475101-71-4Relevant academic research and scientific papers
Synthetic approach toward the partial sequences of betaglycan in the linkage region on solid support and in solution phase
Tamura, Jun-Ichi,Yamaguchi, Akihiro,Tanaka, Junko,Nishimura, Yuko
, p. 61 - 82 (2008/02/09)
We have synthesized, for the first time, the partial sequence of the betaglycan composed of the tetraosyl hexapeptide, which was directly usable as a probe for enzymatic glycosyl transfer. Stepwise elongation afforded the corresponding tetraosyl trichloro
Synthesis and activity of novel glutathione analogues containing an urethane backbone linkage
Cacciatore,Caccuri,Di Stefano,Luisi,Nalli,Pinnen,Ricci,Sozio
, p. 787 - 793 (2007/10/03)
The new GSH analogues H-Glo(-Ser-Gly-OH)-OH (5), its O-benzyl derivative 4, and H-Glo(-Asp-Gly-OH)-OH (9), characterized by the replacement of central cysteine with either serine or aspartic acid, and containing an urethanic fragment as isosteric substitu
Synthesis of betaglycan-type tetraosyl hexapeptide: a possible precursor regulating enzymatic elongation toward heparin.
Tamura, Jun-ichi,Yamaguchi, Akihiro,Tanaka, Junko
, p. 1901 - 1903 (2007/10/03)
TETRAOSYL HEXAPEPTIDE, A PART OF THE SEQUENCE OF BETAGLYCAN: beta-D-GlcA-(1-->3)-beta-D-Gal-(1-->3)-beta-D-Gal-(1-->4)-beta-D-Xyl-(1-->O-SerGlyTrpProAspGly (1), which was designed as a probe for glycan elongation toward heparin, was synthesized in a stere
