Details Top

Internal ID UUID643fe599e99e1396279849
Scientific name Origanum sipyleum
Authority L.
First published in Sp. Pl. : 589 (1753)

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.

In central Anatolia and the Aegean foothills, people gather the leaves of Origanum sipyleum for simple teas and decoctions. Kargıoglu et al., 2010 recorded infusions of the leaves among villagers in the Sultan Mountains region; these were taken as a warming, soothing tea to relieve indigestion and colic, while the accompanying cold maceration (soaking) was used for gargling to ease sore throats. Along the Black Sea coast of northern Turkey, Ertuğ, 2010 likewise noted infusions of O. sipyleum leaves as a stomachic and expectorant tea, commonly drunk after meals. Across the Mediterranean border in the Greek Aegean islands, folk healers also prepare decoctions of the aerial parts for colds and coughs, as reported in Stefanakis et al., 2013. Because the leaflets are densely hairy, users typically remove the upper leaf surface to filter the bitterness, a practice described in detail in Kargıoglu et al., 2010.

Fresh or dried aerial parts are used. A traditional mild tea is prepared by pouring hot (just‑boiled) water over 5 g of crushed leaves and flower buds in 250 ml of water, infusing for 5–7 minutes, then straining; a thinner, “cold maceration” for sore throat gargles is made by soaking 3 g of chopped leaves in 200 ml of cold water for 6–8 hours with occasional stirring. Because commercial references list known intolerances for oregano oils and salicylate‑containing herbs, people with such sensitivities should avoid use; pregnant and breastfeeding individuals are advised to consult a qualified practitioner before taking oregano teas. The plant is sold locally as a wild tea, and in the Sultan Mountains districts one may find both dried loose tea and small leaf bundles.

The bioactivity aligns with well‑documented constituents of Mediterranean oregano. O. sipyleum contains phenolic monoterpenes (notably carvacrol and thymol), flavonoids such as apigenin and luteolin, and rosmarinic acid, as summarized by Şahin & Özçelik, 2003 and Şahin et al., 2004. These compounds account for the carminative, antispasmodic, and antimicrobial effects reported in local preparations.

Today, interest continues in both Turkey and the Aegean. Şahin & Özçelik, 2003 report that dried O. sipyleum leaf tea is locally marketed in Turkey, and local informants in the Sultan Mountains reported continued use of infusions for digestion and colds in Kargıoglu et al., 2010. Pharmacological studies keep evaluating Origanum phenols, while small businesses and rural households continue to make the traditional mild tea.

General Uses Top

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Food and beverages (non-medicinal):
The dried aerial parts of Origanum sipyleum are used as an aromatic herb in Turkish cuisine. The herb is sold under local names such as taş reyhan or dağ reyhanı and typically employed in small quantities to flavor stews, legumes, and grilled meats and vegetables. Processing involves harvesting at the onset of flowering, air-drying in shade, and gently crushing or grinding to release aroma. In spice blends, it complements other Lamiaceae herbs such as Thymus, Origanum, and Satureja, and may be included in regional “kekik” or mixed herb formulations for bakery, meat, and legume products.

Fragrance and cosmetics:
Essential oil from the flowering shoots is distilled in small quantities for fragrance applications. It contains high levels of carvacrol and p-cymene, with variable minor sesquiterpenes, imparting a warm, herbal aroma. The oil is used as a fragrance ingredient in soaps and detergent bases at low levels, where its aroma profile provides herbal top-note character.

Properties relevant to use:
The dried leaf and flower herb owes its aromatic effect to essential oil (commonly 1–3% by air-dry weight) rich in phenolic monoterpenes; the composition can vary with chemotype and harvest stage. Moisture is typically 8–10% at market quality. The ground herb presents fine particulate texture suitable for blending and adherence to food matrices; for perfumery, the oil’s carvacrol dominance confers stability in oxidative environments but limits usage to low concentrations to avoid over-powering notes.

Standards and regulation:
In food, the product is traded as a culinary herb under national spice and dried-vegetable standards governing identity, moisture, purity, and microbiological limits. For fragrance use, the essential oil follows standard fragrance industry good practice for composition disclosure and allergen declaration (e.g., IFRA Standards), with maximum usage levels based on finished product type.

Sustainability and sourcing:
A. sipyleum is wild-collected across the Aegean and central Anatolian highlands during summer flowering. Overharvesting of roots and whole plants poses localized sustainability concerns; recommended practice involves cutting aerial shoots only, allowing regrowth, and implementing seasonal quotas in collection zones. Current supply is artisanal and seasonal, with quantities limited by habitat availability and drying capacity.

Synonyms Top

Scientific name Authority First published in
Majorana sipylea Kostel. Allg. Med.-Pharm. Fl. 3: 770 (1834)
Amaracus sipyleus Raf. Fl. Tellur. 3: 86 (1837)

Common names Top

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Language Common/alternative name
Turkish tahtacı otu

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000260728
Tropicos 17603667
KEW urn:lsid:ipni.org:names:453365-1
The Plant List kew-143919
Open Tree Of Life 807676
Observations.org 144972
NCBI Taxonomy 1132404
IPNI 453365-1
iNaturalist 743245
GBIF 3893904
Elurikkus 435309

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
Research progress of the detection and analysis methods of heavy metals in plants He S, Niu Y, Xing L, Liang Z, Song X, Ding M, Huang W Front Plant Sci 31-Jan-2024
PMCID:PMC10867983
doi:10.3389/fpls.2024.1310328
PMID:38362447
A review of medicinal plant of Middle East and North Africa (MENA) region as source in tuberculosis drug discovery Dehyab AS, Bakar MF, AlOmar MK, Sabran SF Saudi J Biol Sci 10-Jul-2020
PMCID:PMC7451596
doi:10.1016/j.sjbs.2020.07.007
PMID:32884430
A Review of Cytotoxic Plants of the Indian Subcontinent and a Broad-Spectrum Analysis of Their Bioactive Compounds Mazumder K, Biswas B, Raja IM, Fukase K Molecules 20-Apr-2020
PMCID:PMC7221707
doi:10.3390/molecules25081904
PMID:32326113
An Ethnobotanical Study of Medicinal Plants in the Greek Islands of North Aegean Region Axiotis E, Halabalaki M, Skaltsounis LA Front Pharmacol 23-May-2018
PMCID:PMC5974156
doi:10.3389/fphar.2018.00409
PMID:29875656
Medicinal Plants from Near East for Cancer Therapy Abu-Darwish MS, Efferth T Front Pharmacol 31-Jan-2018
PMCID:PMC5797783
doi:10.3389/fphar.2018.00056
PMID:29445343
Composition of the Essential Oil of<i>Origanum sipyleum</i>of Turkish Origin K. H.C. Baser, T. Özek, M. Kürkçüoglu, G. Tümen Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1992.9698035

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
1-Phenyl-2-butene 5356732 Click to see 132.20 unknown https://doi.org/10.1080/10412905.1992.9698035
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
p-Cymen-8-ol 14529 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1992.9698035
> Benzenoids / Benzene and substituted derivatives / Styrenes
1-Phenyl-1-butene 123088 Click to see 132.20 unknown https://doi.org/10.1080/10412905.1992.9698035
> Benzenoids / Phenols / Methoxyphenols
Isoeugenol 853433 Click to see 164.20 unknown https://doi.org/10.1080/10412905.1992.9698035
Propenylguaiacol 7338 Click to see 164.20 unknown https://doi.org/10.1080/10412905.1992.9698035
> Hydrocarbons / Polycyclic hydrocarbons
beta-Patchoulene 101731 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698035
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698035
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1080/10412905.1992.9698035
3-Octanol 11527 Click to see 130.23 unknown https://doi.org/10.1080/10412905.1992.9698035
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698035
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698035
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1992.9698035
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698035
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown https://doi.org/10.1080/10412905.1992.9698035
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1080/10412905.1992.9698035
Carvacryl methyl ether 80790 Click to see 164.24 unknown https://doi.org/10.1080/10412905.1992.9698035
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1080/10412905.1992.9698035
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1992.9698035
Thymyl methyl ether 14104 Click to see 164.24 unknown https://doi.org/10.1080/10412905.1992.9698035
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698035
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698035
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1992.9698035
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698035
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1992.9698035
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698035
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1992.9698035
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1992.9698035
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698035
Tricyclene 79035 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698035
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1992.9698035
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698035
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1992.9698035
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1992.9698035
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1992.9698035
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(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/10.1080/10412905.1992.9698035
(E,Z)-farnesol 1549109 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.1080/10412905.1992.9698035
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/10.1080/10412905.1992.9698035
a Farnesol 3327 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1992.9698035
alpha-Cubebene 442359 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698035
alpha-Patchoulene 521710 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698035
beta-Copaene 57339298 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698035
beta-Cubebene 93081 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698035
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1992.9698035
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698035
Farnesene 5281516 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1992.9698035
> 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/10.1080/10412905.1992.9698035
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
Ethinylestradiol 5991 Click to see 296.40 unknown https://doi.org/10.1080/10412905.1992.9698035
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Hexenal 10460 Click to see 98.14 unknown https://doi.org/10.1080/10412905.1992.9698035
trans-2-Hexenal 5281168 Click to see 98.14 unknown https://doi.org/10.1080/10412905.1992.9698035
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
(4E)-4-Octen-3-one 5369061 Click to see 126.20 unknown https://doi.org/10.1080/10412905.1992.9698035
4-Octen-3-one 84216 Click to see 126.20 unknown https://doi.org/10.1080/10412905.1992.9698035
> Organoheterocyclic compounds / Heteroaromatic compounds
Perillene 68316 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1992.9698035

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