Pectolinarigenin

Last updated

Pectolinarigenin
Pectolinarigenin.svg
Names
IUPAC name
5,7-Dihydroxy-4′,6-dimethoxyflavone
Systematic IUPAC name
5,7-Dihydroxy-6-methoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.007.534 OOjs UI icon edit-ltr-progressive.svg
PubChem CID
UNII
  • InChI=1S/C17H14O6/c1-21-10-5-3-9(4-6-10)13-7-11(18)15-14(23-13)8-12(19)17(22-2)16(15)20/h3-8,19-20H,1-2H3
    Key: GPQLHGCIAUEJQK-UHFFFAOYSA-N
  • InChI=1/C17H14O6/c1-21-10-5-3-9(4-6-10)13-7-11(18)15-14(23-13)8-12(19)17(22-2)16(15)20/h3-8,19-20H,1-2H3
    Key: GPQLHGCIAUEJQK-UHFFFAOYAB
  • COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)O)OC)O
Properties
C17H14O6
Molar mass 314.293 g·mol−1
Related compounds
Related compounds
 Pectolinarin
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Pectolinarigenin is a Cirsium isolate with anti-inflammatory activity and belongs to the flavones. [1]

References

  1. ↑ Lim, H; Son, KH; Chang, HW; Bae, K; Kang, SS; Kim, HP (2008). "Anti-inflammatory activity of pectolinarigenin and pectolinarin isolated from Cirsium chanroenicum". Biological & Pharmaceutical Bulletin. 31 (11): 2063–7. doi: 10.1248/bpb.31.2063 . PMID   18981574.


This page is based on this Wikipedia article
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.