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The Role of the Acidity of N-Heteroaryl Sulfonamides as Inhibitors of Bcl-2 Family Protein-Protein Interactions

  作者 TOURE B BARRY; MILLERMOSLIN KAREN; YUSUFF NAEEM; PEREZ LAWRENCE; DORE MICHAEL; JOUD CAROL; MICHAEL WALTER; DIPIETRO LUCIAN; VAN DER PLAS SIMON; MCEWAN MICHAEL; LENOIR FRANCOIS; HOE MADELENE; KARKI RAJESH; SPRINGER CLAYTON; SULLIVAN JOHN; LEVINE KYMBERLY; FIORILLA CATHERINE; XIE XIAOLING; KULATHILA RAVIRAJ; HERLIHY KARA; PORTER DALE; VISSER MICHAEL  
  选自 期刊  ACS Medicinal Chemistry Letters;  卷期  2013年4-2;  页码  186-190  
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[摘要]Overexpression of the antiapoptotic members of the Bcl-2 family of proteins is commonly associated with cancer cell survival and resistance to chemotherapeutics. Here, we describe the structure-based optimization of a series of N-heteroaryl sulfonamides that demonstrate potent mechanism-based cell death. The role of the acidic nature of the sulfonamide moiety as it relates to potency, solubility, and clearance is examined. This has led to the discovery of novel heterocyclic replacements for the acylsulfonamide core of ABT-737 and ABT-263.

 
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