207686-06-4Relevant academic research and scientific papers
Structure-based design and synthesis of a series of hydroxamic acids with a quaternary-hydroxy group in P1 as inhibitors of matrix metalloproteinases
Jacobson, Irina C.,Reddy, Prabhakar G.,Wasserman, Zelda R.,Hardman, Karl D.,Covington, Maryanne B.,Arner, Elizabeth C.,Copeland, Robert A.,Decicco, Carl P.,Magolda, Ronald L.
, p. 837 - 842 (2007/10/03)
Examination of the S1 area of the active site of pro-stromelysin has led us to the design of novel and potent inhibitors of matrix metalloproteinases containing constrained quaternary-hydroxy group at P1. The synthesis and biological activity of these compounds with variations at P1', P2', and P3' will be described.
