Henna

Also known as: Mignonette, Jamaica-Mignonette, Mignonette Tree

Botanical Overview

Henna (Lawsonia inermis) is a flowering plant in the Lythraceae family. This plant has earned a place in traditional medicine through its consistent therapeutic benefits, recorded across multiple cultures. This species belongs to the Lythraceae family, a group of flowering plants.

General Description

It is used as a traditional medicinal plant. The species is named after the Scottish physician Isaac Lawson, a good friend of Linnaeus.

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

Family Context

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

Geographic Distribution

Henna has been recorded in 10 countries and territories worldwide, including Benin, Brazil, China, Egypt, Indonesia, and others.

Traditional Uses

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

Digestive health.

  • Ache(Stomach)
  • Purgative
  • Vermifuge

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
  • Skin
  • Boil
  • Burn

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.

  • Ache(Head)
  • Inflammation

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
  • Coumarin: aromatic compounds with anticoagulant and anti-inflammatory effects
  • 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.
⚠ Caution
Traditional records: This plant has documented uses including Poison, 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: Benin, Brazil, China, Egypt, Indonesia, India, Kenya, Madagascar, Mexico, Saudi Arabia.

Complete Use Records

CategoryCultural Context
AstringentChina, Dominican Republic, Elsewhere, Turkey
CosmeticChina, Egypt, Iraq
Ache(Head)Dominican Republic, India(Santal)
BactericideElsewhere, India
BruiseChina, Elsewhere
EmmenagogueDominican Republic, Mexico
Hair-DyeElsewhere, Turkey
LeprosyChina, Mexico
SedativeKurdistan, Turkey
SkinElsewhere, Mexico
Ache(Stomach)Dominican Republic
AlterativeTurkey
BoilMalaya
BurnElsewhere
DeodorantDominican Republic
DermatosisMalaya
FungicideIndia
HerpesJava
HysteriaMexico
InflammationElsewhere
JaundiceMexico
LeucorrheaJava
MyalgiaIndia(Santal)
OnychosisMalaya
OphthalmiaMalaya
PoisonMexico
PoulticeTurkey
PurgativeMexico
Sore(Throat)Elsewhere
VermifugeMexico

Complete Chemical Inventory

CompoundFormulaMW
(20S)-3BETA-30-DIHYDROXYLUPANE
1,2-DIHYDROXY-4-GLUCOSYLNAPTHALENE
1,3-DIHYDROXY-6,7-DIMETHOXYXANTHONE
1,3-DIHYDROXYNAPHTHALENEC₁₀H₈O₂160.17 Da
1,4-DIGLUCOSYLOXY-2-HYDROXYNAPTHALENE
1,4-NAPHTHAQUINONEC₁₀H₆O₂158.15 Da
1,4-NAPHTHOQUINONEC₁₀H₆O₂158.15 Da
1-HYDROXY-3,6-DIACETOXY-7-METHOXYXANTHONE
3-BETA-HYDROXY-20-OXO-30-NORLUPANE
30-NOR-LUPAN-3-BETA-OL-20-ONE
3BETA-30-DIHYDROXYLUP-20(29)-ENE
4-GLUCOSYLOXY-1,2-DIHYDROXYNAPTHALENE
ACACETIN-7-O-GLUCOSIDEC₂₂H₂₂O₁₀446.4 Da
AESCULETINC₉H₆O₄178.14 Da
ALPHA-IONONEC₁₃H₂₀O192.30 Da
APIGENIN-4'-GLUCOSIDEC₂₁H₂₀O₁₀432.4 Da
APIGENIN-4'-O-BETA-D-GLUCOSIDE
APIGENIN-7-O-BETA-GLUCOSIDEC₂₁H₂₀O₁₀432.4 Da
ARACHIDIC-ACIDC₂₀H₄₀O₂312.5 Da
ASH
BEHENIC-ACIDC₂₂H₄₄O₂340.6 Da
BETA-IONONEC₁₃H₂₀O192.30 Da
BETA-SITOSTEROLC₂₉H₅₀O414.7 Da
BETA-SITOSTEROL-3-O-GLUCOSIDEC₃₅H₆₀O₆576.8 Da
BETULINC₃₀H₅₀O₂442.7 Da
BETULINIC-ACIDC₃₀H₄₈O₃456.7 Da
CARBOHYDRATES
COSMOSIINC₂₁H₂₀O₁₀432.4 Da
COUMARINSC₁₉H₁₆O₄308.3 Da
CYNAROSIDEC₂₁H₂₀O₁₁448.4 Da

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


References & Further Reading

External Research Links

Data Sources