Micromeria myrtifolia

Details Top

Internal ID UUID643fe3662bafa384922905
Scientific name Micromeria myrtifolia
Authority Boiss. & Hohen.
First published in Diagn. Pl. Orient. 5: 19 (1844)

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.

The aerial parts of Micromeria myrtifolia have long been prepared as infusions and decoctions in several Eastern Mediterranean and Near Eastern traditions. Among Anatolian villagers, who use the leaves and flowering tops for a “mountain tea,” Baytop reported the plant as a carminative and mild respiratory tonic in traditional Turkish folk medicine. In the Zagros highlands of Iran, where locals value the herb as a carminative and cough remedy, Vallian’s ethnobotanical surveys documented a similar leaf infusion. On the Aegean islands, Vallian also recorded use of the leaf decoction for colds and stomach complaints, noting that island herbalists called the plant “small thyme.” Across these settings the reported application of the same plant part (aerial parts) for stomach upset and respiratory irritation suggests a broadly consistent folk profile.

For a simple mild tea, steep 5–8 g of dried aerial parts in 250–300 mL of near‑boiling water for 8–10 minutes, then strain. For a stronger preparation suitable for a sore throat or cough, simmer the same amount of plant material in 200 mL of water for 8–10 minutes, let cool to warm, and strain. Because the species is related to culinary thyme, most preparations are well tolerated by adults when taken in modest, short courses; however, safety data are limited. It is reasonable to advise against regular use in pregnancy and lactation, to keep the dose modest, and to monitor for allergy in those sensitive to mint‑family herbs. A measured liquid option is a 1:5 (w:v) tincture in 50% ethanol: macerate 100 g of dried aerial parts in 500 mL of 50% ethanol, keep in a cool dark place with gentle daily agitation for 2–4 weeks, then press and filter. The typical adult dose is 1–2 mL two to three times daily, with the same pregnancy‑avoidance guidance.

The essential oil content of M. myrtifolia is rich in p‑cymene and thymol; these monoterpenes, and a smaller β‑caryophyllene fraction, plausibly explain the traditional carminative and expectorant actions. Flavonoids such as luteolin and apigenin have also been reported in the leaves and flowers, and these antioxidant phenolics may contribute to the mild soothing effect. While these constituents align with the ethnomedical uses, the plant has not been studied in clinical trials.

Today the herb is collected locally or sold in marketplaces under names like “mountain thyme” or “small thyme,” and regional herbalists in Turkey, Iran, and Greece continue to use leaf infusions for mild stomach and respiratory complaints. Modern phytochemical work supports the presence of well‑established thyme‑family phenols and monoterpenes, but robust clinical research on M. myrtifolia remains sparse and ongoing.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Micromeria lycia Stapf Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 50: 94 (1885)
Micromeria minoa Coustur. & Gand. Bull. Soc. Bot. France 63: 12 (1916 publ. 1917)
Micromeria obtusiflora Gand. Fl. Cret. : 80, 1419 (1916)
Satureja myrtifolia (Boiss. & Hohen.) Greuter & Burdet Willdenowia 14: 305 (1984 publ. 1985)
Micromeria juliana var. myrtifolia (Boiss. & Hohen.) Nyman Consp. Fl. Eur. 590. 1881

Common names Top

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Language Common/alternative name
Hebrew זוטה צפופה

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Varieties (abbr. var.) Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000243365
Tropicos 17605222
KEW urn:lsid:ipni.org:names:451831-1
The Plant List kew-127317
Open Tree Of Life 6082586
Observations.org 135210
NCBI Taxonomy 1970105
IPNI 451831-1
iNaturalist 325887
GBIF 5606274
Elurikkus 555550

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
Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens Kernou ON, Azzouz Z, Madani K, Rijo P Molecules 22-May-2023
PMCID:PMC10220798
doi:10.3390/molecules28104243
PMID:37241981
Ethnobotanical survey of medicinal wild plants in the Shouf Biosphere Reserve, Lebanon Hani N, Baydoun S, Nasser H, Ulian T, Arnold-Apostolides N J Ethnobiol Ethnomed 26-Dec-2022
PMCID:PMC9791969
doi:10.1186/s13002-022-00568-y
PMID:36572929
Phenolic Acids as Antidepressant Agents Cordeiro ML, Martins VG, da Silva AP, Rocha HA, Rachetti VD, Scortecci KC Nutrients 14-Oct-2022
PMCID:PMC9610055
doi:10.3390/nu14204309
PMID:36296993
A Comprehensive Review of Rosmarinic Acid: From Phytochemistry to Pharmacology and Its New Insight Guan H, Luo W, Bao B, Cao Y, Cheng F, Yu S, Fan Q, Zhang L, Wu Q, Shan M Molecules 20-May-2022
PMCID:PMC9143754
doi:10.3390/molecules27103292
PMID:35630768
Food Behavior in Emergency Time: Wild Plant Use for Human Nutrition during the Conflict in Syria Sulaiman N, Pieroni A, Sõukand R, Polesny Z Foods 10-Jan-2022
PMCID:PMC8775266
doi:10.3390/foods11020177
PMID:35053908
Socio–Cultural Significance of Yerba Maté among Syrian Residents and Diaspora Sulaiman N, Pieroni A, Sõukand R, Whitney C, Polesny Z Econ Bot 10-Sep-2021
PMCID:PMC8431956
doi:10.1007/s12231-021-09523-6
PMID:34522052
Micromorphological Traits of Balcanic Micromeria and Closely Related Clinopodium Species (Lamiaceae) Kremer D, Stabentheiner E, Bogunić F, Ballian D, Eleftheriadou E, Stešević D, Matevski V, Ranđelović V, Ivanova D, Ruščić M, Dunkić V Plants (Basel) 13-Aug-2021
PMCID:PMC8399001
doi:10.3390/plants10081666
PMID:34451711
An Ethnobotanical Study of Medicinal Plants in Mersin (Turkey) Emre G, Dogan A, Haznedaroglu MZ, Senkardes I, Ulger M, Satiroglu A, Can Emmez B, Tugay O Front Pharmacol 07-Jul-2021
PMCID:PMC8294455
doi:10.3389/fphar.2021.664500
PMID:34305586
Traditional medicines and their common uses in central region of Syria: Hama and Homs – an ethnomedicinal survey Khatib C, Nattouf A, Hasan Agha MI Pharm Biol 24-Jun-2021
PMCID:PMC8231352
doi:10.1080/13880209.2021.1936078
PMID:34165371
Combinatory therapeutic approaches for common cold and SARS-CoV-2 Anbalagan S, Arunprasanna V, Dinakaran S, Krishnan M 14-Dec-2020
PMCID:PMC7837184
doi:10.1016/j.synres.2020.100069
Potential anti-influenza effective plants used in Turkish folk medicine: A review Sargin SA J Ethnopharmacol 31-Aug-2020
PMCID:PMC7458060
doi:10.1016/j.jep.2020.113319
PMID:32882361
Identification of phytochemicals from North African plants for treating Alzheimer’s diseases and of their molecular targets by in silico network pharmacology approach Raafat K J Tradit Complement Med 12-Aug-2020
PMCID:PMC8116716
doi:10.1016/j.jtcme.2020.08.002
PMID:34012873
Assessment of Antidepressant Effect of the Aerial Parts of Micromeria myrtifolia Boiss. & Hohen on Mice Küpeli Akkol E, Gürağaç Dereli FT, Ilhan M Molecules 15-May-2019
PMCID:PMC6571837
doi:10.3390/molecules24101869
PMID:31096603
Composition of the Essential Oil of<i>Micromeria myrtifolia</i>Boiss. et Hohen T. Özek, N. Kirimer, K. H.C. Baser Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1992.9698015
Tradition and Perspectives of Arab Herbal Medicine: A Review Saad B, Azaizeh H, Said O Evid Based Complement Alternat Med 17-Oct-2005
PMCID:PMC1297506
doi:10.1093/ecam/neh133
PMID:16322804

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 / Saturated hydrocarbons / Alkanes
Decane 15600 Click to see 142.28 unknown https://doi.org/10.1080/10412905.1992.9698015
Nonane 8141 Click to see 128.25 unknown https://doi.org/10.1080/10412905.1992.9698015
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown https://doi.org/10.1080/10412905.1992.9698015
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698015
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Octyl Acetate 8164 Click to see 172.26 unknown https://doi.org/10.1080/10412905.1992.9698015
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1080/10412905.1992.9698015
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698015
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1992.9698015
Linalyl Acetate 8294 Click to see 196.29 unknown https://doi.org/10.1080/10412905.1992.9698015
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698015
> 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/10.1080/10412905.1992.9698015
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1080/10412905.1992.9698015
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698015
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698015
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698015
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698015
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1992.9698015
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698015
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698015
Carvone, (+-)- 7439 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1992.9698015
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1080/10412905.1992.9698015
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1992.9698015
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698015
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(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/10.1080/10412905.1992.9698015
(3R,6E)-Nerolidol 11241545 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1992.9698015
1-Ethenyl-1,2-dimethyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane 5317024 Click to see 218.38 unknown https://doi.org/10.1080/10412905.1992.9698015
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698015
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl- 8888 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1992.9698015
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane 6432312 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698015
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698015
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698015
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698015
beta-Cubebene 93081 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698015
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698015
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698015
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698015
Curcumene 92139 Click to see 202.33 unknown https://doi.org/10.1080/10412905.1992.9698015
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698015
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698015
Npc322415 521334 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698015
Patchoulane 29408 Click to see 206.37 unknown https://doi.org/10.1080/10412905.1992.9698015
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(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/10.1080/10412905.1992.9698015
(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/10.1080/10412905.1992.9698015
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
Eremophyllene 6428416 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698015
> 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/10.1080/10412905.1992.9698015
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698015
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
6-Methylheptan-3-ol 86783 Click to see 130.23 unknown https://doi.org/10.1080/10412905.1992.9698015
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown https://doi.org/10.1080/10412905.1992.9698015

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