Synthesis and Biological Evaluation of Structurally Varied 5'-/6'-Isonucleosides and Theobromine-Containing <i>N</i>-Isonucleosidyl Derivatives
Isonucleosides are rather stable regioisomeric analogs of nucleosides with broad therapeutic potential. We have previously demonstrated the ability of 5′ and 6′-isonucleosides to inhibit the activity of acetylcholinesterase, a major target for Alzheimer’s disease therapy. Continuing with our researc...
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Format: | Book |
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MDPI AG,
2019-07-01T00:00:00Z.
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A1234.567 |
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