Echinacea

Also known as: Eastern Purple-Coneflower, Purple-Coneflower

Botanical Overview

Echinacea (Echinacea purpurea) belongs to the Asteraceae family. Limited but reliable traditional records indicate this plant has recognized medicinal applications in one or more healing traditions. The daisy family (Asteraceae) is one of the largest plant families, characterized by composite flower heads (capitula) that contain many small florets surrounded by bracts. Plants range from tiny alpine herbs to large tropical trees. The family includes many medicinally important species with bitter compounds and essential oils.

General Description

It is native to parts of eastern North America and present to some extent in the wild in much of the eastern, southeastern and midwestern United States, as well as in the Canadian Province of Ontario. It is most common in the Ozarks, the Mississippi Valley, and the Ohio Valley. Its habitats include dry open woods, prairies, and barrens.

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

Family Context

The Asteraceae family is extremely large and diverse. Notable medicinal members include:

Geographic Distribution

Echinacea has been recorded in 10 countries and territories worldwide, including Austria, Belgium, Canada, Germany, France, and others.

Traditional Uses

Echinacea has been traditionally used for skin and wound care, reproductive health, and metabolic and nutritional health.

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.

Reproductive health.

  • Syphilis

In traditional contexts, reproductive health applications typically involve internal preparations such as teas or decoctions. The herb may be taken at specific times during the menstrual cycle.

Metabolic and nutritional health.

  • Depurative

Metabolic applications include consuming the plant as a food, fresh juice, or herbal infusion. Regular use supports the body’s natural metabolic processes and nutritional status.

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
  • 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.

Distribution and Conservation

Reported distribution: Austria, Belgium, Canada, Germany, France, Kazakhstan, Netherlands, Sweden, United States, Unknown.

Complete Use Records

CategoryCultural Context
Bite(Snake)US
DepurativeUS
MedicineUS(Appalachia)
RabiesUS
SkinUS
SyphilisUS

Complete Chemical Inventory

CompoundFormulaMW
13-HYDROXY-OCTADECA-CIS-9-TRANS-11-CIS-15-TRIENNOIC-ACID
2,3-DICAFFEOYL-TARTARIC-ACIDC₂₂H₁₈O₁₂474.4 Da
2-CAFFEOYL-3-COUMAROYL-TARTARIC-ACID
2-CAFFEOYL-3-FERULOYL-TARTARIC-ACID
2-CAFFEOYL-TARTARIC-ACIDC₁₃H₁₂O₉312.23 Da
2-FERULOYL-TARTARIC-ACIDC₁₄H₁₄O₉326.25 Da
3,4-EPOXY-TRIDECA-1,5-DIENE-7,9,11-TRIYNE
4-O-METHYL-GLUCURONOARABINOXYLAN
ALUMINUMAl26.981538 Da
ARABINOGALACTAN
ASCORBIC-ACIDC₆H₈O₆176.12 Da
ASH
BETA-CAROTENEC₄₀H₅₆536.9 Da
BETA-SITOSTEROLC₂₉H₅₀O414.7 Da
BETAINEC₅H₁₁NO₂117.15 Da
BORNEOLC₁₀H₁₈O154.25 Da
BORNYL-ACETATEC₁₂H₂₀O₂196.29 Da
CALCIUMCa40.08 Da
CARYOPHYLLENEC₁₅H₂₄204.35 Da
CARYOPHYLLENE-EPOXIDEC₁₅H₂₄O220.35 Da
CHICHORIC-ACID
CHICHORIC-ACID-DIMETHYL-ETHER
CHICHORIC-ACID-MONOMETHYL-ETHER
CHROMIUMCr51.996 Da
CICHORIC-ACIDC₂₂H₁₈O₁₂474.4 Da
CICHORIENIC-ACID
CINNAMOYL-ECHINADIOLC₂₄H₃₂O₄384.5 Da
CINNAMOYL-ECHINAXANTHOL
COBALTCo58.93319 Da
CYANIDIN-3-O-(6-O-MALONYL-BETA-D-GLUCOPYRANOSIDE)C₂₄H₂₃O₁₄+535.4 Da

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


References & Further Reading

External Research Links

Data Sources