23 results on '"Rossman, Randall"'
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2. Effects of SCH 59228, an orally bioavailable farnesyl protein transferase inhibitor, on the growth of oncogene-transformed fibroblasts and a human colon carcinoma xenograft in nude mice
3. A convergent preparation of the CHK1 inhibitor MK-8776 (SCH 900776)
4. 2′-Modified Guanosine Analogs for the Treatment of HCV
5. Synthesis and SAR of geminal substitutions at the C5′ carbosugar position of pyrimidine-derived HCV inhibitors
6. Synthesis and SAR of pyridothiazole substituted pyrimidine derived HCV replication inhibitors
7. Pyridofuran substituted pyrimidine derivatives as HCV replication (replicase) inhibitors
8. 5-Benzothiazole substituted pyrimidine derivatives as HCV replication (replicase) inhibitors
9. Discovery of pyrazolo[1,5-a]pyrimidine-based CHK1 inhibitors: A template-based approach—Part 1
10. Discovery of pyrazolo[1,5-a]pyrimidine-based CHK1 inhibitors: A template-based approach—Part 2
11. Discovery of Dinaciclib (SCH 727965): A Potent and Selective Inhibitor of Cyclin-Dependent Kinases
12. Pyrazolo[1,5- a]pyrimidines as orally available inhibitors of cyclin-dependent kinase 2
13. Identification of Pharmacokinetically Stable 3,10-Dibromo-8-chlorobenzocycloheptapyridine Farnesyl Protein Transferase Inhibitors with Potent Enzyme and Cellular Activities
14. Tricyclic Farnesyl Protein Transferase Inhibitors: Crystallographic and Calorimetric Studies of Structure−Activity Relationships
15. (+)-4-[2-[4-(8-Chloro-3,10-dibromo-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]- pyridin-11(R)-yl)-1-piperidinyl]-2-oxo-ethyl]-1-piperidinecarboxamide (SCH-66336): A Very Potent Farnesyl Protein Transferase Inhibitor as a Novel Antitumor Agent
16. Inhibitors of Farnesyl Protein Transferase. 4-Amido, 4-Carbamoyl, and 4-Carboxamido Derivatives of 1-(8-Chloro-6,11-dihydro-5H-benzo[5,6]- cyclohepta[1,2-b]pyridin-11-yl)piperazine and 1-(3-Bromo-8-chloro-6,11- dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)piperazine
17. Novel semisynthetic oxo and alkyl macrolide antibacterials and related derivatives.
18. Kijanimicin. Part 3. Structure and absolute stereochemistry of kijanimicin.
19. Semisynthetic macrolide antibacterials derived from tylosin. Synthesis of 23-O-demycinosyltylosin and related compounds.
20. Semisynthetic macrolide antibacterials derived from tylosin. Synthesis of 3-O-acetyl-23-O-demycinosyl-4″-O-isovaleryltylosin and related compounds, as well as the 12,13-epoxy derivatives.
21. Novel 3-O-α-L-cladinosyl sixteen-membered macrolide antibacterials.
22. Kijanimicin. 2. Structure and absolute stereochemistry of kijanimicin
23. Kijanimicin. 1. Structures of the individual sugar components
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