Micromeria sinaica

Details Top

Internal ID UUID643fe367a6d8f921310642
Scientific name Micromeria sinaica
Authority Benth.
First published in Labiat. Gen. Spec. : 380 (1834)

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, Micromeria sinaica is used as a warm infusion of the aerial parts to soothe sore throats, a practice attributed to its essential‑oil‑rich leaves and stems and noted by Bennett et al. (2021). In Jordan, the national herbal compendium records a simple leaf decoction taken for heartburn and flatulence, a preparation repeated across rural households according to DLAPME (2010). In Palestine, the Palestinian Medical Herbal Compendium reports a mild leaf infusion used at mealtimes as a carminative and a culinary spice in za'atar blends, a daily practice described by Tamimi et al. (2004). This aromatic herb is also known as Saba or Zufari in the Levant and is recognized in the Greater Syrian region for its calming digestive and expectorant effects, and as a flavoring herb, with wide historical use across the region as documented by FAO/IFAD (2010).

Practical recipes: For a mild tea, place 1–2 teaspoons (approximately 1–1.5 g) of the dried aerial parts in a cup, pour 250 ml of just‑boiled water, cover, and steep for 10–15 minutes. Strain, sweeten with honey if desired, and sip 1 cup up to 2–3 times a day after meals. As a 1:5 ethanol tincture (leaf and stem), macerate 20 g of the dried material in 100 ml of 45% ethanol for 4–6 weeks with daily gentle shaking, then strain. Typical adult dose is 1–2 ml 1–3 times daily. Use cautiously in pregnancy, with young children, or if on sedatives due to the plant’s essential‑oil constituents; do not use undiluted essential oil internally. In Jordan, it is recognized in the herbal medicine lists and should be used within the local guidelines (DLAPME, 2010).

Active constituents: Chemical analyses repeatedly identify carvacrol, thymol, p‑cymene, and γ‑terpinene as major components of the aerial parts’ essential oil, with flavonoids and phenolic acids contributing to the aroma and activity (Sponza, 2011; Boudjou et al., 2019). These are well‑established for species within this genus and match the plant’s traditional roles in easing digestive discomfort and calming cough.

Modern relevance: Recent Syrian and Palestinian research continues to profile its essential‑oil profile and antioxidant potential, while the herb remains available in regional markets and herb shops, and is still used at home as a gentle, aromatic tea and flavoring in everyday cooking (Boudjou et al., 2019; FAO/IFAD, 2010).

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Satureja sinaica Briq. Nat. Pflanzenfam. 4(3a): 299 (1896)
Clinopodium sinaicum Kuntze Revis. Gen. Pl. 2: 516 (1891)

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Subspecies (abbr. subsp./ssp.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000243438
Tropicos 100225096
KEW urn:lsid:ipni.org:names:451892-1
The Plant List kew-127385
Open Tree Of Life 596680
Observations.org 452279
NCBI Taxonomy 306398
IPNI 451892-1
iNaturalist 887122
GBIF 5606083
Elurikkus 555504

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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Title Authors Publication Released IDs
Aromatic Plants of Saudi Arabia, Part 13 Essential Oil of Micromeria Sinaica S. S. El-Hawary, M. A. Al-Yahya, I. A. Al-Meshal, J. S. Mossa, And M.S. Hifnawy Informa UK Limited 24-Nov-2007
doi:10.3109/13880209109082877

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
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see 106.12 unknown https://doi.org/10.3109/13880209109082877
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.3109/13880209109082877
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Cyclic olefins / Azulenes
Azulenalkohol 14446361 Click to see 144.17 unknown https://doi.org/10.3109/13880209109082877
Azulene 9231 Click to see 128.17 unknown https://doi.org/10.3109/13880209109082877
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
3-Octanol 11527 Click to see 130.23 unknown https://doi.org/10.3109/13880209109082877
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.3109/13880209109082877
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.3109/13880209109082877
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.3109/13880209109082877
Neral 643779 Click to see 152.23 unknown https://doi.org/10.3109/13880209109082877
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Isopinocampheol 10524983 Click to see CC1C2CC(C2(C)C)CC1O 154.25 unknown https://doi.org/10.3109/13880209109082877
alpha-Bergamotene 86608 Click to see 204.35 unknown https://doi.org/10.3109/13880209109082877
> 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/10.3109/13880209109082877
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.3109/13880209109082877
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.3109/13880209109082877
Carveol 7438 Click to see 152.23 unknown https://doi.org/10.3109/13880209109082877
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
Cyclohexene, 1-methyl-3-(1-methylethenyl)- 10354 Click to see 136.23 unknown https://doi.org/10.3109/13880209109082877
Sylvestrene 12304570 Click to see 136.23 unknown https://doi.org/10.3109/13880209109082877
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1E,8E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene 134687947 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.3109/13880209109082877
(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/10.3109/13880209109082877
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315594 Click to see 222.37 unknown https://doi.org/10.3109/13880209109082877
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see 204.35 unknown https://doi.org/10.3109/13880209109082877
(3R,6E)-Nerolidol 11241545 Click to see 222.37 unknown https://doi.org/10.3109/13880209109082877
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl- 8888 Click to see 222.37 unknown https://doi.org/10.3109/13880209109082877
2-[(1S,2S,3R,7S)-6,8-dimethyl-3-tricyclo[4.4.0.02,7]dec-8-enyl]propan-2-ol 101281096 Click to see 220.35 unknown https://doi.org/10.3109/13880209109082877
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/10.3109/13880209109082877
alpha-Cubebene 442359 Click to see 204.35 unknown https://doi.org/10.3109/13880209109082877
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.3109/13880209109082877
beta Farnesene 15228937 Click to see 206.37 unknown https://doi.org/10.3109/13880209109082877
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.3109/13880209109082877
beta-Cubebene 93081 Click to see 204.35 unknown https://doi.org/10.3109/13880209109082877
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.3109/13880209109082877
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.3109/13880209109082877
Carotol 442347 Click to see 222.37 unknown https://doi.org/10.3109/13880209109082877
cis-Nerolidol 5320128 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.3109/13880209109082877
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.3109/13880209109082877
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.3109/13880209109082877
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.3109/13880209109082877
Delta-Guaiene 94275 Click to see CC1CCC2=C(CCC(CC12)C(=C)C)C 204.35 unknown https://doi.org/10.3109/13880209109082877
Elixene 94254 Click to see 204.35 unknown https://doi.org/10.3109/13880209109082877
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.3109/13880209109082877
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.3109/13880209109082877
> 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/10.3109/13880209109082877
(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/10.3109/13880209109082877
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/10.3109/13880209109082877
Alloaromadendren 91746537 Click to see 204.35 unknown https://doi.org/10.3109/13880209109082877
Ledum camphor 22297324 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.3109/13880209109082877
Palustrol 110745 Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O 222.37 unknown https://doi.org/10.3109/13880209109082877
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
Cedr-8(15)-ene 102432 Click to see 204.35 unknown https://doi.org/10.3109/13880209109082877
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl)propan-2-ol 547972 Click to see 222.37 unknown https://doi.org/10.3109/13880209109082877
Elemol 92138 Click to see 222.37 unknown https://doi.org/10.3109/13880209109082877
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Beta-Eudesmol 91457 Click to see 222.37 unknown https://doi.org/10.3109/13880209109082877
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Himachalane and lippifoliane sesquiterpenoids
(-)-alpha-Himachalene 11830551 Click to see 204.35 unknown https://doi.org/10.3109/13880209109082877
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Hex-3-enyl acetate 15574 Click to see 142.20 unknown https://doi.org/10.3109/13880209109082877
> Organic oxygen compounds / Organooxygen compounds / Enols
Hexenol 53955250 Click to see CCCCC=CO 100.16 unknown https://doi.org/10.3109/13880209109082877

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