742102-76-7

Upstream product

• 100-39-0 benzyl bromide 
• 742102-74-5 2,3-dideoxy-6-O-triphenylmethyl-1-{N-[(tert-butyloxycarbonyl)amino]methyl}-β-D-glucopyranose 
• 24424-99-5 di-tert-butyl dicarbonate 
• 229473-28-3 2,3-dideoxy-1-{N-[(tert-butyloxycarbonyl)amino]methyl}-β-D-glucopyranose 

Downstream Products

• 742102-80-3 2,3-dideoxy-4-O-benzyl-1-{N-[(tert-butyloxycarbonyl)amino]methyl}-β-D-glucopyranose 
• 742102-83-6 (1R,4S,5S)-4-O-benzyl-1-{N-[(tert-butyloxycarbonyl)amino]methyl}-tetrahydropyran-6-carboxylic acid 
• 742102-87-0 (1R,4S,5S)-4-O-benzyl-1-{N-[(tert-butyloxycarbonyl)amino]methyl}tetrahydropyran-6-N-L-leucine methyl ester 
• 742102-95-0 N-[(1R)-1-({N-[(tert-butoxy)carbonyl]amino}methyl)-1,2,3-trideoxy-4-benzyloxy-6-oxo-D-arabino-hexopyranos-6-yl]-L-leucine methyl ester 
• 742102-97-2 N-[(1R)-1-({N-[(tert-butoxy)carbonyl]amino}methyl)-1,2,3-trideoxy-4-benzyloxy-6-oxo-D-arabino-hexopyranos-6-yl]-L-methionine methyl ester 
• 742102-91-6 (1R,4S,5S)-4-O-benzyl-1-{(N-[(S-(tert-butyl)sulfanyl)]-N-{[9H-fluoren-9-ylmethoxy]carbonyl}-L-cysteinyl)aminomethyl}tetrahydropyran-6-N-L-leucine methyl ester 
• 742102-89-2 (1R,4S,5S)-4-O-benzyl-1-{(N-[(S-(tert-butyl)sulfanyl)]-N-{[9H-fluoren-9-ylmethoxy]carbonyl}-L-cysteinyl)aminomethyl}tetrahydropyran-6-N-L-methionine methyl ester 
• 742102-99-4 N-[(1R)-1-{(N-(S-(tert-butyl)sulfanyl)-N-{[(9H-fluoren-9-yl)methoxy]carbonyl}-L-cysteinyl)aminomethyl}-1,2,3-trideoxy-4-benzyloxy-6-oxo-D-arabino-hexopyranos-6-yl]-L-leucine methyl ester 
• 742103-01-1 N-[(1R)-1-({N-(S-(tert-butyl)sulfanyl)-N-{[(9H-fluoren-9-yl)methoxy]carbonyl}-L-cysteinyl}aminomethyl)-1,2,3-trideoxy-4-benzyloxy-6-oxo-D-arabino-hexopyranos-6-yl]-L-methionine methyl ester 

Relevant academic research and scientific papers

Design, synthesis, and evaluation of sugar amino acid based inhibitors of protein prenyl transferases PFT and PGGT-1

Eleven analogues of the C-terminal Ca1a2X motif found in natural substrates of the prenyl transferases PFT and PGGT-1 were synthesized and evaluated for their inhibition potency and selectivity against PFT and PGGT-1. Replacement of