Echinops ritro - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Echinops ritro - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID643fc7babdcf9328375585
Scientific name Echinops ritro
Authority L.
First published in Sp. Pl. : 815 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Echinops ritro var. tenuifolius DC. Prodr. 6: 524 (1837)

Common names Top

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Language Common/alternative name
English southern globethistle
Spanish cocodrilo de montpellier
Spanish cardo abadejo
Spanish cabeza de erizo
Arabic قنفذي أزرق
Azerbaijani adi toppuztikan
Bulgarian бодлив челядник
Catalan cardet de sang
Czech bělotrn modrý
Danish glatbladet tidselkugle
Danish glat tidselkugle
German ruthenische kugeldistel
Estonian sinine mesiohakas
Persian شکرتیغال جنوبی
Finnish otapallo-ohdake
French oursin bleu
French azurite
Armenian Ոզնագլխիկ սովորական
Italian cardo-pallottola coccodrillo
Japanese ルリタマアザミ
Malayalam എക്കിനോപ്സ് റിട്രോ
os Пакасæрсындз
Russian Мордовник обыкновенный
Slovak ježibaba belasá
Slovenian navadni bodoglavec
Serbian Плави чичак
Chinese 硬叶蓝刺头
Chinese 硬叶蓝刺头气新疆蓝刺头)
Chinese 禹州漏芦
Chinese 硬葉藍刺頭

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Echinops ritro subsp. meyeri (DC.) Kožuharov Bot. J. Linn. Soc. 71(1): 42 (1975)
Echinops ritro subsp. ritro Unknown
Echinops ritro subsp. ruthenicus (M.Bieb.) Nyman Consp. Fl. Eur. 2: 399 (1879)
Echinops ritro subsp. sartorianus (Boiss. & Heldr.) Kožuharov Bot. J. Linn. Soc. 71(1): 42 (1975)
Echinops ritro subsp. siculus (Strobl) Greuter Willdenowia 33(1): 58 (2003) (2003)
Echinops ritro subsp. thracicus (Velen.) Kožuharov Bot. J. Linn. Soc. 71(1): 42 (1975)

Varieties (abbr. var.) Top

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Name Authority First published in
Echinops ritro var. elbursensis (Rech.f.) Parsa Fl. Iran 10: 84 (1980)

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
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Turkmenistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Siberia
      • Altay
      • West Siberia
    • Western Asia
      • East Aegean Islands
      • Iran
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Central European Russia
      • East European Russia
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Germany
      • Hungary
      • Poland
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • France
      • Spain
  • Northern America
    • Northeastern U.S.A.
      • New York
    • Northwestern U.S.A.
      • Washington

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000016873
USDA Plants ECRI
Tropicos 2702402
INPN 95709
Flora of Italy 6144
KEW urn:lsid:ipni.org:names:202652-1
The Plant List gcc-116324
Missouri Botanical Garden 277311
PFAF Echinops ritro
PaleoBotany 71928
Open Tree Of Life 643726
Observations.org 80206
NCBI Taxonomy 41571
Nature Serve 2.161682
IPNI 202652-1
iNaturalist 162202
GBIF 5392950
Freebase /m/03qhprd
EPPO ECPRI
EOL 467551
Elurikkus 4476
USDA GRIN 14848
Wikipedia Echinops_ritro

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
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Antioxidant and Hepatoprotective Potential of Echinops ritro L. Extracts on Induced Oxidative Stress In Vitro/In Vivo Zheleva-Dimitrova D, Simeonova R, Kondeva-Burdina M, Savov Y, Balabanova V, Zengin G, Petrova A, Gevrenova R Int J Mol Sci 10-Jun-2023
PMCID:PMC10298086
doi:10.3390/ijms24129999
PMID:37373147
In Vitro and In Silico Investigation of Polyacetylenes from Launaea capitata (Spreng.) Dandy as Potential COX-2, 5-LOX, and BchE Inhibitors Abdel Bar FM, Mira A, Foudah AI, Alossaimi MA, Alkanhal SF, Aldaej AM, ElNaggar MH Molecules 17-Apr-2023
PMCID:PMC10145610
doi:10.3390/molecules28083526
PMID:37110760
Characterization of the Slovene Autochthonous Rose Hybrid Rosa pendulina × spinosissima (Rosa reversa Waldst. and Kit) Using Biochemical Patterns of the Plant Blossoms Kunc N, Hudina M, Bavcon J, Vreš B, Luthar Z, Gostinčar K, Mikulič-Petkovšek M, Osterc G, Ravnjak B Plants (Basel) 22-Jan-2023
PMCID:PMC9920101
doi:10.3390/plants12030505
PMID:36771590
Biochemical Analyses of Bioactive Extracts from Plants Native to Lampedusa, Sicily Minor Island Di Lecce R, Mérindol N, Pérez MG, Karimzadegan V, Berthoux L, Boari A, Zidorn C, Vurro M, Surico G, Desgagné-Penix I, Evidente A Plants (Basel) 09-Dec-2022
PMCID:PMC9788634
doi:10.3390/plants11243447
PMID:36559555
Effects of Prickly Burnet (Sarcopoterium spinosum (L.) Spach.) Control and Sheep Grazing on Hay Yield and Quality on Gökçeada Island, Turkey Alatürk F, Gökkuş A, Özaslan Parlak A, Baytekin H, Tölü C Animals (Basel) 08-Nov-2022
PMCID:PMC9686760
doi:10.3390/ani12223073
PMID:36428300
Thiophenes—Naturally Occurring Plant Metabolites: Biological Activities and In Silico Evaluation of Their Potential as Cathepsin D Inhibitors Ibrahim SR, Omar AM, Bagalagel AA, Diri RM, Noor AO, Almasri DM, Mohamed SG, Mohamed GA Plants (Basel) 17-Feb-2022
PMCID:PMC8877444
doi:10.3390/plants11040539
PMID:35214871
Medicinal Plants Used by Traditional Healers in Algeria: A Multiregional Ethnobotanical Study Belhouala K, Benarba B Front Pharmacol 29-Nov-2021
PMCID:PMC8666619
doi:10.3389/fphar.2021.760492
PMID:34912221
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
Fructans as Immunomodulatory and Antiviral Agents: The Case of Echinacea Dobrange E, Peshev D, Loedolff B, Van den Ende W Biomolecules 16-Oct-2019
PMCID:PMC6843407
doi:10.3390/biom9100615
PMID:31623122
Cleonis pigra (Scopoli, 1763) (Coleoptera: Curculionidae: Lixinae): Morphological Re-Description of the Immature Stages, Keys, Tribal Comparisons and Biology Skuhrovec J, Volovnik S, Gosik R, Stejskal R, Trnka F Insects 30-Sep-2019
PMCID:PMC6836170
doi:10.3390/insects10100325
PMID:31574984
The resilience of perennial grasses under two climate scenarios is correlated with carbohydrate metabolism in meristems Volaire F, Morvan-Bertrand A, Prud’homme MP, Benot ML, Augusti A, Zwicke M, Roy J, Landais D, Picon-Cochard C J Exp Bot 26-Sep-2019
PMCID:PMC6913708
doi:10.1093/jxb/erz424
PMID:31557303
Technological Aspects of the Production of Fructo and Galacto-Oligosaccharides. Enzymatic Synthesis and Hydrolysis Martins GN, Ureta MM, Tymczyszyn EE, Castilho PC, Gomez-Zavaglia A Front Nutr 31-May-2019
PMCID:PMC6554340
doi:10.3389/fnut.2019.00078
PMID:31214595
Novel Substituted Thiophenes and Sulf-Polyacetylene Ester from Echinops ritro L. Li LB, Xiao GD, Xiang W, Yang X, Cao KX, Huang RS Molecules 22-Feb-2019
PMCID:PMC6413031
doi:10.3390/molecules24040805
PMID:30813374
An update of the Worldwide Integrated Assessment (WIA) on systemic insecticides. Part 2: impacts on organisms and ecosystems Pisa L, Goulson D, Yang EC, Gibbons D, Sánchez-Bayo F, Mitchell E, Aebi A, van der Sluijs J, MacQuarrie CJ, Giorio C, Long EY, McField M, Bijleveld van Lexmond M, Bonmatin JM Environ Sci Pollut Res Int 09-Nov-2017
PMCID:PMC7921077
doi:10.1007/s11356-017-0341-3
PMID:29124633

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
methyl (2R)-2-[(1R,2R,4aS,8S,8aR)-1,8-dihydroxy-4a,8-dimethyl-5-oxo-2,3,4,8a-tetrahydro-1H-naphthalen-2-yl]propanoate 162845835 Click to see CC(C1CCC2(C(C1O)C(C=CC2=O)(C)O)C)C(=O)OC 296.36 unknown https://doi.org/10.1002/HLCA.200900361
methyl 2-(1,8-dihydroxy-4a,8-dimethyl-5-oxo-2,3,4,8a-tetrahydro-1H-naphthalen-2-yl)propanoate 45359922 Click to see CC(C1CCC2(C(C1O)C(C=CC2=O)(C)O)C)C(=O)OC 296.36 unknown https://doi.org/10.1002/HLCA.200900361
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-[(4aR,8R,8aR)-8-hydroxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]prop-2-enoic acid 137795140 Click to see CC12CCCC(C1CC(CC2)C(=C)C(=O)O)(C)O 252.35 unknown https://doi.org/10.1016/S0031-9422(00)82392-4
Costic acid 6451579 Click to see CC12CCCC(=C)C1CC(CC2)C(=C)C(=O)O 234.33 unknown https://doi.org/10.1016/S0031-9422(00)82392-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,5aS,6R,9aR,9bR)-6-hydroxy-5a,9-dimethyl-3-methylidene-3a,4,5,6,9a,9b-hexahydrobenzo[g][1]benzofuran-2,7-dione 162911590 Click to see CC1=CC(=O)C(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O 262.30 unknown https://doi.org/10.1002/HLCA.200900361
(3aR,5aS,6S,9aR,9bR)-6-hydroxy-5a,9-dimethyl-3-methylidene-4,5,6,7,9a,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one 124708200 Click to see CC1=CCC(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O 248.32 unknown https://doi.org/10.1002/HLCA.200900361
(3R,3aR,5aS,6S,8S,9aR,9bR)-6,8-dihydroxy-3,5a-dimethyl-9-methylidene-3a,4,5,6,7,8,9a,9b-octahydro-3H-benzo[g][1]benzofuran-2-one 163025229 Click to see CC1C2CCC3(C(CC(C(=C)C3C2OC1=O)O)O)C 266.33 unknown https://doi.org/10.1002/HLCA.200900361
6-Hydroxy-5a,9-dimethyl-3-methylidene-3a,4,5,6,9a,9b-hexahydrobenzo[g][1]benzofuran-2,7-dione 162911589 Click to see CC1=CC(=O)C(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O 262.30 unknown https://doi.org/10.1002/HLCA.200900361
6,8-dihydroxy-3,5a-dimethyl-9-methylidene-3a,4,5,6,7,8,9a,9b-octahydro-3H-benzo[g][1]benzofuran-2-one 5256436 Click to see CC1C2CCC3(C(CC(C(=C)C3C2OC1=O)O)O)C 266.33 unknown https://doi.org/10.1002/HLCA.200900361
Barrelin 619337 Click to see CC1C2CCC3(C(C2OC1=O)C(C=CC3=O)(C)O)C 264.32 unknown https://doi.org/10.1002/HLCA.200900361
Sesquiterpene lactone CP-1 331391 Click to see CC1=CCC(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O 248.32 unknown https://doi.org/10.1002/HLCA.200900361
Vulgarin 94253 Click to see CC1C2CCC3(C(C2OC1=O)C(C=CC3=O)(C)O)C 264.32 unknown https://doi.org/10.1002/HLCA.200900361
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3aR,6aS,8R,9R,9aS,9bS)-8-hydroxy-9-methyl-3,6-dimethylidene-4,5,6a,7,8,9,9a,9b-octahydro-3aH-azuleno[4,5-b]furan-2-one 163069974 Click to see CC1C(CC2C1C3C(CCC2=C)C(=C)C(=O)O3)O 248.32 unknown https://doi.org/10.1002/HLCA.200900361
(3S,3aR,6aS,8R,9R,9aS,9bR)-8-hydroxy-3,9-dimethyl-6-methylidene-3,3a,4,5,6a,7,8,9,9a,9b-decahydroazuleno[4,5-b]furan-2-one 162886957 Click to see CC1C(CC2C1C3C(CCC2=C)C(C(=O)O3)C)O 250.33 unknown https://doi.org/10.1002/HLCA.200900361
(3S,3aR,6aS,9R,9aS,9bR)-3,9-dimethyl-6-methylidene-3a,4,5,6a,7,9,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2,8-dione 162872679 Click to see CC1C2CCC(=C)C3CC(=O)C(C3C2OC1=O)C 248.32 unknown https://doi.org/10.1002/HLCA.200900361
(3S,3aS,6aS,8S,9S,9aS,9bS)-3,8-dihydroxy-3,9-dimethyl-6-methylidene-4,5,6a,7,8,9,9a,9b-octahydro-3aH-azuleno[4,5-b]furan-2-one 162975533 Click to see CC1C(CC2C1C3C(CCC2=C)C(C(=O)O3)(C)O)O 266.33 unknown https://doi.org/10.1002/HLCA.200900361
(6aS,8S,9R,9aS,9bS)-8-hydroxy-3-(hydroxymethyl)-9-methyl-6-methylidene-4,5,6a,7,8,9,9a,9b-octahydroazuleno[4,5-b]furan-2-one 162959259 Click to see CC1C(CC2C1C3C(=C(C(=O)O3)CO)CCC2=C)O 264.32 unknown https://doi.org/10.1002/HLCA.200900361
3,8-dihydroxy-3,9-dimethyl-6-methylidene-4,5,6a,7,8,9,9a,9b-octahydro-3aH-azuleno[4,5-b]furan-2-one 162975532 Click to see CC1C(CC2C1C3C(CCC2=C)C(C(=O)O3)(C)O)O 266.33 unknown https://doi.org/10.1002/HLCA.200900361
8-Hydroxy-3-(hydroxymethyl)-9-methyl-6-methylidene-4,5,6a,7,8,9,9a,9b-octahydroazuleno[4,5-b]furan-2-one 162959258 Click to see CC1C(CC2C1C3C(=C(C(=O)O3)CO)CCC2=C)O 264.32 unknown https://doi.org/10.1002/HLCA.200900361
8-Hydroxy-3,9-dimethyl-6-methylidene-3,3a,4,5,6a,7,8,9,9a,9b-decahydroazuleno[4,5-b]furan-2-one 14314689 Click to see CC1C(CC2C1C3C(CCC2=C)C(C(=O)O3)C)O 250.33 unknown https://doi.org/10.1002/HLCA.200900361
8-hydroxy-9-methyl-3,6-dimethylidene-4,5,6a,7,8,9,9a,9b-octahydro-3aH-azuleno[4,5-b]furan-2-one 155036897 Click to see CC1C(CC2C1C3C(CCC2=C)C(=C)C(=O)O3)O 248.32 unknown https://doi.org/10.1002/HLCA.200900361
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)82392-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)82392-4
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 https://doi.org/10.1016/S0031-9422(00)82392-4
> Organoheterocyclic compounds / Bi- and oligothiophenes
[(2R)-2-acetyloxy-4-(5-thiophen-2-ylthiophen-2-yl)but-3-ynyl] acetate 163006171 Click to see CC(=O)OCC(C#CC1=CC=C(S1)C2=CC=CS2)OC(=O)C 334.40 unknown https://doi.org/10.1021/JF052702J
2-Thiophen-2-yl-5-[2-[2-[2-(5-thiophen-2-ylthiophen-2-yl)ethynyl]cyclobutyl]ethynyl]thiophene 14825794 Click to see C1CC(C1C#CC2=CC=C(S2)C3=CC=CS3)C#CC4=CC=C(S4)C5=CC=CS5 432.70 unknown https://doi.org/10.1021/JF052702J
https://doi.org/10.1016/S0031-9422(00)95194-X
2,2':5',2''-Terthiophene 65067 Click to see C1=CSC(=C1)C2=CC=C(S2)C3=CC=CS3 248.40 unknown https://doi.org/10.1021/JF052702J
5-(3-Buten-1-ynyl)-2,2'-bithiophene 70813 Click to see C=CC#CC1=CC=C(S1)C2=CC=CS2 216.30 unknown https://doi.org/10.1021/JF052702J
5-(3,4-Diacetoxybut-1-ynyl)-2,2'-bithiophene 440404 Click to see CC(=O)OCC(C#CC1=CC=C(S1)C2=CC=CS2)OC(=O)C 334.40 unknown https://doi.org/10.1021/JF052702J
5-(4-Hydroxybut-1-ynyl)-2,2'-bithiophene 440357 Click to see C1=CSC(=C1)C2=CC=C(S2)C#CCCO 234.30 unknown https://doi.org/10.1021/JF052702J
5-(4-Isovaleryloxy-1-butynyl)-2,2'-bithiophene 9840009 Click to see CC(C)CC(=O)OCCC#CC1=CC=C(S1)C2=CC=CS2 318.50 unknown https://doi.org/10.1021/JF052702J
5,5''-[[(1S)-Cyclobutane-1alpha,2beta-diyl]bisethynylene]bis(2,2'-bithiophene) 14825795 Click to see C1CC(C1C#CC2=CC=C(S2)C3=CC=CS3)C#CC4=CC=C(S4)C5=CC=CS5 432.70 unknown https://doi.org/10.1016/S0031-9422(00)95194-X
https://doi.org/10.1021/JF052702J
Isocardopatine 76330007 Click to see C1CC(C1C#CC2=CC=C(S2)C3=CC=CS3)C#CC4=CC=C(S4)C5=CC=CS5 432.70 unknown https://doi.org/10.1021/JF052702J
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3S,3aR,8S,9R,9aR,9bR)-8-hydroxy-6-(hydroxymethyl)-3,9-dimethyl-3a,4,5,7,8,9,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 163093359 Click to see CC1C(CC2=C(CCC3C(C(=O)OC3C12)C)CO)O 266.33 unknown https://doi.org/10.1002/HLCA.200900361
8-hydroxy-6-(hydroxymethyl)-3,9-dimethyl-3a,4,5,7,8,9,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 163093358 Click to see CC1C(CC2=C(CCC3C(C(=O)OC3C12)C)CO)O 266.33 unknown https://doi.org/10.1002/HLCA.200900361
> Organoheterocyclic compounds / Quinolines and derivatives
Echinorine 442898 Click to see C[N+]1=CC=C(C2=CC=CC=C21)OC 174.22 unknown https://doi.org/10.1016/S0031-9422(00)82392-4
https://doi.org/10.1002/RECL.19000191104
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
2,4-Diamino-3-(4-methoxy-1-methylquinolin-4-yl)-4-oxobutanoic acid 71438787 Click to see CN1C=CC(C2=CC=CC=C21)(C(C(C(=O)O)N)C(=O)N)OC 305.33 unknown https://doi.org/10.1016/S0031-9422(00)82392-4
Echinopsine 6748 Click to see CN1C=CC(=O)C2=CC=CC=C21 159.18 unknown https://doi.org/10.1002/RECL.19000191104
https://doi.org/10.1016/S0031-9422(00)82392-4
> Organoheterocyclic compounds / Thiophenes / 2,5-disubstituted thiophenes
4-[5-(1,3-Pentadiynyl)-2-thienyl]-3-butyne-1-ol 14890287 Click to see CC#CC#CC1=CC=C(S1)C#CCCO 214.28 unknown https://doi.org/10.1021/JF052702J
> 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/10.1002/RECL.19000191104
https://doi.org/10.3724/SP.J.1009.2012.00084
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/10.3724/SP.J.1009.2012.00084
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.3724/SP.J.1009.2012.00084
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 154496169 Click to see C1=CC(=CC=C1C2=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/10.1002/RECL.19000191104
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1002/RECL.19000191104
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 125528541 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1002/RECL.19000191104
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 26339717 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1002/RECL.19000191104
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-[4-[(3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxyphenyl]-3,5-dihydroxy-7-[(3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 162985503 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)OC5C(C(C(C(O5)C)O)O)OC6C(C(C(CO6)O)O)O)O)O)O)O 710.60 unknown https://doi.org/10.1002/HLCA.200900361
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 154496342 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1002/RECL.19000191104
> 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 https://doi.org/10.1002/RECL.19000191104

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