Osage-Orange

Also known as: Hedge Apple

Botanical Overview

Osage-Orange (Maclura pomifera) belongs to the Moraceae family. While not among the most extensively documented medicinal plants, this species has recorded uses that warrant attention from researchers and practitioners. The fig family (Moraceae) includes trees, shrubs, and climbers with milky sap and alternate leaves. The flowers are small and clustered inside a fleshy receptacle (the fig). Many species produce latex containing proteolytic enzymes and have traditional uses for skin conditions and parasitic infections.

General Description

It is a member of the mulberry family, Moraceae. It typically grows about 8 to 15 m (30–50 ft) tall. The distinctive multiple fruit resembles an immature orange, is roughly spherical, bumpy, 8 to 15 cm (3–6 in) in diameter, and turns bright yellow-green in the fall. The fruit excretes a sticky white latex when cut or damaged. Despite the name “Osage orange”, it is not related to the orange. Due to its latex secretions and woody pulp, the fruit is not usually eaten by humans and rarely by foraging animals. Ecologists Daniel H. Janzen and Paul S. Martin proposed in 1982 that the fruit of this species might be an example of what has come to be called an evolutionary anachronism—that is, a fruit coevolved with a large animal seed dispersal partner that is now extinct. This hypothesis is controversial. Maclura pomifera has many common names, including mock orange, horse apple, and hedge apple. The name bois d’arc (French, meaning “bow-wood”) has also been corrupted into bodark and bodock.

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

Family Context

The Moraceae family is widely distributed. Notable medicinal members include:

Geographic Distribution

Osage-Orange has been recorded in 10 countries and territories worldwide, including Argentina, Australia, Canada, France, Greece, and others.

Traditional Uses

Osage-Orange has been traditionally used for cardiovascular health.

Cardiovascular health.

  • Cardiac

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
  • Sterol: cholesterol-like compounds with anti-inflammatory 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.
⚠ Caution
Traditional records: This plant has documented uses including Poison. Self-medication with herbs carries risks including allergic reactions, drug interactions, and toxicity. Only use under the supervision of a qualified healthcare professional.

Distribution and Conservation

Reported distribution: Argentina, Australia, Canada, France, Greece, Italy, Portugal, Romania, Ukraine, United States.

Complete Use Records

CategoryCultural Context
CardiacElsewhere
PoisonUS
StimulantElsewhere
TenderizerElsewhere
WartUS
CollyriumUS

Complete Chemical Inventory

CompoundFormulaMW
1,3,6,7-TETRAHYDROXYXANTHONEC₁₃H₈O₆260.20 Da
18-ALPHA-OLEOMANE-3-BETA-19-ALPHA-DIOL
19-ALPHA-H-LUPEOL
2'',3',4',5-TETRAHYDROXY-6-(3''-METHYL-3''-BUTENYL)-ISOFLAVONE
2',4',5,7-TETRAHYDROXY-6-(3-METHYL-BUT-3-ENYL)-FLAVONE
2,2',4,4'-TETRAHYDROXY-3-(3-METHYL-2-BUTENYL)-CHALCONE
2-3-4'-5-TETRAHYDROXYSTILBENE
3,6,7,2'-TETRAMETHOXY-4,5-DIHYDROXYFLAVONE
4',5,7-TRIHYDROXY-6-(3-METHYL-BUT-3-ENYL)-FLAVONE
6-DEOXYJACAREUBINC₁₈H₁₄O₅310.3 Da
6-DEOXYJAKAREUBIN
8,8'-BIS-NARINGENIN
8-C-PRENYLNARINGENIN
8-DEOXYGARTANINC₂₃H₂₄O₅380.4 Da
8-PRENYL-TOXYLOXANTHONE
8-PRENYL-TOXYLOXANTHONE-C
ALKALOIDS
ALPINUMISOFLAVONEC₂₀H₁₆O₅336.3 Da
ALVAXANTHONEC₂₃H₂₄O₆396.4 Da
AMYRINC₃₀H₅₀O426.7 Da
APIGENINC₁₅H₁₀O₅270.24 Da
ARACHIDIC-ACIDC₂₀H₄₀O₂312.5 Da
AROMADENDRINC₁₅H₁₂O₆288.25 Da
AROMADENDRIN-7-O-BETA-D-GLUCOSIDE
ARTOCARPESINC₂₀H₁₈O₆354.4 Da
ASCORBIC-ACIDC₆H₈O₆176.12 Da
ASH
ASTRAGALINC₂₁H₂₀O₁₁448.4 Da
AURICULASINC₂₅H₂₄O₆420.5 Da
BETA-SITOSTEROLC₂₉H₅₀O414.7 Da

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


References & Further Reading

External Research Links

Data Sources