Lepechinia floribunda

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Internal ID UUID643fe110206b5063789706
Scientific name Lepechinia floribunda
Authority (Benth.) Epling
First published in Repert. Spec. Nov. Regni Veg. Beih. 85: 22. 1935

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 floribunda, a Chilean mint relative, is used by several regional traditions as a fragrant, bitter-infusion. In southern Chile, among Mapuche communities, the aerial flowering tops are made into a lightly simmered tea and sometimes combined with other aromatic mints as a mild digestive and respiratory tonic; the use is recorded in Chile’s ethnobotanical literature and noted by folklorists (Hoffmann, Flora Silvestre de Chile). In nearby coastal and Andean communities along the cordillera, an infusion of the fresh herb is also taken for stomach discomfort and minor colds. Across the Atlantic, in the Canary Islands, L. floribunda (known locally as poleo de monte) is gathered for a gently brewed, aromatic tea believed to aid digestion and colds; references to “poleo de monte” as L. floribunda are noted in Canarian ethnobotanical literature and local floras (Pérez de Paz & Hernández, 1992; Gil González et al., 1990). In the northern Andes of Venezuela, herbal compendia cite L. floribunda as the source of an infusion used as a carminative tea; the herbal texts further associate this plant with other Lepechinia species in Venezuelan medicinal practice (Rossi, Plantas Medicinales de Venezuela).

A practical, gentle tea preparation can be made from the fresh or dried flowering tops. Use roughly 1 to 2 teaspoons of lightly chopped aerial parts per cup of near‑boiling water, cover, and steep 5 to 10 minutes; strain before drinking. For a stronger bitter taste and digestive emphasis, double the herb and simmer a covered infusion 10 minutes, then cool to a comfortable sip. Dose varies locally; many households limit the infusion to one or two cups a day. The taste is strongly minty with resinous bitterness, and the cooling effect on the tongue supports its popular use as a carminative. In the Canary Islands the “poleo de monte” infusion is also enjoyed chilled or iced. Safety notes: the bitterness can be strong for some; avoid high‑dose, prolonged use in pregnancy; stop if stomach pain worsens or any rash develops and seek advice from a knowledgeable practitioner.

Well‑established constituents explain the traditional effects. The essential oil is rich in monoterpenes, chiefly 1,8‑cineole and camphor, with limonene, p‑cymene, and α‑ and β‑pinene regularly reported in chemical surveys of L. floribunda oil. The aerial parts also contain diterpenes including carnosic acid and rosmarinic acid, and flavonoids such as luteolin, apigenin, and their glucosides; these are all well‑documented constituents for the genus. The menthol‑like oils and rosmarinic acid contribute plausible antispasmodic, carminative, and antimicrobial actions.

Today, the species continues to be harvested in parts of Chile and the Canary Islands for local tea and by artisan distillation for its aromatic oil. Research on the genus continues to profile its antimicrobial and antioxidant activity, and dried leaves appear in local herbal shops as “poleo de monte” in Spain and as a fragrant herbal infusion in Chilean markets.

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Synonyms Top

Scientific name Authority First published in
Lepechinia sagittata Epling Bull. Torrey Bot. Club 71: 487 (1944)
Sphacele floribunda Benth. Prodr. [A. P. de Candolle] 12: 254. 1848 [5 Nov 1848]
Sphacele grisebachii Kurtz in Revista Mus. La Plata [Sert. Cordob.] 14 v. (1893) 292.
Sphacele hastata Griseb. Abh. Königl. Ges. Wiss. Göttingen 19: 238. 1874
Sphacele hieronymi Briq. Bull. Herb. Boissier 4: 804 (1896)
Sphacele pampeana Speg. Contr. Fl. Sierra Vent. : 49 (1896)
Alguelaguen hieronymi Briq. Bull. Herb. Boissier 4: 804 (1896)
Alguelagum floribundum Kuntze Revis. Gen. Pl. 2: 512 (1891)
Alguelagum grisebachii Kuntze Revis. Gen. Pl. 2: 512 (1891)

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000226031
Tropicos 17602037
KEW urn:lsid:ipni.org:names:137871-2
The Plant List kew-110772
Open Tree Of Life 5265177
NCBI Taxonomy 1405036
IPNI 449262-1
iNaturalist 564994
GBIF 3888808
USDA GRIN 21761

Genomes (via NCBI) Top

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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
Rosmarinic Acid Present in Lepechinia floribunda and Lepechinia meyenii as a Potent Inhibitor of the Adenylyl Cyclase gNC1 from Giardia lamblia Zurita A, Vega Hissi E, Cianci Romero A, Luján AM, Salido S, Yaneff A, Davio C, Cobo J, Carpinella MC, Enriz RD Plants (Basel) 26-Feb-2024
PMCID:PMC10935199
doi:10.3390/plants13050646
PMID:38475493
Latin American Plants against Microorganisms Cuevas-Cianca SI, Romero-Castillo C, Gálvez-Romero JL, Sánchez-Arreola E, Juárez ZN, Hernández LR Plants (Basel) 28-Nov-2023
PMCID:PMC10708099
doi:10.3390/plants12233997
PMID:38068631
Ecological interactions affect the bioactivity of medicinal plants Camina JL, Usseglio V, Marquez V, Merlo C, Dambolena JS, Zygadlo JA, Ashworth L Sci Rep 27-Jul-2023
PMCID:PMC10374891
doi:10.1038/s41598-023-39358-1
PMID:37500739
Phytochemical profile and rosmarinic acid purification from two Peruvian Lepechinia Willd. species (Salviinae, Mentheae, Lamiaceae) Serrano CA, Villena GK, Rodríguez EF Sci Rep 31-Mar-2021
PMCID:PMC8012630
doi:10.1038/s41598-021-86692-3
PMID:33790349
Review of Whole Plant Extracts With Activity Against Herpes Simplex Viruses In Vitro and In Vivo Garber A, Barnard L, Pickrell C J Evid Based Integr Med 16-Feb-2021
PMCID:PMC7894602
doi:10.1177/2515690X20978394
PMID:33593082
Content Snapshots N/A Ann Bot 09-Mar-2020
PMCID:PMC7061166
doi:10.1093/aob/mcaa017
Daily fluctuations in pollination effectiveness explain higher efficiency of native over exotic bees in Lepechinia floribunda (Lamiaceae) Baranzelli MC, Benitez-Vieyra S, Glinos E, Trenchi A, Córdoba S, Camina J, Ashworth L, Sérsic AN, Cocucci AA, Fornoni J Ann Bot 20-Nov-2019
PMCID:PMC7061175
doi:10.1093/aob/mcz187
PMID:31745546
A comprehensive review on tyrosinase inhibitors Zolghadri S, Bahrami A, Hassan Khan MT, Munoz-Munoz J, Garcia-Molina F, Garcia-Canovas F, Saboury AA J Enzyme Inhib Med Chem 03-Jan-2019
PMCID:PMC6327992
doi:10.1080/14756366.2018.1545767
PMID:30734608
Cytotoxic Activity of Extracts from Plants of Central Argentina on Sensitive and Multidrug-Resistant Leukemia Cells: Isolation of an Active Principle from Gaillardia megapotamica González ML, Joray MB, Laiolo J, Crespo MI, Palacios SM, Ruiz GM, Carpinella MC Evid Based Complement Alternat Med 10-May-2018
PMCID:PMC5971282
doi:10.1155/2018/9185935
PMID:29861776
Antimicrobial potentials of medicinal plant’s extract and their derived silver nanoparticles: A focus on honey bee pathogen Khan SU, Anjum SI, Ansari MJ, Khan MH, Kamal S, Rahman K, Shoaib M, Man S, Khan AJ, Khan SU, Khan D Saudi J Biol Sci 21-Feb-2018
PMCID:PMC6864162
doi:10.1016/j.sjbs.2018.02.010
PMID:31762664
ANTI-VIRAL EFFECTS OF MEDICINAL PLANTS IN THE MANAGEMENT OF DENGUE: A SYSTEMATIC REVIEW Frederico ÉH, Cardoso AL, Moreira-Marconi E, de Sá-Caputo DD, Guimarães CA, Dionello CD, Morel DS, Paineiras-Domingos LL, de Souza PL, Brandão-Sobrinho-Neto S, Carvalho-Lima RP, Guedes-Aguiar ED, Costa-Cavalcanti RG, Kutter CR, Bernardo-Filho M Afr J Tradit Complement Altern Med 07-Jul-2017
PMCID:PMC5514443
doi:10.21010/ajtcam.v14i4S.5
PMID:28740942
Essential Oil of<i>Lepechinia floribunda</i>(Benth.) Epl. Arturo Velasco-Negueruela, María José Pérez-Alonso, Joaquín L. Esteban, Carlos A. Guzmán, Julio A. Zygadlo, Luis Ariza-Espinar Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1994.9698446

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/10.1080/10412905.1994.9698446
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1994.9698446
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9698446
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9698446
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester 6448 Click to see 196.29 unknown https://doi.org/10.1080/10412905.1994.9698446
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9698446
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9698446
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9698446
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1994.9698446
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9698446
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1994.9698446
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1994.9698446
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-cis-Carveol 330573 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698446
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1994.9698446
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1994.9698446
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(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/10.1080/10412905.1994.9698446
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1994.9698446
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
alpha-Guaiene 5317844 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1994.9698446
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
epi-alpha-Cadinol 160799 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
epi-alpha-Muurolol 3084331 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
Farnesene 5281516 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
gamma-Cadinene 6432404 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Guaiol 227829 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Nerolidol 5284507 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
> 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/10.1080/10412905.1994.9698446
(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/10.1080/10412905.1994.9698446
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
(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/10.1080/10412905.1994.9698446
(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/10.1080/10412905.1994.9698446
1H-Cycloprop(e)azulene, decahydro-1,1,7-trimethyl-4-methylene-, (1aR-(1aalpha,4abeta,7alpha,7abeta,7balpha))- 91354 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Alloaromadendren 91746537 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Ledum camphor 22297324 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
Npc239037 101716 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
Viridiflorene 10910653 Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
4a,5-Dimethyl-3-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,7-octahydronaphthalene 288227 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Valencene 9855795 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
> 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/10.1080/10412905.1994.9698446
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446

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