17 results on '"Roberts, Susan B."'
Search Results
2. Discovery and initial optimization of alkoxyanthranilic acid derivatives as inhibitors of HCV NS5B polymerase
3. Discovery and preclinical evaluation of potent, orally bioavailable, metabolically stable cyclopropylindolobenzazepine acylsulfonamides as thumb site 1 inhibitors of the hepatitis c virus NS5B RNA-dependent, RNA polymerase
4. Identification of a novel series of potent HCV NS5B Site I inhibitors
5. 2-(N-Benzyl-N-phenylsulfonamido)alkyl amide derivatives as γ-secretase inhibitors
6. Synthesis and SAR studies of novel heteroaryl fused tetracyclic indole-diamide compounds: Potent allosteric inhibitors of the hepatitis C virus NS5B polymerase
7. Syntheses and initial evaluation of a series of indolo-fused heterocyclic inhibitors of the polymerase enzyme (NS5B) of the hepatitis C virus
8. 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
9. Carbamate-appended N-alkylsulfonamides as inhibitors of γ-secretase
10. Nitrogen-appended N-alkylsulfonamides as inhibitors of γ-secretase
11. 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]
12. Amino-caprolactam derivatives as γ-secretase inhibitors
13. 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
14. Discovery of (S)-2-((S)-2-(3,5-difluorophenyl)-2-hydroxyacetamido)-N-((S,Z)-3-methyl-4-oxo-4,5-dihydro-3H-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
15. 2,3-Benzodiazepin-1,4-diones as peptidomimetic inhibitors of γ-secretase
16. Hydroxytriamides as potent γ-secretase inhibitors
17. Corrigendum to “Hydroxytriamides as potent γ-secretase inhibitors”: [Bioorg. Med. Chem. Lett. 14 (2004) 1917]
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.