PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 33527177-3 2021 Upadacitinib is a once-daily, oral Janus kinase (JAK) inhibitor with increased selectivity for JAK1 over JAK2, JAK3, and tyrosine kinase 2. upadacitinib 0-12 Janus kinase 2 Homo sapiens 105-109 34471993-11 2021 Simulations indicated that tofacitinib, upadacitinib, and baricitinib at steady state exhibited varying degrees of JAK 1/3 (daily average inhibition, 70-94%) and JAK 2/2 (23%-67%) inhibition at therapeutic concentrations, with Cmax values 17- to 33-fold lower than their TYK2 IC50 levels. upadacitinib 40-52 Janus kinase 2 Homo sapiens 162-169 34023008-1 2021 BACKGROUND: Upadacitinib is an oral Janus kinase (JAK) inhibitor with greater inhibitory potency for JAK1 than JAK2, JAK3, and tyrosine kinase 2. upadacitinib 12-24 Janus kinase 2 Homo sapiens 111-115 34023009-2 2021 Upadacitinib is an oral Janus kinase (JAK) inhibitor with greater inhibitory potency for JAK1 than JAK2, JAK3, or tyrosine kinase 2 that is being tested for atopic dermatitis. upadacitinib 0-12 Janus kinase 2 Homo sapiens 99-103 30394138-2 2019 Upadacitinib selectively inhibits Janus Kinase 1 (JAK1) which could potentially reduce JAK2 and JAK3-related side effects. upadacitinib 0-12 Janus kinase 2 Homo sapiens 87-91 31375130-9 2019 Notably, baricitinib inhibited JAK1/3 signaling to a lesser extent than upadacitinib and tofacitinib, while upadacitinib, baricitinib, and tofacitinib inhibited the signaling of JAK2/2-dependent cytokines, including GM-CSF and IL-3, as well as the signaling of the JAK2/TYK2-dependent cytokine G-CSF. upadacitinib 108-120 Janus kinase 2 Homo sapiens 178-182 32539713-5 2020 RESULTS: Treatment with JAKi (tofacitinib, baricitinib, upadacitinib) prevented GM-CSF-induced JAK2/STAT5 phosphorylation at higher concentrations (400 nM) in THP-1 cells. upadacitinib 56-68 Janus kinase 2 Homo sapiens 95-99 32539713-11 2020 Although baricitinib and upadacitinib almost completely blocked GM-CSF-mediated JAK2/STAT5 signaling, the inhibitory effects of tofacitinib were weaker at lower concentrations suggesting that variation exists among these JAKi in the inhibition of JAK2 signaling pathways. upadacitinib 25-37 Janus kinase 2 Homo sapiens 80-84