Japanese Honeysuckle

Botanical Overview

Japanese Honeysuckle (Lonicera japonica) is a flowering plant in the Caprifoliaceae family. This plant has earned a place in traditional medicine through its consistent therapeutic benefits, recorded across multiple cultures. This species belongs to the Caprifoliaceae family, a group of flowering plants.

General Description

It is often grown as an ornamental plant, but has become an invasive species in a number of countries. It is used in traditional Chinese medicine.

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

Family Context

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

Geographic Distribution

Japanese Honeysuckle has been recorded in 10 countries and territories worldwide, including Australia, Switzerland, China, Spain, France, and others.

Traditional Uses

Japanese Honeysuckle has been traditionally used for digestive health, skin and wound care, and urinary tract health, among other applications.

Digestive health.

  • Stomachic
  • Diarrhea
  • 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.

  • Boil
  • Scabies
  • Skin
  • 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.

Urinary tract health.

  • Diuretic

Urinary tract applications typically involve drinking the herb as a mild tea, which increases urine production and helps flush the urinary system. It may be combined with other demulcent herbs to soothe irritated tissues.

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:

  • 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: Australia, Switzerland, China, Spain, France, United Kingdom, Japan, South Korea, New Zealand, United States.

Complete Use Records

CategoryCultural Context
TumorChina, Elsewhere, Japan
AntidoteChina, Elsewhere
BactericideChina, Elsewhere
DiureticElsewhere, Japan
StomachicChina, Japan
TeaChina, Japan
ArthritisChina
BoilChina
Cancer(Breast)China
Cancer(Esophagus)China
DiarrheaChina
DysenteryChina
FebrifugeJapan
FeverChina
FluChina
InflammationChina
LongevityChina
LymphadenitisChina
RefrigerantChina
ScabiesJapan
SkinChina
SoreChina
SwellingJapan
Ache(Head)China
EnteritisChina
RheumatismChina
AstringentChina
CancerChina
FungicideElsewhere
InfectionChina

Complete Chemical Inventory

CompoundFormulaMW
(Z)-3-HEXEN-1-OLC₆H₁₂O100.16 Da
(Z)-3-HEXENYL-BENZOATE
(Z)-3-HEXENYL-TIGLATE
1-HEXENEC₆H₁₂84.16 Da
2,4-DECADIENALC₁₀H₁₆O152.23 Da
3,5-DICAFFEOYL-QUINIC-ACIDC₂₅H₂₄O₁₂516.4 Da
3,5-DICAFFEOYL-QUINIC-ACID-BUTYL-ESTER
3,5-DICAFFEOYL-QUINIC-ACID-METHYL-ESTER
3-CAFFEOYL-QUINIC-ACID-METHYL-ESTER
3-CAFFEOYLQUINIC-ACIDC₁₆H₁₈O₉354.31 Da
ALPHA-FARNESENEC₁₅H₂₄204.35 Da
ALPHA-TERPINEOLC₁₀H₁₈O154.25 Da
ARACHIDIC-ACIDC₂₀H₄₀O₂312.5 Da
AROMADENDRENEC₁₅H₂₄204.35 Da
ARSENICAs74.92159 Da
AUROXANTHINC₄₀H₅₆O₄600.9 Da
BENZYL-ALCOHOLC₇H₈O108.14 Da
BENZYL-BENZOATEC₁₄H₁₂O₂212.24 Da
BENZYL-SALICYLATEC₁₄H₁₂O₃228.24 Da
BETA-BOURBONENEC₁₅H₂₄204.35 Da
BETA-CARYOPHYLLENEC₁₅H₂₄204.35 Da
BETA-CITRONELLOLC₁₀H₂₀O156.26 Da
BETA-PHENYLETHANOLC₈H₁₀O122.16 Da
CALCIUMCa40.08 Da
CARVACROLC₁₀H₁₄O150.22 Da
CERYL-ALCOHOLC₂₆H₅₄O382.7 Da
CHLOROGENIC-ACIDC₁₆H₁₈O₉354.31 Da
CIS-JASMONEC₁₁H₁₆O164.24 Da
COPPERCu63.55 Da
CRYPTOXANTHINC₄₀H₅₆O552.9 Da

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


References & Further Reading

External Research Links

Data Sources