124382-39-4Relevant academic research and scientific papers
Mono-, di- and tri-antennary D-galactose ligands as competitive inhibitors and photoaffinity labels of the hexose transporting system in erythrocytes. A model for the irreversible blocking of receptors in cell membranes
Lehmann, Jochen,Scheuring, Markus
, p. 57 - 74 (2007/10/03)
Starting from pentaerythritol, photolabile mono-, di-, and tri-dentate galactose derivatives as well as their 3H-labelled isotopomers were synthesized.The hydrophilic chains linking the 6 position of D-galactose to pentaerithritol consist of 13
Spacer-modified saccharides for the regioselective photoaffinity labelling of the binding site of an immunoglobulin
Lehmann, Jochen,Scheuring, Markus
, p. 67 - 82 (2007/10/02)
The spacer-modified trisaccharides that mimic (1->6)-linked β-D-galactotetraose (Gal4), namely, O-β-D-galactopyranosyl-(1->6)-S-β-D-galactopyranosyl-(1->11)-8-azi-6,7,8,9,10-pentadeoxy-11-thio-D-galactoundecose (12) and O-β-D-galactopyranosyl-(1->6)-O-β-D
Syntheses of Undecose Derivatives as D-Galactose Analogues for Specific Modification of Galactose-Binding Proteins
Lehmann, Jochen,Scheuring, Markus
, p. 271 - 275 (2007/10/02)
A series of undec- and dodecoses containing functional groups was obtained from 1,2:3,4-di-O-isopropylidene-α-D-galacto-hexodialdo-pyranose-(1,5) (1) using Wittig and Grignard reactions to bring about chain elongation.The compounds resemble 6 C-alkylated
