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.

Satureja montana, commonly known as wild marjoram, has a long history of use in Mediterranean folk medicine. Among the Turkish people, dried leaves are steeped in hot water to produce a soothing tea that is traditionally taken for stomach upset, indigestion, and mild colds (Yildirim et al., 2015). In Greece, the same leaves are used in a decoction to relieve coughs and sore throats, and the infusion is also applied topically as a poultice for minor skin irritations and insect bites (Papadopoulos et al., 2018). Italian herbalists have recorded the use of a mild tea made from the leaves to calm gastrointestinal cramps and to aid digestion, while the leaves are also crushed and applied to bruises and sprains for their anti‑inflammatory effect (Smith et al., 2019). In the French and Spanish traditions, a poultice of crushed leaves is wrapped around small wounds to promote healing and reduce infection (Kovač et al., 2020). These preparations all involve infusions or decoctions of the aerial parts, with the leaves being the primary material used.

A simple, safe recipe for a mild digestive tea is as follows: take 2 g (about one teaspoon) of dried Satureja montana leaves and steep them in 200 ml of boiling water for 5 minutes. Strain the liquid and sip slowly. This dose is well within the traditional range and is considered safe for most adults. However, because the plant contains compounds that can stimulate uterine contractions, it is advisable to avoid this tea during pregnancy and to limit intake to no more than one cup per day for individuals with a history of uterine hyperactivity.

The therapeutic effects of Satureja montana are largely attributed to its essential oil constituents. Thymol and carvacrol are the dominant phenolic compounds, providing strong antimicrobial and anti‑inflammatory activity. Linalool and borneol also contribute to the plant’s soothing aroma and mild analgesic properties. These well‑established phytochemicals have been isolated from the leaves and are known to inhibit the growth of common gastrointestinal pathogens, which helps explain the plant’s traditional use for digestive complaints.

Today, wild marjoram is still sold as a culinary spice in many markets, and its essential oil is marketed as a natural preservative and flavoring agent. Ongoing research is exploring its potential as a natural antimicrobial additive in food and as a complementary therapy for inflammatory bowel conditions, underscoring the continued relevance of this age‑old herb.

General Uses Top

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Common products:
Satureja montana provides an essential oil used by the flavor and fragrance industries as a natural flavoring component. The dried aerial parts are traded as a culinary herb and spice; leafy sprigs are used whole or ground for seasoning.

Food and beverages (non-medicinal):
The dried herb is employed as a seasoning in processed meats, sausages, cured products, pickles, and preserves; it is also used in sauces, Stuffings, stews, and vegetable dishes. As a culinary spice it appears in spice blends. The herb or its essential oil is used to flavor condiments, aromatic vinegars, and processed foods such as olives and cheese spreads. As a botanical ingredient it is used in the production of liqueurs, bitters, and flavored spirits.

Scientific/model-organism use:
Satureja montana serves as a model in flavor research and in studies of Oregano–Savory essential oil chemistry and chemotyping; its variability in major oil constituents (e.g., carvacrol, thymol) is used to analyze genotype–environment relations. It has been the subject of community resources and standardized protocols for oil extraction and GC-based compositional analysis that support comparative studies within Lamiaceae.

Properties relevant to use:
The essential oil is rich in monoterpenes, notably carvacrol and thymol, which contribute to the characteristic aromatic profile and the flavoring utility. Total phenolics and specific flavonoids have been quantified in extracts used for sensory profiling, informing composition–flavor relationships relevant to spice applications.Oil composition and yields vary among subspecies and populations, reflecting genetic and environmental controls relevant to product sourcing and quality assurance.

Synonyms Top

Scientific name	Authority	First published in
Micromeria montana	Rchb.	Fl. Germ. Excurs. : 311 (1831)
Satureja montana f. subquadrangula	(Rohlena) Šilić	Glasn. Zemaljsk. Muz. Bosne Hercegovine Sarajevu. Prir. Nauke 13: 107. 1975 [1974 publ. 1975]
Satureja montana var. subquadrangula	Rohlena	Unknown
Saturiastrum montanum	Fourr.	Ann. Soc. Linn. Lyon , n.s., 17: 133 (1969)
Thymus montanus	Dum.Cours.	Bot. Cult. , ed. 2, 3: 32 (1811)
Satureja montana var. chamaebuxus	Briq.	Lab. Alp. Mar. 398. 1893
Satureja montana var. communis	Vis.	Fl. Dalmat. 2: 194. 1847
Satureja montana var. stenophylla	Boiss.	Fl. Orient. 4: 563. 1879
Clinopodium montanum	Kuntze	Revis. Gen. Pl. 2: 515 (1891)

Common names Top

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Filter by language:

Language	Common/alternative name
English	perennial savory
English	winter savory
Spanish	axedrea
Spanish	ajedrea
Spanish	hisopillo
Spanish	ajedrea de montana
Spanish	ajedrea de montaña
Spanish	ajedrea montesina
Spanish	ajedrea salvaje
Spanish	ajedrea silvestre
Spanish	axedrea de montana
Spanish	axedrea de montaña
Spanish	axedrea montana
Spanish	axedrea salvaje
Spanish	isopillo
Spanish	isopo montano
Spanish	isopo montesino
Arabic	مصنع الخمر
Arabic	زوباع البر
Arabic	زعتر الجبل
Arabic	المخمرة
Arabic	ندغ جبلي
Azerbaijani	dağ çölnanəsi
Azerbaijani	dağ kəkotusu
Bulgarian	балканска чубрица
Bulgarian	Чубрица
Bosnian	vrijesak
Catalan	sajolida
Catalan	sajolida silvestre
Czech	saturejka horská
Welsh	safri fach
Danish	vinter-sar
German	winter-bohnenkraut
German	berg-bohnenkraut
German	bergbohnenkraut
German	winterbohnenkraut
Esperanto	monta satureo
Finnish	talvikynteli
French	sarriette vivace
French	sarriette des montagnes
Croatian	primorski vrisak
Upper Sorbian	hórska poprica
Hungarian	hegyi pereszlény
Korean	겨울세이버리
Cornish	sawor gwav
Macedonian	планинска чубрика
Macedonian	планинска чубрица
Norwegian Bokmål	vintersar
Dutch	bonenkruid
Dutch	doorlevend bonenkruid
Dutch	winter bonenkruid
oc	isòp
oc	pebre-d'ase
Polish	cząber górski
Portuguese	segurelha-das-montanhas
Russian	Чабер горный
Serbo-Croatian	rtanjski čaj
Serbo-Croatian	planinski čubar
Serbo-Croatian	vrijesak
Slovak	saturejka horská
Slovenian	kraški žepek
Slovenian	kraški šetraj
Serbian	Ртањски чај
Swedish	vinterkyndel
Ukrainian	Чабер гірський
Chinese	欧香料
Chinese	冬塔花

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Satureja montana subsp. macedonica	(Formánek) Baden	Mount. Fl. Greece 2: 123 (1991)
Satureja montana subsp. montana		Unknown
Satureja montana subsp. pisidia	(Wettst.) Šilić	Glasn. Zemaljsk. Muz. Bosne Hercegovine Sarajevu Prir. Nauke 13: 108 (1974 publ. 1975)
Satureja montana subsp. variegata	(Host) P.W.Ball	Bot. J. Linn. Soc. 65: 352 (1972)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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

Africa click to expand
- Macaronesia
  - Azores

Asia-temperate click to expand
- Western Asia
  - Lebanon-Syria
  - Turkey

Europe click to expand
- Middle Europe
  - Austria
- Southeastern Europe
  - Albania
  - Greece
  - Italy
  - Yugoslavia
- Southwestern Europe
  - France
  - Portugal
  - Spain

Northern America click to expand
- South-central U.S.A.
  - Texas

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000304338
UNII	X1A2B19EPY
USDA Plants	SAMO6
Tropicos	17600325
INPN	120908
Flora of Italy	4566
KEW	urn:lsid:ipni.org:names:457736-1
The Plant List	kew-185794
Missouri Botanical Garden	281431
Open Tree Of Life	382237
Observations.org	7412
NCBI Taxonomy	49988
NBN Atlas	NBNSYS0000004212
Nature Serve	2.161590
IPNI	457736-1
iNaturalist	168442
GBIF	2926884
Freebase	/m/05zbxg
EPPO	STIMO
EOL	485130
USDA GRIN	316819
Wikipedia	Winter_savory
CMAUP	NPO23226

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

Emerging Approaches for Mitigating Biofilm-Formation-Associated Infections in Farm, Wild, and Companion Animals

Araújo D, Silva AR, Fernandes R, Serra P, Barros MM, Campos AM, Oliveira R, Silva S, Almeida C, Castro J

Pathogens

13-Apr-2024

PMCID:	PMC11054384
doi:	10.3390/pathogens13040320
PMID:	38668275

Wild Edible Plants Used in Dalmatian Zagora (Croatia)

Ninčević Runjić T, Jug-Dujaković M, Runjić M, Łuczaj Ł

Plants (Basel)

11-Apr-2024

PMCID:	PMC11053949
doi:	10.3390/plants13081079
PMID:	38674488

Spray-Drying Microencapsulation of Bauhinia ungulata L. var. obtusifolia Aqueous Extract Containing Phenolic Compounds: A Comparative Study Using Different Wall Materials

Remígio MS, Greco T, Silva Júnior JO, Converti A, Ribeiro-Costa RM, Rossi A, Barbosa WL

Pharmaceutics

02-Apr-2024

PMCID:	PMC11054010
doi:	10.3390/pharmaceutics16040488
PMID:	38675149

Deep eutectic solvents: Preparation, properties, and food applications

Negi T, Kumar A, Sharma SK, Rawat N, Saini D, Sirohi R, Prakash O, Dubey A, Dutta A, Shahi NC

Heliyon

30-Mar-2024

PMCID:	PMC11015381
doi:	10.1016/j.heliyon.2024.e28784
PMID:	38617909

Synthesis of eco-friendly layered double hydroxide and nanoemulsion for jasmine and peppermint oils and their larvicidal activities against Culex pipiens Linnaeus

Radwan IT, Khater HF, Mohammed SH, Khalil A, Farghali MA, Mahmoud MG, Selim A, Manaa EA, Bagato N, Baz MM

Sci Rep

22-Mar-2024

PMCID:	PMC10959945
doi:	10.1038/s41598-024-56802-y
PMID:	38519561

Using Essential Oils to Reduce Yersinia enterocolitica in Minced Meat and in Biofilms

Vidaković Knežević S, Knežević S, Vranešević J, Milanov D, Ružić Z, Karabasil N, Kocić-Tanackov S

Foods

06-Mar-2024

PMCID:	PMC10931311
doi:	10.3390/foods13050806
PMID:	38472919

Calocedrus formosana Essential Oils Induce ROS-Mediated Autophagy and Apoptosis by Targeting SIRT1 in Colon Cancer Cells

Islam A, Chang YC, Tsao NW, Wang SY, Chueh PJ

Antioxidants (Basel)

26-Feb-2024

PMCID:	PMC10967316
doi:	10.3390/antiox13030284
PMID:	38539819

Traditional Use of Wild Edible Plants in Slovenia: A Field Study and an Ethnobotanical Literature Review

Papež Kristanc A, Kreft S, Strgulc Krajšek S, Kristanc L

Plants (Basel)

24-Feb-2024

PMCID:	PMC10934440
doi:	10.3390/plants13050621
PMID:	38475472

Identification of essential oils with strong activity against stationary phase Mycobacterium abscessus

Cao D, Jiang X, Wu T, Xiang Y, Liu J, Li Z, Yuan X, Bi K, Dong X, Tønjum T, Xu K, Zhang Y

Heliyon

24-Feb-2024

PMCID:	PMC10920374
doi:	10.1016/j.heliyon.2024.e27073
PMID:	38463856

Plants in Menstrual Diseases: A Systematic Study from Italian Folk Medicine on Current Approaches

Mazzei R, Genovese C, Magariello A, Patitucci A, Russo G, Tagarelli G

Plants (Basel)

22-Feb-2024

PMCID:	PMC10935160
doi:	10.3390/plants13050589
PMID:	38475436

Plant-Based Films and Hydrogels for Wound Healing

Lopes AI, Pintado MM, Tavaria FK

Microorganisms

21-Feb-2024

PMCID:	PMC10972459
doi:	10.3390/microorganisms12030438
PMID:	38543489

Development, physicochemical characterization, and antimicrobial evaluation of niosome-loaded oregano essential oil against fish-borne pathogens

Sirati R, Khajehrahimi AE, Kazempoor R, Kakoolaki S, Ghorbanzadeh A

Heliyon

19-Feb-2024

PMCID:	PMC10920168
doi:	10.1016/j.heliyon.2024.e26486
PMID:	38463865

Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species

Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E

Antibiotics (Basel)

07-Feb-2024

PMCID:	PMC10885947
doi:	10.3390/antibiotics13020163
PMID:	38391549

Clinopodium L. Taxa from the Balkans—Are There Unique Leaf Micromorphological and Phytochemical Patterns?

Janković S, Alimpić Aradski A, Dodoš T, Novaković J, Ivanović S, Vujisić L, Marin PD, Rajčević N

Plants (Basel)

16-Jan-2024

PMCID:	PMC10819394
doi:	10.3390/plants13020251
PMID:	38256803

Ethnobotanical and ethnomedicinal research into medicinal plants in the Mt Stara Planina region (south-eastern Serbia, Western Balkans)

Jarić S, Kostić O, Miletić Z, Marković M, Sekulić D, Mitrović M, Pavlović P

J Ethnobiol Ethnomed

10-Jan-2024

PMCID:	PMC10782642
doi:	10.1186/s13002-024-00647-2
PMID:	38200599

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
2-[(1S,2R,4R,4aR,6R,8R,8aS)-4-acetyloxy-8-benzoyloxy-1-(cyanomethyl)-6-ethenyl-4a-hydroxy-1,6-dimethyl-5-oxo-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]-2-methylpropanoic acid	15548729	Click to see CC(=O)OC1CC(C(C2C1(C(=O)C(CC2OC(=O)C3=CC=CC=C3)(C)C=C)O)(C)CC#N)C(C)(C)C(=O)O	525.60	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
[(2S,3S,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7-diacetyloxy-5-benzoyloxy-3-ethenyl-2,10,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	11802781	Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(C(C(C3=O)(C)O)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C	692.70	unknown	via CMAUP database
[(2S,3S,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-3-ethenyl-2,6,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	10032594	Click to see	692.70	unknown	via CMAUP database
Neoorthosiphol A	10055454	Click to see	692.70	unknown	via CMAUP database
Staminol C	11490943	Click to see	692.70	unknown	via CMAUP database
Staminol D	11455867	Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C)(C)C	568.60	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
6-Methyleugenol	45266909	Click to see	178.23	unknown	https://doi.org/10.1080/10412905.1991.9700495
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	https://doi.org/10.1002/PTR.2650090215 https://doi.org/10.1080/10412905.1991.9700495 https://doi.org/10.1080/10412905.1991.9700494 https://doi.org/10.1080/10412905.1992.9698136
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octanol	957	Click to see CCCCCCCCO	130.23	unknown	https://doi.org/10.1080/10412905.1991.9700495
Nonan-1-ol	8914	Click to see CCCCCCCCCO	144.25	unknown	https://doi.org/10.1080/10412905.1991.9700495
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7-diacetyloxy-4b-(acetyloxymethyl)-5-benzoyloxy-2-ethenyl-10,10a-dihydroxy-2,8,8-trimethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	11828707	Click to see CC(=O)OCC12C(CC(C3(C1C(CC(C3=O)(C)C=C)OC(=O)C4=CC=CC=C4)O)O)C(C(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C	734.80	unknown	via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7-diacetyloxy-5-benzoyloxy-2-ethenyl-10,10a-dihydroxy-4b-(hydroxymethyl)-2,8,8-trimethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	11017910	Click to see	692.70	unknown	via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7,10-triacetyloxy-5-benzoyloxy-2-ethenyl-10a-hydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	9987409	Click to see	718.80	unknown	via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7-acetyloxy-5-benzoyloxy-2-ethenyl-6,10,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	10919284	Click to see CC(=O)OC1C(C(C2(C(C1(C)C)CC(C3(C2C(CC(C3=O)(C)C=C)OC(=O)C4=CC=CC=C4)O)O)C)OC(=O)C5=CC=CC=C5)O	634.70	unknown	via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-2-ethenyl-6,10a-dihydroxy-4b-(hydroxymethyl)-2,8,8-trimethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	11115145	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)CO)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C	692.70	unknown	via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,9S,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-2-ethenyl-6,9,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	10930480	Click to see	692.70	unknown	via CMAUP database
[(2S,3R,4S,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-2-ethenyl-3,6,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	10032595	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C	692.70	unknown	via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-2,9-diacetyloxy-7-ethenyl-3,8a-dihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-4-yl] benzoate	101228590	Click to see	570.60	unknown	via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-3-acetyloxy-7-ethenyl-2,8a,9-trihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-4-yl] benzoate	101228589	Click to see	528.60	unknown	via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-9-acetyloxy-4-benzoyloxy-7-ethenyl-3,8a-dihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-2-yl] benzoate	10258500	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C5=CC=CC=C5)(C)C	632.70	unknown	via CMAUP database
[(4aR,4bR,7R,8aR,9R,10aR)-3-acetyloxy-7-ethenyl-8a-hydroxy-1,1,4a,7-tetramethyl-2,5,8-trioxo-6,9,10,10a-tetrahydro-4bH-phenanthren-9-yl] acetate	10072248	Click to see	446.50	unknown	via CMAUP database
Orthosiphol A	15385858	Click to see	676.70	unknown	via CMAUP database
orthosiphol B	15385859	Click to see	676.70	unknown	via CMAUP database
Orthosiphol D	44583689	Click to see	552.60	unknown	via CMAUP database
Orthosiphol F	10327179	Click to see	676.70	unknown	via CMAUP database
Orthosiphol G	10076785	Click to see	572.60	unknown	via CMAUP database
Orthosiphol I	10674582	Click to see	570.60	unknown	via CMAUP database
Orthosiphol J	10438744	Click to see	612.70	unknown	via CMAUP database
Orthosiphol K	10054824	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)O)(C)C	634.70	unknown	via CMAUP database
Orthosiphol L	10101176	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C	692.70	unknown	via CMAUP database
Orthosiphol M	10030927	Click to see	570.60	unknown	via CMAUP database
Orthosiphol N	10258499	Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(=O)CC(C3=O)(C)C=C)O)O)(C)C)OC(=O)C5=CC=CC=C5	632.70	unknown	via CMAUP database
Orthosiphol O	10032464	Click to see	676.70	unknown	via CMAUP database
Orthosiphol P	10101175	Click to see	692.70	unknown	via CMAUP database
Orthosiphol R	44583688	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C	692.70	unknown	via CMAUP database
Orthosiphol S	10099906	Click to see CC1(C2CC(C3(C(C2(C(C(=O)C1OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)C)C(=O)CC(C3=O)(C)C=C)O)O)C	588.60	unknown	via CMAUP database
Orthosiphol T	11082749	Click to see	634.70	unknown	via CMAUP database
Orthosiphol U	637182	Click to see	614.70	unknown	via CMAUP database
Orthosiphol V	10951947	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C)(C)C	572.60	unknown	via CMAUP database
Orthosiphol W	11071897	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)O)(C)C	572.60	unknown	via CMAUP database
Orthosiphol X	10054823	Click to see	634.70	unknown	via CMAUP database
Orthosiphol Y	11144807	Click to see	448.50	unknown	via CMAUP database
Orthosiphol Z	11090752	Click to see CC(=O)OC1=CC2(C(CC(C3(C2C(=O)CC(C3=O)(C)C=C)O)O)C(C1=O)(C)C)C	404.50	unknown	via CMAUP database
orthosiphonone A	10439492	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C5=CC=CC=C5)(C)C	674.70	unknown	via CMAUP database
Orthosiphonone C	11226314	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)O)OC(=O)C4=CC=CC=C4)O)(C)C	528.60	unknown	via CMAUP database
Siphonol A	10952715	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)CO)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C	734.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citronellol	8842	Click to see	156.26	unknown	https://doi.org/10.1080/10412905.1991.9700495
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1991.9700495
> 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/10.1080/10412905.1991.9700495 https://doi.org/10.1080/10412905.1991.9700494 https://doi.org/10.1080/10412905.1992.9698136 https://doi.org/10.1002/PTR.2650070508
P-Cymene	7463	Click to see	134.22	unknown	https://doi.org/10.1002/PTR.2650090215 https://doi.org/10.1080/10412905.1992.9698136 https://doi.org/10.1080/10412905.1991.9700495 https://doi.org/10.1080/10412905.1991.9700494 https://doi.org/10.1055/S-2006-960081
Thymol	6989	Click to see	150.22	unknown	https://doi.org/10.1080/10412905.1991.9700495 https://doi.org/10.1080/10412905.1992.9698136 https://doi.org/10.1055/S-2006-960081
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1002/PTR.2650090215 https://doi.org/10.1080/10412905.1992.9698136
3-Carene	26049	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.1055/S-2006-960081
4,6,6-Trimethylbicyclo(3.1.1)hept-3-en-2-one	29025	Click to see	150.22	unknown	https://doi.org/10.1002/PTR.2650090215
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester	6448	Click to see	196.29	unknown	https://doi.org/10.1080/10412905.1991.9700495 https://doi.org/10.1002/PTR.2650090215
Beta-Pinene	14896	Click to see	136.23	unknown	https://doi.org/10.1002/PTR.2650090215
Borneol	64685	Click to see	154.25	unknown	https://doi.org/10.1002/PTR.2650090215 https://doi.org/10.1080/10412905.1991.9700495 https://doi.org/10.1080/10412905.1992.9698136
Camphene	6616	Click to see	136.23	unknown	https://doi.org/10.1055/S-2006-960081
CID 44630107	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1002/PTR.2650090215 https://doi.org/10.1080/10412905.1992.9698136 https://doi.org/10.1055/S-2006-960081
Norstaminone A	10414921	Click to see	540.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-PHELLANDRENE	7460	Click to see	136.23	unknown	https://doi.org/10.1002/PTR.2650090215 https://doi.org/10.1080/10412905.1992.9698136
Alpha-Terpinene	7462	Click to see	136.23	unknown	https://doi.org/10.1002/PTR.2650090215 https://doi.org/10.1080/10412905.1992.9698136
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1002/PTR.2650090215
Carvone, (+-)-	7439	Click to see	150.22	unknown	https://doi.org/10.1002/PTR.2650090215 https://doi.org/10.1080/10412905.1992.9698136
Carvone, (+)-	16724	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1002/PTR.2650090215 https://doi.org/10.1080/10412905.1992.9698136
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1002/PTR.2650090215
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,6R,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	84690	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1991.9700495
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1992.9698136 https://doi.org/10.1080/10412905.1991.9700495
Vomifoliol, (+)-	5280462	Click to see	224.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	via CMAUP database
(1R,3aR,4S,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-4,9-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	21604188	Click to see	472.70	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/NP50037A025
Betulinic Acid	64971	Click to see	456.70	unknown	via CMAUP database
Maslinic Acid	73659	Click to see	472.70	unknown	https://doi.org/10.1021/NP50037A025
Oleanolic Acid	10494	Click to see	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Siphonol E	10963687	Click to see	736.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
14-deoxo-14-O-acetylorthosiphol Y	21578028	Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(C(CC3O)(C)C=C)OC(=O)C)O)C)OC(=O)C)(C)C	492.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1021/NP50037A025
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1021/NP50037A025
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
Asperglaucide	10026486	Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3	444.50	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
Norstaminolactone A	11146922	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C14OC(=O)C(O4)(C(C3OC(=O)C5=CC=CC=C5)CNC)C)C)OC(=O)C6=CC=CC=C6)OC(=O)C)O)(C)C	707.80	unknown	via CMAUP database
Staminol A	10628761	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C	734.80	unknown	via CMAUP database
Staminolactone A	10770905	Click to see	690.70	unknown	via CMAUP database
Staminolactone B	10676125	Click to see	690.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
2-[(1S,2R,4R,4aR,6R,8R,8aS)-4-acetyloxy-8-benzoyloxy-1-(carboxymethyl)-6-ethenyl-4a-hydroxy-1,6-dimethyl-5-oxo-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]-2-methylpropanoic acid	15548710	Click to see	544.60	unknown	via CMAUP database
Secoorthosiphol B	15548728	Click to see	558.60	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
L-Tartaric acid	444305	Click to see	150.09	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
[(1S,2R,4S,6S,7S,8R,9S,10R,13S)-12-acetyl-2,7-diacetyloxy-6-hydroxy-5,5,9-trimethyl-15,16-dioxatetracyclo[11.2.1.01,10.04,9]hexadec-11-en-8-yl] benzoate	10951829	Click to see	556.60	unknown	via CMAUP database
[(1S,2S,3R,4S,5S,7S,9R,10R,12R,15S,16S,17S)-4,9-diacetyloxy-3-benzoyloxy-5,10,15-trihydroxy-2,6,6,12-tetramethyl-11,13-dioxatetracyclo[8.7.0.02,7.012,16]heptadecan-17-yl] benzoate	10963538	Click to see	696.70	unknown	via CMAUP database
Norstaminol A	11765116	Click to see	678.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid	639655	Click to see	360.30	unknown	via CMAUP database
3,4-Dihydroxycinnamic acid methyl ester	92202	Click to see	194.18	unknown	via CMAUP database
Ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate	66883	Click to see	208.21	unknown	via CMAUP database
Methyl Rosmarinate	6479915	Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O	374.30	unknown	via CMAUP database
P-Hydroxyphenethyl Trans-Ferulate	637308	Click to see	314.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid	2518	Click to see	180.16	unknown	via CMAUP database
Caffeic Acid	689043	Click to see	180.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Eriocitrin	83489	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O	596.50	unknown	https://doi.org/10.1021/NP50037A025
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-6,7,3',4'-Tetramethoxyflavone	152430	Click to see	358.30	unknown	via CMAUP database
5,6,7,4'-Tetramethoxyflavone	96118	Click to see	342.30	unknown	via CMAUP database
6-Hydroxy-5,7-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one	243760	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)OC	328.30	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
Gonzalitosin I	5272653	Click to see	328.30	unknown	via CMAUP database
Ladanein	3084066	Click to see	314.29	unknown	via CMAUP database
Salvigenin	161271	Click to see	328.30	unknown	via CMAUP database
Sinensetin	145659	Click to see	372.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Demethoxynobiletin	44584772	Click to see	372.40	unknown	via CMAUP database

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Satureja montana

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