165288-18-6

Basic information

• Product Name: tetrakis(mesitylsulfonyl)-N,N'-bis(4-piperidinylmethyl)-1,4-diaminobutane
• Synonyms: tetrakis(mesitylsulfonyl)-N,N'-bis(4-piperidinylmethyl)-1,4-diaminobutane
• CAS NO: 165288-18-6
• Molecular Weight: 1011.45
• Mol File: 165288-18-6.mol

Chemical Properties

• CAS DataBase Reference: tetrakis(mesitylsulfonyl)-N,N'-bis(4-piperidinylmethyl)-1,4-diaminobutane(CAS DataBase Reference)
• NIST Chemistry Reference: tetrakis(mesitylsulfonyl)-N,N'-bis(4-piperidinylmethyl)-1,4-diaminobutane(165288-18-6)
• EPA Substance Registry System: tetrakis(mesitylsulfonyl)-N,N'-bis(4-piperidinylmethyl)-1,4-diaminobutane(165288-18-6)

Safety Data

• Hazardous Substances Data: 165288-18-6(Hazardous Substances Data)

Upstream product

• 7144-05-0 4-Aminomethylpiperidine 
• 773-64-8 2-mesitylenesulphonyl chloride 
• 110-52-1 1,4-dibromo-butane 
• 165288-17-5 N,N'-bis(mesitylsulfonyl)-4-(aminomethyl)piperidine 

Relevant articles and documents

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

The Role of Charge in Polyamine Analogue Recognition

A series of analogues and homologues of N1,N12-diethylspermine (DESPM) was synthesized, and their biological properties were evaluated.These tetraamines include a simple linear analogue of DESPM, N1,N12-bis(2,2,2-trifluoroethyl)spermine (FDESPM), the cyclic analogues of DESPM, N,N'-bis(4-piperidinylmethyl)-1,4-diaminobutane and N,N'-bis-1,4-diaminobutane , and their aromatic counterparts, N,N'-bis(4-pyridylmethyl)-1,4-diaminobutane and N,N'-bis-1,4-diaminobutane .The analogues FDESPM, PIP(4,4,4), and PYR(4,4,4) have distances between their nitrogen atoms almost identical to those of DESPM.The longer analogues PIP(5,4,5) and PYR(5,4,5) are very similar in the spacing of their amino groups.However, the pKa of the nitrogens in the groups differ; thus, the extent of protonation and the charge characteristics among the members of the groups differ.A comparison of the biological properties of these compounds clearly demonstrates that the tetraamines must be charged to be "recognized" by the cell.Analogues with low nitrogen pKa's such that the nitrogens are poorly protonated at physiological pH do not compete well with spermidine for uptake and, as expected, have high 96 h IC50 values and have little effect on S-adenosylmethionine decarboxylase, ornithine decarboxylase, and spermidine/spermine N1-acetyltransferase activities and on intracellular polyamine pools.