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6. Discovery of BMS-961955, an allosteric inhibitor of the hepatitis C virus NS5B polymerase

11. Synthesis and SAR studies of novel heteroaryl fused tetracyclic indole-diamide compounds: Potent allosteric inhibitors of the hepatitis C virus NS5B polymerase

12. Syntheses and initial evaluation of a series of indolo-fused heterocyclic inhibitors of the polymerase enzyme (NS5B) of the hepatitis C virus

13. Investigation of the mode of binding of a novel series of N-benzyl-4-heteroaryl-1-(phenylsulfonyl)piperazine-2-carboxamides to the hepatitis C virus polymerase

16. Amino-caprolactam derivatives as γ-secretase inhibitors

17. Discovery of ( S)-2-(( S)-2-(3,5-difluorophenyl)-2-hydroxyacetamido)- N-(( S, Z)-3-methyl-4-oxo-4,5-dihydro-3 H-benzo[ d][1,2]diazepin-5-yl)propanamide (BMS-433796): A γ-secretase inhibitor with Aβ lowering activity in a transgenic mouse model of Alzheimer’s disease

20. Corrigendum to “Investigation of the mode of binding of a novel series of N-benzyl-4-heteroaryl-1-(phenylsulfonyl)piperazine-2-carboxamides to the hepatitis C virus polymerase” [Bioorg. Med. Chem. Lett. 21 (2011) 2212]

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