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18 articles for JR Miller


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Overcoming mutagenicity and ion channel activity: optimization of selective spleen tyrosine kinase inhibitors.EBI
Merck
Structure guided development of novel thymidine mimetics targeting Pseudomonas aeruginosa thymidylate kinase: from hit to lead generation.EBI
Scripps Florida
Oxetane Promise Delivered: Discovery of Long-Acting IDO1 Inhibitors Suitable for Q3W Oral or Parenteral Dosing.EBI
Pharmaron Beijing
Comprehensive Strategies to Bicyclic Prolines: Applications in the Synthesis of Potent Arginase Inhibitors.EBI
Merck
Structure-Based Discovery of Proline-Derived Arginase Inhibitors with Improved Oral Bioavailability for Immuno-Oncology.EBI
Quantitative Biosciences
Utilization of Metabolite Identification and Structural Data to Guide Design of Low-Dose IDO1 Inhibitors.EBI
Merck
Discovery of Diaminopyrimidine Carboxamide HPK1 Inhibitors as Preclinical Immunotherapy Tool Compounds.EBI
Merck
SAR towards indoline and 3-azaindoline classes of IDO1 inhibitors.EBI
Merck
Identification of Potent Reverse Indazole Inhibitors for HPK1.EBI
Merck
Carbamate and EBI
Merck
Discovery of Potent and Orally Available Bicyclo[1.1.1]pentane-Derived Indoleamine-2,3-dioxygenase 1 (IDO1) Inhibitors.EBI
Merck
Discovery and Optimization of Rationally Designed Bicyclic Inhibitors of Human Arginase to Enhance Cancer Immunotherapy.EBI
Merck
Strategic Incorporation of Polarity in Heme-Displacing Inhibitors of Indoleamine-2,3-dioxygenase-1 (IDO1).EBI
Merck
Discovery of Amino-cyclobutarene-derived Indoleamine-2,3-dioxygenase 1 (IDO1) Inhibitors for Cancer Immunotherapy.EBI
Merck
Discovery of N-(Indazol-3-yl)piperidine-4-carboxylic Acids as ROR��t Allosteric Inhibitors for Autoimmune DiseasesEBI
Merck
1,3,4-thiadiazole compounds and their use in treating cancerBDB
Astrazeneca
Pyridyl analogs of 1-(2-cyano-3,12-dioxooleana-1,9(11)dien-28-oyl) imidazoleBDB
Dartmouth College
1-Sulfonylindazoles as potent and selective 5-HT6 ligands.BDB
Wyeth Research