Fe. Wu et al., NEW BIOACTIVE MONOTETRAHYDROFURAN ANNONACEOUS ACETOGENINS, ANNOMURICIN-C AND MURICATOCIN-C, FROM THE LEAVES OF ANNONA-MURICATA, Journal of natural products, 58(6), 1995, pp. 909-915
The leaves of Annona muricata have yielded two additional monotetrahyd
rofuran Annonaceous acetogenins, annomuricin C [1] and muricatocin C [
2]. Compounds 1 and 2 each possess five hydroxyl groups; two hydroxyl
groups are at the C-10/C-11 and C-10/C-12 positions in 1 and 2, respec
tively. The absolute configurations of 1 and 2, except for positions C
-10 and C-11 or C-12, were determined by Mosher ester methodology. The
C-10/C-11 and C-10/C-12 acetonides (1c, 2c) suggested relative stereo
chemistry and significantly enhanced the cytotoxicities against the A-
549 human lung and the MCF-7 human beast solid tumor cell lines. One k
nown monotetrahydrofuran acetogenin, giganterronenin, not described pr
eviously from this plant, was also found.