64353-16-8

Basic information

• Product Name: 5-chloro-2-methoxy-N-(4-methylbenzyl)benzamide
• Synonyms: 5-chloro-2-methoxy-N-(4-methylbenzyl)benzamide
• CAS NO: 64353-16-8
• Molecular Formula: C₁₆H₁₆ClNO₂
• Molecular Weight: 289.75674
• Mol File: 64353-16-8.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-chloro-2-methoxy-N-(4-methylbenzyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 5-chloro-2-methoxy-N-(4-methylbenzyl)benzamide(64353-16-8)
• EPA Substance Registry System: 5-chloro-2-methoxy-N-(4-methylbenzyl)benzamide(64353-16-8)

Safety Data

• Hazardous Substances Data: 64353-16-8(Hazardous Substances Data)

Upstream product

• 3438-16-2 5-chloro-2-methoxybenzoic acid 
• 104-84-7 para-methylbenzylamine 

Relevant articles and documents

Structure-Activity Relationship Studies on Diversified Salicylamide Derivatives as Potent Inhibitors of Human Adenovirus Infection

The effective treatment of adenovirus (HAdV) infections in immunocompromised patients still poses great challenges. Herein, we reported our continued efforts to optimize a series of salicylamide derivatives as potent inhibitors of HAdV infection. Of these, nine compounds (11, 13, 14, 17, 20, 58, 60, 62, and 70) showed significantly improved anti-HAdV activities with nanomolar to submicromolar IC50 values and high selectivity indexes (SI > 100), indicating better safety windows, compared to those of the lead compound niclosamide. Our mechanistic assays suggest that compounds 13, 62, and 70 exert their activities in the HAdV entry pathway, while compounds 14 and 60 likely target the HAdV DNA replication, and 11, 17, 20, and 58 inhibit later steps after DNA replication. Given the broad anti-viral activity profile of niclosamide, these derivatives may also offer therapeutic potential for other viral infections.