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Saccharide

Chemical Structure Cat. No. Product Name CAS No.
Gentiobiose Chemical Structure
 BCP029067 Gentiobiose 554-91-6
Methyl-2,3-O-isopropylidene-D-ribofuranoside Chemical Structure
 BCP31878 Methyl-2,3-O-isopropylidene-D-ribofuranoside 72402-14-3
α-L-Ribofuranose, 1,2-O-(1-methylethylidene)- Chemical Structure
 BCP31871 α-L-Ribofuranose, 1,2-O-(1-methylethylidene)- 172949-42-7
Ethyl α-Thioglucopyranoside Chemical Structure
 BCP31870 Ethyl α-Thioglucopyranoside 13533-58-9
5-Deoxy-D-ribose Chemical Structure
 BCP31731 5-Deoxy-D-ribose 13039-75-3
5-Deoxy-D-ribose is a deoxypentose that is aldehydo-D-ribose in which the hydroxy group at position 5 is substituted by a hydrogen.
D-Cellohexaose Chemical Structure
 BCP17405 D-Cellohexaose 2478-35-5
1,2,3,4,6-Pentagalloyl glucose Chemical Structure
 BCP29751 1,2,3,4,6-Pentagalloyl glucose 14937-32-7
1,2,3,4,6-Pentagalloylglucose is the pentagallic acid ester of glucose. It is a gallotannin and the precursor of ellagitannins.
D-fructofuranose 1,6-bisphosphate Chemical Structure
 BCP29550 D-fructofuranose 1,6-bisphosphate 488-69-7
Uridine Diphosphate Glucuronic Acid Chemical Structure
 BCP29224 Uridine Diphosphate Glucuronic Acid 2616-64-0
Uridine diphosphate glucuronic acid is a nucleoside diphosphate sugar which serves as a source of glucuronic acid for polysaccharide biosynthesis. It may also be epimerized to UDP iduronic acid, which donates iduronic acid to polysaccharides. In animals, UDP glucuronic acid is used for formation of many glucosiduronides with various aglycones.
6'-methyl-2-pyridinoyl-2-(acetylamino)-2-deoxy-1-thio-B-D-glucopyranoside Chemical Structure
 BCP09633 6'-methyl-2-pyridinoyl-2-(acetylamino)-2-deoxy-1-thio-B-D-glucopyranoside 149263-94-5
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