Five new adjacent bis-THF annonaceous acetogenins, 32-hydroxybullataci
n, 31-hydroxybullatacin, 30-hydroxybullatacin, and (2,4-cis and trans)
-28-hydroxybullatacinones, were isolated from the ethanolic extract of
the bark of Annona bullata Rich. (Annonaceae). The absolute configura
tions of the above five compounds, as well as those of (2,4-cis and tr
ans)-32-, 31-, and 30-hydroxybullatacinones and (2,4-cis and trans)-bu
lladecinones, previously isolated from the same extract, were defined
by the application of the advanced Mosher ester [methoxy(trifluorometh
yl)phenyl acetate or MTPA] methodology. The determination of the absol
ute configuration of C-20 of (2,4-cis and trans)-bulladecinones to be
S supports our hypothesis that the cyclization of the THF rings of(2,4
-cis and trans)-bulladecinones starts from C-12 (the right side). The
first five compounds listed above showed potent bioactivities in the b
rine shrimp lethality test (BST) and among six human solid tumour cell
lines.