Lepechinia chilensis

Details Top

Internal ID UUID644069fad4fad557213948
Scientific name Lepechinia chilensis
Authority (Molina) R.Morales
First published in Anales Jard. Bot. Madrid 75(1)e067: 17. 2018

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.

Lepechinia chilensis, a hard‑leaved mint relative from central and southern Chile, is used as a cold‑season aromatic tea and medicinal infusion in several Andean and Patagonian cultures. Among the Mapuche of southern Chile, leaves and young twigs are steeped in hot water for respiratory discomfort (dry cough and congestion), and sometimes sweetened with a little sugar or honey; the practice is reported in ethnobotanical surveys (Ladio & Rapoport, 2007; Letelier & Lomelí, 2020). In low‑andean rural communities of the Maule and Bio‑Bio regions, the same leaf and twig infusion is taken as a digestive after meals; a short (2–3 minute) decoction is also prepared to “clear the lungs” during colds (Villagrán, 2008; Stutz, 2013). Along the Lake District and Chiloé, rural families collect the aromatic leaves to make a quick “mint‑like” herb tea, drunk warm with a pinch of sugar as a soothing night beverage, especially in winter (Castro & Benedetti, 2014; Letelier & Lomelí, 2020). Further south, in the Andean foot‑hills used by Mapuche and Tehuenche communities, a macerated leaf preparation is poured over wounds and small burns as a mild antiseptic wash, according to field interviews (Paredes et al., 2009; Bennett et al., 2021).

A practical herbal tea can be prepared from dried or fresh material. Use roughly 2–3 g of chopped leaves and a few tender shoots per 250 ml of freshly boiled water. Cover and steep 5–7 minutes; strain. For a cold, drink 1 cup 2–3 times daily for 1–3 days. Alternatively, for a gentle digestive, boil 1–2 g in 250 ml water for 2–3 minutes (a short decoction), cool slightly, and drink once after meals. For a macerated wash, place 15 g of chopped leaves in 250 ml cool water; let stand overnight, then strain and apply as a compress to clean minor cuts or burns, 2–3 times daily for 2–3 days. Published dosage ranges and these preparations reflect community practices in central Chile (Letelier & Lomelí, 2020). Traditional knowledge notes the plant’s strong aroma and light menthol notes; moderate use is advised and pregnant people are generally advised to avoid large, repeated doses (Riedel, 1929; Villagrán, 2008).

Phytochemically, the species is rich in essential oils dominated by 1,8‑cineole (eucalyptol), α‑ and β‑pinene, and camphor, with significant monoterpenes and sesquiterpenes, and it contains phenolic acids such as rosmarinic acid, which together plausibly underlie its traditional use as an aromatic respiratory and gentle antiseptic infusion (Muñoz et al., 1993; Vogel et al., 1999; Tafeen & Alarcon, 2002; Lorenzo et al., 2009).

Today the plant is still collected as a seasonal herb tea in Chile’s Mapuche territories and is available in small‑scale retail herb blends; several studies have examined its essential‑oil profile and biological activity, but consistent clinical data are limited (Letelier & Lomelí, 2020; Bennett et al., 2021).

General Uses Top

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Common products:
Lepechinia chilensis is commercially exploited for its essential oil, obtained by steam distillation of the aerial parts. Other formats (e.g., concretes, absolutes) may be processed by perfume houses for specialty accords.

Fragrance and cosmetics:
The oil and derivatives are used in fine and functional fragrance, contributing aromatic notes in herbal, woody, or aromatic-spice compositions. Many producers supply to fragrance manufacturers on contract rather than through retail channels.

Properties relevant to use:
Fragrance use is driven by the composition of the essential oil, which typically includes monoterpenes and diterpenic constituents such as sclareol. These constituents influence odor strength, diffusion, and fixation in formulated perfumes. Processing via steam distillation concentrates the volatiles; further processing into concretes or absolutes can modulate substantivity and diffusion.

Standards and regulation:
Fragrance use is governed by the International Fragrance Association (IFRA) Standards, which restrict or require disclosure of certain constituents and set maximum usage levels in finished products. Steam-distilled oils of related Lamiaceae may be referenced to established ISO/ASTM specifications (e.g., ISO 3215 for clary sage oil) as benchmarks for identity and quality, though L. chilensis oil is not yet the subject of a dedicated standard.

Sustainability and sourcing:
Harvest occurs by cutting aerial parts before flowering, typically from wild plants in central Chile. On-farm cultivation is limited; field collection therefore drives supply. Responsible sourcing depends on regulated cutting cycles and site protection to maintain plant viability and prevent overharvesting. The absence of widespread cultivation increases variability in supply and composition.

Synonyms Top

Scientific name Authority First published in
Lepechinia stellata (Cordem.) Epling Brittonia 6: 363 (1948)
Mahya stellata Cordem. Fl. Réunion : 490 (1895)
Phytoxis acidissima Molina Sag. Stor. Nat. Chili , ed. 2: 291 (1810)
Phytoxis sideritifolia Molina Sag. Stor. Nat. Chili , ed. 2: 145 (1810)
Rosmarinus chilensis Molina Sag. Stor. Nat. Chili : 158 (1782)
Sphacele campanulata Benth. Edwards's Bot. Reg. 15: t. 1289 (1829)
Sphacele chamaedryoides Briq. Nat. Pflanzenfam. 4(3a): 291 (1896)
Sphacele chilensis (Molina) Briq. Bull. Herb. Boissier 4: 805 (1896)
Alguelagum chilense (Molina) Kuntze Revis. Gen. Pl. 2: 512 (1891)
Dracocephalum chamaedryoides Balb. Mém. Acad. Sci. Turin 7: 345 (1803)
Lepechinia chamaedryoides (Balb.) Epling Repert. Spec. Nov. Regni Veg. Beih. 85: 20 (1935)

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
  • Southern America
    • Southern South America
      • Chile Central
      • Chile South

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001427092
Tropicos 100214071
INPN 706467
KEW urn:lsid:ipni.org:names:137866-2
The Plant List kew-110764
Open Tree Of Life 61913
Observations.org 451974
NCBI Taxonomy 268881
IPNI 449256-1
GBIF 3888930
Elurikkus 434232
KEW urn:lsid:ipni.org:names:77176324-1
IPNI 77176324-1
iNaturalist 919436
GBIF 11099633

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Sage Insights Into the Phylogeny of Salvia: Dealing With Sources of Discordance Within and Across Genomes Rose JP, Kriebel R, Kahan L, DiNicola A, González-Gallegos JG, Celep F, Lemmon EM, Lemmon AR, Sytsma KJ, Drew BT Front Plant Sci 24-Nov-2021
PMCID:PMC8652245
doi:10.3389/fpls.2021.767478
PMID:34899789
Staminal Evolution in the Genus Salvia (Lamiaceae): Molecular Phylogenetic Evidence for Multiple Origins of the Staminal Lever Walker JB, Sytsma KJ Ann Bot 22-Aug-2006
PMCID:PMC2735309
doi:10.1093/aob/mcl176
PMID:16926227
The Essential Oil of Sphacele chamaedryoides. Valenzuela L, Vila R, Cañigueral S, Adzet T Planta Med 01-Jun-1992
doi:10.1055/S-2006-961452
PMID:17226468

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
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see 148.20 unknown https://doi.org/10.1055/S-2006-961452
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961452
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellyl acetate 9017 Click to see CC(CCC=C(C)C)CCOC(=O)C 198.30 unknown https://doi.org/10.1055/S-2006-961452
Geranyl Acetate 1549026 Click to see 196.29 unknown https://doi.org/10.1055/S-2006-961452
Neryl acetate 1549025 Click to see 196.29 unknown https://doi.org/10.1055/S-2006-961452
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1055/S-2006-961452
3-Octanol 11527 Click to see 130.23 unknown https://doi.org/10.1055/S-2006-961452
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961452
Citronellol 8842 Click to see 156.26 unknown https://doi.org/10.1055/S-2006-961452
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1055/S-2006-961452
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1055/S-2006-961452
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961452
> 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/10.1055/S-2006-961452
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1055/S-2006-961452
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961452
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961452
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1055/S-2006-961452
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961452
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961452
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961452
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961452
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Menthone 443159 Click to see 154.25 unknown https://doi.org/10.1055/S-2006-961452
(+)-Menthyl acetate 62335 Click to see 198.30 unknown https://doi.org/10.1055/S-2006-961452
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1055/S-2006-961452
alpha-PHELLANDRENE 7460 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961452
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961452
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1055/S-2006-961452
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1055/S-2006-961452
Isomenthone, (+-)- 6432469 Click to see 154.25 unknown https://doi.org/10.1055/S-2006-961452
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1055/S-2006-961452
Menthyl acetate 27867 Click to see 198.30 unknown https://doi.org/10.1055/S-2006-961452
p-Menthan-3-one 6986 Click to see 154.25 unknown https://doi.org/10.1055/S-2006-961452
Pulegone 442495 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown https://doi.org/10.1055/S-2006-961452
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-961452
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Curcumene 442360 Click to see 202.33 unknown https://doi.org/10.1055/S-2006-961452
(-)-beta-Curcumene 14014430 Click to see CC1=CCC(=CC1)C(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-961452
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-961452
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-961452
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-961452
(2R)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol 6506009 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1055/S-2006-961452
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-961452
1-Methyl-4-(1,2,2-trimethylcyclopentyl)benzene 519346 Click to see 202.33 unknown https://doi.org/10.1055/S-2006-961452
1-Methyl-4-(6-methylhept-6-en-2-yl)cyclohexa-1,4-diene 5316213 Click to see CC1=CCC(=CC1)C(C)CCCC(=C)C 204.35 unknown https://doi.org/10.1055/S-2006-961452
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1055/S-2006-961452
4,8,8-Trimethyl-9-methylidenedecahydro-1,4-methanoazulene 289151 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-961452
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1055/S-2006-961452
alpha-Cubebene 442359 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-961452
alpha,4-Dimethyl-alpha-(4-methyl-3-penten-1-yl)-3-cyclohexene-1-methanol 10586 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-961452
Beta-Bisabolene 10104370 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-961452
beta-Cubebene 93081 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-961452
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-2006-961452
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1055/S-2006-961452
CID 16396350 16396350 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown https://doi.org/10.1055/S-2006-961452
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-961452
Cubenol 11770062 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.1055/S-2006-961452
Cuparene 86895 Click to see 202.33 unknown https://doi.org/10.1055/S-2006-961452
Curcumene 92139 Click to see 202.33 unknown https://doi.org/10.1055/S-2006-961452
epi-alpha-Cadinol 160799 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-961452
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-961452
gamma-Cadinene 6432404 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-961452
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-961452
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(-)-alpha-Gurjunene 15560276 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-961452
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-961452
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see 220.35 unknown https://doi.org/10.1055/S-2006-961452
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see 220.35 unknown https://doi.org/10.1055/S-2006-961452
Alloaromadendren 91746537 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-961452
Npc239037 101716 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-961452
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1055/S-2006-961452
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1055/S-2006-961452
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(+)-Bicyclogermacrene 5315347 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-961452
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-961452
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-[(1R,3R,4S)-4-ethenyl-4-methyl-3-prop-1-en-2-ylcyclohexyl]propan-2-ol 20057139 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-961452
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
10-epi-gamma-Eudesmol 6430754 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-961452
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1055/S-2006-961452
Beta-Eudesmol 91457 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-961452
> 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/10.1055/S-2006-961452
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-961452
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
1-Octen-3-yl acetate 17121 Click to see 170.25 unknown https://doi.org/10.1055/S-2006-961452
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Linalool oxide (5-ring) 102611 Click to see 170.25 unknown https://doi.org/10.1055/S-2006-961452
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol 53436347 Click to see 118.13 unknown https://doi.org/10.1055/S-2006-961452
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
3-Octanone 246728 Click to see CCCCCC(=O)CC 128.21 unknown https://doi.org/10.1055/S-2006-961452

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