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Bioorganic & Medicinal Chemistry Letters|October 4, 2016
N-Arylsulfonyl-α-amino carboxamides are potent and selective inhibitors of the chemokine receptor CCR10 that show efficacy in the murine DNFB model of contact hypersensitivityAsitha Abeywardane, Gary Caviness, Younggi Choi, et al.Journal of Virology|October 29, 2020
Shared Mechanisms Govern HIV Transcriptional Suppression in Circulating CD103<sup>+</sup> and Gut CD4<sup>+</sup> T CellsSteven A Yukl, Shahzada Khan, Tsui-Hua Chen, et al.Journal of Medicinal Chemistry|July 14, 2020
Discovery of an Orally Available Diazabicyclooctane Inhibitor (ETX0282) of Class A, C, and D Serine β-LactamasesThomas F Durand-Réville, Janelle Comita-Prevoir, Jing Zhang, et al.Cellular Oncology (Dordrecht, Netherlands)|July 23, 2022
Novel protein kinase inhibitor TT-00420 inhibits gallbladder cancer by inhibiting JNK/JUN-mediated signaling pathwayHuijie Miao, Yajun Geng, Yang Li, et al.JCI Insight|November 8, 2024
SLC6A19 inhibition facilitates urinary neutral amino acid excretion and lowers plasma phenylalanineHeike J Wobst, Andreu Viader, Giovanni Muncipinto, et al.The Oncologist|February 1, 2024
First-In-Human Phase I Study of Tinengotinib (TT-00420), a Multiple Kinase Inhibitor, as a Single Agent in Patients With Advanced Solid TumorsSarina A Piha-Paul, Binghe Xu, Ecaterina E Dumbrava, et al.Pageof 5