Douglas' Savory

Botanical Overview

Douglas’ Savory (Satureja douglasii) belongs to the Lamiaceae family. While not among the most extensively documented medicinal plants, this species has recorded uses that warrant attention from researchers and practitioners. 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.

General Description

The plant takes the form of a sprawling, mat-forming perennial. The name “yerba buena” derives from Spanish for “good herb” and is applied to various other plants.

ⓘ 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

Traditional Uses

Douglas’ Savory has been traditionally used for cardiovascular health.

Cardiovascular health.

  • 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:

  • 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.

Complete Use Records

CategoryCultural Context
BloodCanada(Salish)
DeodorantCanada(Salish)
TeaCanada(Salish)

Complete Chemical Inventory

CompoundFormulaMW
1,8-CINEOLEC₁₀H₁₈O154.25 Da
ALPHA-PINENEC₁₀H₁₆136.23 Da
ALPHA-TERPINENEC₁₀H₁₆136.23 Da
ALPHA-TERPINEOLC₁₀H₁₈O154.25 Da
BETA-BOURBONENEC₁₅H₂₄204.35 Da
BETA-PINENEC₁₀H₁₆136.23 Da
BICYCLOGERMACRENEC₁₅H₂₄204.35 Da
BORNEOLC₁₀H₁₈O154.25 Da
CAMPHENEC₁₀H₁₆136.23 Da
CAMPHORC₁₀H₁₆O152.23 Da
CARVONEC₁₀H₁₄O150.22 Da
CARYOPHYLLENEC₁₅H₂₄204.35 Da
CIS-OCIMENEC₁₀H₁₆136.23 Da
DELTA-CADINENEC₁₅H₂₄204.35 Da
GAMMA-TERPINENEC₁₀H₁₆136.23 Da
GERMACRENE-DC₁₅H₂₄204.35 Da
ISOMENTHONEC₁₀H₁₈O154.25 Da
LIMONENEC₁₀H₁₆136.23 Da
LINALOLC₁₀H₁₈O154.25 Da
MENTHONEC₁₀H₁₈O154.25 Da
METHYL-CARVACROLC₁₁H₁₆O164.24 Da
MYRCENEC₁₀H₁₆136.23 Da
P-CYMENEC₁₀H₁₄134.22 Da
PIPERITENONEC₁₀H₁₄O150.22 Da
PIPERITONEC₁₀H₁₆O152.23 Da
PULEGONEC₁₀H₁₆O152.23 Da
SABINENEC₁₀H₁₆136.23 Da
TERPINEN-4-OLC₁₀H₁₈O154.25 Da
TERPINOLENEC₁₀H₁₆136.23 Da
THYMOLC₁₀H₁₄O150.22 Da

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


References & Further Reading

External Research Links

Data Sources