Poison Ivy

Botanical Overview

Poison Ivy (Rhus toxicodendron) belongs to the Anacardiaceae family. While not among the most extensively documented medicinal plants, this species has recorded uses that warrant attention from researchers and practitioners. The cashew family (Anacardiaceae) includes trees and shrubs with resinous bark and leaves containing phenolic compounds such as urushiol, which can cause contact dermatitis. The flowers are small and clustered, and the fruits are often drupes with a resinous or oily seed. Many species have traditional uses for their oils and resins.

Family Context

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

Geographic Distribution

Poison Ivy has been recorded in , and Norway.

Traditional Uses

Poison Ivy has been traditionally used for immune system support.

Immune system support.

  • Cancer

Immune support involves taking the herb as a decoction or tincture over extended periods. The active compounds stimulate immune cell activity and provide antimicrobial protection.

Active Compounds

Phytochemical research has identified 15 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:

  • Tannin: astringent compounds that tighten tissues and resist infection
ⓘ 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.

Complete Use Records

CategoryCultural Context
Cancer

Complete Chemical Inventory

CompoundFormulaMW
FISETINC₁₅H₁₀O₆286.24 Da
GALLOTANNIC-ACIDC₇₆H₅₂O₄₆1701.2 Da
GALLOTANNIC-ACID-METHYL-ESTER
HENEICOSANDICARBONIC-ACID
KAEMPFEROLC₁₅H₁₀O₆286.24 Da
LINOLEIC-ACIDC₁₈H₃₂O₂280.4 Da
MYRICETINC₁₅H₁₀O₈318.23 Da
MYRISTIC-ACIDC₁₄H₂₈O₂228.37 Da
OLEIC-ACIDC₁₈H₃₄O₂282.5 Da
PALMITIC-ACIDC₁₆H₃₂O₂256.42 Da
QUERCETINC₁₅H₁₀O₇302.23 Da
RHAMNOSEC₆H₁₂O₅164.16 Da
TANNINS
URUSHENOLC₂₁H₃₄O₂318.5 Da
URUSHIOLC₁₀₅H₁₆₂O₁₀1584.4 Da

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


References & Further Reading

External Research Links

Data Sources