Wheat

Botanical Overview

Wheat (Triticum aestivum) is a flowering plant in the Poaceae family. Traditional medicine systems have documented several valuable applications for this species, supported by its observed therapeutic effects. The grass family (Poaceae) includes annual and perennial herbs with hollow, jointed stems and narrow leaves with parallel venation. The flowers are reduced and arranged in spikelets, and the fruits are grains (caryopses). This family provides the majority of the world’s food calories through cereals.

General Description

It originated around 8,000 years ago, from the hybridization of an already existing domesticated variety of wheat and the wild goatgrass in the South Caucasus or southwestern Caspian area. About 95% of wheat produced worldwide is this species; it is the most widely grown of all crops and the cereal with the highest monetary yield.

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

Family Context

The Poaceae family is very large and globally distributed. Notable medicinal members include:

Traditional Uses

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

Digestive health.

  • 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.

  • Skin

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
  • Gravel

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:

  • 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.

Complete Use Records

CategoryCultural Context
CancerCanada, US
DemulcentChina, Turkey
WartPeru, UK
WhitlowIndia, Uk(Wales)
DiarrheaChina
DiscutientChina
DiureticChina
DysenteryChina
EcchymosisChina
EmollientTurkey
EpistaxisChina
FertilityChina
FeverChina
GravelChina
HematuriaChina
HemoptysisChina
HemorrhageChina
IncontinenceChina
InsomniaChina
MenorrhagiaChina
Night-SweatChina
PoulticeChina
RestorativeTurkey
ScaldChina
SedativeChina
SkinChina
SmallpoxChina
SunstrokeChina
SwellingChina
TuberculosisChina

Complete Chemical Inventory

CompoundFormulaMW
1,3-AMINO-PROPYL-PYRROLINIUM
1,3-DIFERULOYL-GLYCEROL
1-O-(6-O-ACYL-BETA-D-GALACTOPYRANOSYL)-2,3-DI-O-ACYL-D-GLY...
2'-CHLORO-DIAZEPAM
2'-CHLORO-N-DEMETHYL-DIAZEPAM
2(3)-BENZOXAZOLINONEC₇H₅NO₂135.12 Da
2-(2,4-DIHYDROXY-1,4(2H)-BENZOXAZIN-3(4H)-ON-BETA-D-GLUCOSIDE
2-(2,4-DIHYDROXY-7-METHOXY-1-4(2H)-BENZOXAZIN-3-(4H)ON)-BETA-D-GLUCOSIDE
2-(2-HYDROXY-4,7-DIMETHOXY-1-4(2H)-BENZOXAZIN-3-ONE-BETA-D-GLUCOSIDE
2-(2-HYDROXY-7-METHOXY-1,4(2H)-BENZOXAZIN-3(4H)-ON-BETA-D-GLUCOSIDE
3-HYDROXY-2'-CHLORO-DIAZEPAM
4-DECYL-PENTA-TRANS-2,4-DIENAL
5,7,4'-TRIHYDROXY-3',5-DIMETHOXYFLAVONE
6-METHOXY-2(3)1-4(2H)-BENZOXAZOLINONE
8-METHOXYCOUMARINC₁₀H₈O₃176.17 Da
ADENINEC₅H₅N₅135.13 Da
ADENOSINEC₁₀H₁₃N₅O₄267.24 Da
ALANINEC₃H₇NO₂89.09 Da
ALBUMIN
ALLANTOINC₄H₆N₄O₃158.12 Da
ALPHA-AMYLASEC₁₅H₁₇N₃OS₂319.4 Da
ALPHA-AMYRINC₃₀H₅₀O426.7 Da
ALPHA-CARBOXYLASE
ALPHA-DIHYDROXYCAROTENE
ALPHA-TOCOPHEROLC₂₉H₅₀O₂430.7 Da
ALPHA-TRITICENEC₁₅H₂₆O222.37 Da
ALPHA-TRITISTEROL
AMMONIALYASE
APIGENINC₁₅H₁₀O₅270.24 Da
ARABINOSEC₅H₁₀O₅150.13 Da

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


References & Further Reading

External Research Links

Data Sources