125960-59-0

Upstream product

• 55-81-2 4-Methoxyphenethylamine 
• 144818-94-0 5-<2-(trifluoroacetylamino)ethyl>-2-methoxybenzenesulfonyl chloride 
• 81654-47-9 2,2,2-Trifluoro-N-[2-(4-methoxyphenyl)ethyl]acetamide 

Downstream Products

• 308336-31-4 5-(2-aminoethyl)-2-methoxybenzenesulfonamide 
• 181272-10-6 1-[[5-[2-(5-chloro-2-methoxybenzamido)ethyl]-2-(2-methoxyethoxy)phenyl]sulfonyl]-3-methylthiourea 
• 181272-13-9 5-chloro-2-methoxy-N-(2-{4-[2-(2-methoxy-ethoxy)-ethoxy]-3-sulfamoyl-phenyl}-ethyl)-benzamide 
• 1026594-32-0 N-[2-(4-butoxy-3-sulfamoyl-phenyl)-ethyl]-5-chloro-2-methoxy-benzamide 
• 181272-12-8 5-(2-(5-chloro-2-methoxybenzamido)ethyl)-2-(2-methoxyethoxy)-benzenesulfonamide 
• 1027719-74-9 N-[2-(4-allyloxy-3-sulfamoyl-phenyl)-ethyl]-5-chloro-2-methoxy-benzamide 
• 1027378-67-1 5-chloro-2-methoxy-N-[2-(4-propoxy-3-sulfamoyl-phenyl)-ethyl]-benzamide 

Relevant academic research and scientific papers

PYRIMIDINE DERIVATIVES USED AS ITK INHIBITORS

The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I): and salts thereof. The compounds of the invention are inhibitors of kinase activity, in particular ltk activity.

Acylaminoalkyl-substituted benzenesulfonamide derivatives, their preparation, their use and pharmaceutical preparations comprising them

One embodiment of the present invention relates to acylaminoalkyl-substituted benzenesulfonamide derivatives of the formula (I), 1in which A, R(1), R(2), X, Y, and Z have the meanings indicated in the specification, and to pharmaceutically tolerable salt

Heteroarylacryloylaminoalkyl-substituted benzenesulfonamide derivatives, their preparation, their use and pharmaceutical preparations comprising them

One embodiment of the present invention relates to heteroarylacryloylaminoalkyl-substituted benzenesulfonamide derivatives of the formula (I), in which R(1), R(2), R(3), R(4), Het, X, Y and Z have the meanings indicated in the specification, and to pharma

Novel phenoxyalkylamine derivatives. VII. Synthesis and pharmacological activities of 2-alkoxy-5-[(phenoxyalkylamino)alkyl]benzenesulfonamide derivatives

To find a novel α-blocker with high α-blocking selectivity against dopamine D2-receptor affinity, we performed structural modification of the alkylene chains and the substituents on two benzene rings of 2-alkoxy-5-[(phenoxyalkylamino)alkyl]benzenesulfonamide derivatives. The modification of the alkylene chain between the amino moiety in the center of the molecule and the benzene ring (ring A) was found to be the most significant. 5-[2-[[2-(5-Fluoro-2-methoxyphenoxy)ethyl]amino]propyl]-2-methoxybenze nesulfonamide (II-4), which possesses 1-methylethyl as the alkylene chain, exhibited high α-blocking selectivity as well as potent α-blocking activity.