855662-12-3

Usage

Chemical Properties

White Solid

InChI:InChI=1/C27H23BrO7/c1-17-21(33-25(29)18-11-5-2-6-12-18)22(34-26(30)19-13-7-3-8-14-19)23(24(28)32-17)35-27(31)20-15-9-4-10-16-20/h2-17,21-24H,1H3/t17-,21+,22-,23-,24?/m0/s1

Upstream product

• 135266-93-2 1,2,3,4-tetra-O-benzoyl-α-L-fucopyranoside 
• 98-88-4 benzoyl chloride 
• 73-34-7 6-deoxy-L-galactose 
• 1294500-99-4 2,3,4-tri-O-benzoyl-L-fucopyranose 

Downstream Products

• 1294500-99-4 2,3,4-tri-O-benzoyl-L-fucopyranose 

Relevant academic research and scientific papers

THIOPYRANOSE COMPOUND AND METHOD FOR PRODUCING SAME

There is provided a production method of a thiopyranose compound represented by the following Formula (2) by reacting a compound represented by the following Formula (1) with a sulfur compound. X represents a leaving group. A represents an oxygen atom or

Synthesis of a chlorogenin glycoside library using an orthogonal protecting group strategy

Naturally occurring spirostanol saponins bear a chacotriose, α-l-rhamnopyranosyl-(1→2)-[α-l-rhamnopyranosyl-(1→4)] -β-d-glucopyranose residue as the oligosaccharide moiety which is believed to be important for biological activity. Herein the development of a concise, combinatorial method for the synthesis of two series of glycan variants at the 2′ and/or 4′ positions of chacotriose is described and the structure-activity relationships of the glycone part at 3-OH of chlorogenin investigated. These compounds were found to be weakly-cytotoxic toward leukemia cell lines CCRF and HL-20, indicating that the chacotriose moiety is important for anticancer activity.