Clove

Also known as: Clovetree

Botanical Overview

Clove (Syzygium aromaticum) is a flowering plant in the Myrtaceae family. This plant has earned a place in traditional medicine through its consistent therapeutic benefits, recorded across multiple cultures. 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

They are native to the Maluku Islands, or Moluccas, in Indonesia, and are commonly used as a spice, flavoring, or fragrance in consumer products, such as toothpaste, soaps, or cosmetics. Cloves are available throughout the year owing to different harvest seasons across various countries.

ⓘ 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

Clove has been recorded in 10 countries and territories worldwide, including Brazil, Indonesia, India, Sri Lanka, Malaysia, and others.

Traditional Uses

Clove has been traditionally used for digestive health, pain and inflammation, and nervous system disorders, among other applications.

Digestive health.

  • Carminative
  • Dyspepsia
  • Stomachic
  • Vermifuge
  • Diarrhea

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.

  • Anodyne

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.

Nervous system disorders.

  • Spasm

Nervous system support involves taking the herb as a warm tea, often in the evening or before bed. The calming compounds interact with neurotransmitter systems to promote relaxation and restful sleep.

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
  • 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: Brazil, Indonesia, India, Sri Lanka, Malaysia, Nigeria, Seychelles, Tanzania, United States, Unknown.

Complete Use Records

CategoryCultural Context
StimulantChina, Elsewhere, Haiti, Turkey
AntisepticChina, Haiti, Turkey
CarminativeChina, Elsewhere, Turkey
Ache(Tooth)China, Elsewhere, Haiti
AnalgesicElsewhere, Haiti
DyspepsiaElsewhere, France
NauseaChina, Elsewhere
RubefacientElsewhere, Turkey
SpasmElsewhere, Turkey
StomachicChina, Turkey
TonicChina, Turkey
VermifugeChina, Haiti
AnestheticElsewhere
AnodyneChina
Antidote(Scorpion)China
CallusMalaya
CholeraChina
DentifriceElsewhere
DeodorantChina
DiarrheaChina
DigestiveTurkey
GargleElsewhere
GastritisElsewhere
GestationHaiti
HairblackChina
HalitosisChina
HerniaChina
Repellant(Insect)Elsewhere
IntestineChina
SterilityChina

Complete Chemical Inventory

CompoundFormulaMW
1,2,3,4,6-PENTA-O-GALLOYL-BETA-D-GLUCOSEC₄₁H₃₂O₂₆940.7 Da
1,2,3,6-TETRA-O-GALLYOL-BETA-D-GLUCOSE
1-BETA-O-GALLOYLPEDUNCULAGIN
1-DEGALLOYL-EUGENIIN
10-(ALPHA)-CADINOL
2-3-DI-O-GALLOYL-GLUCOSEC₂₀H₂₀O₁₄484.4 Da
2-3-HEXAHYDROXY-DIPHENOYL-GLUCOSE
2-HEPTANOLC₇H₁₆O116.20 Da
2-HEPTANONEC₇H₁₄O114.19 Da
2-HEPTYL-ACETATEC₉H₁₈O₂158.24 Da
2-HEPTYL-BENZOATEC₁₄H₂₀O₂220.31 Da
2-NONANOLC₉H₂₀O144.25 Da
2-NONANONEC₉H₁₈O142.24 Da
2-NONYL-ACETATEC₁₁H₂₂O₂186.29 Da
2-UNDECANONEC₁₁H₂₂O170.29 Da
2ALPHA-HYDROXYOLEANOLIC-ACID-METHYL-ESTER
3'-O-METHYL-3-4-METHYLENEDIOXY-ELLAGIC ACID
3,3',4-TRI-O-METHYL-ELLAGIC-ACID
3,3'-DI-O-METHYL-ELLAGIC-ACID
3,4-DIHYDROXYBENZOIC-ACIDC₁₄H₁₂O₈308.24 Da
3,4-DIHYDROXYPHENYLETHANOLC₈H₁₀O₃154.16 Da
3-METHOXYBENZALDEHYDEC₈H₈O₂136.15 Da
4,4-DIMETHYLTRICYCLO[6,3,2,0]TRIDECA-8-ENE-1-OL
5,7-DIHYDROXY-2-METHYLCHROMONE-8-C-BETA-D-GLUCOPYRANOSIDEC₁₆H₁₈O₉354.31 Da
5,7-DIHYDROXY-2-METHYLCHROMONE-8-C-BETA-D-GLUCOSIDE
5,7-DIHYDROXY-2-METHYLCHROMONE-8-C-BETA-GLUCOPYRANOSIDE
5-METHYLFURALDEHYDE
6-METHYL-HEPT-5-EN-2-ONEC₈H₁₄O126.20 Da
ACETOPHENONEC₈H₈O120.15 Da
ACETYL-EUGENOLC₁₂H₁₄O₃206.24 Da

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


References & Further Reading

External Research Links

Data Sources