Guar

Also known as: Cluster-Bean, Siam-Bean

Botanical Overview

Guar (Cyamopsis tetragonoloba) belongs to the Fabaceae family. Limited but reliable traditional records indicate this plant has recognized medicinal applications in one or more healing traditions. The legume family (Fabaceae) includes trees, shrubs, and herbs that produce pods (legumes) and form nitrogen-fixing root nodules through symbiosis with bacteria. The flowers are typically pea-shaped with five petals. This large family provides food staples, timber, and numerous medicinal species.

General Description

It is also known as gavar, gawar, or guvar bean. The genus name Cyamopsis means bean-like. The specific name is from Greek: τετράγωνον, romanized: tetrágōnon and Latin: lobus meaning four-squared-lobed.

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

Family Context

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

Geographic Distribution

Guar has been recorded in 10 countries and territories worldwide, including Afghanistan, Australia, Brazil, Cameroon, China, and others.

Traditional Uses

Guar has been traditionally used for digestive health and pain and inflammation.

Digestive health.

  • Laxative

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.

Pain and inflammation.

  • Swelling

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
ⓘ 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: Afghanistan, Australia, Brazil, Cameroon, China, India, Pakistan, Russia, United States, Unknown.

Complete Use Records

CategoryCultural Context
Boil(Veterinary)Elsewhere
HeadElsewhere
HepatomegalyElsewhere
Poultice(Veterinary)Elsewhere
SwellingElsewhere
LaxativeElsewhere
Night-BlindnessElsewhere
PlagueElsewhere
SmallpoxElsewhere

Complete Chemical Inventory

CompoundFormulaMW
2,3,4-TRIHYDROXY-BENZOIC-ACID
3-EPIKATONIC-ACIDC₃₀H₄₈O₃456.7 Da
7-O-BETA-(2-RHAMNOSYL-GLUCOSYL)-MYRICETIN
7-O-BETA-D-GLUCOSIDE-3-O-(2-DIRHAMNOSYL-GLUCOSYL)-KAEMPFEROL
ASCORBIC-ACIDC₆H₈O₆176.12 Da
ASH
ASTRAGALINC₂₁H₂₀O₁₁448.4 Da
BETA-CAROTENEC₄₀H₅₆536.9 Da
CAFFEIC-ACIDC₉H₈O₄180.16 Da
CALCIUMCa40.08 Da
CARBOHYDRATES
CHLOROGENIC-ACIDC₁₆H₁₈O₉354.31 Da
CONIFERYL-ALCOHOLC₁₀H₁₂O₃180.20 Da
DAIDZEIN-7-O-BETA-D-GLUCOSIDE
ELLAGIC-ACIDC₁₄H₆O₈302.19 Da
FATC₁₆H₃₂O₂256.42 Da
FIBER
FLUOROACETIC-ACIDC₂H₃FO₂78.04 Da
FLUROACETIC-ACID
GALLIC-ACIDC₇H₆O₅170.12 Da
GENTISIC-ACIDC₇H₆O₄154.12 Da
GUARAN
IRONFe55.84 Da
JUGLANINC₂₀H₁₈O₁₀418.3 Da
KAEMPFEROLC₁₅H₁₀O₆286.24 Da
KAEMPFEROL-3-0-RUTINOSIDE
KAEMPFEROL-7-O-BETA-D-GLUCOSIDE-3-GLYCOSIDE
LINOLEIC-ACIDC₁₈H₃₂O₂280.4 Da
MYRICETIN-7-O-BETA-D-GLUCOSIDE-3-GLYCOSIDE
MYRISTIC-ACIDC₁₄H₂₈O₂228.37 Da

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


References & Further Reading

External Research Links

Data Sources