Jump to content

Scillavone A

From Wikipedia, the free encyclopedia
Scillavone A
Chemical structure of scillavone A
Names
Preferred IUPAC name
(3R)-1′,5,7-Trihydroxy-2′,3′-dimethoxy-2H,4H-spiro[[1]benzopyran-3,6′-bicyclo[4.2.0]octane]-1′(8′),2′,4′-trien-4-one
Other names
(+)-Scillavone A
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C18H16O7/c1-23-13-5-10-9(15(21)16(13)24-2)6-18(10)7-25-12-4-8(19)3-11(20)14(12)17(18)22/h3-5,19-21H,6-7H2,1-2H3/t18-/m1/s1
    Key: DXRXYPLZQXGUBC-GOSISDBHSA-N
  • InChI=1/C18H16O7/c1-23-13-5-10-9(15(21)16(13)24-2)6-18(10)7-25-12-4-8(19)3-11(20)14(12)17(18)22/h3-5,19-21H,6-7H2,1-2H3/t18-/m1/s1
    Key: DXRXYPLZQXGUBC-GOSISDBHBI
  • COc1cc2c(c(c1OC)O)C[C@@]23COc4cc(cc(c4C3=O)O)O
Properties
C18H16O7
Molar mass 344.31 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Scillavone A is a homoisoflavone that can be isolated from the bulbs of Scilla scilloides[1] (Barnardia japonica).

References

[edit]
  1. ^ Nishida, Yoichiro; Eto, Masashi; Miyashita, Hiroyuki; Ikeda, Tsuyoshi; Yamaguchi, Koki; Yoshimitsu, Hitoshi; Nohara, Toshihiro; Ono, Masateru (2008). "A new homostilbene and two new homoisoflavones from the bulbs of Scilla scilloides". Chemical and Pharmaceutical Bulletin. 56 (7): 1022–1025. doi:10.1248/cpb.56.1022. PMID 18591825.
[edit]