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

Acutifolin A

From Wikipedia, the free encyclopedia
Acutifolin A
Names
IUPAC name
(1S,5S,6S)-1-Hydroxy-6-(4-hydroxyphenyl)-5-(3-methylbut-2-enyl)bicyclo[3.3.1]non-2-ene-4,9-dione
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
UNII
  • InChI=1S/C20H22O4/c1-13(2)7-12-20-16(14-3-5-15(21)6-4-14)8-10-19(24,18(20)23)11-9-17(20)22/h3-7,9,11,16,21,24H,8,10,12H2,1-2H3/t16-,19-,20-/m0/s1
  • CC(=CC[C@@]12[C@@H](CC[C@@](C1=O)(C=CC2=O)O)C3=CC=C(C=C3)O)C
Properties
C20H22O4
Molar mass 326.392 g·mol−1
Solubility Methanol
+94.7° (589.3 nm)[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Acutifolin A is bio-active isolate of the bark of Brosimum acutifolium, a Brazilian folk medicine ("Mururé").[1]

References

[edit]
  1. 1 2 Takashima, Junko; Ohsaki, Ayumi (December 2001). "Acutifolins A−F, a New Flavan-Derived Constituent and Five New Flavans from". Journal of Natural Products. 64 (12): 1493–1496. doi:10.1021/np010389j. PMID 11754597.