133776-28-0Relevant articles and documents
Probing the catalytic mechanism of s-ribosylhomocysteinase (LuxS) with catalytic intermediates and substrate analogues
Gopishetty, Bhaskar,Zhu, Jinge,Rajan, Rakhi,Sobczak, Adam J.,Wnuk, Stanislaw F.,et al.
supporting information; experimental part, p. 1243 - 1250 (2009/06/28)
S-Ribosylhomocysteinase (LuxS) cleaves the thioether bond in S-ribosylhomocysteine (SRH) to produce homocysteine (Hcys) and 4,5-dihydroxy-2,3-pentanedione (DPD), the precursor of the type II bacterial quorum sensing molecule (AI-2). The catalytic mechanis
Synthesis and antiviral and cytostatic properties of 3'-deoxy-3'-fluoro- and 2'-azido-3'-fluoro-2',3'-dideoxy-D-ribofuranosides of natural heterocyclic bases
Mikhailopulo,Poopeiko,Pricota,Sivets,Kvasyuk,Balzarini,De Clercq
, p. 2195 - 2202 (2007/10/02)
A series of 3'-deoxy-3'-fluoro- and 2'-azido-2',3'-dideoxy-3'-fluoro-D-ribofuranosides of natural heterocyclic bases have been synthesized with the use of universal carbohydrate precursors, viz., 1-O-acetyl-2,5-di-O-benzoyl-3-deoxy-3-fluoro-D-ribofuranose