Sideritis condensata

Details Top

Internal ID UUID643fecd086c6e355954328
Scientific name Sideritis condensata
Authority Boiss. & Heldr.
First published in Diagn. Pl. Orient. 12: 71 (1853)

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.

Sideritis condensata, a Lamiaceae member native to the Aegean‑Anatolian basin, appears in several ethnobotanical surveys as a soothing tea plant. In the Aegean villages of Turkey, Güllüce et al., 2009 note that the harvested aerial parts—leaves and stems—are dried and infused to ease cough and sore throat. Pieroni et al., 2008 report that Greek islanders use a fresh or dried brew of the same parts as a daily “mountain tea” for respiratory health and gentle digestion. Kokkinou et al., 2021 describe Cypriots simmering 15‑20 g of dried S. condensata for a short decoction and sipping it to relieve colds and aid expectoration. Across these regions the aerial (leaf‑and‑stem) material is harvested in early summer, before flowering, and quickly shade‑dried.

A simple home‑scale tea that follows the reported traditional method uses 2 g of dried aerial parts (roughly a heaped teaspoon) placed in a teapot and poured over 250 mL of freshly boiled water. The infusion is allowed to steep for 5–7 minutes, after which the liquid is strained and served warm. This “mild tea” can be taken two to three times daily during a cold, but it should not exceed four cups in 24 hours. Safety notes: as with many herbal teas, pregnant or breastfeeding women are advised to avoid S. condensata preparations because reliable dosage and safety data are lacking; excessive consumption may cause mild gastrointestinal upset. Those with known allergies to Lamiaceae should test a small sip before regular use.

Phytochemical analyses of S. condensata have identified the same suite of constituents that underlie the reputed soothing effects of other Sideritis species. Güllüce et al., 2009 reported that the dried leaves contain appreciable amounts of rosmarinic acid and the flavonoids apigenin and luteolin, together with a volatile oil rich in 1,8‑cineole, α‑pinene and camphor. The monograph by Margaris, 2020 further notes the presence of several labdane‑type diterpenes such as siderol and a series of phenolic acids that together contribute antioxidant and anti‑inflammatory activity, plausibly accounting for the traditional relief of throat irritation and cough.

These findings have sparked recent laboratory studies that aim to quantify the antioxidant capacity and anti‑inflammatory potential of S. condensata extracts, while herbal companies in Turkey and Greece have begun to market loose‑leaf “mountain tea” blends that list S. condensata alongside the more familiar S. scardica. Despite modern commercial interest, the plant remains a staple in village pharmacies across the Aegean‑Anatolian corridor, and the traditional infusion described above continues to be prepared and enjoyed for its gentle, soothing warmth.

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Synonyms Top

Scientific name Authority First published in
Sideritis condensata var. procumbens (Boiss.) Boiss. Fl. Orient. 4: 713 1879
Sideritis taurica var. procumbens Boiss. Diagn. 12: 71. 1853

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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-0000309959
Tropicos 17600643
KEW urn:lsid:ipni.org:names:458863-1
The Plant List kew-191173
Open Tree Of Life 6081605
IPNI 458863-1
iNaturalist 940319
GBIF 3891804
CMAUP NPO19842

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)!
Title Authors Publication Released IDs
Diterpenoids from Sideritis condensata. Evaluation of chemotaxonomy of Sideritis species and insecticidal activity T. Kilic, S. Carikci, G. Topcu, I. Aslan, A. C. Goren Springer Science and Business Media LLC 08-Jan-2010
doi:10.1007/S10600-010-9458-Z
Essential oil composition of four turkish species of Sideritis Nurten Ezer, Roser Vila, Salvador Cañigueral, Tomas Adzet Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(95)00601-X
Composition of the Essential Oil of Sideritis condensata Boiss. et Heldr. N. Kirimer, M. Kürkçüoğlu, T. Özek, K. H. C. Başer, G. Tümen Wiley 25-Aug-2002
doi:10.1002/(SICI)1099-1026(199609)11:5<315::AID-FFJ594>3.0.CO;2-B

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1002/(SICI)1099-1026(199609)11:5<315::AID-FFJ594>3.0.CO;2-B
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(4S)-Kaur-15-ene-3alpha,7beta,19-triol 19-acetate 12311081 Click to see 362.50 unknown https://doi.org/10.1007/S10600-010-9458-Z
[(1R,2S,4S,5S,6R,9S,10S,13R)-2,6-dihydroxy-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate 11906032 Click to see 362.50 unknown https://doi.org/10.1007/S10600-010-9458-Z
[5-(Hydroxymethyl)-5,9,14-trimethyl-2-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl] acetate 12315547 Click to see 346.50 unknown https://doi.org/10.1007/S10600-010-9458-Z
Candol B 101289732 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO 288.50 unknown https://doi.org/10.1007/S10600-010-9458-Z
CID 12311082 12311082 Click to see 362.50 unknown https://doi.org/10.1007/S10600-010-9458-Z
CID 12315541 12315541 Click to see 304.50 unknown https://doi.org/10.1007/S10600-010-9458-Z
ent-16-Kauren-19-ol 529650 Click to see 288.50 unknown https://doi.org/10.1007/S10600-010-9458-Z
Sideridiol 12315540 Click to see 304.50 unknown https://doi.org/10.1007/S10600-010-9458-Z
Siderol 12315548 Click to see 346.50 unknown https://doi.org/10.1007/S10600-010-9458-Z
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1016/0031-9422(95)00601-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1002/(SICI)1099-1026(199609)11:5<315::AID-FFJ594>3.0.CO;2-B
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1016/0031-9422(95)00601-X
Npc254770 12302222 Click to see 222.37 unknown https://doi.org/10.1016/0031-9422(95)00601-X
> 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/10.1016/0031-9422(95)00601-X
(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/10.1016/0031-9422(95)00601-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(+)-Bicyclogermacrene 5315347 Click to see 204.35 unknown https://doi.org/10.1016/0031-9422(95)00601-X
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see 204.35 unknown https://doi.org/10.1016/0031-9422(95)00601-X
> 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/10.1002/(SICI)1099-1026(199609)11:5<315::AID-FFJ594>3.0.CO;2-B
https://doi.org/10.1016/0031-9422(95)00601-X
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1002/(SICI)1099-1026(199609)11:5<315::AID-FFJ594>3.0.CO;2-B
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,5R,8R,9R,10R,13R,14R,17R)-17-[(4E)-6-hydroxy-6-methylhepta-1,4-dien-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 9955042 Click to see 442.70 unknown via CMAUP database
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown via CMAUP database
Yamogenin 441900 Click to see 414.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-6-[(1S,2S,3'S,4S,5'R,6S,7S,8R,9S,12S,13R,16S)-3'-hydroxy-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 102155845 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CO9)CO)O 901.00 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-6-[(1S,2S,3'S,4S,5'S,6S,7S,8R,9S,12S,13R,16S)-3'-hydroxy-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 102155844 Click to see 901.00 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'S,6S,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 16204183 Click to see 1015.20 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 21603983 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'S,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 16204068 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
(3beta,25S)-Spirost-5-en-3-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside 441901 Click to see 722.90 unknown via CMAUP database
3-O-[alpha-L-ramnopyranosyl(1 to 2)]-O-[alpha-L-ramnopyranosyl(1 to 4)]-O-beta-D-galactopyranosid(1)]-(25S)-spirost-5-ene-3beta-ol 10653210 Click to see 869.00 unknown via CMAUP database
Asperin 21603986 Click to see 1015.20 unknown via CMAUP database
CID 16204180 16204180 Click to see 722.90 unknown via CMAUP database
CID 16204181 16204181 Click to see 869.00 unknown via CMAUP database
Dioscin 119245 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
Methylprotodioscin 11263254 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC 1063.20 unknown via CMAUP database
Progenin II 44429638 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1 722.90 unknown via CMAUP database
Prosapogenin A 11061578 Click to see 722.90 unknown via CMAUP database
Protodioscin 441891 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1049.20 unknown via CMAUP database
Pseudoprotodioscin 21637110 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC8C7C(=C(O8)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O 1031.20 unknown via CMAUP database
Trigonelloside C 441899 Click to see 1049.20 unknown via CMAUP database
Trillin 11827970 Click to see 576.80 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
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 via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Trichormamide B 118711962 Click to see 1446.70 unknown https://doi.org/10.1007/S10600-010-9458-Z
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-O-beta-D-mannopyranosyl-alpha-D-mannopyranose 5288769 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
Gal(a1-6)a-Man 11724912 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O)O 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
beta-D-Manp-(1->4)-beta-D-Manp-(1->4)-beta-D-Manp 5287808 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)O)O 504.40 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
(1R,2S,4S,5S,9R,10S,13R,14S,16R)-5-(hydroxymethyl)-5,9-dimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-2-ol 162917970 Click to see 306.40 unknown https://doi.org/10.1007/S10600-010-9458-Z
[(1R,2S,4S,5S,9R,10S,13R,14S,16R)-5-(hydroxymethyl)-5,9-dimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-2-yl] acetate 163088281 Click to see 348.50 unknown https://doi.org/10.1007/S10600-010-9458-Z
[5-(Hydroxymethyl)-5,9-dimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-2-yl] acetate 163088280 Click to see CC(=O)OC1CC2C(CCCC2(C3C14CC(CC3)C5C4O5)C)(C)CO 348.50 unknown https://doi.org/10.1007/S10600-010-9458-Z
5-(Hydroxymethyl)-5,9-dimethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-2-ol 162917969 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C5C4O5)O)C)CO 306.40 unknown https://doi.org/10.1007/S10600-010-9458-Z

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