Synthesis of diphenoxyadamantane alkylamines with pharmacological interest
Ημερομηνία
2019Γλώσσα
en
Λέξη-κλειδί
Επιτομή
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. © 2019 Elsevier Ltd
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