Garden Camomile

Also known as: Perennial Camomile, Roman Camomile

Botanical Overview

Garden Camomile (Chamaemelum nobile) belongs to the Asteraceae family. While not among the most extensively documented medicinal plants, this species has recorded uses that warrant attention from researchers and practitioners. The daisy family (Asteraceae) is one of the largest plant families, characterized by composite flower heads (capitula) that contain many small florets surrounded by bracts. Plants range from tiny alpine herbs to large tropical trees. The family includes many medicinally important species with bitter compounds and essential oils.

General Description

Its synonym is Anthemis nobilis, with various common names, such as Roman chamomile, English chamomile, garden chamomile, ground apple, low chamomile, mother’s daisy or whig plant. C. nobile is one source of the herbal product known as chamomile using dried flowers for flavoring teas or as a fragrance used in aromatherapy. Chamomile has no established medicinal properties.

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

Family Context

The Asteraceae family is extremely large and diverse. Notable medicinal members include:

Geographic Distribution

Garden Camomile has been recorded in 10 countries and territories worldwide, including Australia, Belgium, Germany, Spain, France, and others.

Traditional Uses

Garden Camomile has been traditionally used for digestive health, nervous system disorders, and metabolic and nutritional health.

Digestive health.

  • Carminative
  • Dyspepsia
  • Colic

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.

Nervous system disorders.

  • Nervine
  • Hysteria

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.

Metabolic and nutritional health.

  • Tonic

Metabolic applications include consuming the plant as a food, fresh juice, or herbal infusion. Regular use supports the body’s natural metabolic processes and nutritional status.

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:

  • 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.
⚠ Caution
Traditional records: This plant has documented uses including Emetic. Self-medication with herbs carries risks including allergic reactions, drug interactions, and toxicity. Only use under the supervision of a qualified healthcare professional.

Distribution and Conservation

Reported distribution: Australia, Belgium, Germany, Spain, France, United Kingdom, Ireland, Portugal, United States, Unknown.

Complete Use Records

CategoryCultural Context
CarminativeIraq, Mexico
DyspepsiaIraq, Mexico
StimulantMexico, Turkey
DebilityMexico
EmeticIraq
TonicIraq
Ache(Tooth)Kurdistan
NervineIraq
ColicMexico
HysteriaMexico

Complete Chemical Inventory

CompoundFormulaMW
(-)-BUTANE-1,3-DIYL-1-((Z)-2'-METHYL-2'-BUTENOATE)-3-ISOB...
1,10-EPOXYNOBILINC₂₀H₂₆O₆362.4 Da
1,8-CINEOLEC₁₀H₁₈O154.25 Da
2,3-DIHYDROXYCINNAMIC-ACIDC₉H₈O₄180.16 Da
2-METHYL-2-PROPYL-ANGELATE
2-METHYL-BUTYL-2-METHYL-BUTYRATE
2-METHYL-PROPANE-1,3-DIYL-1-(Z)-2'-METHYL-2'BUTEONATE...
2-METHYLBUTYL-2-METHYLPROPIONATE
2-METHYLBUTYL-BUTYRATE
2-METHYLIDENEPROPANE-1,3-DIYL-1-(Z)-2'-METHYL-2'BUTENOATE...
2-METHYLPROPYL-2-METHYL-BUTYRATE
2-METHYLPROPYL-3-METHYL-BUTYRATE
2-METHYLPROPYL-BUTYRATE
3,4-DIHYDROXYCINNAMIC-ACIDC₉H₈O₄180.16 Da
3-DEHYDRONOBILINC₂₀H₂₄O₅344.4 Da
3-EPINOBILINC₂₀H₂₆O₅346.4 Da
3-HYDROXY-2-METHYLIDENE-BUTYRIC-ACID-ANGELATE
3-METHYL-1-BUTANOLC₅H₁₂O88.15 Da
3-METHYLAMYL-ANGELATE
3-METHYLBUTYL-ANGELATE
3-METHYLIDENE-4-OXPENTYL-ANGELATE
3-METHYLPENTYL-ANGELATE
4-ISOPROPENYL-BENZALDEHYDEC₁₀H₁₀O146.19 Da
4-ISOPROPENYL-TOLUENEC₁₀H₁₂132.20 Da
5-(3-FURYL)-2-METHYL-1-PENTEN-3-OL
5-(3-FURYL)-2-METHYL-1-PENTEN-3-ONEC₁₀H₁₂O₂164.20 Da
5-ISOPROPENYL-2'-(2-METHYLPROPYL)-2-CYCLOHEXEN-1-ONE
ALPHA-BISABOLENE-OXIDE-A
ALPHA-BISABOLOL-OXIDE-AC₁₅H₂₆O₂238.37 Da
ALPHA-BISABOLOL-OXIDE-BC₁₅H₂₆O₂238.37 Da

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


References & Further Reading

External Research Links

Data Sources