86704-37-2

Upstream product

• 108-24-7 acetic anhydride 
• 934826-39-8 benzyl 2-acetamido-2-deoxy-4,6-O-isopropylidene-3-O--α-D-glucopyranoside 

Downstream Products

• 88831-44-1 2-acetamido-1-O-benzoyl-3-O-(D-carboxyethyl)-2-deoxy-4,6-O-isopropylidene-α-D-glucopyranose 
• 88831-57-6 N-<2-O-(2-acetamido-1-O-acetyl-2,3-dideoxy-D-glucopyranose-3-yl)-D-lactoyl>-L-alanyl-D-isoglutamine benzyl ester 
• 88831-45-2 N-<2-O-(2-acetamido-1-O-benzoyl-2,3-dideoxy-4,6-O-isopropylidene-α-D-glucopyranose-3-yl)-D-lactoyl>-L-alanyl-D-isoglutamine methyl ester 
• 88831-51-0 N-<2-O-(2-acetamido-1-O-acetyl-2,3-dideoxy-4,6-O-isopropylidine-D-glucopyranose-3-yl)-D-lactoyl>-L-alanyl-D-isoglutamine benzyl ester 
• 88831-58-7 N-<2-O-(2-acetamido-1-O-decanoyl-2,3-dideoxy-D-glucopyranose-3-yl)-D-lactoyl>L-alanyl-D-isoglutamine benzyl ester 
• 88831-52-1 N-<2-O-(2-acetamido-1-O-decanoyl-2,3-dideoxy-4,6-O-isopropylidene-D-glucopyranose-3-yl)-D-lactoyl>-L-alanyl-D-isoglutamine benzyl ester 
• 88831-59-8 N-<2-O-(2-acetamido-2,3-dideoxy-1-O-hexadecanoyl-D-glucopyranose-3-yl)-D-lactoyl>-L-alanyl-D-isoglutamine benzyl ester 
• 88831-53-2 N-<2-O-(2-acetamido-2,3-dideoxy-1-O-hexadecanoyl-4,6-O-isopropylidene-D-glucopyranose-3-yl)-D-lactoyl>-L-alanyl-D-isoglutamine benzyl ester 
• 92921-71-6 2-acetamido-1-O-benzoyl-2-deoxy-3-O--α-D-glucopyranose 
• 92921-72-7 2-acetamido-1-O-benzoyl-6-bromo-2,6-dideoxy-3-O--α-D-glucopyranose 
• 92921-73-8 2-acetamido-4-O-acetyl-1-O-benzoyl-6-bromo-2,6-dideoxy-3-O--α-D-glucopyranose 
• 83375-11-5 N-<2-O-(2-acetamido-2,3-dideoxy-1-thio-β-D-glucopyranose-3-yl)-D-lactoyl>-L-alanyl-D-isoglutamine 

Relevant academic research and scientific papers

Muramyldipeptide derivatives

Muramyldipeptide derivatives represented by the formula: STR1 wherein Ala represents alanine; Acyl represents an acyl group; R1 and R2 each represents a hydrogen atom or, when taken together, may form an alkylidene group; R3 represents a hydrogen atom, an acyl group or an alkyl group; and R4 represents a hydrogen atom or an alkyl group. These compounds have excellent immunoadjuvant activity, prophylactic and therapeutic effects against microbial infections, and antitumor activity.

Synthesis and biological activities of N-acetyl-1-thiomuramoyl-L-alanyl-D-isoglutamine and some of its lipophilic derivatives.

N-Acetyl-1-thiomuramoyl-L-alanyl-D-isoglutamine and some lipophilic analogs were synthesized from benzyl 2-acetamido-2-deoxy-4,6-O-isopropylidene-3-O-[D-1-(methoxycarbonyl)ethyl ]- alpha-D-glucopyranoside (1). O-Debenzoylation of 2, derived from 1 by oxid