Elecampane

Botanical Overview

Elecampane (Inula helenium) is a flowering plant in the Asteraceae family. Traditional medicine systems have documented several valuable applications for this species, supported by its observed therapeutic effects. 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 Eurasia from Spain to Xinjiang province in western China, and naturalized in parts of North America.

ⓘ 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

Elecampane has been recorded in 10 countries and territories worldwide, including Belgium, Canada, Germany, France, United Kingdom, and others.

Traditional Uses

Elecampane has been traditionally used for digestive health, respiratory conditions, and skin and wound care, among other applications.

Digestive health.

  • Vermifuge
  • Stomachic
  • Carminative
  • Laxative

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.

  • Expectorant
  • Asthma
  • Bronchitis
  • 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:

  • Terpene: aromatic compounds with anti-inflammatory and antimicrobial 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: Belgium, Canada, Germany, France, United Kingdom, Netherlands, Russia, Sweden, Ukraine, United States.

Complete Use Records

CategoryCultural Context
DiureticChina, Elsewhere, Europe, Turkey
AntisepticChina, Europe, Turkey
ExpectorantChina, Europe, Turkey
VermifugeChina, Europe, Turkey
PertussisElsewhere, Turkey
StomachicChina, Turkey
TonicChina, Turkey
AlterativeChina
ApertifTurkey
AsthmaElsewhere
BronchitisTurkey
CarminativeChina
CholagogueTurkey
DeobstruentChina
DiaphoreticElsewhere
DiscutientChina
LaxativeChina
LeukemiaArgentina
LungElsewhere
SclerosisIndia
SkinElsewhere
SudorificTurkey
TeaChina
Tumor(Lung)China
VulneraryChina
WenUK
CoughElsewhere
HemoptysisSpain

Complete Chemical Inventory

CompoundFormulaMW
(-)-INOSITOLC₆H₁₂O₆180.16 Da
1-(1-ISO-BUTYROXY-METHYL-1-2-OXIDO-ETHYL)-2-ISO-BUTYROXY-4-METHYL-BENZENE
1-BETA-HYDROXYISOALANTOLACTONE
1-DEOXY-8-EPIIVANGUSTIN
11(13)-DEHYDRO-ERIOLIN
1BETA,10ALPHA-EPOXY-1,10-H-CIS-INUNOLIDE
1BETA-HYDROXYALANTOLACTONEC₁₅H₂₀O₃248.32 Da
2-ALPHA-HYDROXYALANTOLACTONE
2-OXOALANTOLACTONEC₁₅H₁₈O₃246.30 Da
3-METHYLQUERCETINC₁₆H₁₂O₇316.26 Da
4,5-DIHYDRO-5,6-DEHYDROALANTOLACTONE
4-ALPHA-5-ALPHA-EPOXY-10-14(H)-INUVISCOLIDE
4-ALPHA-5-ALPHA-EPOXY-10-ALPHA-4(H)-INUVISCOLIDE
4-EPIISOINUVISCOLIDEC₁₅H₂₀O₃248.32 Da
4ALPHA-H-CONFERTIN
4BETA,5ALPHA-EPOXY-4,5-CIS-INUNOLIDE
4H-TOMENTOSINC₁₅H₂₂O₃250.33 Da
8,9-EPOXY-10-ISOBUTYRYLOXYTHYMOL-ISOBUTYRATE
8-EPI-ISOVANGUSTIN
8-EPIIVANGUSTINC₁₅H₂₀O₃248.32 Da
8-EPITOMENTOSIN
9-BETA-(2-METHYL-BUTYROYL-OXY)-COSTUNOLIDE
9-BETA-HYDROXYCOSTUNOLIDE
9-BETA-ISO-BUTYROYL-OXY-COSTUNOLIDE
9-BETA-ISO-VALEROYL-OXY-COSTUNOLIDE
9-ISOBUTYRYLOXY-COSTULONIDE
9-ISOVALERYLOXY-COSTULONIDE
9BETA-(2-METHYLBUTYRYLOXY)-COSTULONIDE
9BETA-HYDROXYCOSTULONIDE
ALANTIC-ACID

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


References & Further Reading

External Research Links

Data Sources