Chives

Botanical Overview

Chives (Allium schoenoprasum) belongs to the Liliaceae family. While not among the most extensively documented medicinal plants, this species has recorded uses that warrant attention from researchers and practitioners. The lily family (Liliaceae) includes bulbous herbs with erect stems, alternate leaves, and showy six-parted flowers with prominent stamens. The underground bulbs serve as storage organs rich in carbohydrates. Many species contain steroidal saponins and alkaloids with medicinal properties.

General Description

Chives, scientific name Allium schoenoprasum, is a species of flowering plant in the family Amaryllidaceae.

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

Family Context

The Liliaceae family is widely distributed in temperate regions. Notable medicinal members include:

Geographic Distribution

Chives has been recorded in 10 countries and territories worldwide, including Switzerland, Germany, Finland, France, United Kingdom, and others.

Traditional Uses

Chives has been traditionally used for digestive health, urinary tract health, and cardiovascular health, among other applications.

Digestive health.

  • Carminative

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.

Urinary tract health.

  • Diuretic

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.

Cardiovascular health.

  • Anemia
  • Blood

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
  • Sterol: cholesterol-like compounds with anti-inflammatory properties
  • Alkaloid: nitrogenous compounds with diverse pharmacological activities
ⓘ 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: Switzerland, Germany, Finland, France, United Kingdom, Netherlands, Norway, Russia, Sweden, United States.

Complete Use Records

CategoryCultural Context
DigestiveHaiti, Iraq, Turkey
AntisepticIraq, Turkey
CarminativeIraq, Turkey
DiureticIraq, Turkey
AnemiaTurkey
BloodIraq
SpiceIraq
WenUK

Complete Chemical Inventory

CompoundFormulaMW
1-O-FERULOYL-BETA-D-GLUCOSEC₁₆H₂₀O₉356.32 Da
1-O-P-COUMAROYL-BETA-D-GLUCOSEC₁₅H₁₈O₈326.30 Da
2-METHYL-2-BUTENALC₅H₈O84.12 Da
2-METHYL-2-PENTENALC₆H₁₀O98.14 Da
3,5-DIETHYL-1,2,4-TRITHIOLANEC₆H₁₂S₃180.4 Da
ALANINEC₃H₇NO₂89.09 Da
ALLITHIAMINEC₁₅H₂₂N₄O₂S₂354.5 Da
ALLIUM-LECTIN
ALLYL-DISULFIDEC₆H₁₀S₂146.3 Da
ALLYL-MERCAPTANC₃H₆S74.15 Da
ALPHA-LINOLENIC-ACIDC₁₈H₃₀O₂278.4 Da
ARGININEC₆H₁₄N₄O₂174.20 Da
ASCORBIC-ACIDC₆H₈O₆176.12 Da
ASH
ASPARTIC-ACIDC₄H₇NO₄133.10 Da
BETA-CAROTENEC₄₀H₅₆536.9 Da
CAFFEIC-ACIDC₉H₈O₄180.16 Da
CALCIUMCa40.08 Da
CAMPESTEROLC₂₈H₄₈O400.7 Da
CARBOHYDRATES
CHRYSANTHEMINC₂₁H₂₁ClO₁₁484.8 Da
CIS-PENTYL-HYDRO-DISULFIDE
CIS-PROPENYL-PROPYL-DISULFIDE
CIS-PROPYL-2-PROPENYLDISULFIDE
CITRIC-ACIDC₆H₈O₇192.12 Da
COPPERCu63.55 Da
CYANIDIN-3-O-BETA-(3''-6''-DIMALONYL-GLUCOSIDE)
CYANIDIN-3-O-BETA-(3''-O-BETA-D-GLUCOSYL-GLUCOSIDE)
CYANIDIN-3-O-BETA-(6''-MALONYL-3''-O-BETA-D-GLUCOPYRANOSYL-GLUCOPYRANOSIDE)
CYANIDIN-3-O-BETA-(6''-MALONYL-3''-O-BETA-GLUCOPYRANOSYL-GLUCOPYRANOSIDE)

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


References & Further Reading

External Research Links

Data Sources