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Gaillardia aristata

Gaillardia aristata - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fd23bc166e244876609
Scientific name Gaillardia aristata
Authority Pursh
First published in Fl. Amer. Sept. 2: 573 (1813)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Gaillardia perennis Loisel. Herb. Gen. Amat. 5: t. 328.
Gaillardia rustica Cass. Dict. Sci. Nat., ed. 2. 18: 20 (1821)
Polatherus scaber Raf. Amer. Monthly Mag. & Crit. Rev. 2(4): 268 (1818)
Gaillardia richardsonii hort. ex Kew Bull. 3: 41. 1889
Gaillardia aristata var. foliacea Lunell Amer. Midl. Naturalist 2: 122 (1911)
Gaillardia aristata var. foliosa Lunell
Gaillardia bracteosa Standl. Smithsonian Misc. Collect. 56, n.° 33: 2 (1912)
Virgilia grandiflora Nutt. in Fras. Cat. n. 87. 1813
Gaillardia bicolor Pursh Fl. Amer. Sept. (Pursh) ii. 572; Hook. Fl. Bor. Am. i. 315. 1813
Gaillardia hallii Rydb. N. Amer. Fl. 34(2): 135 (1915)
Gaillardia roezlii Regel Gartenflora (1875) 289.

Common names Top

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Language Common/alternative name
English common gaillardia
English common perennial gaillardia
English common blanketflower
English blanket flower
Arabic غيردية سفوية
Belarusian гайлардыя асцюкаватая
Czech kokarda osinatá
Estonian ohtene mõrsjalill
Persian رعنای زیبای معمولی
Lithuanian akuotuotoji gailiardija
Macedonian обична кокарда
Russian Гайлардия остистая
Russian Гайярдия остистая
Slovak kokarda ostitá
Chinese 宿根天人菊
Chinese 车轮菊

Subspecies (abbr. subsp./ssp.) Top

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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
  • Africa
    • Macaronesia
      • Azores
    • South Tropical Africa
      • Mozambique
    • Southern Africa
      • Namibia
  • Asia-temperate
    • Middle Asia
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • India
    • Indo-China
      • Vietnam
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Belgium
      • Czechoslovakia
      • Hungary
      • Poland
    • Southeastern Europe
      • Italy
      • Romania
    • Southwestern Europe
      • France
      • Spain
  • Northern America
    • North-central U.S.A.
      • Minnesota
      • North Dakota
      • South Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Massachusetts
      • New Hampshire
      • New York
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Washington
      • Wyoming
    • Southwestern U.S.A.
      • Utah
    • Subarctic America
      • Northwest Territorie
      • Yukon
    • Western Canada
      • Alberta
      • British Columbia
      • Manitoba
      • Saskatchewan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000121921
Canadensys 3171
USDA Plants GAAR
Tropicos 2700780
INPN 99217
KEW urn:lsid:ipni.org:names:317387-2
The Plant List gcc-8312
Open Tree Of Life 893837
Observations.org 118051
NCBI Taxonomy 55624
NBN Atlas NHMSYS0000458929
Nature Serve 2.138481
IPNI 317387-2
iNaturalist 77183
GBIF 5387859
Freebase /m/03qntdy
WisFlora 3655
EPPO GAIAR
EOL 467374
Elurikkus 4819
Calflora (Californian flora) 3649
USDA GRIN 70935
Wikipedia Gaillardia_aristata

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
Impacts of Soil Properties on Species Diversity and Structure in Alternanthera philoxeroides-Invaded and Native Plant Communities Wu H, Liu Y, Zhang T, Xu M, Rao B Plants (Basel) 25-Apr-2024
PMCID:PMC11085794
doi:10.3390/plants13091196
PMID:38732411
In vitro activities and mechanisms of action of anti-cancer molecules from African medicinal plants: a systematic review Adico MD, Bayala B, Zoure AA, Lagarde A, Bazie JT, Traore L, Buñay J, Yonli AT, Djigma F, Bambara HA, Baron S, Simporé J, Lobaccaro JM Am J Cancer Res 15-Mar-2024
PMCID:PMC10998760
doi:10.62347/AUHB5811
PMID:38590420
Oil-Contaminated Soil Remediation with Biodegradation by Autochthonous Microorganisms and Phytoremediation by Maize (Zea mays) Wojtowicz K, Steliga T, Kapusta P, Brzeszcz J Molecules 17-Aug-2023
PMCID:PMC10459520
doi:10.3390/molecules28166104
PMID:37630356
Beyond Cleansing: Ecosystem Services Related to Phytoremediation Guidi Nissim W, Castiglione S, Guarino F, Pastore MC, Labra M Plants (Basel) 24-Feb-2023
PMCID:PMC10005053
doi:10.3390/plants12051031
PMID:36903892
Biological Activity of Selenium and Its Impact on Human Health Genchi G, Lauria G, Catalano A, Sinicropi MS, Carocci A Int J Mol Sci 30-Jan-2023
PMCID:PMC9917223
doi:10.3390/ijms24032633
PMID:36768955
Pest categorisation of Icerya aegyptiaca Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Papachristos D, MacLeod A EFSA J 09-Jan-2023
PMCID:PMC9827230
doi:10.2903/j.efsa.2023.7739
PMID:36628331
A critical analysis of sources, pollution, and remediation of selenium, an emerging contaminant Ullah H, Lun L, Rashid A, Zada N, Chen B, Shahab A, Li P, Ali MU, Lin S, Wong MH Environ Geochem Health 16-Aug-2022
PMCID:PMC9379879
doi:10.1007/s10653-022-01354-1
PMID:35972610
The Modulation of Melanogenesis in B16 Cells Upon Treatment with Plant Extracts and Isolated Plant Compounds Merecz-Sadowska A, Sitarek P, Kowalczyk T, Zajdel K, Kucharska E, Zajdel R Molecules 07-Jul-2022
PMCID:PMC9324663
doi:10.3390/molecules27144360
PMID:35889231
Effects of Water Availability on Leaf Trichome Density and Plant Growth and Development of Shepherdia ×utahensis Chen JJ, Sun Y, Kopp K, Oki L, Jones SB, Hipps L Front Plant Sci 18-May-2022
PMCID:PMC9158747
doi:10.3389/fpls.2022.855858
PMID:35665162
First Population Study on Winter Breeding Monarch Butterflies, Danaus plexippus (Lepidoptera: Nymphalidae) in the Urban South Bay of San Francisco, California James DG, Schaefer MC, Krimmer Easton K, Carl A Insects 18-Oct-2021
PMCID:PMC8537757
doi:10.3390/insects12100946
PMID:34680715
Pest categorisation of Phenacoccus solenopsis Bragard C, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Gregoire J, Malumphy C, Campese C, Czwienczek E, Kertesz V, Maiorano A, MacLeod A EFSA J 18-Aug-2021
PMCID:PMC8371560
doi:10.2903/j.efsa.2021.6801
PMID:34429782
Extracts Prepared from a Canadian Toxic Plant Induce Light-Dependent Perinuclear Vacuoles in Human Cells Tuescher JM, Beck CR, Spencer L, Yeremy B, Shi Y, Andersen RJ, Golsteyn RM Toxins (Basel) 12-Feb-2021
PMCID:PMC7917763
doi:10.3390/toxins13020138
PMID:33673235
Selenium Toxicity in Plants and Environment: Biogeochemistry and Remediation Possibilities Hasanuzzaman M, Bhuyan MH, Raza A, Hawrylak-Nowak B, Matraszek-Gawron R, Nahar K, Fujita M Plants (Basel) 04-Dec-2020
PMCID:PMC7762096
doi:10.3390/plants9121711
PMID:33291816
Autotoxicity of Diterpenes Present in Leaves of Cistus ladanifer L. Chaves Lobón N, Ferrer de la Cruz I, Alías Gallego JC Plants (Basel) 22-Jan-2019
PMCID:PMC6410244
doi:10.3390/plants8020027
PMID:30678267
Emerging Anti-Mitotic Activities and Other Bioactivities of Sesquiterpene Compounds upon Human Cells Bosco A, Golsteyn RM Molecules 13-Mar-2017
PMCID:PMC6155193
doi:10.3390/molecules22030459
PMID:28335397

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
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
[3-hydroxy-4-[(2R)-2-hydroxy-1-(2-methylpropanoyloxy)propan-2-yl]phenyl]methyl 2-methylpropanoate 162916505 Click to see CC(C)C(=O)OCC1=CC(=C(C=C1)C(C)(COC(=O)C(C)C)O)O 338.40 unknown https://doi.org/10.1002/CBER.19691020319
[3-Hydroxy-4-[2-hydroxy-1-(2-methylpropanoyloxy)propan-2-yl]phenyl]methyl 2-methylpropanoate 162916504 Click to see CC(C)C(=O)OCC1=CC(=C(C=C1)C(C)(COC(=O)C(C)C)O)O 338.40 unknown https://doi.org/10.1002/CBER.19691020319
> Benzenoids / Phenol esters
[4-[(2R)-2-methyloxiran-2-yl]-3-(2-methylpropanoyloxy)phenyl]methyl (2S)-2-methylbutanoate 163003973 Click to see CCC(C)C(=O)OCC1=CC(=C(C=C1)C2(CO2)C)OC(=O)C(C)C 334.40 unknown https://doi.org/10.1002/CBER.19691020319
[4-[(2R)-2-methyloxiran-2-yl]-3-(2-methylpropanoyloxy)phenyl]methyl 2-methylpropanoate 162953457 Click to see CC(C)C(=O)OCC1=CC(=C(C=C1)C2(CO2)C)OC(=O)C(C)C 320.40 unknown https://doi.org/10.1002/CBER.19691020319
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(1S)-1-[(3aR,6S,7R,8aR)-5,7-dimethyl-3-methylidene-2-oxo-6,7,8,8a-tetrahydro-3aH-cyclohepta[b]furan-6-yl]-3-hydroxypropyl] acetate 14137167 Click to see CC1CC2C(C=C(C1C(CCO)OC(=O)C)C)C(=C)C(=O)O2 308.40 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
Pulchellin B 261574 Click to see CC(=O)OC1CC2(CC3C(CC(=C)C2C1O)OC(=O)C3=C)C 306.40 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones
(3aR,5R,6S,8R,8aS,9S,9aS)-6,8,9-trihydroxy-5,8a-dimethyl-1-methylidene-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,5-b]furan-2-one 163080696 Click to see CC1CC2C(C(C3(C1C(CC3O)O)C)O)C(=C)C(=O)O2 282.33 unknown https://doi.org/10.1080/14786419.2011.606219
(6-acetyloxy-8-hydroxy-5,8a-dimethyl-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,5-b]furan-9-yl) 2-methylbut-2-enoate 162916916 Click to see CC=C(C)C(=O)OC1C2C(CC(C3C1(C(CC3OC(=O)C)O)C)C)OC(=O)C2=C 406.50 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
(6,9-dihydroxy-5,8a-dimethyl-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,7-b]furan-8-yl) 3-methylbutanoate 162962147 Click to see CC1CC2C(C(C3(C1C(CC3OC(=O)CC(C)C)O)C)O)C(=C)C(=O)O2 366.40 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
(9-acetyloxy-4,8-dihydroxy-5,8a-dimethyl-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,5-b]furan-6-yl) 2-methylbut-2-enoate 75072283 Click to see CC=C(C)C(=O)OC1CC(C2(C1C(C(C3C(C2OC(=O)C)C(=C)C(=O)O3)O)C)C)O 422.50 unknown https://doi.org/10.1016/0031-9422(83)83059-3
(9-acetyloxy-4,8-dihydroxy-5,8a-dimethyl-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,5-b]furan-6-yl) 2-methylbutanoate 162981129 Click to see CCC(C)C(=O)OC1CC(C2(C1C(C(C3C(C2OC(=O)C)C(=C)C(=O)O3)O)C)C)O 424.50 unknown https://doi.org/10.1016/0031-9422(83)83059-3
[(3aR,4R,5S,5aS,6S,8R,8aS,9R,9aS)-4,8,9-trihydroxy-5,8a-dimethyl-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,5-b]furan-6-yl] (Z)-2-methylbut-2-enoate 14137163 Click to see CC=C(C)C(=O)OC1CC(C2(C1C(C(C3C(C2O)C(=C)C(=O)O3)O)C)C)O 380.40 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
[(3aR,4R,5S,5aS,6S,8R,8aS,9R,9aS)-9-acetyloxy-4,8-dihydroxy-5,8a-dimethyl-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,5-b]furan-6-yl] (2R)-2-methylbutanoate 162981130 Click to see CCC(C)C(=O)OC1CC(C2(C1C(C(C3C(C2OC(=O)C)C(=C)C(=O)O3)O)C)C)O 424.50 unknown https://doi.org/10.1016/0031-9422(83)83059-3
[(3aR,4R,5S,5aS,6S,8R,8aS,9R,9aS)-9-acetyloxy-4,8-dihydroxy-5,8a-dimethyl-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,5-b]furan-6-yl] (Z)-2-methylbut-2-enoate 14733787 Click to see CC=C(C)C(=O)OC1CC(C2(C1C(C(C3C(C2OC(=O)C)C(=C)C(=O)O3)O)C)C)O 422.50 unknown https://doi.org/10.1016/0031-9422(83)83059-3
[(3aR,5R,5aS,6S,8R,8aR,9S,9aS)-6,9-dihydroxy-5,8a-dimethyl-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,7-b]furan-8-yl] 3-methylbutanoate 162962148 Click to see CC1CC2C(C(C3(C1C(CC3OC(=O)CC(C)C)O)C)O)C(=C)C(=O)O2 366.40 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
[(3aR,5R,5aS,6S,8R,8aS,9S,9aR)-6-acetyloxy-8-hydroxy-5,8a-dimethyl-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,5-b]furan-9-yl] (Z)-2-methylbut-2-enoate 162916917 Click to see CC=C(C)C(=O)OC1C2C(CC(C3C1(C(CC3OC(=O)C)O)C)C)OC(=O)C2=C 406.50 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
[(3aR,5R,5aS,6S,8R,8aS,9S,9aR)-6-hydroxy-5,8a-dimethyl-8-(3-methylbutanoyloxy)-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,5-b]furan-9-yl] (Z)-2-methylbut-2-enoate 163017544 Click to see CC=C(C)C(=O)OC1C2C(CC(C3C1(C(CC3O)OC(=O)CC(C)C)C)C)OC(=O)C2=C 448.50 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
[6-hydroxy-5,8a-dimethyl-8-(3-methylbutanoyloxy)-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,5-b]furan-9-yl] 2-methylbut-2-enoate 163017541 Click to see CC=C(C)C(=O)OC1C2C(CC(C3C1(C(CC3O)OC(=O)CC(C)C)C)C)OC(=O)C2=C 448.50 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
Spathulin 12442910 Click to see CC1C2C(CC(C2(C(C3C(C1OC(=O)C)OC(=O)C3=C)OC(=O)C)C)O)O 382.40 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
(3aR,8aS,9aR)-6,8-dihydroxy-5,8a-dimethyl-1-methylidene-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,5-b]furan-2-one 366039 Click to see CC1CC2C(CC3(C1C(CC3O)O)C)C(=C)C(=O)O2 266.33 unknown https://doi.org/10.1080/14786419.2011.606219
5,7-Dihydroxy-4a,8-dimethyl-3-methylenedecahydroazuleno[6,5-b]furan-2(3H)-one 98168 Click to see CC1CC2C(CC3(C1C(CC3O)O)C)C(=C)C(=O)O2 266.33 unknown https://doi.org/10.1080/14786419.2011.606219
https://doi.org/10.1016/S0031-9422(00)84954-7
Pulchellin 50990212 Click to see CC1CC2C(CC3(C1C(CC3O)O)C)C(=C)C(=O)O2 266.33 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(6-Hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-7-yl) acetate 162843075 Click to see CC(=O)OC1CC2(CC3C(CC2C(=C)C1O)C(=C)C(=O)O3)C 306.40 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
(7-Hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-6-yl) acetate 314622 Click to see CC(=O)OC1C(CC2(CC3C(CC2C1=C)C(=C)C(=O)O3)C)O 306.40 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
[(3aR,4aR,6R,7R,8aR,9aR)-7-hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-6-yl] acetate 101297637 Click to see CC(=O)OC1C(CC2(CC3C(CC2C1=C)C(=C)C(=O)O3)C)O 306.40 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
[(3aR,4aR,6R,7R,8aS,9aR)-6-hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-7-yl] acetate 101297634 Click to see CC(=O)OC1CC2(CC3C(CC2C(=C)C1O)C(=C)C(=O)O3)C 306.40 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
Pulchellin C 14241091 Click to see CC12CC(C(C(=C)C1CC3C(C2)OC(=O)C3=C)O)O 264.32 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
Sesquiterpene lactone TS-8 314621 Click to see CC12CC(C(C(=C)C1CC3C(C2)OC(=O)C3=C)O)O 264.32 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Florilenalin 442243 Click to see CC1(CC(C2C1CC3C(CC2=C)OC(=O)C3=C)O)O 264.32 unknown https://doi.org/10.1016/S0031-9422(00)84954-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1080/14786419.2011.606219
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/10.1080/14786419.2011.606219
> 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/10.1080/14786419.2011.606219
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1080/14786419.2011.606219
> 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/10.1080/14786419.2011.606219
https://doi.org/10.1002/CBER.19691020319
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-dihydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-5-[(2R,3R,4R,5S)-3,4-dihydroxy-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]-5-hydroxy-7-methoxychromen-4-one 162964344 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)C4C(C(C(C(O4)CO)OC5C(C(C(CO5)OC6C(C(C(C(O6)CO)O)O)O)O)O)O)O 756.70 unknown https://doi.org/10.1016/0031-9422(83)83059-3
2-(3,4-Dihydroxyphenyl)-6-[5-[3,4-dihydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]-5-hydroxy-7-methoxychromen-4-one 162964343 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)C4C(C(C(C(O4)CO)OC5C(C(C(CO5)OC6C(C(C(C(O6)CO)O)O)O)O)O)O)O 756.70 unknown https://doi.org/10.1016/0031-9422(83)83059-3
6-beta-D-Glucopyranosyl-4',5-dihydroxy-7-methoxyflavone 369636 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1016/0031-9422(83)83059-3
Swertisin 124034 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1016/0031-9422(83)83059-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2R,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 163011125 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(83)83059-3
Homo-orientin 5382105 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(83)83059-3
Luteolin 6-C-glucoside 8-C-arabinoside 3549960 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(83)83059-3
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(83)83059-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(83)83059-3
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5318574 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(83)83059-3
Quercetin 3-alloside 12304327 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1002/CBER.19691020319
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxyphenyl)-3-methoxy-7-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 163088873 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC)C4=CC=C(C=C4)O)O)O)O)O 446.40 unknown https://doi.org/10.1080/14786419.2011.606219
7-[(2R,3R,4R,5S)-3,4-dihydroxy-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(4-hydroxyphenyl)-5-[[(2S,3R,4R,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl]-6-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 163073764 Click to see C1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)CC5C(C(C(C(O5)O)O)O)O)C6C(C(C(C(O6)CO)O)O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O 872.80 unknown https://doi.org/10.1016/0031-9422(83)83059-3
7-[3,4-Dihydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(4-hydroxyphenyl)-5-[(3,4,5,6-tetrahydroxyoxan-2-yl)methyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 163073763 Click to see C1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)CC5C(C(C(C(O5)O)O)O)O)C6C(C(C(C(O6)CO)O)O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O 872.80 unknown https://doi.org/10.1016/0031-9422(83)83059-3

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