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Identifying the Roles of Amino Acids, Alcohols and 1,2-Diamines as Mediators in Coupling of Haloarenes to Arenes
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December 2014 |
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Placebo-Controlled Trial of an Oral BTK Inhibitor in Multiple Sclerosis
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June 2019 |
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Oxetane Substrates of Human Microsomal Epoxide Hydrolase
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June 2017 |
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Zanubrutinib: First Approval
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January 2020 |
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Applications of Fluorine in Medicinal Chemistry
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July 2015 |
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Managing toxicities of Bruton tyrosine kinase inhibitors
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December 2020 |
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Synthesis and evaluation of CS-2100, a potent, orally active and S1P3- sparing S1P1 agonist
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May 2012 |
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Specific Btk inhibition suppresses B cell– and myeloid cell–mediated arthritis
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November 2010 |
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In vitro models for liver toxicity testing
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January 2013 |
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B-Cell Receptor Signaling Inhibitors for Treatment of Autoimmune Inflammatory Diseases and B-Cell Malignancies
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July 2013 |
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Structures of human Bruton's tyrosine kinase in active and inactive conformations suggest a mechanism of activation for TEC family kinases: Crystal Structures of Human BTK Kinase Domain
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January 2010 |
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Population Pharmacokinetics and Exposure Response Assessment of CC-292, a Potent BTK Inhibitor, in Patients With Chronic Lymphocytic Leukemia: Journal of Clinical Pharmacology
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May 2017 |
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Mechanistic Investigation of the Staudinger Ligation
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March 2005 |
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HM71224, a novel Bruton’s tyrosine kinase inhibitor, suppresses B cell and monocyte activation and ameliorates arthritis in a mouse model: a potential drug for rheumatoid arthritis
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April 2016 |
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Antiarthritis Effect of a Novel Bruton's Tyrosine Kinase (BTK) Inhibitor in Rat Collagen-Induced Arthritis and Mechanism-Based Pharmacokinetic/Pharmacodynamic Modeling: Relationships between Inhibition of BTK Phosphorylation and Efficacy
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April 2011 |
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Next‐generation Bruton's tyrosine kinase inhibitor BIIB091 selectively and potently inhibits B cell and Fc receptor signaling and downstream functions in B cells and myeloid cells
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January 2021 |
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Tec Family Kinases in t Lymphocyte Development and Function
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April 2005 |
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Discovery of BIIB068: A Selective, Potent, Reversible Bruton’s Tyrosine Kinase Inhibitor as an Orally Efficacious Agent for Autoimmune Diseases
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July 2020 |
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Discovery of GDC-0853: A Potent, Selective, and Noncovalent Bruton’s Tyrosine Kinase Inhibitor in Early Clinical Development
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February 2018 |
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The Exploration of Chirality for Improved Druggability within the Human Kinome
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September 2019 |
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Phase I study of single-agent CC-292, a highly selective Brutons tyrosine kinase inhibitor, in relapsed/refractory chronic lymphocytic leukemia
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May 2016 |
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The Cytokine GM-CSF Drives the Inflammatory Signature of CCR2+ Monocytes and Licenses Autoimmunity
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September 2015 |
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The use of liquid chromatography/thermospray mass spectrometry with on-line ultraviolet diode array and radiochemical detection: Characterization of the putative metabolites of U-78875 in female rat faeces
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January 1994 |
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CCR2+Ly-6Chi monocytes are crucial for the effector phase of autoimmunity in the central nervous system
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June 2009 |
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Inhibition of Bruton´s tyrosine kinase as a novel therapeutic approach in multiple sclerosis
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August 2020 |
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Fenebrutinib Versus Placebo or Adalimumab in Rheumatoid Arthritis: A Randomized, Double‐Blind, Phase II Trial
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August 2020 |
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Ability of Bruton’s Tyrosine Kinase Inhibitors to Sequester Y551 and Prevent Phosphorylation Determines Potency for Inhibition of Fc Receptor but not B-Cell Receptor Signaling
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journal
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January 2017 |
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Safety, Pharmacokinetics, and Pharmacodynamics in Healthy Volunteers Treated With GDC‐0853, a Selective Reversible Bruton's Tyrosine Kinase Inhibitor
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journal
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March 2018 |
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Ocrelizumab versus Interferon Beta-1a in Relapsing Multiple Sclerosis
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journal
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January 2017 |
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Über neue organische Phosphorverbindungen III. Phosphinmethylenderivate und Phosphinimine
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journal
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January 1919 |
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Spebrutinib (CC-292) Affects Markers of B Cell Activation, Chemotaxis, and Osteoclasts in Patients with Rheumatoid Arthritis: Results from a Mechanistic Study
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journal
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November 2019 |
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Tricyclic Pyrazoles. 3. Synthesis, Biological Evaluation, and Molecular Modeling of Analogues of the Cannabinoid Antagonist 8-Chloro-1-(2‘,4‘-dichlorophenyl)- N -piperidin-1-yl-1,4,5,6- tetrahydrobenzo[6,7]cyclohepta[1,2- c ]pyrazole-3-carboxamide
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journal
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October 2005 |
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The influence of drug-like concepts on decision-making in medicinal chemistry
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journal
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November 2007 |
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phenix.model_vs_data : a high-level tool for the calculation of crystallographic model and data statistics
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journal
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May 2010 |
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The Role of Tec Family Kinases in Mononuclear Phagocytes
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journal
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January 2009 |
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Acalabrutinib and its use in treatment of chronic lymphocytic leukemia
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journal
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February 2019 |
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BTK: a two-faced effector in cancer and tumour suppression
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journal
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October 2018 |
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Drug development to overcome resistance to EGFR inhibitors in lung and colorectal cancer
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journal
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December 2011 |
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Conformational restriction: an effective tactic in 'follow-on'-based drug discovery
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May 2014 |
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Chiral Brønsted Acid Catalyzed Enantioselective Mannich-Type Reaction
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journal
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May 2007 |
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Population Pharmacokinetics, Efficacy Exposure-response Analysis, and Model-based Meta-analysis of Fenebrutinib in Subjects with Rheumatoid Arthritis
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journal
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January 2020 |
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In silico toxicology: computational methods for the prediction of chemical toxicity: Computational methods for the prediction of chemical toxicity
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journal
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January 2016 |