Anise-Scented Basil

Botanical Overview

Anise-Scented Basil (Ocimum tenuiflorum) is a species in the Lamiaceae family. The mint family (Lamiaceae) includes aromatic herbs and shrubs with square stems, opposite leaves, and two-lipped flowers. Many species produce essential oils in glandular trichomes on their leaves and stems. This family is one of the most important sources of culinary and medicinal herbs worldwide. Although comprehensive ethnobotanical records are limited, phytochemical studies have identified 30 compounds in this species, suggesting potential medicinal value.

General Description

It is widely cultivated throughout the Southeast Asian tropics. It is native to tropical and subtropical regions of Asia, Australia and the western Pacific. This plant has escaped from cultivation and has naturalized in many tropical regions of the Americas. It is an agricultural and environmental weed. Tulasi is cultivated for religious and traditional medicine purposes, and also for its essential oil. It is widely used as an herbal tea, commonly used in Ayurveda. It has a place within the Vaishnava tradition of Hinduism, in which devotees perform worship involving the plant or its leaves.

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

Family Context

The Lamiaceae family is large and widely distributed. Notable medicinal members include:

  • Basil — 86 documented uses
  • Rosemary — 60 documented uses
  • Agbo — 54 documented uses
  • Sage — 49 documented uses

Geographic Distribution

Anise-Scented Basil has been recorded in 10 countries and territories worldwide, including Australia, Cuba, Micronesia, Indonesia, India, 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
  • Alkaloid: nitrogenous compounds with diverse pharmacological activities

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: Australia, Cuba, Micronesia, Indonesia, India, Sri Lanka, Philippines, Thailand, United States, Unknown.

Complete Chemical Inventory

CompoundFormulaMW
(+)-DELTA-CADINENEC₁₅H₂₄204.35 Da
(-)-LINALOOLC₁₀H₁₈O154.25 Da
(-)-TRANS-CARYOPHYLLENEC₁₅H₂₄204.35 Da
(1S)-ALPHA-PINENE
(E)-ANETHOLEC₁₀H₁₂O148.20 Da
(Z)-ALPHA-BISABOLENEC₁₅H₂₄204.35 Da
1,2-BIS(4-ALLYL-2-METHOXYPHENOXY)-3-(4-HYDROXY-3-METHOXYPHENYL)-3-METHOXYPROPANE
1,8-CINEOLEC₁₀H₁₈O154.25 Da
1-(4-HYDROXY-3-METHOXYPHENYL)-1,2,3-TRIS(4-ALLYL-2-METHOXYPHENOXY)PROPANE
1-ALLYL-4-(5-ALLYL-2-HYDROXY-3-METHOXYPHENOXY)-3-(4-ALLYL-2-METHOXYPHENOXY)-5-METHOXYBENZENE
16-HYDROXY-4,4,10,13-TETRAMETHYL-17-(4-METHYL-PENTYL)-HEXADECAHYDRO-CYCLOPENTA[A]PHENANTHREN-3-ONEC₂₇H₄₆O₂402.7 Da
3-(5-ALLYL-2-HYDROXY-3-METHOXYPHENYL)-1-(4-HYDROXY-3-METHOXYPHENOXY)-PROP-1-ENE
4-ALLYL-1-O-BETA-D-GLUCOPYRONOSYL-2-HYDROXYBENZENE
5-ALLYL-3-(4-ALLYL-2-METHOXYPHENOXYMETHYL)-2-(4-HYDROXY-3-METHOXYPHENYL)-7-METHOXY-2,3-DIHYDROBENZOFURAN
6-ALLYL-3',8-DIMETHOXY-FLAVAN-3,4'-DIOL
6-ALLYL-3-(4-ALLYL-2-METHOXYPHENOXY)-3',8-DIMETHOXYFLAVAN-4'-OL
ACETIC-ACIDC₂H₄O₂60.05 Da
ALDEHYDESC₂₀H₃₀O₅350.4 Da
ALKALOIDS
ALPHA-HUMULENEC₁₅H₂₄204.35 Da
ALPHA-LINOLENIC-ACIDC₁₈H₃₀O₂278.4 Da
ALPHA-PINENEC₁₀H₁₆136.23 Da
ANTISTAPHYLOCOAGULASE
APIGENINC₁₅H₁₀O₅270.24 Da
APIGENIN-7-O-BETA-D-GLUCOPYRANOSIDEC₂₁H₂₀O₁₀432.4 Da
APIGENIN-7-O-BETA-D-GLUCURONIC-ACID
APIGENIN-7-O-BETA-D-GLUCURONIC-ACID-6''-METHYL-ESTER
APIGENIN-7-O-GLUCURONIDEC₂₁H₁₈O₁₁446.4 Da
ASCORBIC-ACIDC₆H₈O₆176.12 Da
ASH

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


References & Further Reading

External Research Links

Data Sources