Indian Mulberry

Also known as: Noni

Botanical Overview

Commonly known as Indian Mulberry, this species belongs to the Rubiaceae family. Traditional healers across continents have independently recognized the medicinal value of this species, leading to one of the most extensive ethnobotanical records available. The coffee family (Rubiaceae) includes trees, shrubs, and herbs with opposite leaves and interpetiolar stipules. The flowers are typically tubular with four or five petals. The family includes coffee (Coffea), quinine-producing Cinchona, and numerous other medicinal species with alkaloid constituents.

General Description

It is commonly known as noni or Indian mulberry, among many other names. Native to Southeast Asia and Australasia, the species was spread across the Pacific by Polynesian sailors. It is now cultivated throughout the tropics and is widely naturalised. The plant contains anthraquinones, which can be harmful to human health. Although the fresh fruit is edible, its pungent odour makes it worthwhile only as a famine food. It is also used in traditional medicine and processed into products such as juices.

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

Family Context

The Rubiaceae family is large and primarily tropical. Notable medicinal members include:

Geographic Distribution

Indian Mulberry has been recorded in 10 countries and territories worldwide, including Australia, Costa Rica, Guadeloupe, Indonesia, India, and others.

Traditional Uses

Indian Mulberry has been traditionally used for digestive health, respiratory conditions, and skin and wound care, among other applications.

Digestive health.

  • Diarrhea
  • Laxative
  • Colic

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.

Respiratory conditions.

  • Cough

Respiratory conditions are addressed through steam inhalation of the herb’s vapors or internal use as a warm tea. The hot infusion acts as an expectorant, helping to loosen phlegm and clear congestion. Some traditions combine it with honey for coughs.

Skin and wound care.

  • Wound
  • Boil

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.

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:

  • Flavonoid: antioxidant compounds that protect cells from oxidative damage
  • Terpene: aromatic compounds with anti-inflammatory and antimicrobial properties
ⓘ 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, Costa Rica, Guadeloupe, Indonesia, India, Mexico, Panama, French Polynesia, Philippines, United States.

Complete Use Records

CategoryCultural Context
FeverElsewhere, Malaya, Samoa
WoundHaiti, Hawaii, Samoa
AgueMalaya, Samoa
AnodyneElsewhere, St.Thomas
ArthritisDominica, Tonga
BoilSamoa, Tonga I
CoughJava, Samoa
DiarrheaPhilippines, Tonga
EmmenagogueMalaya, Philippines
GingivitisElsewhere, Tonga
LaxativeJava, Samoa
RheumatismDominica, Samoa
SapraemiaElsewhere, Malaya
SwellingJava, Samoa
Ache(Tooth)Samoa, Tonga
NauseaMalaya, Samoa
BeriberiJava
Bite(Bug)Samoa
ChestMalaya
ColicMalaya
CollyriumSamoa
ConvulsionMalaya
DiabetesJava
DiureticSamoa
DysuriaJava
ElephantiasisSamoa
EyeSamoa
FilariasisSamoa
GoutElsewhere
InflammationSamoa

Complete Chemical Inventory

CompoundFormulaMW
(E)-6-DODECENO-GAMMA-LACTONE
(Z)-6-DODECENO-GAMMA-LACTONE
(Z,Z)-2,5-UNDECADIEN-1-OLC₁₁H₂₀O168.28 Da
(Z,Z,Z)-8,11,14-EICOSATRIENOIC-ACID
1-5-6-TRIHYDROXY-ANTHRAQUINONE
1-BUTANOLC₄H₁₀O74.12 Da
1-HEXANOLC₆H₁₄O102.17 Da
2,6-DI-O-(BETA-D-GLUCOPYRANOSYL)-1-O-OCTANOYL-BETA-D-GLUCOPYRANOSEC₂₆H₄₆O₁₇630.6 Da
2-HEPTANONEC₇H₁₄O114.19 Da
2-HYDROXY-1-METHOXY-7-METHYL-ANTHRAQUINONE
2-METHYL-3-METHYLTHIO-PROPANOATE
2-METHYL-BUTANOIC-ACID
2-METHYL-HEXANOATEC₇H₁₄O₂130.18 Da
2-METHYL-PROPANOIC-ACID
3-5-6-TRIHYDROXY-2-METHYL-ANTHRAQUINONE
3-HYDROXY-2-BUTANONEC₄H₈O₂88.11 Da
3-HYDROXY-MORINDONEC₁₅H₁₀O₆286.24 Da
3-METHYL-2-BUTEN-1-OLC₅H₁₀O86.13 Da
3-METHYL-3-BUTEN-1-OLC₅H₁₀O86.13 Da
3-METHYL-THIOPROPANOIC-ACID
5,7-DIMETHYL-APIGENIN-4'-O-BETA-D(+)-GALACTOPYRANOSIDE
5-6-DIHYDROXY-LUCIDIN
6,8-DIMETHOXY-3-METHYLANTHRAQUINONE-1-O-BETA-RHAMNOSYL-GLUCOPYRANOSIDE
7-HYDROXY-8-METHOXY-2-METHYL-ANTHRAQUINONE
ACACETIN-7-O-BETA-D(+)-GLUCOPYRANOSIDE
ACACETIN-7-O-BETA-D-GLUCOPYRANOSIDEC₂₂H₂₂O₁₀446.4 Da
ACETIC-ACIDC₂H₄O₂60.05 Da
ALIZARINC₁₄H₈O₄240.21 Da
ALIZARIN-ALPHA-METHYL-ETHER
ALPH-METHOXY-ALIZARIN

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


References & Further Reading

External Research Links

Data Sources