Sheep Sorrel

Botanical Overview

Sheep Sorrel (Rumex acetosella) is a flowering plant in the Polygonaceae family. This plant has earned a place in traditional medicine through its consistent therapeutic benefits, recorded across multiple cultures. The buckwheat family (Polygonaceae) includes herbs, shrubs, and vines with swollen stem nodes (joints) and simple, alternate leaves with sheathing stipules called ochreae. The flowers are small and clustered. Many species contain anthraquinone glycosides and tannins.

General Description

Native to Eurasia including the British Isles, the plant and its subspecies are common perennial weeds. It has green arrowhead-shaped leaves and red-tinted deeply ridged stems, and it sprouts from an aggressive and spreading rhizome. The flowers emerge from a tall, upright stem. Female flowers are maroon in color.

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

Family Context

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

Geographic Distribution

Sheep Sorrel has been recorded in 10 countries and territories worldwide, including Belgium, Germany, Denmark, Finland, France, and others.

Traditional Uses

Sheep Sorrel has been traditionally used for digestive health, skin and wound care, and urinary tract health, among other applications.

Digestive health.

  • Purgative

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.

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.

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.

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:

  • Phenolic: antioxidant compounds that neutralize free radicals
  • 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.
⚠ Caution
Traditional records: This plant has documented uses including Poison, Purgative. Self-medication with herbs carries risks including allergic reactions, drug interactions, and toxicity. Only use under the supervision of a qualified healthcare professional.

Distribution and Conservation

Reported distribution: Belgium, Germany, Denmark, Finland, France, United Kingdom, Netherlands, Poland, Sweden, United States.

Complete Use Records

CategoryCultural Context
CancerCanada(Amerindian), Elsewhere, US
DiureticElsewhere, Italian
ScurvyElsewhere, Spanish
WartNa(Aleutian I), Uk(Wales)
PoisonElsewhere, Sanscrit
DepurativeUS
DiaphoreticElsewhere
PurgativeDutch
SkinIndia
SudorificFrench
Tumor(Eye)Europe
Cancer(Throat)Tasmania
StypticVenezuela
FeverGerman
RefrigerantElsewhere
TumorElsewhere

Complete Chemical Inventory

CompoundFormulaMW
ADENOSINEC₁₀H₁₃N₅O₄267.24 Da
ANTHRAQUINONESC₁₄H₈O₂208.21 Da
ASCORBIC-ACIDC₆H₈O₆176.12 Da
ASH
AUXINC₁₈H₃₂O₅328.4 Da
CALCIUM-OXALATEC₂CaO₄128.10 Da
CALCIUM-OXIDECaO56.08 Da
CATECHIN-TANNIN
CHALCONES
CHRYSOPHANIC-ACIDC₁₅H₁₀O₄254.24 Da
CHRYSOPHANOLC₁₅H₁₀O₄254.24 Da
COUMARINSC₁₉H₁₆O₄308.3 Da
CYTOKININC₁₀H₉N₅O215.21 Da
EMODINC₁₅H₁₀O₅270.24 Da
FATC₁₆H₃₂O₂256.42 Da
FLOROGLUCOTANNOID
GIBBERELINC₁₉H₂₂O₆346.4 Da
HYPERINC₂₁H₂₀O₁₂464.4 Da
ISOPENTENYL-ADENINEC₁₀H₁₃N₅203.24 Da
MAGNESIUM-OXIDES
OXALIC-ACIDC₂H₂O₄90.03 Da
PHOSPHORUS-OXIDES
PHYSCIONC₁₆H₁₂O₅284.26 Da
POTASSIUM-BINOXALATEC₂HKO₄128.13 Da
POTASSIUM-OXALATEC₈KO₁₆-₇391.17 Da
POTASSIUM-OXIDES
PROTEIN
RUTINC₂₇H₃₀O₁₆610.5 Da
SILICON-OXIDES
TANNIN

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


References & Further Reading

External Research Links

Data Sources