Author/Authors :
Stuart Bailey، نويسنده , , Brian Bolognese، نويسنده , , Derek R. Buckle، نويسنده , , Andrew Faller، نويسنده , , Sally Jackson، نويسنده , , Pearl Louis-Flamberg، نويسنده , , Mark McCord، نويسنده , , Ruth J. Mayer، نويسنده , , Lisa A. Marshall، نويسنده , , David G. Smith، نويسنده ,
Abstract :
A series of hydroxamic acids related to the non-selective matrix metalloprotease inhibitor Batimastat is described, which inhibits the proteolytic cleavage of the low affinity IgE receptor from cell membrane preparations. Limited SAR studies suggest that the structural requirements for effective inhibition are distinct from those required for the inhibition of collagenase.
We have examined the P1′ requirements for hydroxamate based inhibitors of the novel metalloprotease responsible for processing of the low affinity IgE receptor (CD23).
