Guava

Botanical Overview

Commonly known as Guava, this species belongs to the Myrtaceae family. This species holds a prominent place in the global materia medica, with an extensive record of traditional use spanning diverse cultures and medical systems. The myrtle family (Myrtaceae) includes trees and shrubs with opposite leaves that contain aromatic oil glands. The flowers are showy with numerous stamens, and the fruits are often fleshy berries or capsules. Many species produce essential oils with antiseptic and antimicrobial properties.

General Description

It is pollinated by insects. When cultivated, it is pollinated mainly by the common honey bee, Apis mellifera.

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

Family Context

The Myrtaceae family is primarily tropical and subtropical. Notable medicinal members include:

Geographic Distribution

Guava has been recorded in 10 countries and territories worldwide, including Benin, Brazil, Colombia, Ecuador, India, and others.

Traditional Uses

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

Digestive health.

  • Diarrhea
  • Dysentery
  • Ache(Stomach)
  • Laxative
  • 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.

Respiratory conditions.

  • Catarrh
  • Cough
  • Bronchitis
  • Cold

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.

  • Sore
  • Wound
  • Itch
  • Scabies

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:

  • Phenolic: antioxidant compounds that neutralize free radicals
  • Alkaloid: nitrogenous compounds with diverse pharmacological activities
  • Tannin: astringent compounds that tighten tissues and resist infection
ⓘ 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: Benin, Brazil, Colombia, Ecuador, India, Mexico, Taiwan, Tanzania, United States, South Africa.

Complete Use Records

CategoryCultural Context
DiarrheaBahamas, Elsewhere, Ghana, Haiti, Hawaii, Malaya, Mexico, Philippines, Trinidad
AstringentElsewhere, English, Ghana, Haiti, Philippines, Tahiti, Trinidad, Venezuela
DysenteryElsewhere, Ghana, Haiti, Panama, Trinidad, Venezuela
Ache(Stomach)Haiti, Johore, Mexico, Tonga
SoreElsewhere, Haiti, India(Santal), Philippines
EpilepsyElsewhere, Haiti, Malaya
WoundElsewhere, Hawaii, Philippines
BactericideElsewhere, Trinidad
CatarrhDutch, Elsewhere
CoughGhana, Samoa
ItchHaiti, Mexico
LaxativeGhana, Sanscrit
ScabiesHaiti, Mexico
SwellingJava, Mexico
Ache(Tooth)Elsewhere, Ghana
VermifugeJohore, Mexico
BronchitisElsewhere
CachexiaElsewhere
CarbuncleIndia(Santal)
CholeraElsewhere
ChoreaElsewhere
ColdCuba
ConvulsionElsewhere
DermatosisMalaya
DropsyDominican Republic
Evil eyeNew Zealand(Niue)
FatteningElsewhere
FeverElsewhere
GingivitisElsewhere
HysteriaMalaya

Complete Chemical Inventory

CompoundFormulaMW
(+)-GALLOCATECHINC₁₅H₁₄O₇306.27 Da
(+)-LIMONENEC₁₀H₁₆136.23 Da
2-3-4-6-TETRA-O-GALLOYL-GLUCOSEC₃₄H₂₈O₂₂788.6 Da
2-ETHYL-THIOPHENEC₆H₈S112.19 Da
2-FURFURALC₅H₄O₂96.08 Da
2-METHYL-PROPAN-2-OLC₄H₁₀O74.12 Da
2-METHYL-PROPANE-1-THIOLC₄H₁₀S90.19 Da
2-METHYL-THIO-BENZOTHIAZOLE
2-METHYL-THIOPHENEC₅H₆S98.17 Da
2-PHENETHYLACETATEC₁₀H₁₂O₂164.20 Da
2ALPHA-HYDROXYURSOLIC-ACID
3,3'-DI-O-METHYL-ELLAGIC-ACID
3-METHYL-BUTAN-1-OLC₅H₁₂O88.15 Da
3-METHYL-BUTYL-ACETATE
3-METHYL-THIOPHENEC₅H₆S98.17 Da
3-O-METHYL-ELLAGIC-ACID
5-ETHOXY-THIAZOLE
6-MERCAPTO-HEXAN-1-OLC₆H₁₄OS134.24 Da
ACETALDEHYDEC₂H₄O44.05 Da
ACETONEC₃H₆O58.08 Da
ACETYLFURANC₆H₆O₂110.11 Da
ACUTISSIMIN-AC₅₆H₃₈O₃₁1206.9 Da
ACUTISSIMIN-BC₅₆H₃₈O₃₁1206.9 Da
ALANINEC₃H₇NO₂89.09 Da
ALPHA-AMYRINC₃₀H₅₀O426.7 Da
ALPHA-AMYRIN-ACETATEC₃₂H₅₂O₂468.8 Da
ALPHA-HUMULENEC₁₅H₂₄204.35 Da
ALPHA-LINOLENIC-ACIDC₁₈H₃₀O₂278.4 Da
ALPHA-PINENEC₁₀H₁₆136.23 Da
ALPHA-SELINENEC₁₅H₂₄204.35 Da

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


References & Further Reading

External Research Links

Data Sources