Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

Jump to content

Arcapillin

From Wikipedia, the free encyclopedia
Arcapillin
Names
IUPAC name
2′,4′,5-Trihydroxy-5′,6,7-trimethoxyflavone
Systematic IUPAC name
2-(2,4-Dihydroxy-5-methoxyphenyl)-5-hydroxy-6,7-dimethoxy-4H-1-benzopyran-4-one
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
UNII
  • InChI=1S/C18H16O8/c1-23-13-4-8(9(19)5-10(13)20)12-6-11(21)16-14(26-12)7-15(24-2)18(25-3)17(16)22/h4-7,19-20,22H,1-3H3
    Key: IZWKTABKAJGBFW-UHFFFAOYSA-N
  • InChI=1/C18H16O8/c1-23-13-4-8(9(19)5-10(13)20)12-6-11(21)16-14(26-12)7-15(24-2)18(25-3)17(16)22/h4-7,19-20,22H,1-3H3
    Key: IZWKTABKAJGBFW-UHFFFAOYAR
  • COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O)O
Properties
C18H16O8
Molar mass 360.318 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Arcapillin is an α-glucosidase and protein tyrosine phosphatase inhibitor isolated from Artemisia capillaris.[1]

References

[edit]
  1. Nurul Islam, M; Jung, HA; Sohn, HS; Kim, HM; Choi, JS (2013). "Potent α-glucosidase and protein tyrosine phosphatase 1B inhibitors from Artemisia capillaris". Archives of Pharmacal Research. 36 (5): 542–52. doi:10.1007/s12272-013-0069-7. PMID 23435948. S2CID 207410409.