Marsh Skullcap

Botanical Overview

Marsh Skullcap (Scutellaria galericulata) belongs to the Lamiaceae family. While not among the most extensively documented medicinal plants, this species has recorded uses that warrant attention from researchers and practitioners. The mint family (Lamiaceae) includes aromatic herbs and shrubs with square stems, opposite leaves, and two-lipped flowers. Many species produce essential oils in glandular trichomes on their leaves and stems. This family is one of the most important sources of culinary and medicinal herbs worldwide.

General Description

It is a member of the mint family. The form is upright and is usually 20-45 centimeters in height, sometimes reaching up to 80 cm. It is a wetland-loving species and grows along fens and shorelines. The blue flowers are 1 to 2 centimeters long. The flowers are in pairs and are all on the same side of the stem. The flowers do not appear at the top of the stem. The plant is native to many parts of the world and, as such, is known by a variety of names. The Latin galericulata means “hooded”, relating to the length of the flower’s tube being much longer than the calyx. The variation epilobiifolia translates as leaves like willow-herb, and refers to the slightly serrated long thin leaves which look similar to those of the genus Epilobium.

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

Family Context

The Lamiaceae family is large and widely distributed. Notable medicinal members include:

  • Basil — 86 documented uses
  • Rosemary — 60 documented uses
  • Agbo — 54 documented uses
  • Sage — 49 documented uses

Geographic Distribution

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

Traditional Uses

Marsh Skullcap has been traditionally used for digestive health, skin and wound care, and pain and inflammation, among other applications.

Digestive health.

  • Laxative
  • Stomachic

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.

  • 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.

Pain and inflammation.

  • Anodyne

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 21 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
  • Tannin: astringent compounds that tighten tissues and resist infection
ⓘ 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, Germany, Denmark, Finland, France, United Kingdom, Netherlands, Russia, Sweden, United States.

Complete Use Records

CategoryCultural Context
FeverElsewhere, Spain, Turkey
AnodyneElsewhere, Turkey
LaxativeElsewhere, Turkey
NervineElsewhere, Turkey
SpasmElsewhere, Turkey
StomachicElsewhere, Turkey
AgueElsewhere
EpilepsyElsewhere
SoreElsewhere
AstringentTurkey
MalariaElsewhere
TonicTurkey

Complete Chemical Inventory

CompoundFormulaMW
6-HYDROXY-LUTEIN
ALPHA-HUMULENEC₁₅H₂₄204.35 Da
APIGENINC₁₅H₁₀O₅270.24 Da
BAICALEINC₁₅H₁₀O₅270.24 Da
BAICALEIN-7-BETA-L-RHAMNOSIDE
BAICALINC₂₁H₁₈O₁₁446.4 Da
BETA-CUBEBENEC₁₅H₂₄204.35 Da
CARYOPHYLLENEC₁₅H₂₄204.35 Da
CHRYSINC₁₅H₁₀O₄254.24 Da
CHRYSIN-7-GLUCURONIDEC₂₁H₁₈O₁₀430.4 Da
DIHYDROBAICALEINC₁₅H₁₂O₅272.25 Da
DIHYDRONORWOGONINC₁₅H₁₂O₅272.25 Da
GERMACRENE-DC₁₅H₂₄204.35 Da
LIMONENEC₁₀H₁₆136.23 Da
LUTEOLINC₁₅H₁₀O₆286.24 Da
MENTHONEC₁₀H₁₈O154.25 Da
OROXYLIN-AC₁₆H₁₂O₅284.26 Da
SCUTELLAREINC₁₅H₁₀O₆286.24 Da
TANNIN
TRANS-BETA-FARNESENEC₁₅H₂₄204.35 Da
WOGONINC₁₆H₁₂O₅284.26 Da

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


References & Further Reading

External Research Links

Data Sources