Bidens pilosa

Botanical Overview

Bidens pilosa is a flowering plant in the Asteraceae family. The traditional uses of this species reflect its genuine medicinal value, validated by generations of practical experience. The daisy family (Asteraceae) is one of the largest plant families, characterized by composite flower heads (capitula) that contain many small florets surrounded by bracts. Plants range from tiny alpine herbs to large tropical trees. The family includes many medicinally important species with bitter compounds and essential oils.

General Description

Its many common names include hitch hikers, black-jack, beggarticks, farmer’s friends and Spanish needle, but most commonly referred to as cobblers pegs. It is native to the Americas but is widely distributed as an introduced species in other regions including Eurasia, Africa, Australia, South America and the Pacific Islands, and is classified as an invasive species in some regions of the world.

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

Family Context

The Asteraceae family is extremely large and diverse. Notable medicinal members include:

Geographic Distribution

Bidens pilosa has been recorded in 10 countries and territories worldwide, including Australia, Brazil, China, Spain, Japan, and others.

Traditional Uses

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

Digestive health.

  • Dysentery
  • Colic

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
  • Pectoral
  • Bronchitis
  • Catarrh

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.

  • Boil
  • Itch

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:

  • Flavonoid: antioxidant compounds that protect cells from oxidative damage
  • Terpene: aromatic compounds with anti-inflammatory and antimicrobial properties
  • Sterol: cholesterol-like compounds with anti-inflammatory properties
ⓘ 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, Brazil, China, Spain, Japan, Mexico, Nepal, Taiwan, United States, South Africa.

Complete Use Records

CategoryCultural Context
CoughMalaya, Malaysia, Upper Volta
DiureticBahamas, Dominican Republic, Mexico
BoilJava, Philippines
ConjunctivitisMalaya, W Africa
DiabetesHaiti, Mexico
DysenteryTanzania, Venezuela
EyeDominica, Ghana
PectoralDominican Republic, Mexico
RheumatismElsewhere, S Africa
StypticElsewhere, Ghana
Ache(Tooth)Dominican Republic, Java
AftosaHaiti
AllergyGhana
AmygdalitisHaiti
AnginaHaiti
BronchitisUpper Volta
CatarrhHaiti
ColicUpper Volta
EarGhana
EmmenagogueDominican Republic
FeverBahamas
Food-PoisonTonga
Heat rashBahamas
InflammationAfrica
IntestineUpper Volta
IntoxicantPhilippines
ItchBahamas
LactogogueDominican Republic
LiqueurElsewhere
LiverElsewhere

Complete Chemical Inventory

CompoundFormulaMW
1-PHENYL-HEPTA-1-3-5-TRIYNE
2-O-CAFFEOYL-2-C-METHYL-D-ERYTHRONIC-ACID
3-O-CAFFEOYL-2-C-METHYL-D-ERYTHRONO-1-4-LACTONE
7-PHENYL-HEPTA-2-4-6-TRIYNE
ALPHA-CADINOLC₁₅H₂₆O222.37 Da
BEHENIC-ACIDC₂₂H₄₄O₂340.6 Da
BETA-AMYRINC₃₀H₅₀O426.7 Da
BETA-CARYOPHYLLENEC₁₅H₂₄204.35 Da
BORNEOLC₁₀H₁₈O154.25 Da
CAPRIC-ACIDC₁₀H₂₀O₂172.26 Da
DAUCOSTEROLC₃₅H₆₀O₆576.8 Da
ELAIDIC-ACIDC₁₈H₃₄O₂282.5 Da
ESCULETINC₉H₆O₄178.14 Da
FRIEDELAN-3-BETA-OL
FRIEDELINC₃₀H₅₀O426.7 Da
GERMACRENE-DC₁₅H₂₄204.35 Da
ISOQUERCITRINC₂₁H₂₀O₁₂464.4 Da
L-INOSITOLC₆H₁₂O₆180.16 Da
LAURIC-ACIDC₁₂H₂₄O₂200.32 Da
LIMONENEC₁₀H₁₆136.23 Da
LINOLEIC-ACIDC₁₈H₃₂O₂280.4 Da
LINOLENIC-ACIDC₁₈H₃₀O₂278.4 Da
LUPEOLC₃₀H₅₀O426.7 Da
LUPEOL-ACETATEC₃₂H₅₂O₂468.8 Da
MYRISTIC-ACIDC₁₄H₂₈O₂228.37 Da
OKANIN-3'-4'-DIGLUCOSIDE
OKANIN-3'-GLUCOSIDEC₂₁H₂₂O₁₁450.4 Da
OKANIN-3'-O-BETA-D-GLUCOSIDE
OKANIN-4'-(6'-O-ACETYL)-GLUCOSIDE
OKANIN-4'-DIGLUCOSIDE

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


References & Further Reading

External Research Links

Data Sources