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ACS Medicinal Chemistry Letters|March 19, 2020
Structure-Activity Relationship Evaluation of Wasp Toxin β-PMTX Leads to Analogs with Superior Activity for Human Neuronal Sodium ChannelsCatherine E Garrison, Wendy Guan, Mitsunori Kato, et al.
ACS Medicinal Chemistry Letters|January 8, 2019
Analogues of the Lignan Pinoresinol as Novel Lead Compounds for P-glycoprotein (P-gp) InhibitorsJerónimo Laiolo, Tihomir Tomašič, D Mariano A Vera, et al.
ACS Medicinal Chemistry Letters|January 8, 2019
Hybrid Inhibitors of Malarial Dihydrofolate Reductase with Dual Binding Modes That Can Forestall ResistanceBongkoch Tarnchompoo, Penchit Chitnumsub, Aritsara Jaruwat, et al.
ACS Medicinal Chemistry Letters|January 8, 2019
New in Vitro Assay Measuring Direct Interaction of Nonsense Suppressors with the Eukaryotic Protein Synthesis MachineryMartin Y Ng, Haibo Zhang, Amy Weil, et al.
ACS Medicinal Chemistry Letters|December 21, 2017
Identification of an Indazole-Based Pharmacophore for the Inhibition of FGFR Kinases Using Fragment-Led de Novo DesignLewis D Turner, Abbey J Summers, Laura O Johnson, et al.
ACS Medicinal Chemistry Letters|December 21, 2017
Antitubercular Nitroimidazoles Revisited: Synthesis and Activity of the Authentic 3-Nitro Isomer of PretomanidAndrew M Thompson, Muriel Bonnet, Ho H Lee, et al.
ACS Medicinal Chemistry Letters|December 21, 2017
Discovery of a Slow Tight Binding LPA1 Antagonist (ONO-0300302) for the Treatment of Benign Prostatic HyperplasiaMasahiko Terakado, Hidehiro Suzuki, Kazuya Hashimura, et al.
ACS Medicinal Chemistry Letters|December 21, 2017
Design and Synthesis of Piperazine Sulfonamide Cores Leading to Highly Potent HIV-1 Protease InhibitorsChristopher J Bungard, Peter D Williams, Jurgen Schulz, et al.
ACS Medicinal Chemistry Letters|December 21, 2017
Correction to "Structure-Based Design of ASK1 Inhibitors as Potential Agents for Heart Failure"Marion Lanier, Jason Pickens, Simone V Bigi, et al.
ACS Medicinal Chemistry Letters|December 24, 2013
Bisubstrate Inhibitors of Biotin Protein Ligase in Mycobacterium tuberculosis Resistant to Cyclonucleoside FormationCe Shi, Divya Tiwari, Daniel J Wilson, et al.
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