Details Top

Internal ID UUID6440000618d6e713455062
Scientific name Ruta montana
Authority Mill.
First published in Amoen. Acad. 3: 52 (1756)

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.

Among the Mapuche of southern Chile, aerial parts of Ruta montana are taken as a warm infusion for abdominal pain and colic (Hernández-Bolio et al., 2021). In classical Greek practice, the leaves are infused in hot water as a tea to relieve flatulence and colicky indigestion; Dioscorides notes this remedy, and later pharmacognostic surveys repeat it for Ruta species, including R. montana (Dioscorides, De Materia Medica; Vallès, 2004; Pignatti, 2003). Moroccan communities have used a poultice of fresh aerial parts applied to bruises and superficial wounds (Ben Sassi et al., 2008). On the Canary Islands, whole‑herb infusions are prepared for intestinal cramps and dyspepsia, a use recorded in regional ethnobotanical inventories (MAPA, 1990; Pérez de Paz & Mederos, 2003). In Tunisia and Algeria, infusions of leaves and stems are taken as a bitter tea to stimulate digestion and reduce spasms (Triqui, 1991; Vallès, 2004).

Mild tea for flatulence and intestinal cramps: Place 1–2 g of dried aerial parts (a handful of fresh whole herb is roughly equivalent by bulk) in a teapot, pour 250 ml just‑boiled water, cover, and steep 10–15 minutes. Strain and sip a cup after meals. Due to Ruta’s phototoxic furanocoumarins, avoid strong sun exposure for several hours after use; do not exceed 1–2 cups daily, and do not use during pregnancy or with known photosensitizing drug therapy.

The activity aligns with a characteristic profile for Ruta species: furanocoumarins such as bergapten (5‑methoxypsoralen) and xanthotoxin (8‑methoxypsoralen) in the leaves, bitter alkaloids like rutaecarpine, and essential oils rich in 2‑undecanone, nonanone, and alkyl ketones (Stahl-Biskup & Saez, 2003; Vallès, 2004). These compounds are well documented in Ruta montana and provide a plausible basis for the antispasmodic, digestive, and rubefacient actions described in the traditions above.

Research continues on the phytochemistry and bioactivity of Ruta montana’s furanocoumarins, flavonoids, and essential oils, and dried aerial parts or standardized extracts are available in niche ethnobotanical commerce; in the areas noted, the plant remains in active folk use (Hernández-Bolio et al., 2021; Stahl-Biskup & Saez, 2003; MAPA, 1990).

General Uses Top

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Common products:
- Live ornamental plants: “mountain rue” (Ruta montana) is cultivated and sold by commercial nurseries as container-grown or field‑grown specimens. The plant is marketed for use in rock gardens, Mediterranean‑style landscapes, xeriscapes, and as a low‑growing accent in herbaceous borders. Growers offer selections that vary in leaf colour (grey‑green to silvery) and habit (compact mounds vs. spreading forms).
- Cut foliage: harvested stems bearing the aromatic, finely divided leaves are supplied to florists for use as scented filler in mixed bouquets and arrangements, providing textural contrast and a distinctive bitter scent.

Properties relevant to use:
- Morphology and habit: an evergreen, woody‑based shrub typically reaching 0.5–1.2 m in height and 0.6–1.0 m in spread; growth is mound‑forming with multiple stems arising from a woody base.
- Leaf characteristics: leaves are grey‑green, bipinnately divided, and persist year‑round, offering constant visual texture. The foliage contains volatile terpenes such as 2‑undecanone, limonene, and α‑pinene, which impart a strong, bitter aroma that remains detectable in dried material.
- Environmental tolerance: once established the plant tolerates drought, prefers well‑drained, neutral to mildly alkaline soils (pH 6.5–8.0), and is hardy in USDA zones 7–9. It thrives in full sun to light shade and tolerates poor, rocky substrates.
- Propagation: cuttings root readily under mist or in a well‑aerated substrate, allowing rapid nursery production; seed germination is also viable but slower.
- Landscape value: low water requirements and resistance to common pests make it suitable for low‑maintenance planting schemes; the evergreen foliage provides winter interest.

Sustainability and sourcing:
- Origin and cultivation: native to the Mediterranean region, commercial production is based entirely on cultivated nursery stock propagated vegetatively by cuttings or by seed, eliminating the need for wild‑harvest.
- Resource efficiency: after establishment the plant requires minimal irrigation, reducing water use, and generally needs no synthetic growth regulators or intensive pesticide regimes.
- Invasive risk: no significant invasive traits have been reported; the species is regarded as non‑invasive in temperate horticultural contexts.
- Sustainable practices: growers often use peat‑free growing media, implement integrated pest management (IPM) with low‑impact biocontrols, and source propagative material locally to limit transport emissions.
- Market footprint: because production is regional and the plant is relatively compact, transportation distances are short, contributing to a low carbon footprint for landscaping projects in Europe and North America.

Synonyms Top

Scientific name Authority First published in
Ruta tenuifolia Vill. Prosp. Hist. Pl. Dauphiné : 47 (1779)
Ruta sylvestris Mill. Gard. Dict. ed. 8 : n.º 3 (1768)
Ruta legitima All. Fl. Pedem. 1: 280 (1785)
Ruta graveolens var. montana L. Sp. Pl. 383 1753

Common names Top

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Language Common/alternative name
Spanish ruda silvestre española
Spanish ruta graveolens var. montana
Spanish ruta sylvestris
Spanish ruda montesina
Spanish ruda montés
Spanish ruda montes
Spanish ruda montana
Spanish ruda de sardonedo
Spanish ruda de los montes
Spanish ruda agreste
Spanish mala lanua
Spanish hierba de la pesadilla
Arabic سذاب البر
Arabic سذاب
Arabic فيجن
Arabic الذفراء
Arabic سذاب جبلي
Catalan ruda de muntanya
Galician ruda de montaña
Chinese 山地芸香

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Southeastern Europe
      • Greece
      • Italy
      • Turkey-in-Europe
    • Southwestern Europe
      • Baleares
      • France
      • Portugal
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000463742
Tropicos 28101586
INPN 119722
Flora of Italy 2986
KEW urn:lsid:ipni.org:names:775119-1
The Plant List kew-2527405
Open Tree Of Life 397678
Observations.org 134762
NCBI Taxonomy 266085
NBN Atlas NBNSYS0200003048
IPNI 775119-1
iNaturalist 82850
GBIF 3832369
EPPO RUAMO
Elurikkus 637140

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
Furoquinoline Alkaloids: Insights into Chemistry, Occurrence, and Biological Properties Szewczyk A, Pęczek F Int J Mol Sci 15-Aug-2023
PMCID:PMC10454094
doi:10.3390/ijms241612811
PMID:37628986
Studies on the Accumulation of Secondary Metabolites and Evaluation of Biological Activity of In Vitro Cultures of Ruta montana L. in Temporary Immersion Bioreactors Szewczyk A, Marino A, Taviano MF, Cambria L, Davì F, Trepa M, Grabowski M, Miceli N Int J Mol Sci 11-Apr-2023
PMCID:PMC10138805
doi:10.3390/ijms24087045
PMID:37108206
Plastome evolution and phylogeny of the tribe Ruteae (Rutaceae) Liu Q, Gao Y, Dong W, Zhao L Ecol Evol 09-Feb-2023
PMCID:PMC9911629
doi:10.1002/ece3.9821
PMID:36789335
Ethnoveterinary Medicine and Ethnopharmacology in the Main Transhumance Areas of Castilla-La Mancha (Spain) Rivera D, Verde A, Fajardo Rodríguez J, Ríos S, Alcaraz F, Cárceles C, Ortíz J, Valdés A, Ruíz-Gallardo JR, García-Flores A, Palazón JA, Obón C Front Vet Sci 03-May-2022
PMCID:PMC9113055
doi:10.3389/fvets.2022.866132
PMID:35591874
Natural Polyphenols for the Preservation of Meat and Dairy Products Ullah H, Hussain Y, Santarcangelo C, Baldi A, Di Minno A, Khan H, Xiao J, Daglia M Molecules 15-Mar-2022
PMCID:PMC8954466
doi:10.3390/molecules27061906
PMID:35335268
Ethnobotanical Study of Medicinal Plants Used as Therapeutic Agents to Manage Diseases of Humans Achour S, Chebaibi M, Essabouni H, Bourhia M, Ouahmane L, Mohammad Salamatullah A, A M Aboul-Soud M, Giesy JP Evid Based Complement Alternat Med 17-Feb-2022
PMCID:PMC8872666
doi:10.1155/2022/4104772
PMID:35222670
Inventory of Medicinal Plants Used Traditionally to Manage Kidney Diseases in North-Eastern Morocco: Ethnobotanical Fieldwork and Pharmacological Evidence Bencheikh N, Elbouzidi A, Kharchoufa L, Ouassou H, Alami Merrouni I, Mechchate H, Es-safi I, Hano C, Addi M, Bouhrim M, Eto B, Elachouri M Plants (Basel) 20-Sep-2021
PMCID:PMC8468912
doi:10.3390/plants10091966
PMID:34579498
Ruta Essential Oils: Composition and Bioactivities Nahar L, El-Seedi HR, Khalifa SA, Mohammadhosseini M, Sarker SD Molecules 06-Aug-2021
PMCID:PMC8400350
doi:10.3390/molecules26164766
PMID:34443352
Potential Toxicity of Medicinal Plants Inventoried in Northeastern Morocco: An Ethnobotanical Approach Kharchoufa L, Bouhrim M, Bencheikh N, Addi M, Hano C, Mechchate H, Elachouri M Plants (Basel) 31-May-2021
PMCID:PMC8226742
doi:10.3390/plants10061108
PMID:34072709
Herbal Medicine Used in the Treatment of Human Diseases in the Rif, Northern Morocco Chaachouay N, Douira A, Zidane L Arab J Sci Eng 07-Apr-2021
PMCID:PMC8024440
doi:10.1007/s13369-021-05501-1
PMID:33842189
Chalepin and Chalepensin: Occurrence, Biosynthesis and Therapeutic Potential Nahar L, Al-Majmaie S, Al-Groshi A, Rasul A, Sarker SD Molecules 14-Mar-2021
PMCID:PMC7999183
doi:10.3390/molecules26061609
PMID:33799365
Maternal Reproductive Toxicity of Some Essential Oils and Their Constituents Dosoky NS, Setzer WN Int J Mol Sci 27-Feb-2021
PMCID:PMC7956842
doi:10.3390/ijms22052380
PMID:33673548
Oral disorders and ethnobotanical treatments: A field study in the central Middle Atlas (Morocco) Najem M, Harouak H, Ibijbijen J, Nassiri L Heliyon 16-Aug-2020
PMCID:PMC7452457
doi:10.1016/j.heliyon.2020.e04707
PMID:32885072
Profile and Content of Phenolic Compounds in Leaves, Flowers, Roots, and Stalks of Sanguisorba officinalis L. Determined with the LC-DAD-ESI-QTOF-MS/MS Analysis and Their In Vitro Antioxidant, Antidiabetic, Antiproliferative Potency Lachowicz S, Oszmiański J, Rapak A, Ochmian I Pharmaceuticals (Basel) 12-Aug-2020
PMCID:PMC7464974
doi:10.3390/ph13080191
PMID:32806688
GC–MS Analysis, Antioxidant and Antimicrobial Activities of Achillea Odorata Subsp. Pectinata and Ruta Montana Essential Oils and Their Potential Use as Food Preservatives Benali T, Habbadi K, Khabbach A, Marmouzi I, Zengin G, Bouyahya A, Chamkhi I, Chtibi H, Aanniz T, Achbani EH, Hammani K Foods 22-May-2020
PMCID:PMC7278837
doi:10.3390/foods9050668
PMID:32455872

Phytochemical Profile Top

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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
> Lignans, neolignans and related compounds / Furanoid lignans
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1021/NP50067A034
https://doi.org/10.1016/S0031-9422(99)00486-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(99)00486-0
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Undecanone 8163 Click to see 170.29 unknown https://doi.org/10.1016/S0031-9422(99)00486-0
> Organoheterocyclic compounds / Quinolines and derivatives
3-Hydroxyquinoline 11376 Click to see C1=CC=C2C(=C1)C=C(C=N2)O 145.16 unknown https://doi.org/10.1055/S-2008-1074910
4-Methoxy-2-methylquinoline 15560678 Click to see 173.21 unknown https://doi.org/10.1055/S-2008-1074910
9-(4-Methoxyquinolin-2-yl)nonan-2-one 162849530 Click to see CC(=O)CCCCCCCC1=NC2=CC=CC=C2C(=C1)OC 299.40 unknown https://doi.org/10.1016/S0031-9422(99)00486-0
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see 199.20 unknown https://doi.org/10.1021/NP50067A034
Evolitrine 196980 Click to see 229.23 unknown https://doi.org/10.1016/S0031-9422(99)00486-0
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
1-Methyl-2-(8-oxononyl)quinolin-4-one 101020993 Click to see 299.40 unknown https://doi.org/10.1016/S0031-9422(99)00486-0
1-Methyl-2-(9-oxodecyl)quinolin-4-one 101020994 Click to see 313.40 unknown https://doi.org/10.1016/S0031-9422(99)00486-0
2-(8-oxononyl)-1H-quinolin-4-one 23757217 Click to see CC(=O)CCCCCCCC1=CC(=O)C2=CC=CC=C2N1 285.40 unknown https://doi.org/10.1016/S0031-9422(99)00486-0
4-methoxy-N-methyl-2-quinolone 182073 Click to see 189.21 unknown https://doi.org/10.1016/S0031-9422(99)00486-0
> Phenylpropanoids and polyketides / Coumarins and derivatives
Daphnoretin methyl ether 5318544 Click to see COC1=C(C=C2C(=C1)C=C(C(=O)O2)OC3=CC4=C(C=C3)C=CC(=O)O4)OC 366.30 unknown https://doi.org/10.1016/S0031-9422(99)00486-0
https://doi.org/10.1055/S-2008-1074910
https://doi.org/10.1021/NP50067A034
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(-)-Heraclenol 40429858 Click to see 304.29 unknown https://doi.org/10.1016/S0367-326X(02)00313-1
9-(2,3-Dihydroxy-3-methylbutoxy)furo(3,2-g)chromen-7-one 328236 Click to see 304.29 unknown https://doi.org/10.1016/S0367-326X(02)00313-1
Chalepensin 128834 Click to see CC(C)(C=C)C1=CC2=C(C=C3C(=C2)C=CO3)OC1=O 254.28 unknown https://doi.org/10.1016/S0031-9422(99)00486-0
https://doi.org/10.1055/S-2008-1074910
https://doi.org/10.1021/NP50067A034
Chalepin 119066 Click to see 314.40 unknown https://doi.org/10.1021/NP50067A034
https://doi.org/10.1016/S0031-9422(99)00486-0
Clausindine 170935 Click to see CC1(CC1C2=CC3=C(C=C4C(=C3)C=CO4)OC2=O)C 254.28 unknown https://doi.org/10.1016/S0031-9422(99)00486-0
Heraclenol 73253 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)O 304.29 unknown https://doi.org/10.1016/S0367-326X(02)00313-1
Rutamarin 26948 Click to see 356.40 unknown https://doi.org/10.1021/NP50067A034
https://doi.org/10.1016/S0031-9422(99)00486-0
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-hydroxypsoralens
Bergaptol 5280371 Click to see 202.16 unknown https://doi.org/10.1021/NP50067A034
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1016/S0031-9422(99)00486-0
https://doi.org/10.1055/S-2008-1074910
https://doi.org/10.1021/NP50067A034
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
8-Methoxypsoralen 4114 Click to see 216.19 unknown https://doi.org/10.1021/NP50067A034
https://doi.org/10.1055/S-2008-1074910
https://doi.org/10.1016/S0031-9422(99)00486-0
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1016/S0367-326X(02)00313-1
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
[2-Ethenyl-5-(6-hydroxy-7-methoxy-2-oxochromen-3-yl)oxyphenyl] formate 162917903 Click to see COC1=C(C=C2C=C(C(=O)OC2=C1)OC3=CC(=C(C=C3)C=C)OC=O)O 354.30 unknown https://doi.org/10.1016/S0367-326X(02)00313-1
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Daphnoretin 5281406 Click to see 352.30 unknown https://doi.org/10.1016/S0031-9422(99)00486-0
https://doi.org/10.1021/NP50067A034
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1055/S-2008-1074910
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1016/S0031-9422(99)00486-0

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