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Basic Information

ID: ALA1146026

Journal: Bioorg Med Chem Lett

Title: Novel, potent, selective, and orally bioavailable human betaII-tryptase inhibitors.

Authors: Sperandio D, Tai VW, Lohman J, Hirschbein B, Mendonca R, Lee CS, Spencer JR, Janc J, Nguyen M, Beltman J, Sprengeler P, Scheerens H, Lin T, Liu L, Gadre A, Kellogg A, Green MJ, McGrath ME.

Abstract: The synthesis of novel [1,2,4]oxadiazoles and their structure-activity relationship (SAR) for the inhibition of tryptase and related serine proteases is presented. Elaboration of the P'-side afforded potent, selective, and orally bioavailable tryptase inhibitors.

CiteXplore: 16725321

DOI: 10.1016/j.bmcl.2006.04.088