Garden Myrrh

Also known as: Myrrh, Sweet Chervil, Sweet Cicely, Cicely

Botanical Overview

Garden Myrrh (Myrrhis odorata) is a flowering plant in the Apiaceae family. Traditional medicine systems have documented several valuable applications for this species, supported by its observed therapeutic effects. The carrot family (Apiaceae) includes herbs with hollow stems, alternate leaves, and distinctive umbrella-shaped flower clusters called umbels. Many species have aromatic roots and seeds used as culinary spices and medicines. The family includes both nutritious vegetables and highly toxic species.

General Description

It is the only species in the genus Myrrhis.

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

Family Context

The Apiaceae family is widely distributed in temperate regions. Notable medicinal members include:

Geographic Distribution

Garden Myrrh has been recorded in 10 countries and territories worldwide, including Belgium, Switzerland, Germany, Denmark, Finland, and others.

Traditional Uses

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

Digestive health.

  • Carminative
  • Dysentery

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

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.

  • Abscess
  • Sore

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:

  • Flavonoid: antioxidant compounds that protect cells from oxidative damage
  • 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: Belgium, Switzerland, Germany, Denmark, Finland, France, United Kingdom, Netherlands, Norway, Sweden.

Complete Use Records

CategoryCultural Context
DepurativeEnglish, Europe
ExpectorantDutch, Europe
AbdomenChina
AbscessChina
AmenorrheaChina
Cancer(Breast)Europe
CarbuncleChina
CarminativeFrench
ChestChina
DiureticItalian
DysenteryUS(Blackfoot)
DysmenorrheaChina
Lactogogue(Veterinary)Europe
LiqueurEnglish
RheumatismChina
SoreChina
TonicSwedish
VulneraryGerman
AnodyneChina
EmmenagogueSpanish

Complete Chemical Inventory

CompoundFormulaMW
2-ACETOXYFURANO-TRANS-1(10)-TRANS-4-DIENE
2-METHOXYFURANO-TRANS-1(10)-TRANS-4-DIENE
ALLO-AROMADENDRENEC₁₅H₂₄204.35 Da
ALPHA-PINENEC₁₀H₁₆136.23 Da
ALPHA-TERPINENEC₁₀H₁₆136.23 Da
ALPHA-TERPINEOLC₁₀H₁₈O154.25 Da
ANETHOLEC₁₀H₁₂O148.20 Da
ANISALDEHYDEC₈H₈O₂136.15 Da
APIGENIN-7-O-GLUCOSIDEC₂₁H₂₀O₁₀432.4 Da
BETA-BISABOLENEC₁₅H₂₄204.35 Da
BETA-CARYOPHYLLENEC₁₅H₂₄204.35 Da
BETA-CYMENEC₁₀H₁₄134.22 Da
BETA-PINENEC₁₀H₁₆136.23 Da
BETA-SELINENEC₁₅H₂₄204.35 Da
CHAVICOL-METHYL-ETHERC₁₀H₁₂O148.20 Da
COSMOSIINC₂₁H₂₀O₁₀432.4 Da
CYNAROSIDEC₂₁H₂₀O₁₁448.4 Da
ELEMOLC₁₅H₂₆O222.37 Da
ESTRGOLE
EUGENOL-METHYL-ETHERC₁₁H₁₄O₂178.23 Da
FUMARIC-ACIDC₄H₄O₄116.07 Da
GAMMA-MUUROLENEC₁₅H₂₄204.35 Da
GAMMA-TERPINENEC₁₀H₁₆136.23 Da
GAMMA-TERPINEOLC₁₀H₁₈O154.25 Da
GERMACRENE-DC₁₅H₂₄204.35 Da
LIMONENEC₁₀H₁₆136.23 Da
LONGIFOLENEC₁₅H₂₄204.35 Da
LUTEOLIN-7-O-GLUCOSIDEC₂₁H₂₀O₁₁448.4 Da
MYRCENEC₁₀H₁₆136.23 Da
OLEIC-ACIDC₁₈H₃₄O₂282.5 Da

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


References & Further Reading

External Research Links

Data Sources