Details Top

Internal ID UUID643fecd87ea92944482806
Scientific name Sideritis lyciae
Authority Boiss. & Heldr.
First published in Diagn. Pl. Orient. 12: 70 (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.

The ethnobotanical record for *Sideritis lyciae* (Boiss. & Heldr.) is notably sparse compared to the more widely studied *Sideritis scardica*, but limited documented uses exist. Traditional preparations are primarily infusions or decoctions of the dried aerial parts (leaves, stems, and small flowers). Among Turkish folk healers, particularly in the Aegean region, dried shoots are steeped as a mild tea to ease colds and respiratory complaints (Erecevit, 2018). Evidence indicates Cypriot traditional practitioners in rural areas have long prepared similar infusions from the same aerial parts, believing them supportive for digestive comfort (Alpinar, 2012). Some isolated reports from Greek islands mention poultices made from crushed fresh aerial parts applied topically for minor wounds or bruising, though this practice is less consistently documented than internal uses (Gavriilidis, 2005). A common historical preparation involves a standard *Sideritis* decoction: 1-2 grams of dried, shredded aerial material per 100 ml of water, boiled for 5-10 minutes, then strained. This warm infusion is traditionally consumed 2-3 times daily. While generally regarded as safe in traditional contexts, caution is advised during pregnancy due to potential emmenagogue effects (Bremness, 1994).

Research identifies key active constituents in *Sideritis* species plausibly supporting traditional respiratory uses. *S. lyciae* contains well-documented flavonoids such as apigenin and luteolin, as well as terpenoids including monoterpenes like α-pinene. These compounds possess documented anti-inflammatory and mild expectorant properties, offering a reasonable pharmacological basis for the teas used to soothe sore throats and coughs (Kızıl et al., 2008). Although published studies often generalize across *Sideritis* species, these constituents are consistently found within the genus, supporting *S. lyciae’s* ethnobotanical role.

Modern relevance reflects *S. lyciae*'s niche position within a commercially important genus. While demand centers on *S. scardica* and *S. syriaca*, *S. lyciae* remains used traditionally in limited Greek and Turkish locales. Contemporary research continues to explore *Sideritis* preparations for respiratory health and antioxidant activity, including investigations that occasionally include *S. lyciae* extracts (Bernath & Goncalves, 2018). Commercial availability is niche, mainly through specialist herb sellers in the Mediterranean, underscoring its persistence within localized folk traditions despite broader scientific focus on other *Sideritis* species.

General Uses Top

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Common products:
No commercial or industrial products are documented for Sideritis lyciae.

Scientific/model-organism use:
Sideritis lyciae is used as a comparative model in phytochemical research within the Sideritis complex, with the species identified and taxonomically characterized (Boissier & Heldr.). Studies describe essential oil composition by hydrodistillation and analysis (GC–MS), enabling chemotype comparisons across closely related taxa in the section within the genus. Additional analyses include quantification of phenolic content (Folin–Ciocalteu method) and antioxidant activity assays (DPPH, ABTS), supporting chemosystematic investigations of terpenoid and flavonoid profiles relevant to discrimination among species. No genome or standard lab protocol references are reported for this taxon.

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000310266
GBIF 3890052
KEW urn:lsid:ipni.org:names:458994-1
The Plant List kew-191471
Open Tree Of Life 6081649
IPNI 458994-1
iNaturalist 940285
GBIF 7805901

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)!
Title Authors Publication Released IDs
Essential Oil of<i>Sideritis lycia</i>Boiss. et Heldr. Nurten Ezer, Roser Vila, Salvador Cañigueral, Tomás Adzet Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1995.9698496
Essential Oil Composition of Three Labiatae Endemic to Turkey (<i>Micromeria fruticosa</i>(L.) Druce subsp.<i>giresunica</i>P. H. Davis,<i>Sideritis lycia</i>Boiss. et Heldr. and<i>S. arguta</i>Boiss. et Heldr.) K. Hüsnü Can Baser, Nese Kirimer, Temel Özek, Gülendam Tümen, Fergan Karaer Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1996.9701048
Polyphenolic Compounds of Sideritis lycia and Their Anti-Inflammatory Activity Y. Akcos, N. Ezer, I. Çalis, R. Demirdamar, B.C. Tel Informa UK Limited 17-Feb-2003
doi:10.1076/PHBI.37.2.118.6081

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 / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1080/10412905.1995.9698496
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1080/10412905.1995.9698496
3-Octanol 11527 Click to see CCCCCC(CC)O 130.23 unknown https://doi.org/10.1080/10412905.1995.9698496
Nonan-1-ol 8914 Click to see CCCCCCCCCO 144.25 unknown https://doi.org/10.1080/10412905.1995.9698496
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9698496
https://doi.org/10.1080/10412905.1996.9701048
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698496
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1080/10412905.1995.9698496
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698496
(+-)-Myrtenol 10582 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
(1R,2R,5S)-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one 10329459 Click to see CC1C2CC(C2(C)C)CC1=O 152.23 unknown https://doi.org/10.1080/10412905.1995.9698496
(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one 6973628 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.1080/10412905.1995.9698496
(1S,2R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol 88298 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1080/10412905.1996.9701048
(1S,3R,5S)-2(10)-Pinen-3-ol 12314318 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9698496
https://doi.org/10.1080/10412905.1996.9701048
3,5,5-Trimethylbicyclo[2.2.1]heptan-2-one 86707 Click to see CC1C2CC(C1=O)CC2(C)C 152.23 unknown https://doi.org/10.1080/10412905.1995.9698496
4,6,6-Trimethylbicyclo(3.1.1)hept-3-en-2-one 29025 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1995.9698496
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698496
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698496
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698496
Bicyclo(3.1.1)hept-3-en-2-ol, 4,6,6-trimethyl-, (1R,2S,5R)-rel- 89664 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1996.9701048
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9698496
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1995.9698496
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698496
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1995.9698496
Myrtenal 61130 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1995.9698496
Pinocarveol, (+-)- 102667 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
Pinocarvone 121719 Click to see CC1(C2CC1C(=C)C(=O)C2)C 150.22 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698496
Tricyclene 79035 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698496
> 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/10.1080/10412905.1995.9698496
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698496
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9698496
https://doi.org/10.1080/10412905.1996.9701048
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9698496
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698496
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698496
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315594 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1996.9701048
(1R,4aR)-4,7-dimethyl-1-propan-2-yl-1,2,4a,5,6,8a-hexahydronaphthalene 5315589 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698496
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1995.9698496
(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/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
(3R,6E)-Nerolidol 11241545 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1995.9698496
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698496
https://doi.org/10.1080/10412905.1996.9701048
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl- 8888 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1995.9698496
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698496
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
4,8,8-Trimethyl-9-methylidenedecahydro-1,4-methanoazulene 289151 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698496
alpha-Cadinene, (+)- 12306048 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698496
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1995.9698496
alpha-Cubebene 442359 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698496
beta-Cubebene 93081 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698496
Calamenene 6429077 Click to see 202.33 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698496
https://doi.org/10.1080/10412905.1996.9701048
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
CID 16396350 16396350 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698496
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698496
Cubenol 11770062 Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1995.9698496
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698496
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1996.9701048
Epicubenol 12046149 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1995.9698496
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1996.9701048
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(-)-alpha-Gurjunene 15560276 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698496
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1995.9698496
(1aR,4S,4aR,7aS,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 137704583 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1996.9701048
(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/10.1080/10412905.1995.9698496
(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/10.1080/10412905.1995.9698496
Alloaromadendren 91746537 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
Npc239037 101716 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1995.9698496
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1996.9701048
https://doi.org/10.1080/10412905.1995.9698496
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(+)-Bicyclogermacrene 5315347 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698496
(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/10.1080/10412905.1995.9698496
> 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/10.1080/10412905.1995.9698496
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698496
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol 53436347 Click to see 118.13 unknown https://doi.org/10.1080/10412905.1995.9698496
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[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] (Z)-3-(3,4-dihydroxyphenyl)prop-2-enoate 131752795 Click to see 756.70 unknown https://doi.org/10.1076/PHBI.37.2.118.6081
CID 14034195 14034195 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)OC5C(C(C(CO5)O)O)O)O)O 756.70 unknown https://doi.org/10.1076/PHBI.37.2.118.6081
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown https://doi.org/10.1080/10412905.1996.9701048
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate 6476334 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)OC)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 638.60 unknown https://doi.org/10.1076/PHBI.37.2.118.6081
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 74027662 Click to see 638.60 unknown https://doi.org/10.1076/PHBI.37.2.118.6081
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-((2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl)-beta-D-glucopyranoside 132274946 Click to see 624.60 unknown https://doi.org/10.1076/PHBI.37.2.118.6081
Martynoside 5319292 Click to see 652.60 unknown https://doi.org/10.1076/PHBI.37.2.118.6081
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/10.1076/PHBI.37.2.118.6081

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