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Journal of Medicinal Chemistry|March 4, 2005
Structure-based design, synthesis, and study of potent inhibitors of beta-ketoacyl-acyl carrier protein synthase III as potential antimicrobial agentsZhe Nie, Carin Perretta, Jia Lu, et al.Journal of Medicinal Chemistry|December 12, 2003
Structure-based design, synthesis, and antimicrobial activity of indazole-derived SAH/MTA nucleosidase inhibitorsXiaoming Li, Sam Chu, Victoria A Feher, et al.ACS Medicinal Chemistry Letters|June 22, 2019
Discovery of Orally Active Hydroxyethylamine Based SPPL2a InhibitorsJuraj Velcicky, Casey J N Mathison, Victor Nikulin, et al.Bioorganic & Medicinal Chemistry Letters|April 23, 2014
Discovery of structurally novel, potent and orally efficacious GPR119 agonistsPhil Alper, Mihai Azimioara, Christopher Cow, et al.Bioorganic & Medicinal Chemistry Letters|December 3, 2014
Novel tricyclic pyrazolopyrimidines as potent and selective GPR119 agonistsMihai Azimioara, Phil Alper, Christopher Cow, et al.Journal of Medicinal Chemistry|April 6, 2021
Structure-Based Design of Selective LONP1 Inhibitors for Probing In Vitro BiologyLaura J Kingsley, Xiaohui He, Matthew McNeill, et al.Journal of Medicinal Chemistry|May 19, 2026
Targeting Multiple KRAS Mutations with High-Affinity Macrocyclic Inhibitors: From Discovery to Preclinical ValidationDean P Phillips, Phil B Alper, Charles Y Cho, et al.Pageof 1