Curry Leaf Tree

Also known as: Curry Leaf, Indian Curry Tree

Botanical Overview

Curry Leaf Tree (Murraya koenigii) belongs to the Rutaceae family. While not among the most extensively documented medicinal plants, this species has recorded uses that warrant attention from researchers and practitioners. The citrus family (Rutaceae) includes trees and shrubs with gland-dotted leaves that release aromatic oils when crushed. The flowers are typically white with four or five petals, and the fruits are often modified berries with a leathery rind. Most species produce alkaloids and limonoids with medicinal activity.

General Description

It is native to the Indian subcontinent, southern China and mainland Southeast Asia, and it has been introduced to other parts of southeast Asia and to Australia. Its leaves are used in many culinary dishes in India, Sri Lanka and Bangladesh.

ⓘ Information
Description adapted from Wikipedia (CC BY-SA 4.0).

Family Context

The Rutaceae family is primarily tropical and subtropical. Notable medicinal members include:

Geographic Distribution

Curry Leaf Tree has been recorded in 10 countries and territories worldwide, including Australia, China, Indonesia, India, Sri Lanka, and others.

Traditional Uses

Curry Leaf Tree has been traditionally used for digestive health, skin and wound care, and urinary tract health, among other applications.

Digestive health.

  • Carminative
  • Dysentery
  • Stomachic
  • Diarrhea

For digestive complaints, the herb is typically prepared as a tea or decoction taken before meals. The bitter compounds stimulate digestive secretions and improve nutrient absorption. Some traditions use the powdered root or leaves in small doses as a stomachic tonic.

Skin and wound care.

  • Eruption

For skin conditions, the fresh or dried plant is applied topically as a poultice, wash, or compress. A strong decoction can be used to clean wounds and sores. The antimicrobial properties help prevent infection while promoting tissue repair.

Urinary tract health.

  • Kidney

Urinary tract applications typically involve drinking the herb as a mild tea, which increases urine production and helps flush the urinary system. It may be combined with other demulcent herbs to soothe irritated tissues.

Active Compounds

Phytochemical research has identified 30 compounds in this species, including a diverse array of phytochemical classes (see the Complete Chemical Inventory below for the full list).

The identified compounds include the following categories:

  • Alkaloid: nitrogenous compounds with diverse pharmacological activities
ⓘ Information
Information on this page is compiled from Dr. Duke’s Phytochemical and Ethnobotanical Databases (USDA ARS), a public domain resource. Consult a healthcare professional before using any herbal preparation.

Distribution and Conservation

Reported distribution: Australia, China, Indonesia, India, Sri Lanka, Malaysia, Nepal, Thailand, United States, South Africa.

Complete Use Records

CategoryCultural Context
AnodyneElsewhere
CarminativeElsewhere
DysenteryElsewhere
EruptionElsewhere
KidneyElsewhere
NauseaElsewhere
StomachicElsewhere
TonicElsewhere
BruiseElsewhere
DiarrheaElsewhere

Complete Chemical Inventory

CompoundFormulaMW
(E)-BETA-OCIMENEC₁₀H₁₆136.23 Da
(E,E)-2,4-HEPTADIENALC₇H₁₀O110.15 Da
(Z)-2-HEXENALC₆H₁₀O98.14 Da
(Z)-2-PENTENOLC₅H₁₀O86.13 Da
(Z)-3-HEXENOLC₆H₁₂O100.16 Da
(Z)-3-HEXENYL-ACETATE
(Z)-3-HEXENYL-BUTANOATE
1,2,4-TRIMETHYL-BENZENEC₉H₁₂120.19 Da
1-METHYL-2-(2-PROPENYL)-BENZENE
2,3-DIHYDROBENZOFURANC₈H₈O120.15 Da
2-ACETYL-FURANC₆H₆O₂110.11 Da
2-ETHYL-4-METHYLMALEIMIDE
2-FURANCARBOXALDEHYDEC₅H₄O₂96.08 Da
2-HYDROXY-6-METHYLCARBAZOLE
2-METHYL-BUTANALC₅H₁₀O86.13 Da
2-NONANONEC₉H₁₈O142.24 Da
2-OCTANONEC₈H₁₆O128.21 Da
3-(1,1-DIMETHYLALLYL)-XANTHYLETIN
3-METHYL-BUT-2-EN-1-OLC₅H₁₀O86.13 Da
3-METHYLCARBAZOLEC₁₃H₁₁N181.23 Da
6-METHYLHEP-5-EN-2-ONE
9-CARBETHOXY-3-METHYLCARBAZOLE
9-FORMYL-3-METHYLCARBAZOLEC₁₄H₁₁NO209.24 Da
ALPHA-COPAENEC₁₅H₂₄204.35 Da
ALPHA-CUBEBENEC₁₅H₂₄204.35 Da
ALPHA-HUMULENEC₁₅H₂₄204.35 Da
ALPHA-PHELLANDRENEC₁₀H₁₆136.23 Da
ALPHA-PINENEC₁₀H₁₆136.23 Da
ALPHA-SELINENEC₁₅H₂₄204.35 Da
ALPHA-TERPINENEC₁₀H₁₆136.23 Da

Data from PubChem (NIH/NLM, public domain).


References & Further Reading

External Research Links

Data Sources