125488-16-6

Basic information

• Product Name: 4-(4-bromophenyl)-2-(piperidin-1-yl)thiazole
• Synonyms: 4-(4-bromophenyl)-2-(piperidin-1-yl)thiazole
• CAS NO: 125488-16-6
• Molecular Weight: 323.256
• Mol File: 125488-16-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 4-(4-bromophenyl)-2-(piperidin-1-yl)thiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-bromophenyl)-2-(piperidin-1-yl)thiazole(125488-16-6)
• EPA Substance Registry System: 4-(4-bromophenyl)-2-(piperidin-1-yl)thiazole(125488-16-6)

Safety Data

• Hazardous Substances Data: 125488-16-6(Hazardous Substances Data)

Upstream product

• 110-89-4 piperidine 
• 3884-33-1 2-chloro-4-(p-bromophenyl)-thiazole 
• 14294-09-8 piperidine-1-carbothioamide 
• 99-73-0 para-bromophenacyl bromide 
• 4540-33-4 piperdinium acetate 
• 65679-14-3 1-(4-bromophenyl)-2-thiocyanatoethanone 

Relevant articles and documents

Synthesis and structure-activity relationship of aminoarylthiazole derivatives as correctors of the chloride transport defect in cystic fibrosis

Abstract The cystic fibrosis transmembrane conductance regulator (CFTR) is a chloride channel present in the membrane of epithelial cells. Mutations affecting the CFTR gene cause cystic fibrosis (CF), a multi-organ severe disease. The most common CF mutation, F508del, impairs the processing and activity (gating) of CFTR protein. Other mutations, like G551D, only cause a gating defect. Processing and gating defects can be targeted by small molecules called generically correctors and potentiators, respectively. Aminoarylthiazoles (AATs) represent an interesting class of compounds that includes molecules with dual activity, as correctors and potentiators. With the aim to improve the activity profile of AATs, we have now designed and synthesized a library of novel compounds in order to establish an initial SAR that may provide indications about the chemical groups that are beneficial or detrimental for rescue activity. The new compounds were tested as correctors and potentiators in CFBE41o-expressing F508del-CFTR using a functional assay. A dual active compound, AAT-4a, characterized by improved efficacy and marked synergy when combined with the corrector VX-809 has been identified. Moreover, by computational methods, a possible binding site for AATs in nucleotide binding domain NBD1 has been detected. These results will direct the synthesis of new analogues with possibly improved activity.

ARYLTHIAZOLYL PIPERIDINES AND RELATED COMPOUNDS AS MODULATORS OF SURVIVAL MOTOR NEURON (SMN) PROTEIN PRODUCTION

Aryl substituted thiazol-2-yl-piperidines and related compounds useful as modulators of survival motor neuron (SMN) protein production are provided herein. Without being bound to any particular theory it is believed the aryl substituted thiazol-2-yl-piper

Substituted 2-Aminothiazoles from α-Thiocyanato-acetophenones and Dialkylamines

α-Thiocyanato-acetophenones 1 react with dialkylammonium salts of weak acids (acetates, propionates, benzoates) to give 2-dialkylamino-4-aryl-thiazoles 4.As reaction medium aliphatic alcohols (methanol, ethanol), dipolar-aprotic solvents (acetonitrile, di