作者:Kateryna Prysiazhniuk、Oleksandr P. Datsenko、Oleksandr Polishchuk、Stanislav Shulha、Oleh Shablykin、Yelyzaveta Nikandrova、Kateryna Horbatok、Iryna Bodenchuk、Petro Borysko、Dmytro Shepilov、Iryna Pishel、Vladimir Kubyshkin、Pavel K. Mykhailiuk
DOI:10.1002/anie.202316557
日期:2024.2.26
The spiro[3.3]heptane core, with the non-coplanar exit vectors, was shown to be a saturated benzene bioisostere. This scaffold was incorporated into the anticancer drug sonidegib (instead of the meta-benzene), the anticancer drug vorinostat (instead of the phenyl ring), and the anesthetic drug benzocaine (instead of the para-benzene). The patent-free saturated analogs obtained showed a high potency
具有非共面退出向量的螺[3.3]庚烷核心被证明是饱和苯生物等排体。该支架被整合到抗癌药物索尼吉布(代替间苯)、抗癌药物伏立诺他(代替苯环)和麻醉药物苯佐卡因(代替对苯)中。获得的无专利饱和类似物在相应的生物测定中显示出高效力。