.1248/CPB.40.2325
https://doi.org/10.1248/CPB.40.2639
Rutaecarpine 65752 Click to see 287.30 unknown https://doi.org/10.1248/CPB.40.2639
https://doi.org/10.1248/CPB.40.2325
https://doi.org/10.1248/YAKUSHI1947.116.12_911
> Organoheterocyclic compounds / Quinolines and derivatives / Dihydrofuranoquinolines
Platydesmine 6451457 Click to see CC(C)(C1CC2=C(C3=CC=CC=C3N=C2O1)OC)O 259.30 unknown https://doi.org/10.2307/4117899
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1248/CPB.40.2639
https://doi.org/10.1248/CPB.40.2325
https://doi.org/10.1248/YAKUSHI1947.116.12_911
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
Zanthobungeanine 5315422 Click to see 271.31 unknown https://doi.org/10.1248/CPB.40.2325
https://doi.org/10.1248/CPB.40.2639
https://doi.org/10.1248/YAKUSHI1947.116.12_911
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthyletin 65188 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 228.24 unknown https://doi.org/10.1016/S0367-326X(00)00214-8

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