| Literature DB >> 15178399 |
Yasuhiro Kajihara1, Daisuke Kamiyama, Naoki Yamamoto, Tohru Sakakibara, Masayuki Izumi, Hironobu Hashimoto.
Abstract
We reported the synthesis of beta-D-lactosaminide with a 2-aminopyridyl group that is linked to a glycosyl tether at the reducing end. This fluorescent disaccharide acts as an acceptor for both alpha-(2-->6)- and alpha-(2-->3)-sialyltransferases. In addition, the acceptor ability of this disaccharide was evaluated and compared with that of beta-D-lactosaminide having a dansyl or a 4-methylumbelliferyl group. Copyright 2004 Elsevier Ltd.Entities:
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Year: 2004 PMID: 15178399 DOI: 10.1016/j.carres.2004.03.015
Source DB: PubMed Journal: Carbohydr Res ISSN: 0008-6215 Impact factor: 2.104