Maca

Also known as: Peruvian Ginseng

Botanical Overview

Maca (Lepidium meyenii) is a species in the Brassicaceae family. The mustard family (Brassicaceae) includes herbs with alternate leaves and four-petaled flowers arranged in cross-like clusters. The fruits are typically elongated capsules called siliques. Most species produce glucosinolates and isothiocyanates, pungent sulfur-containing compounds with anticancer and antimicrobial properties. Although comprehensive ethnobotanical records are limited, phytochemical studies have identified 30 compounds in this species, suggesting potential medicinal value.

General Description

It was rediscovered for commercial purposes at the Meseta de Bombón plateau close to Lake Junin in the late 1980s. It is grown for its fleshy hypocotyl that is fused with a taproot, which is typically dried but may also be freshly cooked as a root vegetable. As a cash crop, it is primarily exported as a powder that may be raw or processed further as a gelatinized starch or as an extract. If dried, it may be processed into a flour for baking or as a dietary supplement. Its Spanish and Quechua names include maca-maca, maino, ayak chichira, and ayak willku.

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

Family Context

The Brassicaceae family is widely distributed in temperate regions. Notable medicinal members include:

Geographic Distribution

Maca has been recorded in 9 countries and territories worldwide, including Argentina, Bolivia, Chile, China, 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:

  • Sterol: cholesterol-like compounds with anti-inflammatory properties
  • Alkaloid: nitrogenous compounds with diverse pharmacological activities

Research Status

Although this species has documented phytochemical constituents, its ethnobotanical and clinical documentation remains incomplete. Systematic pharmacological studies are needed to validate the traditional uses attributed to this species.

ⓘ 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: Argentina, Bolivia, Chile, China, Spain, United Kingdom, Norway, Peru, Russia.

Complete Chemical Inventory

CompoundFormulaMW
(1R,3S)-1-METHYL-TETRAHYDRO-BETA-CARBOLINE-3-CARBOXYLIC-ACID
4-METHOXY-GLUCOBRASSICIN
4-METHOXY-INDOYL-3-METHYLGLUCOSINOLATE
5-METHYLSULFINYLPENTYL-GLUCOSINOLATEC₁₃H₂₅NO₁₀S₃451.5 Da
ALANINEC₃H₇NO₂89.09 Da
ALKALOIDS
ALLYL-GLUCOSINOLATEC₁₀H₁₆NO₉S₂-358.4 Da
ARGININEC₆H₁₄N₄O₂174.20 Da
ASCORBIC-ACIDC₆H₈O₆176.12 Da
ASH
ASPARTIC-ACIDC₄H₇NO₄133.10 Da
BENZYL-GLUCOSINOLATEC₁₄H₁₉NO₉S₂409.4 Da
BETA-ECDYSONEC₂₇H₄₄O₇480.6 Da
BETA-SITOSTEROLC₂₉H₅₀O414.7 Da
CALCIUMCa40.08 Da
CAMPESTEROLC₂₈H₄₈O400.7 Da
CARBOHYDRATES
COPPERCu63.55 Da
FATC₁₆H₃₂O₂256.42 Da
FIBER
GLUCOALYSSINC₁₃H₂₅NO₁₀S₃451.5 Da
GLUCOBRASSICANAPINC₁₂H₂₁NO₉S₂387.4 Da
GLUCOBRASSICINC₁₆H₂₀N₂O₉S₂448.5 Da
GLUCOLIMNANTHINC₁₅H₂₁NO₁₀S₂439.5 Da
GLUCOSINALBINC₁₄H₁₉NO₁₀S₂425.4 Da
GLUCOSINOLATES
GLUCOTROPAEOLINC₁₄H₁₉NO₉S₂409.4 Da
GLUTAMIC-ACIDC₅H₉NO₄147.13 Da
GLYCINEC₂H₅NO₂75.07 Da
HISTIDINEC₆H₉N₃O₂155.15 Da

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


References & Further Reading

External Research Links

Data Sources