Tamarixetin

Last updated
Tamarixetin
Tamarixetin.svg
Names
IUPAC name
3,3′,5,7-Tetrahydroxy-4′-methoxyflavone
Systematic IUPAC name
3,5,7-Trihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one
Other names
4'-Methylquercetin; 4'-O-Methylquercetin; Quercetin 4'-methyl ether
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.009.137 OOjs UI icon edit-ltr-progressive.svg
PubChem CID
UNII
  • InChI=1S/C16H12O7/c1-22-11-3-2-7(4-9(11)18)16-15(21)14(20)13-10(19)5-8(17)6-12(13)23-16/h2-6,17-19,21H,1H3
    Key: FPLMIPQZHHQWHN-UHFFFAOYSA-N
  • InChI=1/C16H12O7/c1-22-11-3-2-7(4-9(11)18)16-15(21)14(20)13-10(19)5-8(17)6-12(13)23-16/h2-6,17-19,21H,1H3
    Key: FPLMIPQZHHQWHN-UHFFFAOYAK
  • COC1=CC=C(C=C1O)C1=C(O)C(=O)C2=C(O1)C=C(O)C=C2O
Properties
C16H12O7
Molar mass 316.265 g·mol−1
Melting point 307 °C (585 °F; 580 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Tamarixetin is an O-methylated flavonol, a naturally occurring flavonoid. It has been isolated from Tamarix ramosissima . [1]

See also

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Anna Amelia Sher is an American plant ecologist who is a professor at the University of Denver. She works on conservation and the restoration of areas invaded by Tamarix. She is the author of two textbooks, Ecology:Concepts and Applications and Introduction to conservation biology.

References

  1. Sultanova, N.; Makhmoor, T.; Abilov, Z.A; Parween, Z.; Omurkamzinova, V.B; Ur-Rahman, Atta-; Choudhary, M.Iqbal (2001). "Antioxidant and antimicrobial activities of Tamarix ramosissima". Journal of Ethnopharmacology. 78 (2–3): 201–205. doi:10.1016/S0378-8741(01)00354-3. PMID   11694365.