| Literature DB >> 9873535 |
C O Ogbu1, M N Qabar, P D Boatman, J Urban, J P Meara, M D Ferguson, J Tulinsky, C Lum, S Babu, M A Blaskovich, H Nakanishi, F Ruan, B Cao, R Minarik, T Little, S Nelson, M Nguyen, A Gall, M Kahn.
Abstract
The general approach of using a bicyclic template to produce inhibitors of the protease superfamily of enzymes has been investigated. The Diels Alder cycloaddition reaction on solid support has been found to be highly efficient for the synthesis of libraries of compounds that mimic the beta-strand secondary structure of proteins. Several potent and selective inhibitors of proteases have been discovered.Mesh:
Substances:
Year: 1998 PMID: 9873535 DOI: 10.1016/s0960-894x(98)00420-x
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823