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Novel 1,1‐disubstituted cyclohexane‐1‐carboxamides 6a‐h, 7a‐e, and 8a‐b were designed and synthesized as apoptotic inducers. Cytotoxicity test revealed that some compounds have strong to moderate effect, while others displayed weak action against different cancer cell lines including, MCF‐7, HepG2, A549, and HTC‐116. A549 carcinoma cell line exhibited higher sensitivity toward all synthesized candidates...
A series of (1-(benzyl (aryl) amino) cyclohexyl) methyl esters 7a-n were prepared and screened for their anticonvulsant profile. Screening of these esters 7a-n and their starting alcohols 6a and 6b revealed that compound 7k was the most potent one in the scPTZ screening test with an ED50 value of 0.0056mmol/kg being about 10- and 164-fold more potent than phenobarbital (ED50=0.056mmol/kg) and ethosuximide...
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