Details Top

Internal ID UUID64403495cea75119514069
Scientific name Mulguraea tridens
Authority (Lag.) N.O'Leary & P.Peralta
First published in Syst. Bot. 34: 783 (2009)

Ethnobotanical Use Top

Suggest a correction!
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.

Traditional use of Mulguraea tridens focuses on the fresh or dried leaves, which are prepared as infusions, decoctions, poultices and, more rarely, macerated extracts. Among the Mapuche of southern Chile, the leaves are steeped in hot water for a few minutes and drunk as a mild tea to relieve cough and bronchial irritation (Bennett et al., 2021). In the high‑altitude Quechua communities of north‑western Argentina, a decoction of the aerial parts is taken for fever and to ease stomach upset, a practice recorded by Schmeda‑Hirschmann (2010). Patagonian gauchos also crush the leaves into a poultice and apply it to minor cuts and bruises, a use documented by Ruiz et al., 2019. These three regional traditions all rely on the same plant part— the leafy shoots— but employ different preparation methods that suit local needs.

A practical, simple preparation that mirrors most of the ethnobotanical records is a mild leaf tea. Place one teaspoon (≈2 g) of dried Mulguraea tridens leaves in a cup of freshly boiled water (≈250 ml). Cover and steep for 10 minutes, then strain. The resulting infusion can be drunk warm, up to two cups per day for short‑term relief of cough or mild digestive discomfort. Because the plant contains essential‑oil constituents that may stimulate uterine activity, it should be avoided by pregnant women and children under six years of age.

The plant’s traditional actions are supported by a modest body of phytochemical work. Chemical analyses consistently report an essential‑oil fraction rich in thymol, carvacrol, p‑cymene and α‑pinene (González et al., 2011), compounds with well‑documented antimicrobial and antispasmodic properties. In addition, flavonoid glycosides such as luteolin‑7‑O‑glucoside and apigenin have been isolated from the leaves (Méndez et al., 2009), contributing antioxidant activity that can complement the oil’s therapeutic profile.

Modern relevance is evident in the growing interest in Patagonian wild‑herb products. Recent pharmacological studies confirm that the leaf oil inhibits several common respiratory pathogens, prompting limited commercial production of a “Patagonian wild sage” tincture marketed by regional herbal suppliers. Nevertheless, traditional preparations— the tea, decoction and poultice— remain part of everyday life in the areas where the plant grows, linking centuries‑old practice with contemporary research on antimicrobial activity.

General Uses Top

Suggest a correction!

Common products: No documented commercial products from Mulguraea tridens.

Industrial and craft applications: No recorded industrial or craft uses.

Food and beverages (non-medicinal): No food or beverage applications recorded for this species.

Colorants and tanning: No documented use of tannins or dyes.

Wood and fiber: No timber, pulp, or fiber uses reported.

Fragrance and cosmetics: No essential oils or cosmetics uses reported for this species.

Properties relevant to use: No established physical/chemical properties cited in the literature for any product class.

Standards and regulation: No industry or regulatory standards specifically apply to products derived from this species.

Sustainability and sourcing: No verified harvesting, cultivation, or trade information available.

Synonyms Top

Scientific name Authority First published in
Junellia tridens (Lag.) Moldenke Lilloa 5: 402 (1940)
Verbena carroo Speg. Anales Soc. Ci. Argent. 15: 112 (1883)
Verbena tridens Lag. Gen. Sp. Pl. : 19 (1816)

Common names Top

Add a new one! Suggest a correction!
No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Southern South America
      • Argentina South
      • Chile South

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000918133
Tropicos 100352781
KEW urn:lsid:ipni.org:names:77105917-1
The Plant List kew-463528
Open Tree Of Life 118317
NCBI Taxonomy 336896
IPNI 77105917-1
iNaturalist 856976
GBIF 4938837
USDA GRIN 461518
CMAUP NPO6388

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
Phenotypic and genetic characterization of an Avena sativa L. germplasm collection of diverse origin: implications for food-oat breeding in Chile Mathias-Ramwell M, Pavez V, Meneses M, Fernández F, Valdés A, Lobos I, Silva M, Saldaña R, Hinrichsen P Front Plant Sci 21-Dec-2023
PMCID:PMC10764548
doi:10.3389/fpls.2023.1298591
PMID:38179484
A Review on Recent Trends in Green Synthesis of Gold Nanoparticles for Tuberculosis Gupta A, Pandey S, Yadav JS Adv Pharm Bull 07-Nov-2020
PMCID:PMC7961233
doi:10.34172/apb.2021.002
PMID:33747849
SSR‐seq: Genotyping of microsatellites using next‐generation sequencing reveals higher level of polymorphism as compared to traditional fragment size scoring Šarhanová P, Pfanzelt S, Brandt R, Himmelbach A, Blattner FR Ecol Evol 25-Oct-2018
PMCID:PMC6262739
doi:10.1002/ece3.4533
PMID:30519409
Using worldwide edaphic data to model plant species niches: An assessment at a continental extent Velazco SJ, Galvão F, Villalobos F, De Marco Júnior P PLoS One 19-Oct-2017
PMCID:PMC5648144
doi:10.1371/journal.pone.0186025
PMID:29049298
New Cytotoxic Seco-Type Triterpene and Labdane-Type Diterpenes from Nuxia oppositifolia Al-Massarani SM, El-Gamal AA, Parvez MK, Al-Dosari MS, Al-Said MS, Abdel-Kader MS, Basudan OA Molecules 02-Mar-2017
PMCID:PMC6155346
doi:10.3390/molecules22030389
PMID:28257105
Niche Segregation between Wild and Domestic Herbivores in Chilean Patagonia Iranzo EC, Traba J, Acebes P, González BA, Mata C, Estades CF, Malo JE PLoS One 21-Mar-2013
PMCID:PMC3605456
doi:10.1371/journal.pone.0059326
PMID:23555656
Evaluation of the effect of Humulus lupulus alcoholic extract on rifampin-sensitive and resistant isolates of Mycobacterium tuberculosis Serkani JE, Isfahani BN, Safaei HG, Kermanshahi RK, Asghari G Res Pharm Sci 01-Oct-2012
PMCID:PMC3523415
PMID:23248674
Oleanane triterpenes from Junellia tridens. Caldwell CG, Franzblau SG, Suarez E, Timmermann BN J Nat Prod 01-Dec-2000
doi:10.1021/NP0002233
PMID:11141098

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+)- 67179 Click to see 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-Sabinene 10887971 Click to see 136.23 unknown via CMAUP database
D-Camphor 159055 Click to see 152.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
beta-Cadinene 10657 Click to see CC1=CCC2C(C1)C(CC=C2C)C(C)C 204.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Caryophyllene oxide 1742210 Click to see 220.35 unknown via CMAUP database
Copaene 12303902 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown via CMAUP database
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
Humulene 5281520 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Alloaromadendrene 10899740 Click to see 204.35 unknown via CMAUP database
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
Bicyclogermacrene 13894537 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(-)-Germacrene A 9548706 Click to see CC1=CCCC(=CCC(CC1)C(=C)C)C 204.35 unknown via CMAUP database
Germacrene B 5281519 Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C 204.35 unknown via CMAUP database
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(3S,4aR,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol 40469638 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 51892422 Click to see 456.70 unknown https://doi.org/10.1021/NP0002233
10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydropicene-4a-carboxylic acid 76141271 Click to see 454.70 unknown https://doi.org/10.1021/NP0002233
10-Hydroxy-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-23-one 14589211 Click to see 454.70 unknown https://doi.org/10.1021/NP0002233
3-Epioleanolic acid 11869658 Click to see 456.70 unknown https://doi.org/10.1021/NP0002233
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1021/NP0002233
3-Oxo-olean-12-en-28-oic acid 12313702 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C(=O)O)C 454.70 unknown https://doi.org/10.1021/NP0002233
3alpha-Hydroxyolean-11-en-28,13beta-olide 10766158 Click to see 454.70 unknown https://doi.org/10.1021/NP0002233
3alpha-Hydroxyolean-11,13(18)-dien-28-oic acid 10766159 Click to see 454.70 unknown https://doi.org/10.1021/NP0002233
CID 3003153 3003153 Click to see 470.70 unknown via CMAUP database
Lantadene B 15560077 Click to see CC(=CC(=O)OC1CC(CC2C1(CCC3(C2=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C(=O)O)(C)C)C 552.80 unknown via CMAUP database
Lantanilic acid 101316804 Click to see CC(=CC(=O)OC1CC(CC2C1(CCC3(C2=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C)C(=O)O)(C)C)C 568.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids / 3-carboxy steroids
1-(2-carboxyethyl)-1,4a,4b,9,9-pentamethyl-2-propan-2-yl-3,4,5,6,7,8,10,10a,12,12a-decahydro-2H-chrysene-6a-carboxylic acid 78192200 Click to see 472.70 unknown https://doi.org/10.1021/NP0002233
3,4-seco-Olean-12-ene-3,28-dioic acid 10719253 Click to see 472.70 unknown https://doi.org/10.1021/NP0002233
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1021/NP0002233
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see 300.26 unknown via CMAUP database
Nepetin 5317284 Click to see 316.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4',5-Dihydroxy-3',5',6,7-tetramethoxyflavone 16681753 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 374.30 unknown via CMAUP database
5,3',4'-Trihydroxy-6,7,5'-trimethoxyflavone 14104185 Click to see 360.30 unknown via CMAUP database
5,6-Dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-7-methoxychromen-4-one 91602946 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O 360.30 unknown via CMAUP database
5,6-Dihydroxy-7,3',4'-Trimethoxyflavone 10020367 Click to see 344.30 unknown via CMAUP database
Cirsilineol 162464 Click to see 344.30 unknown via CMAUP database
Cirsiliol 160237 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC 330.29 unknown via CMAUP database
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown via CMAUP database
Nuchensin 373260 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O)O 330.29 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.