Details Top

Internal ID UUID643febe13878f141478184
Scientific name Salvia pratensis
Authority L.
First published in Sp. Pl. : 25 (1753)

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.

Salvia pratensis (L.)—commonly called meadow clary—has been used in traditional European practice mainly as an aromatic infusion and occasionally as a poultice. In the Czech Republic and Poland, decoctions of the above‑ground herb were taken to ease coughs and as a mild expectorant, while infusions of leaves and flowering tops were used as carminatives and for digestive “wind” according to Hobhouse (1986). In Italy (Trentino–Alto Adige/South Tyrol), a leaf infusion was drunk for sore throat and mouth irritation, with some herbalists also preparing compresses of the same material for inflamed eyes; these uses are noted in Zanetti et al. (2013). In Austria, a traditional poultice of crushed leaves was applied to minor wounds and bruises, as recorded by Vogl et al. (2013), and in Hungary a mild leaf infusion was used as a diaphoretic for colds, following Horn and Leonhartsberger (2014). These accounts consistently involve preparations of aerial parts, especially the leaves, in water‑based infusions or decoctions, reflecting the plant’s aromatic constituents.

For a practical cold‑and‑sore‑throat infusion, use 1–2 grams of dried aerial herb (mostly leaves) per 200 milliliters of just‑boiled water, cover and steep 10–15 minutes, then strain; sip 1–2 cups daily. A 1:5 tincture can be made by macerating 20 grams of dried aerial parts in 100 milliliters of 45–50% ethanol for 2–3 weeks, shaking daily, then pressing and filtering. There are no widely accepted clinical dose limits for Salvia pratensis, but caution is advised for pregnancy and in people with sage‑allergy, and infusions should be kept modest; traditional practice suggests avoiding higher or prolonged doses.

The activity aligns with well‑known Salvia constituents: carnosic acid and carnosol from the essential‑oil fraction, together with rosmarinic acid, caffeic acid derivatives, and the flavonoids luteolin and apigenin. These polyphenols and phenolics are documented for Salvia pratensis and plausibly account for the observed mild anti‑inflammatory and antispasmodic properties in traditional infusions, while the essential‑oil monoterpenes support the aromatic and expectorant traditions.

Modern relevance is modest: extracts are occasionally present in European herbal formulas, but Salvia officinalis remains the dominant culinary and medicinal species, and meadow clary is mainly a specialty or niche item used in some regional herbal traditions today.

General Uses Top

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Common products:
Salvia pratensis yields an essential oil obtained by steam distillation of the aerial parts. Commercial profiles report major constituents including thujone, camphor, and 1,8-cineole, with other oxygenated monoterpenes such as α- and β-thujone, borneol, and camphor frequently reported in GC analyses of wild-growing material.

Fragrance and cosmetics:
The essential oil is used as a fragrance component in perfumery and aromatic compositions. Its terpene profile and odor characteristics fit standard fragrance applications. Established cosmetic standards for Salvia oil exist, and formulations using S. pratensis oil are typically aligned with general limits and requirements applied to sage oils.

Properties relevant to use:
The oil’s scent and volatility are driven by its oxygenated monoterpene content (e.g., thujone and camphor). This chemistry imparts the characteristic sharp, camphoraceous aroma used in fragrance accords. Regulatory guidance for sage oils—where thujone is a key toxicological marker—applies to Salvia oils in general.

Sustainability and sourcing:
Salvia pratensis occurs widely across Europe and is used as a source material for essential oil production from wild-collected or cultivated plants. Its perennial habit and broad ecological amplitude support moderate harvesting, but collection should follow established sustainable wild-crafting practices to maintain local populations.

Synonyms Top

Scientific name Authority First published in
Plethiosphace pratensis Opiz Seznam : 75 (1852)
Salvia barrelieri Ten. Fl. Napol. 1: 9 (1811)
Salvia ceratophylla Ten. Syll. Pl. Fl. Neapol. 21. 1831 (1831)
Salvia dubia K.Koch Linnaea 21: 657 (1849)
Salvia oblongata Schur Enum. Pl. Transsilv. : 961 (1866)
Salvia variegata Host Fl. Austriac. 1: 27 (1827)
Sclarea pratensis Mill. Gard. Dict. ed. 8 : n.º 4 (1768)
Salvia pratensis var. variegata (Waldst. & Kit. ex Willd.) Nyman Consp. Fl. Eur. 569. 1881
Salvia pratensis var. rostrata (F.W.Schmidt) Rchb.f. Icon. Fl. Germ. Helv. 18: 29. 1856
Salvia haematodes subsp. tiberina (Mauri) Nyman Consp. Fl. Eur. 569. 1881 (1881)
Salvia pratensis var. albiflora T.Durand Prodr. Fl. Belg. 3: 663. 1903
Salvia pratensis var. submollis Jakucs Ann. Hist.-Nat. Mus. Natl. Hung. n.s., 3: 90. 1953
Salvia pratensis var. nicaeensis Briq. Lab. Alp. Mar. 528. 1895
Salvia pratensis var. parviflora Lecoq & Lamotte Cat. Pl. Plateau Central 296. 1848
Salvia pratensis var. modesta Briq. Lab. Alp. Mar. 529. 1895
Gallitrichum pratense Fourr. Ann. Soc. Linn. Lyon , n.s., 17: 134 (1869)
Salvia pratensis var. caerulea Schrad. Fl. Germ. : 63 (1806)

Common names Top

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Language Common/alternative name
English meadow sage
English meadow clary
English introduced sage
Spanish plethiosphace leistneriana
Spanish gallitrichum pratense
Spanish plethiosphace pratensis
Spanish salvia barrelieri
Spanish hormigón de prados
Spanish hormigon de prados
Spanish gallocresta rustica
Spanish salvia variegata
Arabic قصعين حقلي
Azerbaijani Çəmənlik adaçayı
Belarusian Шалфей лугавы
Bulgarian ливаден конски босилек
Catalan sauge des prés
Czech šalvěj luční
Welsh saets y waun
Welsh clari'r maes
Danish eng-salvie
German wiesen-salbei
German wiesensalbei
German sauge des prés
Estonian aassalvei
Persian مریم چمنی
Finnish niittysalvia
French sauge des prés
French sauge des pres
Irish tormán léana
Upper Sorbian Łučna želbija
Hungarian mezei zsálya
Igbo meadow clary
Kazakh Дала шалфейі
Lithuanian sauge des prés
Lithuanian pievinis šalavijas
Latvian pļavas salvija
Macedonian полска жалфија
Macedonian ливадска жалфија
Norwegian Bokmål engsalvie
Dutch veldsalie
os Уыгæрдæны лæсыф
Polish szałwia łąkowa
Romanian salvie de câmp
Romanian salvie de camp
Russian Шалфей луговой
Slovak šalvia lúčna
Slovenian travniška kadulja
Swedish Ängssalvia
Swedish sauge des prés
Ukrainian Шавлія лучна
Walloon saedje des tchamps
Chinese 草地鼠尾草

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Salvia pratensis subsp. haematodes (L.) Arcang. Comp. Fl. Ital. , ed. 2: 429 (1894)
Salvia pratensis subsp. laciniosa (Jord.) Briq. Lab. Alp. Mar. : 525 (1895)
Salvia pratensis subsp. pozegensis (Watzl) Diklic Fl. SR Srbije 6: 450 (1974)
Salvia pratensis subsp. pratensis 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.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Romania
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Spain
  • Northern America
    • Eastern Canada
      • Ontario
    • North-central U.S.A.
      • Illinois
      • Kansas
      • South Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Massachusetts
      • Michigan
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Washington
      • Wyoming
    • South-central U.S.A.
      • New Mexico
    • Southeastern U.S.A.
      • Delaware
      • Kentucky
      • Maryland
      • Virginia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000301989
UNII 0RF2RJ6JV2
Canadensys 6448
USDA Plants SAPR2
Tropicos 17600305
INPN 120685
Flora of Italy 4674
KEW urn:lsid:ipni.org:names:457007-1
The Plant List kew-183565
Missouri Botanical Garden 281424
Open Tree Of Life 816902
Observations.org 2728
NCBI Taxonomy 49216
NBN Atlas NBNSYS0000004220
Nature Serve 2.160135
IPNI 457007-1
iNaturalist 85338
GBIF 2927007
Freebase /m/0gjg8h
WisFlora 7624
EPPO SALPR
EOL 579406
Elurikkus 7050
Calflora (Californian flora) 9412
USDA GRIN 32955
Wikipedia Salvia_pratensis

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
Chemometric Analysis Evidencing the Variability in the Composition of Essential Oils in 10 Salvia Species from Different Taxonomic Sections or Phylogenetic Clades Tomou EM, Fraskou P, Dimakopoulou K, Dariotis E, Krigas N, Skaltsa H Molecules 29-Mar-2024
PMCID:PMC11013157
doi:10.3390/molecules29071547
PMID:38611827
Saving the local tradition: ethnobotanical survey on the use of plants in Bologna district (Italy) Chiocchio I, Marincich L, Mandrone M, Trincia S, Tarozzi C, Poli F J Ethnobiol Ethnomed 12-Mar-2024
PMCID:PMC10936038
doi:10.1186/s13002-024-00664-1
PMID:38475780
Land‐use affects pollinator‐specific resource availability and pollinator foraging behaviour Birkenbach M, Straub F, Kiesel A, Ayasse M, Wilfert L, Kuppler J Ecol Evol 07-Mar-2024
PMCID:PMC10918743
doi:10.1002/ece3.11061
PMID:38455145
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
Genetic and Environmental Factors Affecting Seed Germination Šerá B, Hnilička F Plants (Basel) 08-Dec-2023
PMCID:PMC10748122
doi:10.3390/plants12244106
PMID:38140433
A Possible Perspective of Recultivation with Arbuscular Mycorrhiza-Inoculated Drought-Tolerant Herbaceous Plants Papp L, Habtemariam AA, Brandt S, Cseh P, Heller Á, Péter B, Szakály ÁP, Kiszel P, Codogno B, Bratek Z, Tóth Z Plants (Basel) 06-Dec-2023
PMCID:PMC10747347
doi:10.3390/plants12244088
PMID:38140415
In Vitro Antibacterial, Antioxidant, Anticholinesterase, and Antidiabetic Activities and Chemical Composition of Salvia balansae Mokhtar A, Souhila T, Nacéra B, Amina B, Alghonaim MI, Öztürk M, Alsalamah SA, Miara MD, Boufahja F, Bendif H Molecules 27-Nov-2023
PMCID:PMC10708212
doi:10.3390/molecules28237801
PMID:38067531
Epiphytic microflora and mycotoxin content in meadows–Is plant biodiversity affecting fungal contamination? Kolackova I, Smolkova B, Skladanka J, Kouril P, Hrudova E PLoS One 14-Sep-2023
PMCID:PMC10501618
doi:10.1371/journal.pone.0288397
PMID:37708181
Comparing Non-Thermal Plasma and Cold Stratification: Which Pre-Sowing Treatment Benefits Wild Plant Emergence? Gudyniene V, Juzenas S, Stukonis V, Mildaziene V, Ivankov A, Norkeviciene E Plants (Basel) 10-Sep-2023
PMCID:PMC10534388
doi:10.3390/plants12183220
PMID:37765384
Chemical Profile and Bioactivity Evaluation of Salvia Species from Eastern Europe Luca SV, Skalicka-Woźniak K, Mihai CT, Gradinaru AC, Mandici A, Ciocarlan N, Miron A, Aprotosoaie AC Antioxidants (Basel) 28-Jul-2023
PMCID:PMC10451821
doi:10.3390/antiox12081514
PMID:37627509
Sweet Basil between the Soul and the Table—Transformation of Traditional Knowledge on Ocimum basilicum L. in Bulgaria Ivanova T, Bosseva Y, Chervenkov M, Dimitrova D Plants (Basel) 26-Jul-2023
PMCID:PMC10420671
doi:10.3390/plants12152771
PMID:37570924
Plants cultivated for ecosystem restoration can evolve toward a domestication syndrome Conrady M, Lampei C, Bossdorf O, Hölzel N, Michalski S, Durka W, Bucharova A Proc Natl Acad Sci U S A 08-May-2023
PMCID:PMC10193954
doi:10.1073/pnas.2219664120
PMID:37155873
Features of Natural Succession of Ex-Arable Forest Steppe Grassland (from Western Romania) under the Influence of Climate Sărățeanu V, Cotuna O, Paraschivu M, Cojocariu LL, Horablaga NM, Rechițean D, Mircov VD, Sălceanu C, Urlică AA, Copăcean L Plants (Basel) 07-Mar-2023
PMCID:PMC10059065
doi:10.3390/plants12061204
PMID:36986892
Biocontrol Activity of Aromatic and Medicinal Plants and Their Bioactive Components against Soil-Borne Pathogens Greff B, Sáhó A, Lakatos E, Varga L Plants (Basel) 05-Feb-2023
PMCID:PMC9958657
doi:10.3390/plants12040706
PMID:36840053
Biosynthesis of Silver Nanoparticles Using Salvia pratensis L. Aerial Part and Root Extracts: Bioactivity, Biocompatibility, and Catalytic Potential Srećković NZ, Nedić ZP, Monti DM, D’Elia L, Dimitrijević SB, Mihailović NR, Katanić Stanković JS, Mihailović VB Molecules 01-Feb-2023
PMCID:PMC9921037
doi:10.3390/molecules28031387
PMID:36771054

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
2-Methyldecane 23415 Click to see 156.31 unknown https://doi.org/10.1055/S-2008-1074842
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
6-Hydroxy-1,1,4A-trimethyl-7-(propan-2-YL)-1,2,3,4,4A,9,10,10A-octahydrophenanthren-9-one 275529 Click to see 300.40 unknown https://doi.org/10.1055/S-2006-957435
7-Ketoroyleanone 2751800 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2=O)(C)C)C)O 330.40 unknown https://doi.org/10.1055/S-2006-957435
Royleanone 442084 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2)(C)C)C)O 316.40 unknown https://doi.org/10.1055/S-2006-957435
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2S,3R,4S,5S,6R)-2-[2-[(1R,4R,4aR,8aS)-4-hydroxy-4,7-dimethyl-2,3,4a,5,6,8a-hexahydro-1H-naphthalen-1-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162956442 Click to see CC1=CC2C(CC1)C(CCC2C(C)(C)OC3C(C(C(C(O3)CO)O)O)O)(C)O 400.50 unknown https://doi.org/10.1055/S-2008-1074842
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
8a-[3-[5-[4-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxy-6-methyloxan-2-yl]oxycarbonyl-2-hydroxy-6b-(hydroxymethyl)-4,6a,11,11,14b-pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 74081266 Click to see 1237.30 unknown https://doi.org/10.1055/S-2008-1074842
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
kankanoside M 49788109 Click to see 330.33 unknown https://doi.org/10.1055/S-2008-1074842
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,6S,7aR,11aR,11bR,13aR,13bR)-6-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 21672671 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CC(C4(C3(CC2)C)C)O)(C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(00)97947-0
(1R,3aR,5aR,5bR,6S,7aR,9S,11aS,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-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-6,9-diol 21672679 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CC(C4(C3(CC2)C)C)O)(C)C)O)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)97947-0
3a,5a,5b,8,8,11a-Hexamethyl-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-6,9-diol 73821085 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(00)97947-0
6-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 73821081 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CC(C4(C3(CC2)C)C)O)(C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(00)97947-0
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97947-0
Germanicol 122857 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97947-0
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97947-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
methyl (E,6R)-6-[(1R,3R,6S,8S,11R,12S,13S,15R,16R,18R)-6,13-diacetyloxy-18-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methylhept-2-enoate 162863514 Click to see CC(CCC=C(C)C(=O)OC)C1CC(C2(C1(CC(C34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)O)C)C)OC(=O)C 586.80 unknown https://doi.org/10.1055/S-2008-1074842
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
[(2R,3R,5R,6R,9R,10R,11R,13R,14R,17R)-17-[(E,2R,5S)-5,6-dimethylhept-3-en-2-yl]-2,3,5,6,9-pentahydroxy-10-(hydroxymethyl)-13-methyl-2,3,4,6,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate 21609792 Click to see 536.70 unknown https://doi.org/10.1055/S-2008-1074842
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
5-[[4-Amino-5-[[1-[[1-carboxy-4-[(4-carboxy-3-methylbut-2-enoyl)-hydroxyamino]butyl]amino]-5-[(4-carboxy-3-methylbut-2-enoyl)-hydroxyamino]-1-oxopentan-2-yl]amino]-5-oxopentyl]-hydroxyamino]-3-methyl-5-oxopent-3-enoic acid 163059045 Click to see CC(=CC(=O)N(CCCC(C(=O)NC(CCCN(C(=O)C=C(C)CC(=O)O)O)C(=O)NC(CCCN(C(=O)C=C(C)CC(=O)O)O)C(=O)O)N)O)CC(=O)O 786.80 unknown https://doi.org/10.1055/S-2008-1074842
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(3aR,4R,5R,9aR,9bS)-5-acetyloxy-6,9-dimethyl-3-methylidene-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-4-yl] (2R,3R)-2,3-dimethyloxirane-2-carboxylate 162926507 Click to see 416.40 unknown https://doi.org/10.1055/S-2008-1074842
> 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 https://doi.org/10.1021/NP50048A050
https://doi.org/10.1016/S0031-9422(01)00415-0
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 https://doi.org/10.1021/NP50048A050
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Delphinidin 3-glucosylglucoside 5316496 Click to see 627.50 unknown https://doi.org/10.1021/NP50048A050
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1016/S0031-9422(01)00415-0
https://doi.org/10.1021/ACS.JNATPROD.7B00155
Tilianin 5321954 Click to see 446.40 unknown https://doi.org/10.1021/NP50048A050
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/S0031-9422(01)00415-0

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