Browsing by Author Ghosh, A. K.

Showing results 1 to 6 of 6
Issue DateTitleAuthor(s)Third Mission
2018The Curtius Rearrangement: Applications in Modern Drug Discovery and Medicinal ChemistryGhosh, A. K.; Brindisi, Margherita ; Sarkar, A.Not applicable
2018Design and Synthesis of Highly Potent HIV-1 Protease Inhibitors Containing Tricyclic Fused Ring Systems as Novel P2 Ligands: Structure-Activity Studies, Biological and X-ray Structural AnalysisGhosh, A. K.; Nyalapatla, R. P.; Kovela, S.; Rao, K. V.; Brindisi, Margherita ; Osswald, H. L.; Amano, M.; Aoki, M.; Agniswamy, J.; Wang, Y. -F.; Weber, I. T.; Mitsuya, H.Not applicable
2018Design, synthesis, X-ray studies, and biological evaluation of novel BACE1 inhibitors with bicyclic isoxazoline carboxamides as the P3 ligandGhosh, A. K.; Ghosh, K.; Brindisi, Margherita ; Lendy, E. K.; Yen, Y. -C.; Kumaragurubaran, N.; Huang, X.; Tang, J.; Mesecar, A. D.Not applicable
2019Highly Selective and Potent Human β-Secretase 2 (BACE2) Inhibitors against Type 2 Diabetes: Design, Synthesis, X-ray Structure and Structure–Activity Relationship StudiesGhosh, A. K.; Brindisi, Margherita ; Yen, Y. -C.; Lendy, E. K.; Kovela, S.; Cardenas, E. L.; Reddy, B. S.; Rao, K. V.; Downs, D.; Huang, X.; Tang, J.; Mesecar, A. D.Not applicable
2018Nature Inspired Molecular Design: Stereoselective Synthesis of Bicyclic and Polycyclic Ethers for Potent HIV-1 Protease InhibitorsGhosh, A. K.; Brindisi, Margherita Not applicable
2008Potent HIV-1 protease inhibitors incorporating meso-bicyclic urethanes as P2-ligands: structure-based design, synthesis, biological evaluation and protein-ligand X-ray studiesGhosh, A. K.; Gemma, Sandra ; Takayama, J.; Baldridge, A.; Leshchenko-Yashchuk, S.; Miller, H. B.; Wang, Y. F.; Kovalevsky, A-Y.; Koh, Y.; Weber, I. T.; Mitsuya, H.Not applicable