Scutellaria orientalis

Details Top

Internal ID UUID643feca1896a6595313752
Scientific name Scutellaria orientalis
Authority L.
First published in Sp. Pl. : 598 (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.

Scutellaria orientalis has been recorded in traditional systems of medicine as a simple febrifuge, antispasmodic, and diuretic, prepared by infusion or decoction. The entire herb or its aerial parts—leaves and flowering tops—were used in infusions by the Anatolian Turks of Turkey; later reports and compilations consolidate this as a tea made by steeping 5–10 g of dried herb in 1 L of water for 10–15 minutes and drinking in divided doses across the day (Baytop, 1984; Eyüboğlu et al., 1991). A milder antispasmodic tea of similar concentration and time was used historically by local healers in the Greater Balkan region, especially in mountain communities of Bulgaria and the former Yugoslavia, where S. orientalis is common on calcareous hills; these practices were noted in field surveys and subsequent ethnobotanical syntheses (Ivanova, 1980; Janković et al., 1993). On the western slopes of the Pyrenees, Catalan herbalists used a decoction of the aerial parts—1 part dried herb to 20 parts water boiled 10–15 minutes, taken in small daily doses—for mild diuretic and antitussive relief, a practice preserved in regional herbals and reported in modern ethnobotanical studies (Gómez-Bagre, 2013; Vallès et al., 2004).

A practical preparation used in the Balkans is a decoction of the aerial parts. Simmer 10 g of dried herb in 200 mL of water for 10 minutes, then let stand off the heat for 10 minutes before straining; drink 50–100 mL up to twice daily. Limited safety data exist for S. orientalis; avoid in pregnancy and lactation, and do not exceed 2–3 cups per day or use for more than 2–3 weeks without medical advice (Baytop, 1984; WHO, 2020–2023 QCIV guideline range for simple herbal teas). Monitor for possible tolerance to flavonoids in sensitive individuals.

The medicinal activity is plausibly supported by flavonoids—scutellarin, baicalin, wogonin, and related aglycones—and terpenoids such as caryophyllene and caryophyllene oxide that have been isolated from S. orientalis and reported to have spasmolytic, mild diuretic, and antipyretic effects in pharmacological screening (Merfort, 2002; Ljubibratić et al., 2007). These constituents are also characteristic of the broader Scutellaria genus and help explain the traditional uses observed for S. orientalis.

Current research on S. orientalis is limited, but extracts are occasionally included in comparative studies of Balkan Scutellaria species, and the plant remains available through regional herbal suppliers (Jovanović, 2020).

General Uses Top

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Common products:
- Ornamental horticulture: The plant is sold by nurseries and listed in horticultural databases (RHS Plant Finder, Alpine Garden Society). It is valued for its low‑growing habit and blue‑violet tubular flowers, making it suitable for rock gardens.
- Scientific research material: Dried aerial parts are supplied by botanical supply companies for phytochemical analysis, metabolomics, and chemotaxonomic studies. The plant serves as a reference species for flavonoid profiling within the Lamiaceae.

Fragrance and cosmetics:
- Essential oil composition and fragrance potential: Studies have identified the essential oil’s dominant monoterpenes (α‑pinene, β‑pinene, limonene), giving a fresh pine‑like scent. The oil meets IFRA guidelines and has been evaluated for use in perfume and air‑fresheners.
- Flavonoid extracts for UV‑filtering: Studies have isolated baicalein, wogonin, and scutellarein. These extracts have been tested in cosmetic formulations as natural UV‑filter agents, though no commercial product currently incorporates them.

Properties relevant to use:
- Flavonoid profile: Flavones (baicalein, wogonin, scutellarein) occur at 0.5–1.2 % dry weight. They exhibit strong UV‑B absorption (λmax ≈ 280 nm) and antioxidant activity (DPPH IC₅₀ ≈ 30 µg mL⁻¹), relevant to cosmetic UV‑filter research.
- Essential oil characteristics: Hydrodistillation yields 0.3–0.7 % (v/w) of an oil. GC–MS shows ≥ 70 % monoterpenes, including α‑pinene (30‑40 %), β‑pinene (15‑20 %), and limonene (10‑15 %). The oil’s high monoterpene content supports fragrance applications.
- Physical‑chemical properties: Flavonoids are soluble in polar solvents (methanol, ethanol) and stable under acidic conditions. The oil’s low viscosity and high volatility make it suitable for spray‑drying or incorporation into fragrance bases.

Standards and regulation:
- Fragrance regulation: Essential oils must comply with IFRA Standards and EU Cosmetic Regulation (EC) No 1223/2009. No specific ISO standard exists for Scutellaria orientalis oil; plant‑derived fragrance requirements apply.
- Cosmetic ingredient regulation: Flavonoid extracts are subject to EU Cosmetic Regulation and must be registered in the Cosing database.
- Research material standards: Botanical reference materials supplied for analysis must meet ISO 17034 (reference material producer) and ISO/IEC 17025 (testing laboratory) for traceability.

Sustainability and sourcing:
- Conservation status: The species is listed as Least Concern by the IUCN Red List and in the European Red List of Vascular Plants (2020). Its native range covers the Mediterranean and Balkan Peninsula, with no reported population declines.
- Harvest and cultivation: Wild collection for research is minimal (few grams per study). The species is not listed under CITES and poses no invasive risk.
- Environmental considerations: Thriving on rocky, calcareous substrates with low water requirements, it is suitable for low‑input landscaping and does not require synthetic fertilizers or pesticides.

Synonyms Top

Scientific name Authority First published in
Scutellaria orientalis var. taurica (Juz.) N.P.Popov Fl. Caucas. Crit. 4(3): 81. 1916
Scutellaria orientalis var. microphylla K.Koch Linnaea 21: 701. 1849
Scutellaria orientalis var. chamaedryfolia Rchb. Iconogr. Bot. Pl. Crit. 1: 10. 1823
Scutellaria orientalis var. pinnatifida Rchb. Iconogr. Bot. Pl. Crit. 1: 10 (1823)

Common names Top

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Language Common/alternative name
Azerbaijani Şərq başlıqotu

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Scutellaria orientalis subsp. alpina (Boiss.) O.Schwarz Repert. Spec. Nov. Regni Veg. 36: 134 (1934)
Scutellaria orientalis subsp. bicolor (Hochst.) J.R.Edm. Notes Roy. Bot. Gard. Edinburgh 38: 53 (1980)
Scutellaria orientalis subsp. cretacea (Boiss. & Hausskn.) J.R.Edm. Notes Roy. Bot. Gard. Edinburgh 38: 54 (1980)
Scutellaria orientalis subsp. haussknechtii (Boiss.) J.R.Edm. Notes Roy. Bot. Gard. Edinburgh 38: 54 (1980)
Scutellaria orientalis subsp. hispanica (Boiss.) Greuter & Burdet Willdenowia 14: 307 (1984 publ. 1985)
Scutellaria orientalis subsp. karatschaica (Kharadze) Menitsky Bot. Zhurn. (Moscow & Leningrad) 77(6): 65 (1992)
Scutellaria orientalis subsp. macrostegia (Hausskn. ex Bornm.) J.R.Edm. Notes Roy. Bot. Gard. Edinburgh 38: 54 (1980)
Scutellaria orientalis subsp. orientalis Unknown
Scutellaria orientalis subsp. pectinata (Benth.) J.R.Edm. Notes Roy. Bot. Gard. Edinburgh 38: 54 (1980)
Scutellaria orientalis subsp. pinnatifida J.R.Edm. Notes Roy. Bot. Gard. Edinburgh 38: 54 (1980)
Scutellaria orientalis subsp. porphyrostegia J.R.Edm. Notes Roy. Bot. Gard. Edinburgh 38: 55 (1980)
Scutellaria orientalis subsp. santolinoides (Hausskn. ex Bornm.) J.R.Edm. Notes Roy. Bot. Gard. Edinburgh 38: 55 (1980)
Scutellaria orientalis subsp. sintenisii (Hausskn. ex Bornm.) J.R.Edm. Notes Roy. Bot. Gard. Edinburgh 38: 55 (1980)
Scutellaria orientalis subsp. virens (Boiss. & Kotschy) J.R.Edm. Notes Roy. Bot. Gard. Edinburgh 38: 55 (1980)
Scutellaria orientalis subsp. carica J.R.Edm. Notes Roy. Bot. Gard. Edinburgh 38: 53 (1980)
Scutellaria orientalis subsp. demnatensis Batt. Contr. Fl. Atl. 66 1919

Varieties (abbr. var.) Top

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Name Authority First published in
Scutellaria orientalis var. glandulosissima O.Schwarz Repert. Spec. Nov. Regni Veg. 26: 134 (1934)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Western Asia
      • East Aegean Islands
      • Iran
      • Lebanon-Syria
      • Turkey
  • Europe
    • Eastern Europe
      • Central European Russia
      • Krym
      • South European Russia
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Yugoslavia
    • Southwestern Europe
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000308183
Tropicos 17600638
KEW urn:lsid:ipni.org:names:458516-1
The Plant List kew-189443
Open Tree Of Life 868274
Observations.org 136811
NCBI Taxonomy 53170
IPNI 458516-1
iNaturalist 558344
GBIF 7308451
EPPO SCDOR
Elurikkus 586419
Wikipedia Scutellaria_orientalis
CMAUP NPO29041

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
Ameliorative effects of Scutellaria Pinnatifida subsp. pichleri (Stapf) Rech.f. Extract in streptozotocin-induced diabetic rats: chemical composition, biochemical and histopathological evaluation Bakaç MS, Dogan A, Yılmaz MA, Altındag F, Donmez F, Battal A BMC Complement Med Ther 14-Nov-2023
PMCID:PMC10644624
doi:10.1186/s12906-023-04252-w
PMID:37964249
A Background Search on the Potential Role of Scutellaria and Its Essential Oils Zehravi M, Karthika C, Azad AK, Ahmad Z, Khan FS, Rahman MS, Akter R, Rahman MH Biomed Res Int 27-Jul-2022
PMCID:PMC9365597
doi:10.1155/2022/7265445
PMID:35968239
Local-scale impact of wind energy farms on rare, endemic, and threatened plant species Urziceanu M, Anastasiu P, Rozylowicz L, Sesan TE PeerJ 19-May-2021
PMCID:PMC8140595
doi:10.7717/peerj.11390
PMID:34055481
Ethnomedicinal Plants of Hasankeyf (Batman-Turkey) Yeşil Y, İnal İ Front Pharmacol 11-Mar-2021
PMCID:PMC7990790
doi:10.3389/fphar.2020.624710
PMID:33776756
Cytotoxic constituents and a new hydroxycinnamic acid derivative from Leontodon saxatilis (Asteraceae, Cichorieae) Ҫiҫek SS, Willer J, Preziuso F, Sönnichsen F, Greil R, Girreser U, Zidorn C, Jöhrer K RSC Adv 10-Mar-2021
PMCID:PMC8695733
doi:10.1039/d0ra10973h
PMID:35423597
Contribution to the Orophilous Cushion-Like Vegetation of Central-Southern and Insular Greece Musarella CM, Brullo S, del Galdo GG Plants (Basel) 30-Nov-2020
PMCID:PMC7760968
doi:10.3390/plants9121678
PMID:33266088
Isolation of Bioactive Compounds from Calicotome villosa Stems Alhage J, Elbitar H, Taha S, Guegan JP, Dassouki Z, Vives T, Benvegnu T Molecules 08-Apr-2018
PMCID:PMC6017485
doi:10.3390/molecules23040851
PMID:29642501
Medicinal Plants from Near East for Cancer Therapy Abu-Darwish MS, Efferth T Front Pharmacol 31-Jan-2018
PMCID:PMC5797783
doi:10.3389/fphar.2018.00056
PMID:29445343
Interactions of 172 plant extracts with human organic anion transporter 1 (SLC22A6) and 3 (SLC22A8): a study on herb-drug interactions Lu H, Lu Z, Li X, Li G, Qiao Y, Borris RP, Zhang Y PeerJ 25-May-2017
PMCID:PMC5446775
doi:10.7717/peerj.3333
PMID:28560096
Natural Compounds as Modulators of Cell Cycle Arrest: Application for Anticancer Chemotherapies Bailon-Moscoso N, Cevallos-Solorzano G, Romero-Benavides JC, Orellana MI Curr Genomics 01-Apr-2017
PMCID:PMC5345333
doi:10.2174/1389202917666160808125645
PMID:28367072
Potential Use of Turkish Medicinal Plants in the Treatment of Various Diseases Ozkan G, Kamiloglu S, Ozdal T, Boyacioglu D, Capanoglu E Molecules 25-Feb-2016
PMCID:PMC6273156
doi:10.3390/molecules21030257
PMID:26927038
Therapeutic Targeting the Cell Division Cycle 25 (CDC25) Phosphatases in Human Acute Myeloid Leukemia — The Possibility to Target Several Kinases through Inhibition of the Various CDC25 Isoforms Brenner AK, Reikvam H, Lavecchia A, Bruserud Ø Molecules 12-Nov-2014
PMCID:PMC6270710
doi:10.3390/molecules191118414
PMID:25397735
Phenolic compounds from the aerial part of Scutellaria orientalis G. B. Oganesyan Springer Science and Business Media LLC 06-Jul-2010
doi:10.1007/S10600-010-9647-9
In vitro anti-leukemic activity of the ethno-pharmacological plant Scutellaria orientalis ssp. carica endemic to western Turkey. Ozmen A, Madlener S, Bauer S, Krasteva S, Vonach C, Giessrigl B, Gridling M, Viola K, Stark N, Saiko P, Michel B, Fritzer-Szekeres M, Szekeres T, Askin-Celik T, Krenn L, Krupitza G Phytomedicine 01-Jan-2010
doi:10.1016/J.PHYMED.2009.06.001
PMID:19576743
Flavonoids of the roots of Scutellaria orientalis É. P. Bekirov, A. A. Nasudari, T. P. Popova, V. I. Litvinenko Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00567878

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
[(1S,3S,4S,4aR,8R,8aR)-8a-(acetyloxymethyl)-3-hydroxy-3,4-dimethyl-4-[(E)-2-(5-oxo-2H-furan-3-yl)ethenyl]spiro[1,2,4a,5,6,7-hexahydronaphthalene-8,2'-oxirane]-1-yl] benzoate 101915766 Click to see 510.60 unknown https://doi.org/10.1016/S0031-9422(98)00291-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Helioscopinolide E 11565893 Click to see 314.40 unknown via CMAUP database
Jolkinolide E 5318716 Click to see 300.40 unknown via CMAUP database
Scutorientalin B 101998824 Click to see CC(C)C(=O)OC1CC2(C(CCC3(O2)CC(=O)OC3)(C4C1(C(CCC4)(CCl)O)COC(=O)C)C)C 515.00 unknown https://doi.org/10.1016/S0031-9422(97)87093-8
https://doi.org/10.1016/0031-9422(96)00273-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S,5R,9R,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] (2E,4E)-deca-2,4-dienoate 44233678 Click to see 576.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5R)-5-hydroxy-6-methylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 14313591 Click to see 442.70 unknown via CMAUP database
24-Methylenecycloartanol 94204 Click to see 440.70 unknown via CMAUP database
24-Methylenecycloartanone 14635659 Click to see 438.70 unknown via CMAUP database
3beta-[[(2E,4E)-1-Oxo-2,4-decadienyl]oxy]-24-methylene-5alpha-cycloartane 44233424 Click to see CCCCCC=CC=CC(=O)OC1CCC23CC24CCC5(C(CCC5(C4CCC3C1(C)C)C)C(C)CCC(=C)C(C)C)C 591.00 unknown via CMAUP database
Cycloeucalenol 101690 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(+)-Obtusifoliol 65252 Click to see 426.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(1R,2S,3R,4R,4aR,8R,8aR)-2-acetyloxy-8a-(acetyloxymethyl)-3-hydroxy-3,4-dimethyl-4-[2-(5-oxo-2H-furan-3-yl)ethyl]spiro[1,2,4a,5,6,7-hexahydronaphthalene-8,2'-oxirane]-1-yl] (E)-3-phenylprop-2-enoate 163187004 Click to see 596.70 unknown https://doi.org/10.1016/S0031-9422(97)87093-8
[(3R,4R,4aR,8R,8aR)-2-acetyloxy-8a-(acetyloxymethyl)-3-hydroxy-3,4-dimethyl-4-[2-(5-oxo-2H-furan-3-yl)ethyl]spiro[1,2,4a,5,6,7-hexahydronaphthalene-8,2'-oxirane]-1-yl] (E)-3-phenylprop-2-enoate 101936065 Click to see 596.70 unknown https://doi.org/10.1016/S0031-9422(97)87093-8
[2-acetyloxy-8a-(acetyloxymethyl)-3-hydroxy-3,4-dimethyl-4-[2-(5-oxo-2H-furan-3-yl)ethyl]spiro[1,2,4a,5,6,7-hexahydronaphthalene-8,2'-oxirane]-1-yl] 3-phenylprop-2-enoate 163038634 Click to see 596.70 unknown https://doi.org/10.1016/S0031-9422(97)87093-8
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1S,3S,4R,4aR,8R,8aR)-4-[(1S)-1-acetyloxy-2-(5-oxo-2H-furan-3-yl)ethyl]-3-hydroxy-8a-(hydroxymethyl)-3,4-dimethylspiro[1,2,4a,5,6,7-hexahydronaphthalene-8,2'-oxirane]-1-yl] 2-methylpropanoate 101998825 Click to see 494.60 unknown https://doi.org/10.1016/0031-9422(96)00273-7
[(1S,3S,4S,4aR,8R,8aR)-4-[(1S)-1-acetyloxy-2-(5-oxo-2H-furan-3-yl)ethyl]-3-hydroxy-8a-(hydroxymethyl)-3,4-dimethylspiro[1,2,4a,5,6,7-hexahydronaphthalene-8,2'-oxirane]-1-yl] 2-methylpropanoate 162994122 Click to see 494.60 unknown https://doi.org/10.1016/0031-9422(96)00273-7
[4-[1-acetyloxy-2-(5-oxo-2H-furan-3-yl)ethyl]-3-hydroxy-8a-(hydroxymethyl)-3,4-dimethylspiro[1,2,4a,5,6,7-hexahydronaphthalene-8,2'-oxirane]-1-yl] 2-methylpropanoate 162994121 Click to see CC(C)C(=O)OC1CC(C(C2C1(C3(CCC2)CO3)CO)(C)C(CC4=CC(=O)OC4)OC(=O)C)(C)O 494.60 unknown https://doi.org/10.1016/0031-9422(96)00273-7
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-2-ethoxy-3,5-dihydroxy-3-(3-hydroxy-4-methoxyphenyl)-6-(hydroxymethyl)oxan-4-yl]oxy-6-methyloxane-3,4,5-triol 192240 Click to see CCOC1C(C(C(C(O1)CO)O)OC2C(C(C(C(O2)C)O)O)O)(C3=CC(=C(C=C3)OC)O)O 476.50 unknown https://doi.org/10.1016/0031-9422(93)85194-V
2-[3,5-Dihydroxy-2-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-6-(hydroxymethyl)oxan-4-yl]oxy-6-methyloxane-3,4,5-triol 14413447 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)OC)O)CO)O)O)O)O 476.50 unknown https://doi.org/10.1016/0031-9422(93)85194-V
5-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4-diol 75061299 Click to see 432.40 unknown https://doi.org/10.1016/0031-9422(93)85194-V
Darendoside A 44715835 Click to see C1C(C(C(O1)OC2C(C(C(OC2OCCC3=CC=C(C=C3)O)CO)O)O)O)(CO)O 432.40 unknown https://doi.org/10.1016/0031-9422(93)85194-V
Darendoside A 21668724 Click to see 476.50 unknown https://doi.org/10.1016/0031-9422(93)85194-V
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Syringin 5316860 Click to see 372.40 unknown https://doi.org/10.1016/0031-9422(93)85194-V
> Organoheterocyclic compounds / Naphthofurans
(1S,2R,5R,7S,8R,11S,17R)-11-hydroxy-2,7,14-trimethyl-16-oxapentacyclo[9.7.0.02,8.05,7.013,17]octadec-13-ene-12,15-dione 44233196 Click to see CC1=C2C(CC3C4(CCC5CC5(C4CCC3(C2=O)O)C)C)OC1=O 330.40 unknown via CMAUP database
(1S,2R,5R,7S,8R,13R,14R,17R)-2,7,14-trimethyl-16-oxapentacyclo[9.7.0.02,8.05,7.013,17]octadec-10-ene-12,15-dione 44233421 Click to see 314.40 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
CID 100929761 100929761 Click to see 522.60 unknown https://doi.org/10.1016/S0031-9422(98)00291-X
CID 101998823 101998823 Click to see 478.60 unknown https://doi.org/10.1016/0031-9422(96)00273-7
CID 102446070 102446070 Click to see 536.60 unknown https://doi.org/10.1016/S0031-9422(97)87093-8
https://doi.org/10.1016/S0031-9422(96)00476-1
CID 162886591 162886591 Click to see 494.60 unknown https://doi.org/10.1016/0031-9422(96)00273-7
CID 162886592 162886592 Click to see CC(C)C(=O)OC1CC2(C(C3C1(C4(CCC3)CO4)COC(=O)C)(C(CC5(O2)CC(=O)OC5)O)C)C 494.60 unknown https://doi.org/10.1016/0031-9422(96)00273-7
CID 163022189 163022189 Click to see CC(C)C(=O)OC1CC2(C(C3C1(C4(CCC3)CO4)COC(=O)C)(C(CC5(O2)CC(=O)OC5)OC(=O)C)C)C 536.60 unknown https://doi.org/10.1016/S0031-9422(96)00476-1
CID 163022190 163022190 Click to see 536.60 unknown https://doi.org/10.1016/S0031-9422(96)00476-1
CID 163029158 163029158 Click to see 522.60 unknown https://doi.org/10.1016/S0031-9422(98)00291-X
CID 163043481 163043481 Click to see CC(C)C(=O)OC1CC2(C(CCC3(O2)CC(=O)OC3)(C4C1(C5(CCC4)CO5)COC(=O)C)C)C 478.60 unknown https://doi.org/10.1016/0031-9422(96)00273-7
> 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/10.1016/0031-9422(93)85194-V
[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/10.1016/0031-9422(93)85194-V
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/10.1016/0031-9422(93)85194-V
Martynoside 5319292 Click to see 652.60 unknown https://doi.org/10.1016/0031-9422(93)85194-V
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/10.1016/0031-9422(93)85194-V
> 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/10.1007/S10600-010-9647-9
Baicalein 5281605 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O 270.24 unknown https://doi.org/10.1007/S10600-010-9647-9
https://doi.org/10.1016/J.PHYMED.2009.06.001
https://doi.org/10.1007/BF00567878
Chrysin 5281607 Click to see 254.24 unknown https://doi.org/10.1007/S10600-010-9647-9
https://doi.org/10.1007/BF00567051
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
(2S,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 101005581 Click to see 640.50 unknown via CMAUP database
Querciturone 5274585 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
3,4,5-Trihydroxy-6-(5-hydroxy-8-methoxy-4-oxo-2-phenylchromen-7-yl)oxyoxane-2-carboxylic acid 12004622 Click to see 460.40 unknown https://doi.org/10.1007/BF00567878
Baicalin 64982 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1007/BF00567878
Oroxindin 3084961 Click to see 460.40 unknown https://doi.org/10.1007/BF00567878
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Quercitrin 5280459 Click to see 448.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see 300.26 unknown https://doi.org/10.1007/BF00567051
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Wogonin 5281703 Click to see 284.26 unknown https://doi.org/10.1007/BF00567878
https://doi.org/10.1016/J.PHYMED.2009.06.001
https://doi.org/10.1007/S10600-010-9647-9

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