Abstract

High-throughput screening has identified 1-methyl-3-(trifluoromethyl)- N-[4-(pyrrolidinylsulfonyl)phenyl]-1 H-pyrazole-5-carboxamide 16677 as a novel and potent (IC 50 = 35–145 nM) inhibitor against multiple primary isolates of diverse measles virus (MV) genotypes currently circulating worldwide. The synthesis of 16677 and several analogs together with effects on MV replication is described. The most potent analog displays nanomolar inhibition against the MV and a selectivity ratio (CC 50/IC 50) of ca. 16,500.

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