197971-38-3

Upstream product

• 501-53-1 benzyl chloroformate 
• 197971-54-3 (4-{Benzyloxycarbonyl-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-amino}-butyl)-carbamic acid benzyl ester 

Downstream Products

• 197971-55-4 (4-{Benzyloxycarbonyl-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-amino}-butyl)-carbamic acid benzyl ester 
• 197971-43-0 (S)-4-{(S)-1-[(Benzyloxy-{3-[benzyloxycarbonyl-(4-benzyloxycarbonylamino-butyl)-amino]-propoxy}-phosphorylmethyl)-carbamoyl]-ethylcarbamoyl}-2-benzyloxycarbonylamino-butyric acid benzyl ester 
• 197971-51-0 C₃₃H₃₉N₄O₈P 
• 103493-32-9 {4-[(3-amino-propyl)-benzyloxycarbonyl-amino]-butyl}-carbamic acid benzyl ester 
• 197971-41-8 Aminomethyl-phosphonic acid benzyl ester 3-[benzyloxycarbonyl-(4-benzyloxycarbonylamino-butyl)-amino]-propyl ester 

Relevant academic research and scientific papers

Design, synthesis, and biochemical evaluation of phosphonate and phosphonamidate analogs of glutathionylspermidine as inhibitors of glutathionylspermidine synthetase/amidase from Escherichia coli

Three phosphapeptides designed to mimic two distinct tetrahedral intermediates formed during either the synthesis or hydrolysis of glutathionylspermidine (Gsp) were synthesized and evaluated as inhibitors of the bifunctional enzyme Gsp synthetase/amidase.