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Expert Opinion on Therapeutic Patents|January 10, 2022
Selective TYK2 inhibitors as potential therapeutic agents: a patent review (2019-2021)Felix Gonzalez Lopez de Turiso, Kevin GuckianOrganic & Biomolecular Chemistry|July 21, 2005
Synthetic studies towards furanocembrane diterpenes. A total synthesis of bis-deoxylophotoxinManuel Cases, Felix Gonzalez-Lopez de Turiso, Maria S Hadjisoteriou, et al.ACS Medicinal Chemistry Letters|April 16, 2020
Discovery of CNS-Penetrant Apoptosis Signal-Regulating Kinase 1 (ASK1) InhibitorsZhili Xin, Martin K Himmelbauer, J Howard Jones, et al.The Journal of Organic Chemistry|August 19, 2007
An efficient and scalable one-pot double Michael addition-Dieckmann condensation for the synthesis of 4,4-disubstituted cyclohexane beta-keto estersMichael R DeGraffenreid, Sarah Bennett, Sebastien Caille, et al.Journal of Medicinal Chemistry|November 12, 2019
Rational Design and Optimization of a Novel Class of Macrocyclic Apoptosis Signal-Regulating Kinase 1 InhibitorsMartin K Himmelbauer, Zhili Xin, J Howard Jones, et al.Bioorganic & Medicinal Chemistry Letters|November 25, 2010
Synthesis and optimization of novel 4,4-disubstituted cyclohexylbenzamide derivatives as potent 11β-HSD1 inhibitorsDaqing Sun, Zhulun Wang, Seb Caille, et al.Journal of Medicinal Chemistry|October 15, 2021
Discovery of Potent, Selective, and Brain-Penetrant Apoptosis Signal-Regulating Kinase 1 (ASK1) Inhibitors that Modulate Brain Inflammation <i>In Vivo</i>J Howard Jones, Zhili Xin, Martin Himmelbauer, et al.Journal of Medicinal Chemistry|August 11, 2012
Discovery and in vivo evaluation of dual PI3Kβ/δ inhibitorsFelix Gonzalez-Lopez de Turiso, Youngsook Shin, Matthew Brown, et al.ACS Medicinal Chemistry Letters|June 6, 2014
Discovery of AMG 853, a CRTH2 and DP Dual AntagonistJiwen Liu, An-Rong Li, Yingcai Wang, et al.Journal of Medicinal Chemistry|May 4, 2021
Discovery of Potent and Brain-Penetrant Tau Tubulin Kinase 1 (TTBK1) Inhibitors that Lower Tau Phosphorylation In VivoTamara Halkina, Jaclyn L Henderson, Edward Y Lin, et al.Pageof 2