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15 articles for K Hirai


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

PMID
Data
Article Title
Organization
Discovery of orally available spirodiketopiperazine-based CCR5 antagonists.EBI
Minase Research Institute
Discovery of potent, selective, orally active benzoxazepine-based Orexin-2 receptor antagonists.EBI
Takeda Pharmaceutical
Synthesis of a novel series of tricyclic dihydrofuran derivatives: discovery of 8,9-dihydrofuro[3,2-c]pyrazolo[1,5-a]pyridines as melatonin receptor (MT1/MT2) ligands.EBI
Takeda Pharmaceutical
1,6-Dihydro-2H-indeno[5,4-b]furan derivatives: design, synthesis, and pharmacological characterization of a novel class of highly potent MT2-selective agonists.EBI
Takeda Pharmaceutical
Spirodiketopiperazine-based CCR5 antagonists: Improvement of their pharmacokinetic profiles.EBI
Minase Research Institute
Discovery of clinical candidate Sivopixant (S-600918): Lead optimization of dioxotriazine derivatives as selective P2X3 receptor antagonists.EBI
Shionogi
Discovery of a Potent and Orally Bioavailable Melatonin Receptor Agonist.EBI
Takeda Pharmaceutical
Synthesis of a novel series of tricyclic indan derivatives as melatonin receptor agonists.EBI
Takeda Chemical Industries
Synthesis of a novel series of benzocycloalkene derivatives as melatonin receptor agonists.EBI
Takeda Chemical Industries
Design and synthesis of orally bioavailable inhibitors of inducible nitric oxide synthase. Part 1: synthesis and biological evaluation of dihydropyridin-2-imines.EBI
Fukui Research Institute
Central cholinergic agents. 6. Synthesis and evaluation of 3-[1-(phenylmethyl)-4-piperidinyl]-1-(2,3,4,5-tetrahydro-1H-1-benzazepi n-8-yl)-1-propanones and their analogs as central selective acetylcholinesterase inhibitors.EBI
Takeda Chemical Industries
Discovery of a Slow Tight Binding LPA1 Antagonist (ONO-0300302) for the Treatment of Benign Prostatic Hyperplasia.EBI
Ono Pharmaceutical
Cyclobutyl pyrazolopyrimidine PDE9 inhibitorsBDB
Merck Sharp & Dohme
[9,10-dimethoxy-3-(2-methylpropyl)-1H,2H,3H,4H,6H,7H,11BH-pyrido-[2,1-a]isoquinolin-2-yl]methanol and compounds, compositions and methods relating theretoBDB
Neurocrine Biosciences
Tetrahydropyrido[4,3-d]pyrimidine inhibitors of ATR kinaseBDB
University Of Texas