Synthesis of tropolone derivatives and evaluation of their in vitro neuroprotective activity
Maria Koufaki1, Elissavet Theodorou, Xanthippi Alexi
1Institute of Organic and Pharmaceutical Chemistry, National Hellenic Research Foundation, 48 Vas Constantinou Ave, 116 35 Athens, Greece. mkoufa@eie.gr
Abstract:
beta-Thujaplicin (hinokitiol or 2-hydroxy-4-isopropyl-2,4,6-cycloheptatrien-1-one), a natural tropolone, shows numerous activities while its synthetic analogues were found to exhibit anticancer and anti-ischemic activity. However, the ability of tropolone derivatives to protect neuronal cells from oxidative stress-induced cell damage has not been studied so far. As an ongoing effort toward highly effective antioxidants with potential neuroprotective activity, we have synthesized 7-substituted derivatives of beta-thujaplicin and its methoxy analogue. The substituents were heterocycles (piperazine, morpholine) or heteroaromatics (triazoles, pyridine). Only the piperazine derivatives of beta-thujaplicin were able to protect HT22 hippocampal neurons from oxidative stress-induced cell death.

