161452-19-3

Upstream product

• 161452-08-0 N-(tert-butoxycarbonyl)-N-(3-cyanopropyl)mesitylenesulfonamide 
• 161452-09-1 N-(tert-butoxycarbonyl)-N-(4-aminobutyl)mesitylenesulfonamide 
• 151915-07-0 N-ethyl-(2-mesitylene)sulfonamide 
• 21926-49-8 2,4,6-Trimethylbenzol-sulfonylisocyanat 
• 56830-76-3 (2,4,6-trimethylbenzenesulfonyl)carbamic acid tert-butyl ester 
• 4543-58-2 2,4,6-trimethylbenzenesulfonamide 
• 773-64-8 2-mesitylenesulphonyl chloride 
• 161452-15-9 N-(4-bromobutyl)-N-ethylmesitylenesulfonamide 
• 161452-10-4 N-(tert-butoxycarbonyl)-N, N'-bis(mesitylenesulfonyl)-1,4-diaminobutane 

Downstream Products

• 161452-22-8 N¹,N⁵,N¹⁰,N¹⁴-tetrakis(mesitylenesulfonyl)-N¹-(tert-butyl)-N¹⁴-ethylhomospermine 
• 161452-21-7 3,7,12,17-tetrakis(mesitylenesulfonyl)-3,7,12,17-tetraazanonadecane 
• 161452-20-6 1,6,11-tris(mesitylenesulfonyl)-1,6,11-triazatridecane 

Relevant academic research and scientific papers

Analogs of biologically active, naturally occurring polyamines, pharmaceutical compositions and methods of treatment

Polyamines having the formula: or a salt thereof with a pharmaceutically acceptable acid wherein: R1-R6may be the same or different and are alkyl, aryl, aryl alkyl, cycloalkyl, optionally having an alkyl chain interrupted by at least

Antiproliferative Properties of Polyamine Analogues: A Structure-Activity Study

A basis set of polyamine analogues was designed and synthesized.These compounds were used to initiate a systematic investigation of the role of chain length, terminal nitrogen alkyl group size, and symmetry of the methylene backbone in the antineoplastic