141810-60-8Relevant articles and documents
Automated access to well-defined ionic oligosaccharides
Delbianco, Martina,Grafmüller, Andrea,Schiefelbein, Kevin,Seeberger, Peter H.,Tyrikos-Ergas, Theodore,Zhu, Yuntao
, p. 1349 - 1353 (2020/03/03)
Ionic polysaccharides are part of many biological events, but lack structural characterisation due to challenging purifications and complex synthesis. Four monosaccharides bearing modifications not found in nature are used for the automated synthesis of a collection of ionic oligosaccharides. Structural analysis reveals how the charge pattern affects glycan conformation.
Modular synthesis of heparan sulfate oligosaccharides for structure-activity relationship studies
Arungundram, Sailaja,Al-Mafraji, Kanar,Asong, Jinkeng,Leach III, Franklin E.,Amster, I. Jonathan,Venot, Andre,Turnbull, Jeremy E.,Boons, Geert-Jan
scheme or table, p. 17394 - 17405 (2010/03/23)
Although hundreds of heparan sulfate binding proteins have been identified and implicated in a myriad of physiological and pathological processes, very little information is known about the ligand requirements for binding and mediating biological activiti
Preparation of ethyl 2-azido-2-deoxy-1-thio-β-D-mannopyranosides, and their rearrangement to 2-S-ethyl-2-thio-β-D-mannopyranosylamines
Vesely, Jan,Rohlenova, Anna,Dzoganova, Martina,Trnka, Tomas,Tislerova, Iva,Saman, David,Ledvina, Miroslav
, p. 699 - 705 (2007/10/03)
The synthesis of ethyl 2-azido-2-deoxy-1-thio-β-D-mannopyranosides 7-11, starting from appropriate synthons with gluco configuration, via S N2 substitution at C(2), and their rearrangement to 2-S-ethyl-2-thio-β-D-mannopyranosylamines 12-14 are