904813-75-8Relevant academic research and scientific papers
Novel bis-(arylsulfonamide) hydroxamate-based selective MMP inhibitors
Subramaniam, Rajesh,Haldar, Manas K.,Tobwala, Shakila,Ganguly, Bratati,Srivastava,Mallik, Sanku
supporting information; experimental part, p. 3333 - 3337 (2009/04/11)
A series of bis-(arylsulfonamide) hydroxamate inhibitors were synthesized. These compounds exhibit good potency against MMP-7 and MMP-9 depending on the nature, steric bulk, and substitution pattern of the substituents in the benzene ring. In general, the preliminary structure-activity relationships (SAR) suggest that among the DAPA hydroxamates (i) electron-rich benzene rings of the sulfonamides may produce better inhibitors than electron-poor analogs. However, potential H-bond acceptors can reverse the trend depending on the isozyme; (ii) isozyme selectivity between MMP-7 and -9 can be conferred through steric bulk and substitution pattern of the substituents in the benzene ring, and (iii) the MMP-10 inhibition pattern of the compounds paralleled that for MMP-9.
