173067-91-9

Upstream product

• 124-63-0 methanesulfonyl chloride 
• 95037-04-0 (2S,3R,4E)-3-O-benzoyl-2-dichloroacetamido-4-octadecen-1,3-diol 
• 173067-90-8 (2S,3R,4E)-3-O-benzoyl-1-O-tert-butyldiphenylsilyl-2-dichloroacetamido-4-octadecen-1,3-diol 
• 173067-89-5 (2S,3R,4E)-1-O-tert-butyldiphenylsilyl-2-dichloroacetamido-4-octadecen-1,3-diol 
• 80692-62-2 N-dichloroacetylsphingosine 
• 123-78-4 (2S,3R,4E)-2-amino-4-octadecene-1,3-diol 

Downstream Products

• 173067-94-2 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1<*>4)-S-(2,3,6-tri-O-acetyl-β-D-glucopyranosyl)-(1<*>1)-(2R,3R,4E)-3-benzyloxy-2-dichloroacetamido-4-octadecen-1-thiol 
• 173067-93-1 S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-(1<*>1)-(2R,3R,4E)-3-O-benzoyl-2-dichloroacetamido-4-octadecen-1-thiol 
• 173067-92-0 Benzoic acid (E)-(R)-1-[(R)-1-(2,2-dichloro-acetylamino)-2-iodo-ethyl]-hexadec-2-enyl ester 

Relevant academic research and scientific papers

Synthesis of fluorescent and radioactive analogues of two lactosylceramides and glucosylceramide containing β-thioglycosidic bonds that are resistant to enzymatic degradation

Condensation of 2-S-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-2-thiopseudourea hydrobromide with 2,3,6-tri-O-benzoyl-4-O-trifluoromethylsulfonyl-β-D-galactopyranosyl-(1->1)-(2S,3R,4E)-3-O-benzoyl-2-dichloroacetamido-4-octadecen-1,3-diol afforded S-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzoyl-4-thio-β-D-glucopyranosyl-(1->1)-(2S,3R,4E)-3-O-benzoyl-2-dichloroacetamido-4-octadecen-1,3-diol in good yield.Removal of the protecting groups, followed by selective N-acylation of the sphingosine amino group with either a fluorescent or a radioactive fatty acid, gave labeled lactosylceramide analogues in good yield.Since these products contained a β-thioglycosidic bond between the two sugar moieties, they were totally resistant to the action of acid lysosomal glycosidases.Likewise, condensation of 2-S-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2-thiopseudourea hydrobromide and 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1->4)-2,3,6-tri-O-acetyl-1-S-acetyl-1-thio-β-D-glucopyranose with (2R,3R,4E)-3-O-benzoyl-2-dichloroacetamido-1-iodo-4-octadecen-3-ol in methanolic sodium acetate afforded the corresponding β-thioglycosides 14 and 16, respectively, in good yield.These β-thioglycosides were converted into glucosylceramide and lactosylceramide analogues following removal of the protecting groups and by subsequent selective N-acylation using either a fluorescent or radioactive fatty acid N-succinimidyl ester.Whereas the glucosylthioceramides thus obtained proved to be completely undegradable by lysosomal glucocerebrosidase, the lactosylceramides containing the β-thioglycosidic bond between the lactose and the ceramide residues could be degraded by lysosomal GM1-β-galactosidase to give the corresponding glucosylthioceramides.These compounds did not yield to any further enzymatic degradation.Keywords: Thioglycolipids; Glycolipids; labeled; Thioglycosides; Glucosylthioceramide; Lactosylthioceramide