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In this work, the synthesis and the pharmacological evaluation of diphenoxyadamantane alkylamines Ia-f and IIa-f is described. The new diphenoxy-substituted adamantanes share structural features present in trypanocidal and antitubercular agents. 1-Methylpiperazine derivative Ia is the most potent against T. brucei compound, whilst its hexylamine congener IIf exhibits a significant antimycobacterial activity.
Ursula Röthlisberger, Sophia Kathryn Johnson, Andrea Levy
David Lyndon Emsley, Arthur César Pinon, Jasmine Viger-Gravel
Pierre Vogel, Florence Pojer, Somi Reddy Majjigapu, Ute Röhrig, Aline Emma Christine Reynaud