Nicotinamide Benzimidazolide Dinucleotides, Non-Cyclisable Analogues of NAD<sup>+</sup>
Data(s) |
2014
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Resumo |
Benzimidazole-based nucleotides and dinucleotides have been synthesised to increase the range of chemical tools available to probe the NAD+ biology space. They were examined for their reactivity in alkylation-type reactions, where they yielded unstable alkylated heteoaromatic adducts, both chemically and enzymatically. While unsuited for NAD+ cyclases, these NAD+ analogues could be viable substrates for non-adenine modifying NAD+-dependent enzyme classes. |
Formato |
application/pdf |
Identificador | |
Idioma(s) |
eng |
Direitos |
info:eu-repo/semantics/openAccess |
Fonte |
Redpath , P , Haluszczak , J , Macdonald , S J & Migaud , M E 2014 , ' Nicotinamide Benzimidazolide Dinucleotides, Non-Cyclisable Analogues of NAD + ' Synlett , vol 25 , no. 16 , pp. 2331-2336 . DOI: 10.1055/s-0034-1379000 |
Palavras-Chave | #benzimidazoribosyl nucleosides #cyclic adenosine diphosphoribose #enzymes #nucleotides #phosphorylation #/dk/atira/pure/subjectarea/asjc/1600/1605 #Organic Chemistry |
Tipo |
article |