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Bioorg Khim ; 41(6): 731-6, 2015.
Article in Russian | MEDLINE | ID: mdl-27125028

ABSTRACT

It was found that compounds combining diazaadamantane and monoterpenoid fragments are potent inhibitors of new structural type of human recombinant DNA repair enzyme Tyrosyl-DNA phosphodiesterase I (Tdp1). It was demonstrated that the inhibition efficiency depended on the length and flexibility of the aliphatic chain of the substituent.


Subject(s)
Adamantane , Enzyme Inhibitors , Monoterpenes , Nitrogen/chemistry , Phosphoric Diester Hydrolases/chemistry , Adamantane/chemical synthesis , Adamantane/chemistry , Enzyme Inhibitors/chemical synthesis , Enzyme Inhibitors/chemistry , Humans , Monoterpenes/chemical synthesis , Monoterpenes/chemistry
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