Sinensetin

Sinensetin is a methylated flavone. It can be found in Orthosiphon stamineus[2] and in orange oil.[3]

Sinensetin
Skeletal formula of sinensetin
Ball-and-stick model of sinensetin
Names
IUPAC name
3′,4′,5,6,7-Pentamethoxyflavone
Systematic IUPAC name
2-(3,4-Dimethoxyphenyl)-5,6,7-trimethoxy-4H-1-benzopyran-4-one
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.230.396
UNII
  • InChI=1S/C20H20O7/c1-22-13-7-6-11(8-15(13)23-2)14-9-12(21)18-16(27-14)10-17(24-3)19(25-4)20(18)26-5/h6-10H,1-5H3 checkY
    Key: LKMNXYDUQXAUCZ-UHFFFAOYSA-N checkY
  • COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC
Properties
C20H20O7
Molar mass 372.36 g/mol
Hazards
GHS labelling:[1]
GHS06: Toxic
Danger
H301
P264, P270, P301+P310, P321, P330, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references


References
  1. GHS: Pubchem
  2. Akowuah, G. A.; Ismail, Z.; Norhayati, I.; Sadikun, A. (2005). "The effects of different extraction solvents of varying polarities on polyphenols of Orthosiphon stamineus and evaluation of the free radical-scavenging activity". Food Chemistry. 93 (2): 311–317. doi:10.1016/j.foodchem.2004.09.028.
  3. Steinke, Katrin; Jose, Elena; Sicker, Dieter; Siehl, Hans-Ullrich; Zeller, Klaus-Peter; Berger, Stefan (2013). "Sinensetin". Chemie in unserer Zeit (in German). 47 (3): 158–163. doi:10.1002/ciuz.201300627.


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.