Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain Penetrant, and Orally Bioavailable CXCR2 Antagonists
Por um escritor misterioso
Last updated 03 junho 2024
Discovery of CNS Penetrant CXCR2 Antagonists for the Potential Treatment of CNS Demyelinating Disorders
Allosteric Modulation of Class A GPCRs: Targets, Agents, and Emerging Concepts
Discovery, structure-activity relationship study and biological evaluation of 2-thioureidothiophene-3-carboxylates as a novel class of C-X-C chemokine receptor 2 (CXCR2) antagonists - ScienceDirect
Advances in targeting Phosphodiesterase 1: From mechanisms to potential therapeutics - ScienceDirect
WO2014033122A1 - Inhibitors of cd40-traf6 interaction - Google Patents
Discovery of Novel 1-Cyclopentenyl-3-phenylureas as Selective, Brain Penetrant, and Orally Bioavailable CXCR2 Antagonists
Allosteric Modulation of Class A GPCRs: Targets, Agents, and Emerging Concepts. - Abstract - Europe PMC
Xichen Lin's research works China Academy of Building Research Shanghai Branch, Shanghai and other places
Chan–Lam Reaction and Lewis Acid Promoted 1,3-Rearrangement of N–O Bonds to Prepare N-(2-Hydroxyaryl)pyridin-2-ones
1-(3-tert-butylsulfonyl-4-cyano-2-hydroxyphenyl)-3 -[(1R)-2-methylcyclopent-2-en-1-yl]urea, C18H23N3O4S
Directing the Metabolism of Drugs Away from CYP450: The Use of Oxetane Rings
Ting Yang's research works China Academy of Building Research Shanghai Branch, Shanghai and other places
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