Daffodil

Botanical Overview

Daffodil (Narcissus tazetta) is a flowering plant in the Liliaceae family. Traditional medicine systems have documented several valuable applications for this species, supported by its observed therapeutic effects. The lily family (Liliaceae) includes bulbous herbs with erect stems, alternate leaves, and showy six-parted flowers with prominent stamens. The underground bulbs serve as storage organs rich in carbohydrates. Many species contain steroidal saponins and alkaloids with medicinal properties.

General Description

Cultivars of N. tazetta include ‘Caniculatus’, ‘Grand Soleil d’Or’ and ‘Ziva’, which are popularly used for forcing indoors, as is the form of N. tazetta known as Chinese Sacred Lily.

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

Family Context

The Liliaceae family is widely distributed in temperate regions. Notable medicinal members include:

Geographic Distribution

Daffodil has been recorded in 10 countries and territories worldwide, including Australia, Spain, France, United Kingdom, Greece, and others.

Traditional Uses

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

Digestive health.

  • Purgative

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.

  • Abscess
  • Boil

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
  • Edema

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.
⚠ Caution
Traditional records: This plant has documented uses including Poison, Emetic, Purgative. 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, Spain, France, United Kingdom, Greece, Israel, Italy, Japan, Portugal, United States.

Complete Use Records

CategoryCultural Context
PoisonChina, Elsewhere
SwellingChina, Elsewhere
AbscessChina
Abscess(Breast)China
BoilChina
BreastJapan
CancerChina
CosmeticChina
DemulcentChina
DiureticIndia
EdemaJapan
EmeticIndia
Fish-BonesChina
GynecopathyChina
HairChina
MastitisChina
PoulticeChina
PurgativeIndia
Sclerosis(Uterus)Europe
TumorChina
Tumor(Ear)Jerusalem
AnalgesicChina
AntiphlogisticChina
Cancer(Breast)China
OintmentJapan

Complete Chemical Inventory

CompoundFormulaMW
3-O-MARITIDINE
6ALPHA-HYDROXY-3-O-METHYL-EPIMARITIDINE
6BETA-HYDROXY-3-O-METHYL-EPIMARITIDINE
ALKALOIDS
ALPHA-PHENYLPROPYL-ACETATE
ALPHA-PHENYLPROPYL-ALCOHOL
ALPHA-TERPINEOLC₁₀H₁₈O154.25 Da
BENZALDEHYDEC₇H₆O106.12 Da
BENZOIC-ACIDC₇H₆O₂122.12 Da
BENZYL-ACETATEC₉H₁₀O₂150.17 Da
BENZYL-ALCOHOLC₇H₈O108.14 Da
CINEOLEC₁₀H₁₈O154.25 Da
CINNAMYL-ALCOHOLC₉H₁₀O134.17 Da
DEMETHYLHOMOLYCORINEC₁₇H₁₉NO₄301.34 Da
EPIGALANTHAMINEC₁₇H₂₁NO₃287.35 Da
EUGENOLC₁₀H₁₂O₂164.20 Da
FIANCINE
GALANTHAMINEC₁₇H₂₁NO₃287.35 Da
GALANTHINEC₁₈H₂₃NO₄317.4 Da
HAEMANTHAMINEC₁₇H₁₉NO₄301.34 Da
HEPTYL-ALCOHOLC₇H₁₆O116.20 Da
HIPPEASTRINEC₁₇H₁₇NO₅315.32 Da
HOMOLYCORINEC₁₈H₂₁NO₄315.4 Da
INDOLC₈H₇N117.15 Da
ISORHAMNETINC₁₆H₁₂O₇316.26 Da
LINALOLC₁₀H₁₈O154.25 Da
LYCORAMINEC₁₇H₂₃NO₃289.4 Da
LYCORANOLIDINE
LYCORANOLINE
LYCORENINEC₁₈H₂₃NO₄317.4 Da

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


References & Further Reading

External Research Links

Data Sources