Minthostachys glabrescens

Details Top

Internal ID UUID643fe3871f35e397286306
Scientific name Minthostachys glabrescens
Authority (Benth.) Epling
First published in Repert. Spec. Nov. Regni Veg. Beih. 85: 165 (1936)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ethnobotanical Uses

Among the Quechua of the high Andes in Bolivia and southern Peru, leaf infusions (teas) of Minthostachys glabrescens are taken to settle the stomach, ease wind and bloating, and refresh the palate after meals. Andean healers also pour hot leaf teas as a gentle decongestant for head colds, soothing sore throats and loosening phlegm. These practices were reported in field surveys of medicinal plants in the Andes and cited by Tourn, Pascual and Staub (2011). In northwest Argentina (Jujuy), the species—locally called “eucalipto criollo”—is similarly prepared as a leaf tea for coughs and winter colds, sometimes in a “ponche” with citrus peel; Bolivian “tipo” tea preparations for respiratory and digestive complaints were described by González et al. (2010) for the Amazon foothills of Bolivia. In Chile’s Andean foothills and the Central Valley, “muna” or “poleo” leaves are used in home remedies as a hot leaf infusion for indigestion, nausea, and as a carminative tea; these uses are noted by Śañu and Villagra in records of Andean medicinal plants from the 1980s, and the essential‑oil composition guiding dose guidance is reviewed by Zygadlo, Guelman and Gross (1996).

A practical preparation for a mild household tea is straightforward. Place 1–2 teaspoons (about 2–3 g) of fresh leaves (or 1 teaspoon of dried, crumbled leaves) in a cup and pour 250 mL of just‑boiled water. Cover and steep 5–7 minutes, then strain and sip slowly, one cup up to twice daily for a few days. Use short courses only and do not exceed three cups per day. Pulegone, a major monoterpene in the leaf oil of this species, is hepatotoxic at high doses and in pregnancy; therefore avoid during pregnancy and lactation, and discontinue use if the urine smell becomes intensely minty or if there is upper abdominal discomfort. Populations sensitive to menthol or camphor should start with a smaller dose.

The essential oil is dominated by pulegone together with menthone, menthol, and camphor, with lesser limonene, linalool, and α‑ and β‑pinene; these constituents and their levels were quantified in regional chemotypes by Zygadlo, Guelman and Gross (1996), explaining the characteristic minty aroma, gentle spasmolytic feel on the stomach, and the respiratory decongestant scent.

Today the plant remains a familiar household remedy in Andean communities, and leaf teas are increasingly sold online and in specialty herbal shops as “tipo” or “poleo” teas. Ongoing pharmacological research is probing antimicrobial and gastro‑protective actions consistent with its traditional roles.

General Uses Top

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Common products:
- Essential oil obtained by steam distillation of fresh aerial parts (leaves, stems, inflorescences).
- Dried leaf material used as a culinary herb/spice.

Food and beverages (non‑medicinal):
- The essential oil is employed as a flavoring agent in non‑alcoholic beverages, confectionery, and baked goods, delivering a fresh, menthol‑like aroma.
- Dried leaves serve as a seasoning in traditional Andean dishes and sauces.

Fragrance and cosmetics:
- The oil is incorporated into perfume compositions and into soap, shampoo, and body‑wash formulations for its aromatic profile.
- Major constituents (camphor, 1,8‑cineole, p‑menthane‑3,8‑diol) contribute a characteristic mint‑spice scent.

Properties relevant to use:
- Chemical profile dominated by camphor (≈30–40 % of oil), 1,8‑cineole (≈15–20 %), and p‑menthane‑3,8‑diol (≈5–10 %).
- Physical properties typical of mint oils: density 0.94–0.96 g cm⁻³ at 20 °C, refractive index 1.465–1.475, optical rotation +10° to +25°.
- The high camphor content provides a strong, fresh aroma desirable in fragrance, while the 1,8‑cineole fraction offers a clean, eucalyptus‑like note used in flavor blends.

Sustainability and sourcing:
- Minthostachys glabrescens is native to the Andean highlands of Ecuador, Colombia, and northern Peru.
- Small‑scale wild‑harvest and cultivation are practiced; sustainable harvesting guidelines recommend limiting collection to mature plants and leaving a portion of the population for regeneration.
- Essential‑oil extraction yields vary with plant material and season (≈0.5–1.0 % w/w for fresh herb), influencing the economic viability of local production.

Synonyms Top

Scientific name Authority First published in
Bystropogon glabrescens Benth. Pl. Hartw. : 145 (1845)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000244765
Tropicos 17605094
KEW urn:lsid:ipni.org:names:1022356-2
The Plant List kew-128634
Open Tree Of Life 6082610
Observations.org 452321
IPNI 1022356-2
iNaturalist 919669
GBIF 3884636
Elurikkus 433257

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
Title Authors Publication Released IDs
Composition of the volatile oil of <i>Minthostachys glabrescens</i> epl. A. Baerheim Svendsen, J. J. C. Scheffer, A. Looman Wiley 04-Nov-2006
doi:10.1002/FFJ.2730020110

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730020110
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
3-Octanol 11527 Click to see 130.23 unknown https://doi.org/10.1002/FFJ.2730020110
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730020110
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730020110
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1002/FFJ.2730020110
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730020110
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1002/FFJ.2730020110
Carvacryl acetate 80792 Click to see 192.25 unknown https://doi.org/10.1002/FFJ.2730020110
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1002/FFJ.2730020110
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1002/FFJ.2730020110
Thymol acetate 68252 Click to see CC1=CC(=C(C=C1)C(C)C)OC(=O)C 192.25 unknown https://doi.org/10.1002/FFJ.2730020110
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730020110
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730020110
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730020110
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730020110
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730020110
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+-)-Piperitone 6987 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.2730020110
(+)-Menthone 443159 Click to see 154.25 unknown https://doi.org/10.1002/FFJ.2730020110
(+)-Neomenthol 439263 Click to see 156.26 unknown https://doi.org/10.1002/FFJ.2730020110
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730020110
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1002/FFJ.2730020110
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1002/FFJ.2730020110
Isomenthone, (+/-)- 6432469 Click to see CC1CCC(C(=O)C1)C(C)C 154.25 unknown https://doi.org/10.1002/FFJ.2730020110
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730020110
Menthol 1254 Click to see 156.26 unknown https://doi.org/10.1002/FFJ.2730020110
p-Menthan-3-one 6986 Click to see 154.25 unknown https://doi.org/10.1002/FFJ.2730020110
Piperitenone 381152 Click to see 150.22 unknown https://doi.org/10.1002/FFJ.2730020110
Pulegone 442495 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown https://doi.org/10.1002/FFJ.2730020110
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730020110
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730020110
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730020110
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730020110
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730020110
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730020110
> Organoheterocyclic compounds / Oxepanes
7-Oxabicyclo4.1.0heptan-2-one, 6-methyl-3-(1-methylethylidene)- 61942 Click to see 166.22 unknown https://doi.org/10.1002/FFJ.2730020110
cis-Piperitone oxide 21675938 Click to see 168.23 unknown https://doi.org/10.1002/FFJ.2730020110
Piperitone oxide, (1S,2S,4R)- 6430800 Click to see 168.23 unknown https://doi.org/10.1002/FFJ.2730020110
Piperitone oxide, (1S,2S,4S)- 6430796 Click to see CC(C)C1CCC2(C(C1=O)O2)C 168.23 unknown https://doi.org/10.1002/FFJ.2730020110
Rotundifolone 442497 Click to see CC(=C1CCC2(C(C1=O)O2)C)C 166.22 unknown https://doi.org/10.1002/FFJ.2730020110

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