79982-02-8

Upstream product

• 29617-66-1 (S)-2-chloropropanoic acid 
• 75263-30-8 benzyl 2-acetamido-2-deoxy-4,6-isopropylidene-α-D-allopyranosidede 
• 66026-10-6 N-((4aR,6S,7R,8R,8aS)-6-(benzyloxy)-8-hydroxy-2,2-dimethylhexahydropyrano[3,2-d][1,3]dioxin-7-yl)acetamide 
• 75263-33-1 benzyl 2-acetamido-2-deoxy-4,6-O-isopropylidene-α-D-galactopyranoside 
• 3554-93-6 benzyl 2-acetamido-2-deoxy-α-D-galactopyranoside 
• 75263-31-9 benzyl 2-acetamido-2-deoxy-4,6-O-isopropylidene-α-D-gulopyranoside 
• 33423-30-2 benzyl 2-acetamido-2-deoxy-α-D-gulopyranoside 
• 50605-12-4 benzyl 2-acetamido-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranoside 
• 598-78-7 L-2-chloropropionic acid 
• 75263-24-0 benzyl 2-acetamido-2-deoxy-4,6-isopropylidene-3-O-mesyl-α-D-glucopyranoside 

Downstream Products

• 79957-36-1 benzyl 2-acetamido-4,6-di-O-acetyl-2-deoxy-3-O--α-D-galactopyranoside 
• 57816-11-2 N-<2-O-(benzyl 2-acetamido-2,3-dideoxy-β-D-glucopyranosid-3-yl)-D-lactoyl>-L-alanyl-D-isoglutamine benzyl ester 
• 128726-61-4 N-<2-O-(benzyl 2-acetamido-6-O-< 5-(tert-butoxycarbonylamino)pentanoyl>-2,3-dideoxy-β-D-glucopyranosid-3-yl)-D-lactoyl>-L-alanyl-D-isoglutamine benzyl ester 
• 128747-59-1 N-<2-O-(benzyl 2-acetamido-6-O-< 8-(tert-butoxycarbonylamino)octanoyl>-2,3-dideoxy-β-D-glucopyranosid-3-yl)-D-lactoyl>-L-alanyl-D-isoglutamine benzyl ester 
• 128747-55-7 N-(2-O--D-lactoyl)-L-alanyl-D-isoglutamine benzyl ester trifluoroacetate 
• 128726-70-5 N-(2-O--D-lactoyl)-L-alanyl-D-isoglutamine benzyl ester trifluoroacetate 
• 69323-69-9 N-<2-O-(benzyl 2-acetamido-2,3-dideoxy-4,6-O-isopropylidene-β-D-glucopyranosid-3-yl)-D-lactoyl>-L-alanyl-D-isoglutamine benzyl ester 

Relevant academic research and scientific papers

Synthesis and Biological Activity of 6-O-(3-Acyloxytetradecanoyl)-N-acetyl-muramoyl Dipeptide Methyl Esters and Related Compounds

A variety of 6-O-(3-acyloxytetradecanoyl)-MDP methyl esters were synthesized using optically-active (3R)-3-acyloxytetradecanoic acid.Their immunoadjuvant activity was examined.

Synthesis of carbohydrate analogs (positional, configurational, and optical) of n-acetylmuramoyl-L-alanyl-D-isoglutamine, and their immunoadjuvant activities.

2-Acetamido-2-deoxy-4- and -6-O-(D-2-propanoyl-L-alanyl-D-isoglutamine)-D-glucopyranose, 2-acetamido-2-deoxy-3-O-(D-2-propanoyl-L-alanyl-D-isoglutamine)-D-allopyranose, -D-gulopyranose, -D-galactopyranose, -D-mannopyranose, and -L-idopyranose, and 3-O-(D-2-propanoyl-L-alanyl-D-isoglutamine)-D- and -L-glucopyranose were synthesized, in order to clarify the structural requirements for the immunoadjuvant activity of the carbohydrate moiety in N-acetylmuramoyl-L-alanyl-D-isoglutamine. Immunoadjuvant activity of the N-acetylmuramoyl-dipeptide analogs was examined in guinea-pigs.