Synthesis of oligonucleotides containing the oxidatively modified B site: unique binding affinity to the NF B p50 homodimer

Abstract
Synthesis of oligonucleotide 26-mers including single 5-formyl-2′-deoxy-uridine (1) or 5-formyl-2′-O-methyl-uridine (2) in place of thymidine at the κB site has been accomplished. One of the 26-mers with 1 was critically discriminated by the NFκB p50 homodimer in binding.

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