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Internal ID UUID643ff27d85d42026344534
Scientific name Carex fraseriana
Authority Ker Gawl.
First published in Bot. Mag. 33: t. 1391 (1811)

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Synonyms Top

Scientific name Authority First published in
Carex fraseri Andrews Bot. Repos. 10: t. 639 (1811)
Carex lagopus Muhl. Descr. Gram. : 265 (1817)
Cymophyllus fraseri Mack. Ill. Fl. N. U.S. , ed. 2, 1: 441 (1913)
Olamblis fraseri (Andrews) Raf. Good Book : 26 (1840)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Northeastern U.S.A.
      • Pennsylvania
      • West Virginia
    • Southeastern U.S.A.
      • Georgia
      • Kentucky
      • Maryland
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000346813
Tropicos 9906784
KEW urn:lsid:ipni.org:names:274065-2
Open Tree Of Life 8144
NCBI Taxonomy 100288
IPNI 274065-2
iNaturalist 471431
GBIF 2731126
USDA GRIN 415454

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 CentralĀ®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
First study on in vitro antiviral and virucidal effects of flavonoids against feline infectious peritonitis virus at the early stage of infection Triratapiban C, Lueangaramkul V, Phecharat N, Pantanam A, Lekcharoensuk P, Theerawatanasirikul S Vet World 26-Mar-2023
PMCID:PMC10082729
doi:10.14202/vetworld.2023.618-630
PMID:37041840
Treatment Effects of Natural Products on Inflammatory Bowel Disease In Vivo and Their Mechanisms: Based on Animal Experiments Zhou Y, Wang D, Yan W Nutrients 18-Feb-2023
PMCID:PMC9967064
doi:10.3390/nu15041031
PMID:36839389
A new strategy for osteoarthritis therapy: Inhibition of glycolysis Tan C, Li L, Han J, Xu K, Liu X Front Pharmacol 10-Nov-2022
PMCID:PMC9685317
doi:10.3389/fphar.2022.1057229
PMID:36438808
Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T Molecules 09-Sep-2022
PMCID:PMC9501561
doi:10.3390/molecules27185858
PMID:36144591
Flavonoids as Potential Antiviral Agents for Porcine Viruses Zhang X, Chen S, Li X, Zhang L, Ren L Pharmaceutics 26-Aug-2022
PMCID:PMC9501777
doi:10.3390/pharmaceutics14091793
PMID:36145539
Taxonomic implications of the flavonoids of Cymophyllus fraseri (Cyperaceae) Robert H. Johnson, James W. Wallace Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(88)90056-7

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
> 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/10.1016/0305-1978(88)90056-7
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/10.1016/0305-1978(88)90056-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
6-beta-D-glucopyranosyl-3',4',5-trihydroxy-7-methoxyflavone 44258368 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)O)O)O 462.40 unknown https://doi.org/10.1016/0305-1978(88)90056-7
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/10.1016/0305-1978(88)90056-7
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/0305-1978(88)90056-7
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/0305-1978(88)90056-7
Swertiajaponin 442659 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)O)O)O 462.40 unknown https://doi.org/10.1016/0305-1978(88)90056-7
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/10.1016/0305-1978(88)90056-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257674 Click to see C1=CC(=CC=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 594.50 unknown https://doi.org/10.1016/0305-1978(88)90056-7
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,4S,5R)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 44257662 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/0305-1978(88)90056-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/0305-1978(88)90056-7
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/0305-1978(88)90056-7
Scolymoside 5282152 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/0305-1978(88)90056-7
Tricin 7-glucoside 5322022 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 492.40 unknown https://doi.org/10.1016/0305-1978(88)90056-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown https://doi.org/10.1016/0305-1978(88)90056-7

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