Tarragon

Botanical Overview

Tarragon (Artemisia dracunculus) 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 widespread in the wild across much of Eurasia and North America and is cultivated for culinary and medicinal purposes.

ⓘ 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

Tarragon has been recorded in 10 countries and territories worldwide, including Canada, China, Germany, France, Kazakhstan, and others.

Traditional Uses

Tarragon has been traditionally used for digestive health, urinary tract health, and pain and inflammation, among other applications.

Digestive health.

  • Carminative
  • Stomachic
  • 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.

Urinary tract health.

  • Diuretic

Urinary tract applications typically involve drinking the herb as a mild tea, which increases urine production and helps flush the urinary system. It may be combined with other demulcent herbs to soothe irritated tissues.

Pain and inflammation.

  • Swelling

For pain and inflammation, preparations are applied both topically as compresses and taken internally. A warm poultice draws blood to the area and promotes healing, while internal preparations address systemic inflammation.

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
  • Coumarin: aromatic compounds with anticoagulant and anti-inflammatory effects
  • 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: Canada, China, Germany, France, Kazakhstan, Mongolia, Mexico, Russia, Sweden, United States.

Complete Use Records

CategoryCultural Context
ApertifElsewhere, Turkey
DiureticElsewhere, Turkey
EmmenagogueElsewhere, Turkey
AnthelminthicElsewhere
CarminativeTurkey
RefrigerantTurkey
SpiceTurkey
StomachicTurkey
SwellingUS(Flathead)
Ache(Tooth)Elsewhere
VermifugeTurkey
Tumor(Sinew)

Complete Chemical Inventory

CompoundFormulaMW
(E)-2-DIHYDROXY-4-METHOXY-4-METHOXYCINNAMIC-ACID-METHYL-ETHER
(E)-ARTEMIDINC₁₃H₁₂O₂200.23 Da
(Z)-ARTEMIDINC₁₃H₁₂O₂200.23 Da
1,2-DIMETHOXY-4-ALLYL-BENZENE
1,8-CINEOLC₁₀H₁₈O154.25 Da
1,8-CINEOLEC₁₀H₁₈O154.25 Da
1-(BUT-2-YNYL)-ISOCOUMARIN
2,4,6-TRIMETHOXYCINNAMYL-ALCOHOL
2-CARBOXYARABINITOLC₆H₁₂O₇196.16 Da
2-HEPTANONEC₇H₁₄O114.19 Da
2-HYDROXY-4-METHOXY-TRANS-CINNAMIC-ACID
3',5'-DIHYDROXY-4',7-DIMETHOXY-FLAVANONE
3,4',5-TRIHYDROXY-3',7-DIMETHOXY-FLAVANONE
3,4',5-TRIHYDROXY-7-METHOXY-FLAVANONE
3-BUT-CIS-1-ENYL-ISOCOUMARIN
3-BUT-TRANS-1-ENYL-5-HYDROXY-ISOCOUMARIN
3-BUT-TRANS-1-ENYL-8-HYDROXY-ISOCOUMARIN
3-BUT-TRANS-1-ENYL-ISOCOUMARIN
4-ALLYL-1,2-DIMETHOXYBENZENEC₁₁H₁₄O₂178.23 Da
4-HYDROXY-BENZOIC-ACID
4-METHOXYCINNAMALDEHYDEC₁₀H₁₀O₂162.18 Da
6,7-DIMETHOXYCOUMARINC₁₁H₁₀O₄206.19 Da
7-(ALPHA-D-GALACTOPYRANOSIDE)-P-HYDROXYBENZOATE-ISORHAMNETIN
7-METHOXYCOUMARINC₁₀H₈O₃176.17 Da
7-O-METHYLAROMADENDRINC₁₆H₁₄O₆302.28 Da
9-HYDROXYGERANIOLC₁₀H₁₈O₂170.25 Da
AESCULETIDIN-DIMETHYL-ETHER
AESCULETINC₉H₆O₄178.14 Da
ALANINEC₃H₇NO₂89.09 Da
ALLO-OCIMENEC₁₀H₁₆136.23 Da

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


References & Further Reading

External Research Links

Data Sources