1622137-40-9

Basic information

• Product Name: 3-bromo-N-[2-(2-methyl-1H-indol-3-yl)ethyl]benzenesulfonamide
• Synonyms: 3-bromo-N-[2-(2-methyl-1H-indol-3-yl)ethyl]benzenesulfonamide
• CAS NO: 1622137-40-9
• Molecular Weight: 393.304
• Mol File: 1622137-40-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-bromo-N-[2-(2-methyl-1H-indol-3-yl)ethyl]benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-bromo-N-[2-(2-methyl-1H-indol-3-yl)ethyl]benzenesulfonamide(1622137-40-9)
• EPA Substance Registry System: 3-bromo-N-[2-(2-methyl-1H-indol-3-yl)ethyl]benzenesulfonamide(1622137-40-9)

Safety Data

• Hazardous Substances Data: 1622137-40-9(Hazardous Substances Data)

Upstream product

• 2731-06-8 2-methyltryptamine 
• 2905-24-0 3-Bromobenzenesulfonyl chloride 

Relevant articles and documents

Indole-3-ethylsulfamoylphenylacrylamides: Potent histone deacetylase inhibitors with anti-inflammatory activity

A series of 2-methyl-1H-indol-3-ethylsulfamoylphenylacrylamides based on LBH589-PXD101 core have been synthesized and evaluated for their histone deacetylase (HDAC) inhibitory and anti-inflammatory activity. In vitro, compounds 9-12 show 2.6-fold better HDAC inhibition and 3-fold better IL-6 suppression compared to LBH589·HCl (1·HCl). Furthermore, these compounds did not show apparent cell viability suppression on macrophages while in contrast, treatment with 1·HCl resulted in significant reduction in cell viability as demonstrated by an MTT assay. Repressed expression of iNOS, COX-2 and reduced phosphorylation of p65 revealed the inhibitory effect of these analogues on inflammatory mediator release which is related to inhibited NF-KB signals. (N-Hydroxy-3-{3-[2-(2-methyl-1H-indol-3-yl)-ethylsulfamoyl]-phenyl}- acrylamide) (9), exhibited ability superior to that of 1·HCl, was able to reduce carrageenan-induced acute inflammation in an animal model. Compounds 9-12 have potential anti-inflammatory activity and compound 9 can serve as lead compound for further development.