Chinese Alpenrose

Botanical Overview

Chinese Alpenrose (Rhododendron dauricum) is a species in the Ericaceae family. The heath family (Ericaceae) includes shrubs and small trees with simple, often evergreen leaves that are typically thick and leathery. The flowers are urn-shaped or bell-shaped with fused petals. Many species grow in acidic soils and form mycorrhizal associations, and several produce berries used in traditional medicine. Although comprehensive ethnobotanical records are limited, phytochemical studies have identified 28 compounds in this species, suggesting potential medicinal value.

Family Context

The Ericaceae family is widely distributed worldwide. Notable medicinal members include:

Geographic Distribution

Chinese Alpenrose has been recorded in 10 countries and territories worldwide, including China, Japan, North Korea, South Korea, Kazakhstan, and others.

Active Compounds

Phytochemical research has identified 28 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
  • Alkaloid: nitrogenous compounds with diverse pharmacological activities

Research Status

Although this species has documented phytochemical constituents, its ethnobotanical and clinical documentation remains incomplete. Systematic pharmacological studies are needed to validate the traditional uses attributed to this species.

ⓘ 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: China, Japan, North Korea, South Korea, Kazakhstan, Latvia, Mongolia, Russia, United States, Unknown.

Complete Chemical Inventory

CompoundFormulaMW
8-DEMETHYFARREROL
ALPHA-EUDESMOLC₁₅H₂₆O222.37 Da
ANDROMEDOTOXIC
AVICULARINC₂₀H₁₈O₁₁434.3 Da
AZALEATINC₁₆H₁₂O₇316.26 Da
BETA-EUDESMOLC₁₅H₂₆O222.37 Da
BETULINC₃₀H₅₀O₂442.7 Da
CAMPHORC₁₀H₁₆O152.23 Da
DIHYDROQUERCETINC₁₅H₁₂O₇304.25 Da
FARREROLC₁₇H₁₆O₅300.30 Da
GAMMA-EUDESMOLC₁₅H₂₆O222.37 Da
GAMMA-SELINENEC₁₅H₂₄204.35 Da
GERMACRONEC₁₅H₂₂O218.33 Da
GOSSYPETINC₁₅H₁₀O₈318.23 Da
HYDROQUINONEC₆H₆O₂110.11 Da
HYPERINC₂₁H₂₀O₁₂464.4 Da
HYPEROSIDEC₂₁H₂₀O₁₂464.4 Da
ISOHYPEROSIDEC₂₁H₂₀O₁₂464.4 Da
KAEMPFEROLC₁₅H₁₀O₆286.24 Da
MENTHOLC₁₀H₂₀O156.26 Da
MYRICETINC₁₅H₁₀O₈318.23 Da
P-HYDROXY-BENZOIC-ACID
QUERCETINC₁₅H₁₀O₇302.23 Da
SCOPOLETINC₁₀H₈O₄192.17 Da
SELINANEC₁₅H₂₈208.38 Da
UMBELLIFERONEC₉H₆O₃162.14 Da
URSOLIC-ACIDC₃₀H₄₈O₃456.7 Da
VANILLIC-ACIDC₈H₈O₄168.15 Da

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


References & Further Reading

External Research Links

Data Sources