Annual Camomile

Also known as: German Camomile, Wild Camomile

Botanical Overview

Annual Camomile (Matricaria recutita) is a species in the Asteraceae family. 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. Although comprehensive ethnobotanical records are limited, phytochemical studies have identified 30 compounds in this species, suggesting potential medicinal value.

Family Context

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

Geographic Distribution

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

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

Research Status

Although this species has documented phytochemical constituents, its ethnobotanical and clinical documentation remains incomplete. The limited documentation available for this species represents an opportunity for ethnobotanical research.

ⓘ 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: Belgium, Germany, Denmark, Spain, France, Greece, Luxembourg, Netherlands, Russia, United States.

Complete Chemical Inventory

CompoundFormulaMW
2,4-DIHYDROXYBENZOIC-ACIDC₇H₆O₄154.12 Da
2,5-DIHYDROXYBENZOIC-ACIDC₇H₆O₄154.12 Da
3,4-DIHYDROXYCINNAMIC-ACIDC₉H₈O₄180.16 Da
3-CARENEC₁₀H₁₆136.23 Da
3-HYDROXY-2-METHYLIDENE-BUTYRIC-ACID-ANGELATE
4-HYDROXY-3-METHOXY-BENZOIC-ACID
4-METHOXYBENZOIC-ACIDC₈H₈O₃152.15 Da
6,3-DIMETHOXYQUERCETINC₁₇H₁₄O₉362.3 Da
6,7-DIMETHOXYQUERCETINC₁₇H₁₄O₉362.3 Da
6-HYDROXY-LUTEOLIN-7-GLUCOSIDE
6-METHOXYKAEMPFEROLC₁₆H₁₂O₇316.26 Da
ALPHA-BISABOLOLC₁₅H₂₆O222.37 Da
ALPHA-BISABOLOL-OXIDE-AC₁₅H₂₆O₂238.37 Da
ALPHA-BISABOLOL-OXIDE-BC₁₅H₂₆O₂238.37 Da
ALPHA-BISABOLOLOXIDE-C
ALPHA-BISABOLONEOXIDE-A
ALPHA-CUBEBENEC₁₅H₂₄204.35 Da
ALPHA-MUUROLENEC₁₅H₂₄204.35 Da
ANTHECOTULIDEC₁₅H₂₀O₃248.32 Da
ANTHEMIC-ACID
APIGENINC₁₅H₁₀O₅270.24 Da
APIGENIN-7-(6'O-ACETYL)-GLUCOSIDE
APIGENIN-7-ACETYLGLUCOSIDE
APIGENIN-7-APIOSYLGLUCOSIDEC₂₆H₂₈O₁₄564.5 Da
APIGENIN-7-GLUCOSIDEC₂₁H₂₀O₁₀432.4 Da
APIGENIN-7-GLUCOSIDE-(2',3')-DIACETATE
APIGENIN-7-GLUCOSIDE-(3',4')-DIACETATE
APIGENIN-7-O-NEOHESPEROSIDE
APIGENIN-7-O-RUTINOSIDEC₂₇H₃₀O₁₄578.5 Da
APIGETRINC₂₁H₂₀O₁₀432.4 Da

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


References & Further Reading

External Research Links

Data Sources