202065-44-9

Upstream product

• 188966-04-3 {4-[Benzyloxycarbonyl-(4-benzyloxycarbonylamino-butyl)-amino]-butyl}-[(trityl-amino)-methyl]-phosphinic acid ethyl ester 
• 188966-02-1 {4-[[4-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-(2,2,2-trifluoro-acetyl)-amino]-butyl}-[(trityl-amino)-methyl]-phosphinic acid ethyl ester 
• 188965-99-3 {4-[[4-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-(2,2,2-trifluoro-acetyl)-amino]-butyl}-phosphinic acid ethyl ester 
• 188965-98-2 {4-[[4-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-(2,2,2-trifluoro-acetyl)-amino]-butyl}-phosphinic acid 
• 202065-49-4 N-[4-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-2,2,2-trifluoro-N-(4-iodo-butyl)-acetamide 
• 501-53-1 benzyl chloroformate 

Relevant academic research and scientific papers

Investigations on New Strategies for the Facile Synthesis of Polyfunctionalized Phosphinates: Phosphinopeptide Analogues of Glutathionylspermidine

Three possible methods for the facile synthesis of functionalized phosphinates, including the core of complex phosphinopeptide analogues of glutathionylspermidine, were explored. Among these methods, the three-component condensation reaction involving ben

Novel inhibitors of trypanothione biosynthesis: Synthesis and evaluation of a phosphinate analog of glutathionyl spermidine (GSP), a potent, slow-binding inhibitor of GSP synthetase

A phosphinate analog of glutathionyl spermidine (Gsp), 3, has been synthesized and evaluated as an inhibitor of Gsp synthetase (GSPS). In addition, a non-spermidine-containing derivative (4) was synthesized in order to evaluate the role of the polyamine m