Common St. Johnswort

Also known as: Hypericum, Klamath Weed, St. John's-wort, Goatweed

Botanical Overview

Common St. Johnswort (Hypericum perforatum) is a flowering plant in the Clusiaceae family. This plant has earned a place in traditional medicine through its consistent therapeutic benefits, recorded across multiple cultures. The garcinia family (Clusiaceae) includes trees and shrubs with opposite, leathery leaves and resinous sap that is often yellow. The flowers are typically showy with numerous stamens, and the fruits are often fleshy capsules. Many species produce xanthones and polycyclic polyprenylated acylphloroglucinols (PPAPs) with significant biological activity.

General Description

John’s wort (sometimes perforate St. John’s wort or common St. John’s wort), is a flowering plant in the family Hypericaceae. It is a hairless, perennial herb with woody roots, yellow flowers marked by black glands, and leaves that appear perforated due to translucent glands, producing thousands of seeds per plant. H. perforatum is the type species of its genus, known for its historical use in folklore and traditional medicine. Probably a hybrid between the closely related H. attenuatum and H. maculatum (imperforate St. John’s wort) that originated in Siberia, the species has spread worldwide. It can further hybridize with related species due to its allopolyploid nature. It is native to much of Europe, West and Central Asia, and parts of Africa and China and has been widely introduced elsewhere, thriving in well-drained, temperate habitats such as meadows, hillsides, and open woods with moderate rainfall and mild temperatures. It is a resilient, toxic, and invasive plant that reproduces sexually and vegetatively, supports specialized insect herbivores, suffers from plant diseases, and poses ecological and agricultural threats in many parts of the world. H. perforatum has been used for centuries in traditional medicine, especially for treating wounds and depression. To prepare it for use, the oil from its glands can be extracted or its above-ground parts can be dried and ground into a powder called herba hyperici. H. perforatum exhibits antidepressant effects comparable to drugs with fewer side effects for mild to moderate depression (for which it is approved in the European Union); however, it may interact with various medications by accelerating their metabolism.

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

Family Context

The Clusiaceae family is primarily tropical. Notable medicinal members include:

Geographic Distribution

Common St. Johnswort has been recorded in 10 countries and territories worldwide, including Australia, Belgium, Switzerland, Germany, Denmark, and others.

Traditional Uses

Common St. Johnswort has been traditionally used for digestive health, respiratory conditions, and skin and wound care, among other applications.

Digestive health.

  • Vermifuge

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
  • 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.

  • Wound
  • 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:

  • Phenolic: antioxidant compounds that neutralize free radicals
  • 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 Abortifacient, Poison. 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: Australia, Belgium, Switzerland, Germany, Denmark, France, United Kingdom, Netherlands, Sweden, United States.

Complete Use Records

CategoryCultural Context
AstringentElsewhere, Turkey
DiureticElsewhere, Turkey
ExpectorantElsewhere, Turkey
NervineElsewhere, Turkey
VermifugeIndia, Turkey
VulnerarySpain, Turkey
WoundElsewhere, UK
AbortifacientElsewhere
AlopeciaElsewhere
AnodyneTurkey
AntibioticElsewhere
AntisepticTurkey
BactericideElsewhere
Cancer(Stomach)Poland
EmmenagogueIndia
GastrointestinalElsewhere
LungElsewhere
PoisonElsewhere
ResolventTurkey
RheumatismElsewhere
SoreElsewhere
StimulantTurkey
TumorUS(NC)
UrogenitalElsewhere
UterotonicTurkey
VermicideElsewhere
DepressionElsewhere
PhototoxicUS
CatarrhTurkey
CholagogueTurkey

Complete Chemical Inventory

CompoundFormulaMW
(+)-CATECHINC₁₅H₁₄O₆290.27 Da
(+)-EPICATECHINC₁₅H₁₄O₆290.27 Da
(-)-EPICATECHINC₁₅H₁₄O₆290.27 Da
(E)-BETA-FARNESENEC₁₅H₂₄204.35 Da
(E)-OCIMENEC₁₀H₁₆136.23 Da
(Z)-OCIMENEC₁₀H₁₆136.23 Da
1(3)-11(8)-BIAPIGENINC₃₀H₁₈O₁₀538.5 Da
1,3,6,7-TETRAHYDROXYXANTHONEC₁₃H₈O₆260.20 Da
2,2-DIMETHYL-7-ISOBUTYL-2H,5H-PYRANO-(4,3-B)-PYRAN-5-ONE
2,2-DIMETHYL-7-SEC-BUTYL-2H,5H-PYRANO-(4,3-B)-PYRAN-5-ONE
2-METHYL-BUTENOL
2-METHYL-DECANEC₁₁H₂₄156.31 Da
2-METHYL-OCTANEC₉H₂₀128.25 Da
5-METHYLHEPTAN-2,4-DIONE
6-METHYL-HEPT-5-EN-2-ONEC₈H₁₄O126.20 Da
6-METHYLHEPTAN-2,4-DIONEC₈H₁₄O₂142.20 Da
ACETOPHENONEC₈H₈O120.15 Da
ACYLPHLOROGLUCINOLS
ADHYPERFOLIN
ADHYPERIFORIN
ALKANES
ALKANOLS
ALPHA-AMORPHENEC₁₅H₂₄204.35 Da
ALPHA-CAMPHOLENOLC₁₀H₁₈O154.25 Da
ALPHA-CUPRENENEC₁₅H₂₄204.35 Da
ALPHA-EUDESMOLC₁₅H₂₆O222.37 Da
ALPHA-HUMULENEC₁₅H₂₄204.35 Da
ALPHA-PHELLANDRENEC₁₀H₁₆136.23 Da
ALPHA-PINENEC₁₀H₁₆136.23 Da
ALPHA-SELINENEC₁₅H₂₄204.35 Da

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


References & Further Reading

External Research Links

Data Sources