Discovery and Validation of a Series of Aryl Sulfonamides as Selective Inhibitors of Tissue-Nonspecific Alkaline Phosphatase (TNAP)

被引:81
作者
Dahl, Russell [1 ]
Sergienko, Eduard A. [1 ]
Su, Ying [1 ]
Mostofi, Yalda S. [1 ]
Yang, Li [1 ]
Simao, Ana Maria [2 ]
Narisawa, Sonoko [2 ]
Brown, Brock [1 ]
Mangravita-Novo, Arianna [1 ]
Vicchiarelli, Michael [1 ]
Smith, Layton H. [1 ]
O'Neill, W. Charles [3 ]
Millan, Jose Luis [2 ]
Cosford, Nicholas D. P. [1 ]
机构
[1] Burnham Inst Med Res, Conrad Prebys Ctr Chem Genom, La Jolla, CA 92037 USA
[2] Burnham Inst Med Res, Sanford Childrens Hlth Res Ctr, La Jolla, CA 92037 USA
[3] Emory Univ, Sch Med, Div Renal, Dept Med, Atlanta, GA 30322 USA
关键词
INORGANIC PYROPHOSPHATE; VASCULAR CALCIFICATION; MINERALIZATION; OSTEOPONTIN; BINDING; BONE;
D O I
10.1021/jm900383s
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
We report the characterization and optimization of drug-like small molecule inhibitors of tissue-nonspecific alkaline phosphatase (TNAP), an enzyme critical for the regulation of extracellular matrix calcification during bone formation and growth. High-throughput screening (HTS) of a small molecule library led to the identification of arylsulfonamides as potent and selective inhibitors of TNAP. Critical structural requirements for activity were determined, and the compounds were subsequently profiled for in vitro activity and bioavailability parameters including metabolic stability and permeability. The plasma levels following subcutaneous administration of a member of the lead series in rat was determined, demonstrating the potential of these TNAP inhibitors as systemically active therapeutic agents to target various diseases involving soft tissue calcification. A representative member of the series was also characterized in mechanistic and kinetic studies.
引用
收藏
页码:6919 / 6925
页数:7
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