Details Top

Internal ID UUID643fece04f8f8791548787
Scientific name Sideritis trojana
Authority Bornm.
First published in Magyar Bot. Lapok 31: 141 (1932)

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 peoples of western Anatolia and nearby Aegean islands, the dried aerial parts of Sideritis trojana are used for an everyday herbal infusion known as “mountain tea.” Women harvest the herb in the Taurus and Kaz Dağ regions to dry for home use, and small tea suppliers market the herb in local markets and kiosks. Ethnobotanical surveys of medicinal plant use in northern and western Anatolia consistently list S. trojana among plants prepared as an infusion to “cool” the body and support comfort during common colds and flu-like episodes, while residents of nearby Greek islands use the same preparation as a pleasant, everyday beverage (Ecevit et al., 2012; Karaman, 2012; Polunin, 1980). Folk practitioners in Greece and Turkey recommend the same aqueous preparation for sore throats and mild coughs, and older village informants recall that the dried herb was also used to make a short decoction when a stronger, warming drink was desired (Shahat et al., 2009; Polunin, 1980).

For a mild herbal tea, use 2–3 grams of dried aerial parts in 200 milliliters of near‑boiling water; cover and infuse for 8–10 minutes, then strain. This “mountain tea” is often taken one cup at a time. For a short decoction, simmer the same dose in 200 milliliters of water for 10 minutes and cool before drinking (Ecevit et al., 2012; Polunin, 1980). For a 1:5 ethanol tincture, macerate 20 grams of dried aerial parts in 100 milliliters of 45% ethanol for 2–3 weeks, shaking daily, then filter. Because the plant’s safety profile has not been fully established, keep alcohol tinctures to very modest amounts. As a general precaution, traditional teas are used intermittently and not as a daily beverage, and they are best avoided during pregnancy unless advised by a qualified practitioner (Brinker, 2010).

The dried herb’s aroma and taste are associated with known secondary metabolites in Sideritis: flavonoids such as apigenin and luteolin, several phenylpropanoids including chlorogenic acid, and essential‑oil constituents like 1,8‑cineole, pinenes, camphor, and α‑terpineol (Çarıkçı and Kılıçel, 2012; Heinrich et al., 2004; Gülçin, 2011). These compounds are well reported in Sideritis species and plausibly contribute to the plant’s traditional value as an aromatic, comforting infusion.

Sideritis trojana remains common in local markets and household pantries across Turkey and the eastern Aegean, and it has also attracted modern research on its volatile oils (Çarıkçı and Kılıçel, 2012). Alongside wild‑harvested tea supplies, small‑scale cultivated stocks now enter the market, preserving the plant’s role as a gentle, everyday herbal tea.

General Uses Top

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**Common products:**
Sideritis trojana is cultivated and harvested for its essential oil, used in the fragrance industry for perfumery and aromatherapy applications. The oil is typically extracted via steam distillation of aerial parts (leaves and stems) and exhibits a herbaceous, slightly floral aroma.

**Industrial and craft applications:**
Beyond fragrance, the species has limited documented non-fragrance industrial uses. Its stiff stems may be utilized for basic landscaping applications such as soil stabilization due to the plant's adaptation to mountainous terrains.

**Food and beverages (non-medicinal):**
While primarily known in traditional contexts, S. trojana is commercially processed as a flavoring ingredient in certain European herbal beverage blends, particularly in Greek-style herbal teas. The dried aerial parts are used directly as a flavoring agent without health claims.

**Fragrance and cosmetics:**
The essential oil is the primary commercial product. It is incorporated into soaps, detergents, and cosmetics (e.g., scented creams) at low concentrations. Key aromatic constituents documented include α-pinene, β-pinene, limonene, and sesquiterpenes, contributing to its characteristic scent profile.

**Properties relevant to use:**
The essential oil’s aroma profile (monoterpene hydrocarbons like α-pinene and sesquiterpenes) enables its fragrance use. The plant’s adaptation to nutrient-poor soils influences cultivation yield, but chemical composition remains consistent.

**Standards and regulation:**
Essential oil production aligns with general standards for aromatic plants, such as ISO 9235 for aromatic natural raw materials. Food/beverage use as a flavoring ingredient adheres to EU regulations on novel foods where applicable.

**Sustainability and sourcing:**
Overharvesting from wild populations poses conservation risks, particularly in its native Turkish habitats. Sustainable sourcing requires controlled cultivation. Rural economies benefit from harvesting, but sustainable practices are crucial to prevent habitat degradation.

Synonyms Top

No known synonyms.

Common names Top

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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-0000310508
Tropicos 50211437
KEW urn:lsid:ipni.org:names:459122-1
The Plant List kew-191701
Open Tree Of Life 465619
NCBI Taxonomy 703113
IPNI 459122-1
iNaturalist 940250
GBIF 3888471
CMAUP NPO11342

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
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
Cobalt: An Essential Micronutrient for Plant Growth? Hu X, Wei X, Ling J, Chen J Front Plant Sci 16-Nov-2021
PMCID:PMC8635114
doi:10.3389/fpls.2021.768523
PMID:34868165
Transcriptome-Wide Identification of WRKY Transcription Factor and Functional Characterization of RgWRKY37 Involved in Acteoside Biosynthesis in Rehmannia glutinosa Wang F, Li X, Zuo X, Li M, Miao C, Zhi J, Li Y, Yang X, Liu X, Xie C Front Plant Sci 29-Sep-2021
PMCID:PMC8511629
doi:10.3389/fpls.2021.739853
PMID:34659306
Phytotoxic Potential and Phenolic Profile of Extracts from Scrophularia striata Mousavi SS, Karami A, Haghighi TM, Alizadeh S, Maggi F Plants (Basel) 11-Jan-2021
PMCID:PMC7827524
doi:10.3390/plants10010135
PMID:33440883
Assessment of the Antimicrobial, Antioxidant, and Antiproliferative Potential of Sideritis raeseri subps. raeseri Essential Oil Mitropoulou G, Sidira M, Skitsa M, Tsochantaridis I, Pappa A, Dimtsoudis C, Proestos C, Kourkoutas Y Foods 01-Jul-2020
PMCID:PMC7404406
doi:10.3390/foods9070860
PMID:32630203
Iridoid, phenylethanoid and flavonoid glycosides from Sideritis trojana. Kirmizibekmez H, Ariburnu E, Masullo M, Festa M, Capasso A, Yesilada E, Piacente S Fitoterapia 01-Jan-2012
doi:10.1016/J.FITOTE.2011.10.003
PMID:22024633
Phytochemical Analysis of Some Sideritis Species of Turkey T. Kilic, Ya. K. Yildiz, A. C. Goren, G. Tumen, G. Topcu Springer Science and Business Media LLC 13-Jan-2004
doi:10.1023/B:CONC.0000011119.53554.9C
Diterpenes from Sideritis theezans Pietro Venturella, Aurora Bellino, Franco Piozzi Elsevier BV 12-Feb-2003
doi:10.1016/S0031-9422(00)98662-X

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 / Prenol lipids / Diterpenoids
(3S,4aS,4bS,7S,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-3-ol 162855918 Click to see CC1(CC(CC2(C1CCC3=CC(CCC32)(C)C=C)C)O)C 288.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-3-ol 162855917 Click to see CC1(CC(CC2(C1CCC3=CC(CCC32)(C)C=C)C)O)C 288.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(5,5,9-Trimethyl-14-methylidene-2-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 14890425 Click to see 330.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
(5,5,9,14-Tetramethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-2-yl) acetate 163059730 Click to see 346.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
(5,5,9,14-Tetramethyl-2-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl) acetate 13855333 Click to see CC1=CC23CC1CCC2C4(CCCC(C4CC3OC(=O)C)(C)C)C 330.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
[(1R,2S,4R,9R,10S,13R)-5,5,9,14-tetramethyl-2-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl] acetate 162993466 Click to see CC1=CC23CC1CCC2C4(CCCC(C4CC3OC(=O)C)(C)C)C 330.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
[(1S,2R,4S,9S,10R,13S,14R,16S)-5,5,9,14-tetramethyl-15-oxapentacyclo[11.3.1.01,10.04,9.014,16]heptadecan-2-yl] acetate 163059731 Click to see 346.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
[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/10.1023/B:CONC.0000011119.53554.9C
5-(Hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-2-ol 13858160 Click to see 304.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
Candol A acetate 14890426 Click to see CC(=O)OC1CC2C(CCCC2(C3C14CC(CC3)C(=C)C4)C)(C)C 330.50 unknown https://doi.org/10.1016/S0031-9422(00)98662-X
https://doi.org/10.1023/B:CONC.0000011119.53554.9C
CID 12315541 12315541 Click to see 304.50 unknown https://doi.org/10.1016/S0031-9422(00)98662-X
https://doi.org/10.1023/B:CONC.0000011119.53554.9C
Sideridiol 12315540 Click to see 304.50 unknown https://doi.org/10.1023/B:CONC.0000011119.53554.9C
Siderol 12315548 Click to see 346.50 unknown https://doi.org/10.1016/S0031-9422(00)98662-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[(2R,3S,4S,5R,6S)-6-[[(1S,4aS,5R,7aR)-5-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,7a-dihydro-1H-cyclopenta[c]pyran-4a-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 25135705 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC34C=COC(C3C(=CC4O)CO)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O 670.60 unknown https://doi.org/10.1016/J.FITOTE.2011.10.003
[(2S,3R,4S,5R,6R)-2-[[(1S,4aS,5R,7aR)-5-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,7a-dihydro-1H-cyclopenta[c]pyran-4a-yl]oxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 25135704 Click to see 670.60 unknown https://doi.org/10.1016/J.FITOTE.2011.10.003
[(3R,4R,5R,6S)-6-[[(1S,4aR,5S,7aS)-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-5-yl]oxy]-4,5-dihydroxyoxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 102445639 Click to see 624.60 unknown via CMAUP database
[3,4,5-trihydroxy-6-[[5-hydroxy-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,7a-dihydro-1H-cyclopenta[c]pyran-4a-yl]oxy]oxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 74392283 Click to see 670.60 unknown https://doi.org/10.1016/J.FITOTE.2011.10.003
[3,5-dihydroxy-2-[[5-hydroxy-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,7a-dihydro-1H-cyclopenta[c]pyran-4a-yl]oxy]-6-(hydroxymethyl)oxan-4-yl] 3-(4-hydroxyphenyl)prop-2-enoate 74392282 Click to see 670.60 unknown https://doi.org/10.1016/J.FITOTE.2011.10.003
2-[[5-hydroxy-7-(hydroxymethyl)-4a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,7a-dihydro-1H-cyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 15560475 Click to see C1=COC(C2C1(C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 524.50 unknown https://doi.org/10.1016/J.FITOTE.2011.10.003
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown via CMAUP database
Melittoside 11968737 Click to see C1=COC(C2C1(C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 524.50 unknown https://doi.org/10.1016/J.FITOTE.2011.10.003
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Desrhamnosylverbascosaponin 102445401 Click to see 927.10 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Catalpol 91520 Click to see 362.33 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-[4-(hydroxymethyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 13965334 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)CO 346.33 unknown https://doi.org/10.1016/J.FITOTE.2011.10.003
Di-O-Methylcrenatin 10736338 Click to see 346.33 unknown https://doi.org/10.1016/J.FITOTE.2011.10.003
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4R,5R,6R)-4-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 6444244 Click to see 770.70 unknown https://doi.org/10.1016/J.FITOTE.2011.10.003
[4-[4,5-Dihydroxy-6-methyl-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 73156275 Click to see 770.70 unknown https://doi.org/10.1016/J.FITOTE.2011.10.003
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
{6-[2-(3,4-Dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 73323377 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/J.FITOTE.2011.10.003
Acteoside;Kusaginin;TJC160 354009 Click to see 624.60 unknown https://doi.org/10.1016/J.FITOTE.2011.10.003
Isoacteoside 6476333 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/J.FITOTE.2011.10.003
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/J.FITOTE.2011.10.003
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Saccatoside 15736668 Click to see CC1C(C(C(C(O1)OC2C3C=COC(C3C4(C2O4)CO)OC5C(C(C(C(O5)CO)O)O)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O 654.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> 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
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4R,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[5,8-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 21576581 Click to see 652.60 unknown https://doi.org/10.1016/J.FITOTE.2011.10.003
[6-[2-[5,8-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 73802680 Click to see 652.60 unknown https://doi.org/10.1016/J.FITOTE.2011.10.003
[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.FITOTE.2011.10.003
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13093776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
7-(alpha-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one 12304095 Click to see 432.40 unknown via CMAUP database
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.FITOTE.2011.10.003
Hesperidin 10621 Click to see 610.60 unknown via CMAUP database
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Apigenin trimethyl ether 79730 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC 312.30 unknown via CMAUP database

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