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Bioorganic & Medicinal Chemistry Letters|February 17, 2006
Design and synthesis of novel HIV-1 protease inhibitors incorporating oxyindoles as the P2'-ligandsArun K Ghosh, Gary Schiltz, Ramu Sridhar Perali, et al.Journal of Bioenergetics and Biomembranes|November 13, 2008
The yeast mitochondrial citrate transport protein: identification of the Lysine residues responsible for inhibition mediated by Pyridoxal 5'-phosphateSreevidya Remani, Jiakang Sun, Rusudan Kotaria, et al.Journal of Medicinal Chemistry|May 13, 2005
Structure-based design: synthesis and biological evaluation of a series of novel cycloamide-derived HIV-1 protease inhibitorsArun K Ghosh, Lisa M Swanson, Hanna Cho, et al.Bioorganic & Medicinal Chemistry Letters|December 26, 2009
Synthesis and biological evaluation of novel allophenylnorstatine-based HIV-1 protease inhibitors incorporating high affinity P2-ligandsArun K Ghosh, Sandra Gemma, Elena Simoni, et al.Bioorganic & Medicinal Chemistry Letters|August 17, 2019
Potent HIV-1 protease inhibitors incorporating squaramide-derived P2 ligands: Design, synthesis, and biological evaluationArun K Ghosh, Jacqueline N Williams, Satish Kovela, et al.Bioorganic & Medicinal Chemistry Letters|October 26, 2016
Variation of the aryl substituent on the piperazine ring within the 4-(piperazin-1-yl)-2,6-di(pyrrolidin-1-yl)pyrimidine scaffold unveils potent, non-competitive inhibitors of the inflammatory caspasesCourtney R Kent, Magdalena Bryja, Helen A Gustafson, et al.The Journal of Biological Chemistry|July 8, 2010
Conformational changes in BAK, a pore-forming proapoptotic Bcl-2 family member, upon membrane insertion and direct evidence for the existence of BH3-BH3 contact interface in BAK homo-oligomersKyoung Joon Oh, Pawan Singh, Kyungro Lee, et al.Journal of Medicinal Chemistry|August 18, 2006
Structure-based design of novel HIV-1 protease inhibitors to combat drug resistanceArun K Ghosh, Perali Ramu Sridhar, Sofiya Leshchenko, et al.Pageof 4