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27 articles for N Kaila


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

PMID
Data
Article Title
Organization
Discovery of isoquinolinone indole acetic acids as antagonists of chemoattractant receptor homologous molecule expressed on Th2 cells (CRTH2) for the treatment of allergic inflammatory diseases.EBI
Pfizer
Diazine indole acetic acids as potent, selective, and orally bioavailable antagonists of chemoattractant receptor homologous molecule expressed on Th2 cells (CRTH2) for the treatment of allergic inflammatory diseases.EBI
Pfizer
Synthesis and biological evaluation of quinoline salicylic acids as P-selectin antagonists.EBI
Wyeth Research
Beta-C-mannosides as selectin inhibitors.EBI
Wyeth Research
Design and synthesis of sialyl Lewis x mimics as E-selectin inhibitors.EBI
Wyeth Research
Discovery of 2-[1-(4-chlorophenyl)cyclopropyl]-3-hydroxy-8-(trifluoromethyl)quinoline-4-carboxylic acid (PSI-421), a P-selectin inhibitor with improved pharmacokinetic properties and oral efficacy in models of vascular injury.EBI
Pfizer
Identification of a novel class of selective Tpl2 kinase inhibitors: 4-Alkylamino-[1,7]naphthyridine-3-carbonitriles.EBI
Wyeth Research
Discovery of a Potent and Selective Tyrosine Kinase 2 Inhibitor: TAK-279.EBI
Nimbus Therapeutics
2-(4-Chlorobenzyl)-3-hydroxy-7,8,9,10-tetrahydrobenzo[H]quinoline-4-carboxylic acid (PSI-697): identification of a clinical candidate from the quinoline salicylic acid series of P-selectin antagonists.EBI
Wyeth Research
Inhibition of Tpl2 kinase and TNFalpha production with quinoline-3-carbonitriles for the treatment of rheumatoid arthritis.EBI
Wyeth Research
Inhibition of Tpl2 kinase and TNF-alpha production with 1,7-naphthyridine-3-carbonitriles: synthesis and structure-activity relationships.EBI
Wyeth Research
Quinic acid derivatives as sialyl Lewis(x)-mimicking selectin inhibitors: design, synthesis, and crystal structure in complex with E-selectin.EBI
Wyeth
Discovery of 3-Cyano- N-(3-(1-isobutyrylpiperidin-4-yl)-1-methyl-4-(trifluoromethyl)-1 H-pyrrolo[2,3- b]pyridin-5-yl)benzamide: A Potent, Selective, and Orally Bioavailable Retinoic Acid Receptor-Related Orphan Receptor C2 Inverse Agonist.EBI
Karo Pharma
Identification of N-{cis-3-[Methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]cyclobutyl}propane-1-sulfonamide (PF-04965842): A Selective JAK1 Clinical Candidate for the Treatment of Autoimmune Diseases.EBI
Pfizer
DUAL INHIBITORS OF TRYPTOPHAN DIOXYGENASES (IDO1 AND TDO) AND THEIR USE IN THERAPYBDB
Antido Therapeutics International
Substituted piperidines as BTK inhibitorsBDB
Haisco Pharmaceuticals
Small molecule inhibitors of Galectin-3BDB
Bristol-Myers Squibb
Heteroarylsulfonyl-substituted pyridines and their use in the treatment of cancerBDB
Oblique Therapeutics
Indolizine derivatives and their application in medicineBDB
Kind Pharmaceutical
Cyanopyrrolidine derivatives with activity as inhibitors of USP30BDB
Mission Therapeutics
Substituted heterocyclic inhibitors of PTPN11BDB
Navire Pharma
2,4-disubstituted phenylene-1,5-diamine derivatives and applications thereof, and pharmaceutical compositions and pharmaceutically acceptable compositions prepared therefromBDB
Shanghai Haiyan Pharmaceutical Technology
Macrocyclic LRRK2 kinase inhibitorsBDB
Oncodesign
Alkylene derivativesBDB
Shionogi
3,5,N-trihydroxy-alkanamide and derivatives: method for making same and use thereofBDB
National Taiwan University
Cloning, expression and pharmacology of the mouse 5-HT(4L) receptor.BDB
Cnrs Upr 9023
The reversed binding of beta-phenethylamine inhibitors of DPP-IV: X-ray structures and properties of novel fragment and elaborated inhibitors.BDB
Santhera Pharmaceuticals