Fe. Wu et al., MURICATOCIN-A AND MURICATOCIN-B, 2 NEW BIOACTIVE MONOTETRAHYDROFURAN ANNONACEOUS ACETOGENINS FROM THE LEAVES OF ANNONA-MURICATA, Journal of natural products, 58(6), 1995, pp. 902-908
The leaves of Annona muricata have yielded the novel monotetrahydrofur
an Annonaceous acetogenins, muticatocins A [1] and B [2]. Each compoun
d possesses five hydroxyl groups, with two hydroxyl groups at the C-10
and C-12 positions. The absolute configurations of 1 and 2 (except fo
r positions C-10 and C-12) were determined by Mosher ester methodology
. The C-10, C-12 acetonides (1c, 2c) suggested relative stereochemistr
y and significantly enhanced cytotoxicity against the A-549 human lung
tumor cell line. Three known monotetrahydrofuran acetogenins, annonac
in A, (2,4-trans)-isoannonacin, and (2,4-cis)-isoannonacin, were also
found.