Hopwood

Botanical Overview

Hopwood (Dodonaea viscosa) is a flowering plant in the Sapindaceae family. The traditional uses of this species reflect its genuine medicinal value, validated by generations of practical experience. This species belongs to the Sapindaceae family, a group of flowering plants.

General Description

Dodonaea is part of Sapindaceae, the soapberry family. This species is notable for its extremely wide distribution, which it achieved only over the last 2 million years (from its region of origin in Australia) via oceanic dispersal. Harrington and Gadek (2009) referred to D. viscosa as having “a distribution equal to some of the world’s greatest transoceanic dispersers”.

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

Family Context

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

Geographic Distribution

Hopwood has been recorded in 10 countries and territories worldwide, including Australia, Brazil, Colombia, Ecuador, Mexico, and others.

Traditional Uses

Hopwood has been traditionally used for digestive health, skin and wound care, and pain and inflammation, among other applications.

Digestive health.

  • 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.

Skin and wound care.

  • Burn
  • Sore
  • Wound

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.

Pain and inflammation.

  • Gout
  • Rheumatism
  • Swelling

For pain and inflammation, preparations are applied both topically as compresses and taken internally. A warm poultice draws blood to the area and promotes healing, while internal preparations address systemic inflammation.

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.

Distribution and Conservation

Reported distribution: Australia, Brazil, Colombia, Ecuador, Mexico, New Zealand, Reunion, Taiwan, United States, South Africa.

Complete Use Records

CategoryCultural Context
FeverElsewhere, India, Iraq, Mexico, Samoa, Sudan
GoutIndia, Iraq, Mexico
PiscicideElsewhere, India, Iraq
RheumatismIndia, Iraq, Mexico
BruiseIndia, Sudan
BurnIndia, Iraq
SoreIndia, Newguinea
SprainIndia, Sudan
StimulantIraq, Peru
SwellingIndia, Iraq
AstringentIndia
ColicMexico
FlatulenceJava
FunerealNewguinea
LiqueurMexico
PoulticeNewguinea(Dani)
ShoulderNewguinea
SudorificIraq
VenerealMexico
DentifriceElsewhere
StypticElsewhere
WoundIraq

Complete Chemical Inventory

CompoundFormulaMW
21,22-DIANGELOYL-BARRINGTOGENOL-C
21,22-DIANGELOYL-R1-BARRINGENOL
21-ANGELOYL-R1-BARRINGENOL
3,6,4'TRIMETHOXY-5,7-DIHYDROXYFLAVONE
4H-1-BENZOPYRAN-4-ONEC₉H₆O₂146.14 Da
5,7,4'-TRIHYDROXY-3',6'-DIMETHOXYFLAVONE
5,7-DIHYDROXY-3,6-DIMETHOXY-2-(4-METHOXYPHENYL)-FLAVONE
5-HYDROXY-3,6,7,4'-TETRAMETHOXYFLAVONEC₁₉H₁₈O₇358.3 Da
ALIARINC₂₂H₂₄O₈416.4 Da
ALKALOID
ARACHIDIC-ACIDC₂₀H₄₀O₂312.5 Da
BEHENIC-ACIDC₂₂H₄₄O₂340.6 Da
BETA-SITOSTEROLC₂₉H₅₀O414.7 Da
CAFFEIC-ACIDC₉H₈O₄180.16 Da
CLEOMISCOSIN
CYANIDINC₁₅H₁₁O₆+287.24 Da
DODOGENIN
DODONIC-ACID
DODONIN
ERUCIC-ACIDC₂₂H₄₂O₂338.6 Da
FATC₁₆H₃₂O₂256.42 Da
HAUTRIWAIC-ACIDC₂₀H₂₈O₄332.4 Da
HENTRIACONTANEC₃₁H₆₄436.8 Da
HYPERINC₂₁H₂₀O₁₂464.4 Da
ISORHAMNETINC₁₆H₁₂O₇316.26 Da
ISORHAMNETIN-3-O-RHAMNOSYLGALACTOSIDE
ISORHAMNETIN-3-O-RUTINOSIDEC₂₈H₃₂O₁₆624.5 Da
KAEMPFEROLC₁₅H₁₀O₆286.24 Da
KAEMPFEROL-3',4',7-TRIMETHYLETHER
KAEMPFEROL-3,7-DIMETHYLETHER

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


References & Further Reading

External Research Links

Data Sources