Mulguraea tridens
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
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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.
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) |
Germination/Propagation Top
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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 click to expand
-
Southern South America
- Argentina South
- Chile South
-
Southern South America
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)!
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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 |
|---|---|---|---|---|---|
| > 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 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |