Antler Herb

Also known as: Clubmoss

Botanical Overview

Antler Herb (Lycopodium clavatum) is a flowering plant in the Lycopodiaceae family. The traditional uses of this species reflect its genuine medicinal value, validated by generations of practical experience. The clubmoss family (Lycopodiaceae) includes evergreen, moss-like plants with creeping stems and upright branches covered in small, scale-like leaves. These ancient plants reproduce by spores rather than seeds. Several species produce alkaloids used in traditional medicine and as sources of clubmoss powder.

General Description

Lycopodium clavatum (common clubmoss, stag’s-horn clubmoss, running clubmoss, or ground pine) is the most widespread species in the genus Lycopodium in the clubmoss family.

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

Family Context

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

Geographic Distribution

Antler Herb has been recorded in 10 countries and territories worldwide, including Canada, Germany, Finland, France, United Kingdom, and others.

Traditional Uses

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

Digestive health.

  • Carminative
  • Diarrhea
  • Dyspepsia
  • Laxative

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.

  • Catarrh

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.

  • 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.

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
  • 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: Canada, Germany, Finland, France, United Kingdom, Norway, Poland, Russia, Sweden, United States.

Complete Use Records

CategoryCultural Context
Cancer(Skin)France, Italy
DiureticTurkey, US
SkinElsewhere, Turkey
SpasmElsewhere, Turkey
Ache(Head)Lesotho
ApertifUS
CarminativeTurkey
CatarrhSpain
ChestElsewhere
DiarrheaUS
DyspepsiaElsewhere
EmmenagogueTurkey
FeverElsewhere
FumitoryLesotho
HomeopathyElsewhere
LaxativeTurkey
NervesUS
PressorElsewhere
Preventitive(Chafe)US
RheumatismElsewhere
UterotonicElsewhere
AphrodisiacUS
Pill-CoatingElsewhere
UrogenitalElsewhere

Complete Chemical Inventory

CompoundFormulaMW
16-OXOLYCOCLAVANOLC₃₀H₄₈O₄472.7 Da
16-OXOSERRAT-14-EN-3-BETA,21-ALPHA-DIOL
16-OXOSERRAT-14-EN-3-BETA,21-BETA-DIOL
16-OXOSERRAT-14-ENE-3ALPHA,21BETA-DIOL
16-OXOSERRATENEDIOL
16-OXYSERRATENEDIOL
21-EPISERRATENEDIOLC₃₀H₅₀O₂442.7 Da
21-EPISERRATRIOLC₃₀H₅₀O₃458.7 Da
22-DEHYDROCAMPESTEROLC₂₈H₄₆O398.7 Da
24-ALPHA-ETHYLCHOLEST-5-EN-3-BETA-OL
24-ALPHA-ETHYLCHOLESTA-5,22-DIEN-3-BETA-OL
24-ALPHA-METHYL-CHOLEST-5-EN-3-BETA-OL
24-BETA-METHYLCHOLEST-5-EN-3-BETA-OL
9,10-DIHYDROXYSTEARIC-ACIDC₁₈H₃₆O₄316.5 Da
9,10-DIOXYSTEARIC-ACID
9-HEXADECANOIC-ACIDC₁₆H₂₉O₂-₃253.40 Da
ACETYLDIHYDROLYCOPODINE
ACETYLFAWCETTIINEC₂₀H₃₁NO₄349.5 Da
ALANINEC₃H₇NO₂89.09 Da
ALKALOIDS
ALPHA-OBSCURINEC₁₇H₂₆N₂O274.4 Da
ALPHA-ONOCERINC₃₀H₅₀O₂442.7 Da
ANHYDROLYCODOLINEC₁₆H₂₃NO245.36 Da
ANNONTINE
APIGENINC₁₅H₁₀O₅270.24 Da
APIGENIN-4'-GLUCOSIDEC₂₁H₂₀O₁₀432.4 Da
ARGININEC₆H₁₄N₄O₂174.20 Da
ARSENICAs74.92159 Da
AZELAIC-ACIDC₉H₁₆O₄188.22 Da
BETA-OBSCURINEC₁₇H₂₄N₂O272.4 Da

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


References & Further Reading

External Research Links

Data Sources