Evening-Primrose

Botanical Overview

Evening-Primrose (Oenothera biennis) belongs to the Onagraceae family. While not among the most extensively documented medicinal plants, this species has recorded uses that warrant attention from researchers and practitioners. This species belongs to the Onagraceae family, a group of flowering plants.

General Description

Evening primrose oil is produced from the plant. Other common names include evening star, sundrop, weedy evening primrose, German rampion, hog weed, King’s cure-all and fever-plant.

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

Family Context

The Onagraceae family is widely distributed. Notable medicinal members include:

Geographic Distribution

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

Traditional Uses

Evening-Primrose has been traditionally used for respiratory conditions, nervous system disorders, and metabolic and nutritional health, among other applications.

Respiratory conditions.

  • Pectoral

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.

Nervous system disorders.

  • Sedative
  • Spasm

Nervous system support involves taking the herb as a warm tea, often in the evening or before bed. The calming compounds interact with neurotransmitter systems to promote relaxation and restful sleep.

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:

  • 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: Belgium, Canada, Germany, France, United Kingdom, South Korea, Poland, Russia, Sweden, United States.

Complete Use Records

CategoryCultural Context
AstringentElsewhere, Turkey
SedativeElsewhere, Turkey
CyanogeneticUS
DepurativeTurkey
SpasmTurkey
TumorUS
PectoralTurkey

Complete Chemical Inventory

CompoundFormulaMW
2-HYDROXY-4-METHOXYBENZOIC-ACIDC₁₆H₁₆O₈336.29 Da
ALANINEC₃H₇NO₂89.09 Da
ALPHA-AMYRINC₃₀H₅₀O426.7 Da
ALPHA-LINOLEIC-ACID
ALPHA-LINOLENIC-ACIDC₁₈H₃₀O₂278.4 Da
ALPHA-TOCOPHEROLC₂₉H₅₀O₂430.7 Da
AMINO-ACIDS
AMMONIAH₃N17.031 Da
ARGININEC₆H₁₄N₄O₂174.20 Da
ASH
ASPARTIC-ACIDC₄H₇NO₄133.10 Da
BETA-AMYRINC₃₀H₅₀O426.7 Da
BETA-LINOLEIC-ACID
BETA-SITOSTEROLC₂₉H₅₀O414.7 Da
BORONB10.81 Da
CAFFEIC-ACIDC₉H₈O₄180.16 Da
CALCIUMCa40.08 Da
CAMPESTEROLC₂₈H₄₈O400.7 Da
CARBOHYDRATES
CELLULOSE
CIS-6,9,12-OCTADECATRIENOIC-ACID
CIS-GAMMA-LINOLEIC-ACID
CIS-GAMMA-LINOLENIC-ACID
CIS-LINOLEIC-ACIDC₁₇H₃₀O₂266.4 Da
CITROSTADIENIOL
COPPERCu63.55 Da
CYCLOARTENOLC₃₀H₅₀O426.7 Da
CYSTINEC₆H₁₂N₂O₄S₂240.3 Da
DELPHINIDINC₁₅H₁₁O₇+303.24 Da
DIGALLIC-ACIDC₁₄H₁₀O₉322.22 Da

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


References & Further Reading

External Research Links

Data Sources