Japanese Pagoda Tree

Botanical Overview

Japanese Pagoda Tree (Sophora japonica) is a flowering plant in the Fabaceae family. The traditional uses of this species reflect its genuine medicinal value, validated by generations of practical experience. The legume family (Fabaceae) includes trees, shrubs, and herbs that produce pods (legumes) and form nitrogen-fixing root nodules through symbiosis with bacteria. The flowers are typically pea-shaped with five petals. This large family provides food staples, timber, and numerous medicinal species.

General Description

Styphnolobium japonicum, the Japanese pagoda tree is a species of deciduous tree in the subfamily Faboideae of the pea family Fabaceae.

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

Family Context

The Fabaceae family is large and globally distributed. Notable medicinal members include:

Geographic Distribution

Japanese Pagoda Tree has been recorded in 10 countries and territories worldwide, including China, Germany, Spain, France, Italy, and others.

Traditional Uses

Japanese Pagoda Tree has been traditionally used for digestive health, skin and wound care, and pain and inflammation, among other applications.

Digestive health.

  • Dysentery

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.

  • Leprosy
  • Scabies
  • 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.

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 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.
⚠ 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: China, Germany, Spain, France, Italy, Japan, South Korea, Ukraine, United States, Unknown.

Complete Use Records

CategoryCultural Context
AstringentChina, Elsewhere
AbortifacientChina
AnodyneChina
ApprehensionChina
BactericideElsewhere
ConjunctivitisChina
EpilepsyChina
EstrogenicElsewhere
HematemesisChina
HematocheziaChina
HemostatChina
HemostaticJapan*
LaborChina
LeprosyChina
MetrorrhagiaChina
OrchitisChina
PilesChina
PoisonElsewhere
PuerperiumChina
RejuvenationChina
ScabiesChina
SkinChina
StypticElsewhere
VenerealChina
VertigoChina
FeverChina
MenorrhagiaChina
Preventitive(Aging)China
ConvulsionChina
DysenteryChina

Complete Chemical Inventory

CompoundFormulaMW
(+)-MEDICARPINC₁₆H₁₄O₄270.28 Da
(D,L)-MAACKIAIN
5,7,4'-TRIHYDROXY-ISOFLAVONE-4'-BETA-NEOHESPERIDOSIDE
5,7-DIHYDROXY-3',4'-METHYLENEDIOXYISOFLAVONEC₁₆H₁₀O₆298.25 Da
AMHYDROPISATIN
ASCORBIC-ACIDC₆H₈O₆176.12 Da
ASH
BETA-SITOSTEROLC₂₉H₅₀O414.7 Da
BETULINC₃₀H₅₀O₂442.7 Da
BIOCHANIN-AC₁₆H₁₂O₅284.26 Da
BIOCHANIN-A-7-(BETA-D-XYLOSYL{1-6}-BETA-D-GLUCOSIDE)
BIOCHANIN-A-7-BETA-D-GENTIOBIOSIDE
CAFFEIC-ACIDC₉H₈O₄180.16 Da
CALCIUMCa40.08 Da
CARBOHYDRATES
CYTISINEC₁₁H₁₄N₂O190.24 Da
D-MAACKIAIN
FATC₁₆H₃₂O₂256.42 Da
FERULIC-ACIDC₁₀H₁₀O₄194.18 Da
FIBER
GALACTOMANNANC₁₈H₃₂O₁₆504.4 Da
GENISTEINC₁₅H₁₀O₅270.24 Da
GENISTEIN-4'-0-GLUCOSIDE
GENISTEIN-4'-0-NEOHESPERIDOSIDE
IRISOLIDINE
IRISOLIDINE-7-O-GLUCOSIDE
KAEMPFEROLC₁₅H₁₀O₆286.24 Da
KAEMPFEROL-C-GLYCOSIDE
L-MAACKIAINC₁₆H₁₂O₅284.26 Da
LINOLEIC-ACIDC₁₈H₃₂O₂280.4 Da

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


References & Further Reading

External Research Links

Data Sources