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 Greek island communities the dried aerial parts are steeped as a mild infusion for colds, sore throats and mild fevers (Papadopoulos, 2018). In the central Anatolian villages of Turkey the same material is boiled as a short decoction for fever, a use noted by Kotan et al., 2014. In the Lebanese mountain villages fresh leaves are soaked in cold water to make a cold infusion taken as a digestive tonic, recorded by Al‑Mousawi et al., 2015. All three preparations rely on the aerial parts of the plant and are intended for short‑term internal use.

A simple, widely used preparation is a mild tea. Place 2–3 g of dried aerial parts (roughly a small handful of leaves and flowers) in a teapot, pour 200 mL of just‑boiled water, cover and steep for 5–10 minutes. The infusion can be sweetened with honey and drunk while warm. The dose commonly advised in folk practice is one cup taken 2–3 times a day for no more than five consecutive days. Because safety data are limited, pregnant women, nursing mothers and children under 12 years should avoid regular use, and anyone with a known allergy to Lamiaceae should discontinue if irritation occurs.

Phytochemical work on Sideritis syriaca has identified several classes of compounds that plausibly support its traditional actions. The essential oil, described by Kotan et al., 2014, contains α‑pinene, 1,8‑cineole, camphor and borneol, constituents known for mild antimicrobial and decongestant activity. In parallel, phenolic acids such as rosmarinic and caffeic acids, together with flavonoids including apigenin, luteolin and quercetin derivatives, have been quantified in aqueous extracts (Mert & Toprak, 2015). These antioxidants and anti‑inflammatory agents are consistent with the plant’s reputation for soothing respiratory and digestive irritation.

Modern laboratory studies continue to confirm antioxidant and antimicrobial effects of extracts from S. syriaca, and the herb is now sold in commercial “Sideritis tea” blends in Greece and Turkey, where it remains a staple in many households (Kotan et al., 2014; Katsiotis & Angeli, 2017). Ongoing ethnobotanical field work suggests the traditional uses described above are still practiced in remote mountain villages, ensuring that the heritage of Sideritis syriaca persists alongside scientific interest.

General Uses Top

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Food and beverages (non-medicinal):
Sideritis syriaca is commercially supplied as a dried herbal ingredient for brewing “Greek mountain tea.” Its flavor profile—earthy, herbaceous, and mildly resinous—derives from essential oils and diterpenes. Products include bulk dried aerial parts and branded loose-leaf or tea bags, used as a non-medicinal beverage and as a flavoring in confectionery and baked goods.

Synonyms Top

Scientific name	Authority	First published in
Navicularia syriaca	(L.) Soják	Cas. Nár. Mus., Odd. Prír. 148: 79 (1979 publ. 1980)
Sideritis cretica	Boiss.	Fl. Orient. 4: 708 (1879)

Common names Top

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Filter by language:

Language	Common/alternative name
English	ironwort
Arabic	فزر سوري
Bulgarian	кримски миризлив бурен
German	griechischer bergtee
German	malotira
German	syrisches gliedkraut
French	thé de crimée
French	tisane strandzhan
Italian	stregonia siciliana

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Sideritis syriaca subsp. nusairiensis	(Post) Hub.-Mor.	Bauhinia 6: 291 (1978)
Sideritis syriaca subsp. syriaca		Unknown

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

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

Europe click to expand
- Southeastern Europe
  - Kriti

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000310485
Tropicos	17600670
KEW	urn:lsid:ipni.org:names:459111-1
The Plant List	kew-191680
Open Tree Of Life	290040
Observations.org	146857
NCBI Taxonomy	155265
IPNI	459111-1
iNaturalist	358226
GBIF	7307364
Freebase	/m/011bdmyv
EPPO	SIESY
USDA GRIN	411422
Wikipedia	Sideritis_syriaca
CMAUP	NPO1723
PFAF	Sideritis syriaca

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

DNA Barcoding and Fertilization Strategies in Sideritis syriaca subsp. syriaca, a Local Endemic Plant of Crete with High Medicinal Value

Paschalidis K, Fanourakis D, Tsaniklidis G, Tsichlas I, Tzanakakis VA, Bilias F, Samara E, Ipsilantis I, Grigoriadou K, Samartza I, Matsi T, Tsoktouridis G, Krigas N

Int J Mol Sci

04-Feb-2024

PMCID:	PMC10856587
doi:	10.3390/ijms25031891
PMID:	38339166

Chemical profile of the Anatolian Sideritis species with bioactivity studies

Çarıkçı S, Kılıç T, Gören AC, Dirmenci T, Alim Toraman GÖ, Topçu G

Pharm Biol

22-Nov-2023

PMCID:	PMC11001281
doi:	10.1080/13880209.2023.2280253
PMID:	37990887

Chemical Composition of the Essential Oils of Three Popular Sideritis Species Cultivated in Greece Using GC-MS Analysis

Kaparakou EH, Daferera D, Kanakis CD, Skotti E, Kokotou MG, Tarantilis PA

Biomolecules

20-Jul-2023

PMCID:	PMC10377382
doi:	10.3390/biom13071157
PMID:	37509192

Natural Products for the Prevention and Treatment of Common Cold and Viral Respiratory Infections

Mammari N, Albert Q, Devocelle M, Kenda M, Kočevar Glavač N, Sollner Dolenc M, Mercolini L, Tóth J, Milan N, Czigle S, Varbanov M

Pharmaceuticals (Basel)

28-Apr-2023

PMCID:	PMC10220542
doi:	10.3390/ph16050662
PMID:	37242445

Determination of the Total Phenolics Content and Antioxidant Activity of Extracts from Parts of Plants from the Greek Island of Crete

Kalpoutzakis E, Chatzimitakos T, Athanasiadis V, Mitakou S, Aligiannis N, Bozinou E, Gortzi O, Skaltsounis LA, Lalas SI

Plants (Basel)

01-Mar-2023

PMCID:	PMC10005234
doi:	10.3390/plants12051092
PMID:	36903954

Mediterranean Diet: The Role of Phenolic Compounds from Aromatic Plant Foods

Delgado A, Gonçalves S, Romano A

Foods

16-Feb-2023

PMCID:	PMC9957056
doi:	10.3390/foods12040840
PMID:	36832914

Leucosceptosides A and B: Two Phenyl-Ethanoid Glycosides with Important Occurrence and Biological Activities

Frezza C, De Vita D, Toniolo C, Sciubba F, Tomassini L, Venditti A, Bianco A, Serafini M, Foddai S

Biomolecules

02-Dec-2022

PMCID:	PMC9775335
doi:	10.3390/biom12121807
PMID:	36551235

Characterization of Sideritis clandestina subsp. peloponnesiaca Polar Glycosides and Phytochemical Comparison to Other Mountain Tea Populations

Dimaki VD, Zeliou K, Nakka F, Stavreli M, Bakratsas I, Papaioannou L, Iatrou G, Lamari FN

Molecules

06-Nov-2022

PMCID:	PMC9658581
doi:	10.3390/molecules27217613
PMID:	36364439

Medicinal-Cosmetic Potential of the Local Endemic Plants of Crete (Greece), Northern Morocco and Tunisia: Priorities for Conservation and Sustainable Exploitation of Neglected and Underutilized Phytogenetic Resources

Bourgou S, Ben Haj Jilani I, Karous O, Megdiche-Ksouri W, Ghrabi-Gammar Z, Libiad M, Khabbach A, El Haissoufi M, Lamchouri F, Greveniotis V, Avramakis M, Hatzilazarou S, Anestis I, Tsoktouridis G, Krigas N

Biology (Basel)

16-Dec-2021

PMCID:	PMC8698715
doi:	10.3390/biology10121344
PMID:	34943257

GIS-Facilitated Seed Germination and Multifaceted Evaluation of the Endangered Abies marocana Trab. (Pinaceae) Enabling Conservation and Sustainable Exploitation

Hatzilazarou S, El Haissoufi M, Pipinis E, Kostas S, Libiad M, Khabbach A, Lamchouri F, Bourgou S, Megdiche-Ksouri W, Ghrabi-Gammar Z, Aslanidou V, Greveniotis V, Sakellariou MA, Anestis I, Tsoktouridis G, Krigas N

Plants (Basel)

27-Nov-2021

PMCID:	PMC8707146
doi:	10.3390/plants10122606
PMID:	34961077

Agro-Alimentary Potential of the Neglected and Underutilized Local Endemic Plants of Crete (Greece), Rif-Mediterranean Coast of Morocco and Tunisia: Perspectives and Challenges

Libiad M, Khabbach A, El Haissoufi M, Anestis I, Lamchouri F, Bourgou S, Megdiche-Ksouri W, Ghrabi-Gammar Z, Greveniotis V, Tsiripidis I, Dariotis E, Tsiafouli MA, Krigas N

Plants (Basel)

25-Aug-2021

PMCID:	PMC8469186
doi:	10.3390/plants10091770
PMID:	34579305

Optimization of Ultrasound-Assisted Extraction of Phenolics from Sideritis raeseri Using Response Surface Methodology

Šavikin K, Živković J, Janković T, Ćujić-Nikolić N, Zdunić G, Menković N, Drinić Z

Molecules

28-Jun-2021

PMCID:	PMC8272202
doi:	10.3390/molecules26133949
PMID:	34203414

Effect of Cocoa Bean Shell Addition on Metabolite Profile and Antioxidant Activity of Herbal Infusions

Quijano-Avilés M, Chóez-Guaranda I, Viteri R, Barragán-Lucas A, Sosa D, Manzano P

Int J Food Sci

06-May-2021

PMCID:	PMC8121573
doi:	10.1155/2021/9915797
PMID:	34036096

A Comparison Study on Traditional Mixtures of Herbal Teas Used in Eastern Mediterranean Area

Obón C, Rivera D, Fonollá E, Alcaraz F, Attieh L

Front Pharmacol

23-Apr-2021

PMCID:	PMC8103161
doi:	10.3389/fphar.2021.632692
PMID:	33967769

An In Vitro Evaluation of the Molecular Mechanisms of Action of Medical Plants from the Lamiaceae Family as Effective Sources of Active Compounds against Human Cancer Cell Lines

Sitarek P, Merecz-Sadowska A, Śliwiński T, Zajdel R, Kowalczyk T

Cancers (Basel)

13-Oct-2020

PMCID:	PMC7601952
doi:	10.3390/cancers12102957
PMID:	33066157

Phytochemical Profile Top

Add a new one!

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
(S)-Mandelonitrile	439767	Click to see C1=CC=C(C=C1)C(C#N)O	133.15	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(R)-2-Methylbutanoic acid	6950479	Click to see CCC(C)C(=O)O	102.13	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid	10467	Click to see	312.50	unknown	via CMAUP database
Myristic Acid	11005	Click to see	228.37	unknown	via CMAUP database
Palmitoleic Acid	445638	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	via CMAUP database
Stearic Acid	5281	Click to see	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2-Hexen-1-OL	5318042	Click to see CCCC=CCO	100.16	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
Linolenic Acid	5280934	Click to see	278.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4S,5S,9R,10S,13R)-5-(hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-en-2-one	163195101	Click to see	302.50	unknown	https://doi.org/10.1016/0031-9422(83)80158-7
Kaurane-7,18-diol, 15,16-epoxy-, (4beta,7alpha,15alpha)-	163092060	Click to see	320.50	unknown	https://doi.org/10.1016/0031-9422(83)83060-X
Siderone	14681633	Click to see CC1=CC23CC1CCC2C4(CCCC(C4CC3=O)(C)CO)C	302.50	unknown	https://doi.org/10.1016/0031-9422(83)80158-7
Ucriol	12315549	Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C5(C4O5)C)O)C)CO	320.50	unknown	https://doi.org/10.1016/0031-9422(83)83060-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral	638011	Click to see	152.23	unknown	via CMAUP database
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene	7463	Click to see	134.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol	442501	Click to see	154.25	unknown	via CMAUP database
Terpinolene	11463	Click to see	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
I2-Ionone	638014	Click to see	192.30	unknown	via CMAUP database
Vomifoliol, (+)-	5280462	Click to see	224.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Flavoxanthin	5281238	Click to see	584.90	unknown	via CMAUP database
Rubixanthin	5281252	Click to see	552.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin acetate	92842	Click to see	468.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
(8S,9S,13S,14R)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one	670995	Click to see CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O	270.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
[17-[1-(4,5-Dimethyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-10-methyl-3-oxo-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-13-yl]methyl acetate	14102732	Click to see	480.60	unknown	https://doi.org/10.1016/J.FOODCHEM.2010.05.076
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Poriferasterol	5281330	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
Stigmasteryl-beta-d-glucopyranoside	12895774	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	574.80	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron	88113319	Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O	192.12	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucuronides / O-glucuronides
beta-D-GlcpA-(1->6)-beta-D-Galp	70680285	Click to see C(C1C(C(C(C(O1)O)O)O)O)OC2C(C(C(C(O2)C(=O)O)O)O)O	356.28	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Amygdalin	656516	Click to see	457.40	unknown	via CMAUP database
Neoamygdalin	441462	Click to see	457.40	unknown	via CMAUP database
Prunasin	119033	Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O	295.29	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Nonenal	5283335	Click to see CCCCCCC=CC=O	140.22	unknown	via CMAUP database
2,4-Decadienal	5283349	Click to see	152.23	unknown	via CMAUP database
Hexanal	6184	Click to see	100.16	unknown	via CMAUP database
trans-2-Hexenal	5281168	Click to see	98.14	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-5-butyloxolan-2-one	7057972	Click to see CCCCC1CCC(=O)O1	142.20	unknown	via CMAUP database
(R)-gamma-Decalactone	183870	Click to see	170.25	unknown	via CMAUP database
Gamma-dodecalactone, (R)-	10888889	Click to see	198.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
Linalool oxide, cis-	6428573	Click to see	170.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1S,5R,6S,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol	5317050	Click to see	544.50	unknown	via CMAUP database
(1S,5S,6R,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol	73353883	Click to see	544.50	unknown	via CMAUP database
(1S,5S,6S,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol	5317051	Click to see	544.50	unknown	via CMAUP database
[(1S,5R,6R,13R,21S)-6,9,17,19-tetrahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-yl] 4-hydroxybenzoate	10723070	Click to see	664.60	unknown	via CMAUP database
Mahuannin A	5317052	Click to see	544.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
[4-[5,8-Dihydroxy-7-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-4-oxochromen-2-yl]phenyl] 3-(4-hydroxyphenyl)prop-2-enoate	162868104	Click to see C1=CC(=CC=C1C=CC(=O)OC2=CC=C(C=C2)C3=CC(=O)C4=C(O3)C(=C(C=C4O)OC(=O)C=CC5=CC=C(C=C5)O)O)O	578.50	unknown	https://doi.org/10.1016/J.FOODCHEM.2010.05.076
[5,8-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate	101523766	Click to see	432.40	unknown	https://doi.org/10.1016/J.FOODCHEM.2010.05.076
[5,8-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl] 3-(4-hydroxyphenyl)prop-2-enoate	163057819	Click to see C1=CC(=CC=C1C=CC(=O)OC2=C(C3=C(C(=C2)O)C(=O)C=C(O3)C4=CC=C(C=C4)O)O)O	432.40	unknown	https://doi.org/10.1016/J.FOODCHEM.2010.05.076
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see	286.24	unknown	via CMAUP database
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin	5280804	Click to see	464.40	unknown	via CMAUP database
Rutin	5280805	Click to see	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate	162916367	Click to see	578.50	unknown	https://doi.org/10.1016/0031-9422(94)00634-6
[6-[2-[5,8-Dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	73802681	Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C=C(O4)C5=CC=C(C=C5)OC)O)CO)O)O)O)O)O	666.60	unknown	https://doi.org/10.1016/J.FOODCHEM.2010.05.076
7-[[2-O-(6-O-Acetyl-I(2)-D-glucopyranosyl)-I(2)-D-glucopyranosyl]oxy]-5,8-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one	101915840	Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C=C(O4)C5=CC(=C(C=C5)OC)O)O)CO)O)O)O)O)O	682.60	unknown	https://doi.org/10.1016/0031-9422(94)00634-6
7-[2-O-(6-O-Acetyl-beta-D-allopyranosyl)-beta-D-glucopyranosyloxy]-5,8-dihydroxy-4'-methoxyflavone	21576582	Click to see	666.60	unknown	https://doi.org/10.1016/J.FOODCHEM.2010.05.076
8-Hydroxyhesperetin 7-[6-acetylglucosyl-(1->2)-glucoside]	74977927	Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C4=C(C(=C3)O)C(=O)C=C(O4)C5=CC(=C(C=C5)OC)O)O)CO)O)O)O)O)O	682.60	unknown	https://doi.org/10.1016/0031-9422(94)00634-6
Apigenin-7-O-(6''-O-4-coumaroyl)-beta-glucopyranoside	6439941	Click to see	578.50	unknown	https://doi.org/10.1016/0031-9422(94)00634-6

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Sideritis syriaca

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top