Lion's Ear

Botanical Overview

Lion’s Ear (Leonotis leonurus) belongs to the Lamiaceae family. While not among the most extensively documented medicinal plants, this species has recorded uses that warrant attention from researchers and practitioners. The mint family (Lamiaceae) includes aromatic herbs and shrubs with square stems, opposite leaves, and two-lipped flowers. Many species produce essential oils in glandular trichomes on their leaves and stems. This family is one of the most important sources of culinary and medicinal herbs worldwide.

General Description

It is a broadleaf evergreen shrub, native to South Africa, where it is very common, with a wide altitudinal range from 5 m up to 1980 m. It is known to have medicinal and sedating properties. The main psychoactive component of Leonotis leonurus is hypothesized to be either leonurine or a mixture of labdane-type compounds; Leonotis leonurus has been confirmed to contain leonurine according to peer reviewed journal published phytochemical analysis. Like other plants in the mint family, it also contains marrubin. The word “dagga” comes from Afrikaans, and derives in turn from the Khoikhoi “dachab”. The word “dagga” has been extended to include the genus Cannabis in Afrikaans and South African English, so the use of “wild” serves to distinguish Leonotis from Cannabis.

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

Family Context

The Lamiaceae family is large and widely distributed. Notable medicinal members include:

  • Basil — 86 documented uses
  • Rosemary — 60 documented uses
  • Agbo — 54 documented uses
  • Sage — 49 documented uses

Geographic Distribution

Lion’s Ear has been recorded in 10 countries and territories worldwide, including Australia, Brazil, Chile, Colombia, Spain, and others.

Traditional Uses

Lion’s Ear has been traditionally used for digestive health, respiratory conditions, and skin and wound care, among other applications.

Digestive health.

  • Purgative
  • Vermifuge

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.

  • Cold
  • 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.

  • Skin

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:

  • 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.
⚠ Caution
Traditional records: This plant has documented uses including Purgative. 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: Australia, Brazil, Chile, Colombia, Spain, New Zealand, Portugal, United States, South Africa, Unknown.

Complete Use Records

CategoryCultural Context
Bite(Snake)Africa
ColdAfrica
CoughAfrica
PurgativeAfrica
SkinAfrica
TapewormAfrica
EmmenagogueAfrica
VermifugeAfrica

Complete Chemical Inventory

CompoundFormulaMW
(E)-BETA-FARNESENEC₁₅H₂₄204.35 Da
(E)-BETA-OCIMENEC₁₀H₁₆136.23 Da
(Z)-BETA-FARNESENEC₁₅H₂₄204.35 Da
(Z)-BETA-OCIMENEC₁₀H₁₆136.23 Da
2-PENTYL-FURANC₉H₁₄O138.21 Da
ALLO-OCIMENEC₁₀H₁₆136.23 Da
ALPHA-CADINOLC₁₅H₂₆O222.37 Da
ALPHA-COPAENEC₁₅H₂₄204.35 Da
ALPHA-CUBEBENEC₁₅H₂₄204.35 Da
ALPHA-HUMULENEC₁₅H₂₄204.35 Da
ALPHA-P-DIMETHYL-STYRENE
ALPHA-PINENEC₁₀H₁₆136.23 Da
ALPHA-THUJENEC₁₀H₁₆136.23 Da
BETA-BOURBONENEC₁₅H₂₄204.35 Da
BETA-CARYOPHYLLENEC₁₅H₂₄204.35 Da
BETA-CUBEBENEC₁₅H₂₄204.35 Da
BETA-MYRCENEC₁₀H₁₆136.23 Da
BETA-PINENEC₁₀H₁₆136.23 Da
BORNEOLC₁₀H₁₈O154.25 Da
CALAMENENEC₁₅H₂₂202.33 Da
CARYOPHYLLENE-OXIDEC₁₅H₂₄O220.35 Da
DELTA-CADINENEC₁₅H₂₄204.35 Da
DELTA-TERPINEOLC₁₀H₁₈O154.25 Da
GAMMA-MUUROLENEC₁₅H₂₄204.35 Da
GAMMA-TERPINENEC₁₀H₁₆136.23 Da
GERMACRENE-DC₁₅H₂₄204.35 Da
LEONITIN
LIMONENEC₁₀H₁₆136.23 Da
LINALOLC₁₀H₁₈O154.25 Da
MARRUBIINC₂₀H₂₈O₄332.4 Da

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


References & Further Reading

External Research Links

Data Sources