Fishwort

Also known as: Dokudami, Yu Xing Cao

Botanical Overview

Fishwort (Houttuynia cordata) is a flowering plant in the Saururaceae family. The traditional uses of this species reflect its genuine medicinal value, validated by generations of practical experience. This species belongs to the Saururaceae family, a group of flowering plants.

General Description

emeiensis). It is a flowering plant native to Southeast Asia. It grows in moist, shady locations. It was named after Martinus Houttuyn.

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

Family Context

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

Geographic Distribution

Fishwort has been recorded in 10 countries and territories worldwide, including Austria, Belgium, China, Czech Republic, United Kingdom, and others.

Traditional Uses

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

Digestive health.

  • Dysentery
  • Dyspepsia

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.

  • Cough

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
  • Abscess

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:

  • 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: Austria, Belgium, China, Czech Republic, United Kingdom, Japan, South Korea, Netherlands, Taiwan, United States.

Complete Use Records

CategoryCultural Context
DiureticChina, Elsewhere, India, Japan, Japan*
PilesChina, India, Japan
AntidoteChina, Japan*
DysenteryChina, India
EyeIndia, Vietnam
GonorrheaIndia, Japan
SkinChina, India
SwellingChina, Japan
UrethritisChina, Japan
AbscessChina
AlexitericChina
AnodyneChina
AntisepticChina
AnusChina
AperientJapan*
AstringentChina
BactericideElsewhere
Bite(Snake)China
BonesChina
Cancer(Stomach)Japan
CoughChina
DyspepsiaChina
EnteritisChina
FemaleElsewhere
Fertility(Veterinary)Elsewhere
FeverChina
InternulcerElsewhere
LungChina
MalariaChina
MeaslesIndia

Complete Chemical Inventory

CompoundFormulaMW
(+)-LIMONENEC₁₀H₁₆136.23 Da
(+)-SESAMINC₂₀H₁₈O₆354.4 Da
1,3,5-TRIDECANOYLBENZENEC₃₆H₆₀O₃540.9 Da
1,4-DIHYDROPYRIDINEC₅H₇N81.12 Da
1,8-CINEOLEC₁₀H₁₈O154.25 Da
1-DECANOLC₁₀H₂₂O158.28 Da
1-DODECANOLC₁₂H₂₆O186.33 Da
1-NONANOLC₉H₂₀O144.25 Da
2-NONYL-5-DECANOYLPYRIDINE
3,5-DIDECANOYLPYRIDINEC₂₅H₄₁NO₂387.6 Da
3-KETODECANAL
ACETALDEHYDEC₂H₄O44.05 Da
AFZELINC₂₁H₂₀O₁₀432.4 Da
AFZERIN
ALPHA-PINENEC₁₀H₁₆136.23 Da
ARISTOLACTAM-A-IIC₁₆H₁₁NO₃265.26 Da
BETA-CARYOPHYLLENEC₁₅H₂₄204.35 Da
BETA-MYRCENEC₁₀H₁₆136.23 Da
BETA-PINENEC₁₀H₁₆136.23 Da
BETA-SITOSTEROLC₂₉H₅₀O414.7 Da
BORNEOLC₁₀H₁₈O154.25 Da
BORNEOL-ACETATEC₁₂H₂₀O₂196.29 Da
CALCIUMCa40.08 Da
CAMPHENEC₁₀H₁₆136.23 Da
CAPRIC-ACIDC₁₀H₂₀O₂172.26 Da
CAPRIC-ALDEHYDEC₁₀H₂₀O156.26 Da
CAPRYLALDEHYDEC₈H₁₆O128.21 Da
CARVACROLC₁₀H₁₄O150.22 Da
CARYOPHYLLENEC₁₅H₂₄204.35 Da
CARYOPHYLLENE-OXIDEC₁₅H₂₄O220.35 Da

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


References & Further Reading

External Research Links

Data Sources