Nicotinamide Benzimidazolide Dinucleotides, Non-Cyclisable Analogues of NAD<sup>+</sup>


Autoria(s): Redpath, Philip; Haluszczak, Jolanta; Macdonald, Simon J.; Migaud, Marie E.
Data(s)

2014

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

http://pure.qub.ac.uk/portal/en/publications/nicotinamide-benzimidazolide-dinucleotides-noncyclisable-analogues-of-nad(7ce0441f-4930-4718-bce1-b608a988b6cb).html

http://dx.doi.org/10.1055/s-0034-1379000

http://pure.qub.ac.uk/ws/files/13095810/lNettiercotinamide_Benzimidazolide_Dinucleotides_Non_Cyclisable_Analogues_of.pdf

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