Plectranthus coleoides

Botanical Overview

Plectranthus coleoides 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.

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

Plectranthus coleoides has been recorded in 9 countries and territories worldwide, including Belgium, Brazil, Cook Islands, Germany, Spain, 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:

  • Alkaloid: nitrogenous compounds with diverse pharmacological activities

Research Status

Although this species has documented phytochemical constituents, its ethnobotanical and clinical documentation remains incomplete. Additional phytochemical investigation could identify novel bioactive compounds in this plant.

ⓘ 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, Brazil, Cook Islands, Germany, Spain, India, New Zealand, Portugal, United States.

Complete Chemical Inventory

CompoundFormulaMW
1,1-DIPHENYLPROPANEC₁₅H₁₆196.29 Da
1,3-BIS(DIMETHYLAMINO)-BENZENE
1,3-DIMETHYL-BENZENEC₈H₁₀106.16 Da
1,3-TRIMETHYL-BENZENE
1-PHENYLETHYL-ACETATEC₁₀H₁₂O₂164.20 Da
2,2-DIMETHYL-TETRADECANEC₁₆H₃₄226.44 Da
2-ETHYL-HEXANOLC₈H₁₈O130.23 Da
2-METHYL-BUTANOLC₅H₁₂O88.15 Da
2-METHYL-HEPTAN-4-ONE
2-METHYL-UNDEC-2-ENEC₁₂H₂₄168.32 Da
2-PROPYL-HEPT-2-ENAL
3,4-DIMETHYL-(2H)-PYRAN-2-ONE
3-HEXENALC₆H₁₀O98.14 Da
4,6-DECADIENALC₁₀H₁₆O152.23 Da
4-METHYL-PENT-2-ENALC₆H₁₀O98.14 Da
ALPHA-HUMULENEC₁₅H₂₄204.35 Da
BETA-CARYOPHYLLENEC₁₅H₂₄204.35 Da
BORNEOLC₁₀H₁₈O154.25 Da
BORNYL-ACETATEC₁₂H₂₀O₂196.29 Da
BUTYL-ACETATEC₆H₁₂O₂116.16 Da
BUTYL-FORMATEC₅H₁₀O₂102.13 Da
CARVONEC₁₀H₁₄O150.22 Da
CITRONELLYL-FORMATEC₁₁H₂₀O₂184.27 Da
ETHYL-ACETATEC₄H₈O₂88.11 Da
FENCHONEC₁₀H₁₆O152.23 Da
GERANYL-ACETATEC₁₂H₂₀O₂196.29 Da
HEXADECANEC₁₆H₃₄226.44 Da
HEXYL-CINNAMALDEHYDEC₁₅H₂₀O216.32 Da
ISOBORNYL-ACETATEC₁₂H₂₀O₂196.29 Da
ISOPENTYL-FORMATEC₆H₁₂O₂116.16 Da

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


References & Further Reading

External Research Links

Data Sources