Malabaricol is a unique plant natural
product, 3-keto tricarbocyclic
triterpenoid, isolated from Ailanthus malabarica. Malabaricol underwent reaction with aromatic aldehydes under alkaline
conditions to form 2-arylidene analogs. Indoles and pyrazine ring
system fused to the 2,3-position of malabaricol were synthesized.
In this ring system of tricarbocyclic triterpenoid, the conformation
is such that there is no steric hindrance due to C<sub>4</sub> and
C<sub>10</sub> axial methyl groups and other skeletons. Malabaricol
and its synthetic analogues show cytotoxic activity toward lung cancer,
which was compared to that of standard doxorubicin.