1567327-12-1

Basic information

• Product Name: 2-(4-(piperidin-1-ylmethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one
• Synonyms: 2-(4-(piperidin-1-ylmethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one
• CAS NO: 1567327-12-1
• Molecular Weight: 371.341
• Mol File: 1567327-12-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(4-(piperidin-1-ylmethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-(piperidin-1-ylmethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one(1567327-12-1)
• EPA Substance Registry System: 2-(4-(piperidin-1-ylmethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one(1567327-12-1)

Safety Data

• Hazardous Substances Data: 1567327-12-1(Hazardous Substances Data)

Upstream product

• 118-92-3 anthranilic acid 
• 110-89-4 piperidine 
• 59507-44-7 1-(4-nitrobenzyl)piperidine 
• 100-11-8 1-bromomethyl-4-nitro-benzene 
• 29608-05-7 1-(4-aminobenzyl)piperidine 
• 1441-85-6 2-(chloroseleno)benzoyl chloride 
• 6512-83-0 2,2'-diselanediyl-di-benzoic acid 

Relevant articles and documents

Synthesis and biological evaluation of a new series of ebselen derivatives as glutathione peroxidase (GPx) mimics and cholinesterase inhibitors against Alzheimer's disease

A series of ebselen derivatives were designed, synthesised and evaluated as inhibitors of cholinesterases (ChEs) and glutathione peroxidase (GPx) mimics. Most of the compounds were found to be potent against AChEs and BuChE, compounds 5e and 5i, proved to be the most potent against AChE with IC50 values of 0.76 and 0.46 μM, respectively. Among these hybrids, most of the compounds were found to be good GPx mimics compare with ebselen. The selected compounds 5e and 5i were also used to determine the catalytic parameters and in vitro hydrogen peroxide scavenging activity. The results indicate that compounds 5e and 5i may be excellent multifunctional agents for the treatment of AD.