Eucalyptus stoatei

Botanical Overview

Eucalyptus stoatei is a species in the Myrtaceae family. The myrtle family (Myrtaceae) includes trees and shrubs with opposite leaves that contain aromatic oil glands. The flowers are showy with numerous stamens, and the fruits are often fleshy berries or capsules. Many species produce essential oils with antiseptic and antimicrobial properties. Although comprehensive ethnobotanical records are limited, phytochemical studies have identified 30 compounds in this species, suggesting potential medicinal value.

General Description

Eucalyptus stoatei, commonly known as scarlet pear gum or Stoate’s mallee, is a tree that is native to a small area along the south coast of Western Australia.

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

Family Context

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

Geographic Distribution

Eucalyptus stoatei has been recorded in Australia, New Zealand, and United States.

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

Research Status

Although this species has documented phytochemical constituents, its ethnobotanical and clinical documentation remains incomplete. The limited documentation available for this species represents an opportunity for ethnobotanical research.

ⓘ 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, New Zealand, United States.

Complete Chemical Inventory

CompoundFormulaMW
1,8-CINEOLEC₁₀H₁₈O154.25 Da
ALLO-AROMADENDRENEC₁₅H₂₄204.35 Da
ALPHA-BULNESENEC₁₅H₂₄204.35 Da
ALPHA-CAMPHOLENIC-ALDEHYDE
ALPHA-COPAENEC₁₅H₂₄204.35 Da
ALPHA-CUBEBENEC₁₅H₂₄204.35 Da
ALPHA-EUDESMOLC₁₅H₂₆O222.37 Da
ALPHA-FENCHENEC₁₀H₁₆136.23 Da
ALPHA-GURJUNENEC₁₅H₂₄204.35 Da
ALPHA-PHELLANDRENEC₁₀H₁₆136.23 Da
ALPHA-PINENEC₁₀H₁₆136.23 Da
ALPHA-SELINENEC₁₅H₂₄204.35 Da
ALPHA-TERPINEOLC₁₀H₁₈O154.25 Da
AROMADENDRENEC₁₅H₂₄204.35 Da
BETA-CARYOPHYLLENEC₁₅H₂₄204.35 Da
BETA-CIS-OCIMENEC₁₀H₁₆136.23 Da
BETA-CUBEBENEC₁₅H₂₄204.35 Da
BETA-ELEMENEC₁₅H₂₄204.35 Da
BETA-EUDESMOLC₁₅H₂₆O222.37 Da
BETA-PHELLANDRENEC₁₀H₁₆136.23 Da
BETA-PINENEC₁₀H₁₆136.23 Da
BETA-SELINENEC₁₅H₂₄204.35 Da
BETA-TRANS-OCIMENEC₁₀H₁₆136.23 Da
BICYCLOELEMENEC₁₅H₂₄204.35 Da
BICYCLOGERMACRENEC₁₅H₂₄204.35 Da
CADINA-1,4-DIENEC₁₅H₂₄204.35 Da
CALACORENEC₁₅H₂₀200.32 Da
CALAMENENEC₁₅H₂₂202.33 Da
CARYOPHYLLENE-OXIDEC₁₅H₂₄O220.35 Da
CIS-P-MENTH-1,8-DIEN-6-OL

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


References & Further Reading

External Research Links

Data Sources