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17 articles for RC Haltiwanger


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

PMID
Data
Article Title
Organization
Piperidine-3,4-diol and piperidine-3-ol derivatives of pyrrolo[2,1-f][1,2,4]triazine as inhibitors of anaplastic lymphoma kinase.EBI
Teva Branded Pharmaceutical Products R & D
3,4-Diaza-bicyclo[4.1.0]hept-4-en-2-one phenoxypropylamine analogs of irdabisant (CEP-26401) as potent histamine-3 receptor inverse agonists with robust wake-promoting activity.EBI
Teva Global R & D.
Discovery of an orally efficacious inhibitor of anaplastic lymphoma kinase.EBI
Cephalon
The inophyllums, novel inhibitors of HIV-1 reverse transcriptase isolated from the Malaysian tree, Calophyllum inophyllum Linn.EBI
Smithkline Beecham Pharmaceuticals R&D
4-phenoxypiperidine pyridazin-3-one histamine H(3) receptor inverse agonists demonstrating potent and robust wake promoting activity.EBI
Cephalon
Design, synthesis, and anaplastic lymphoma kinase (ALK) inhibitory activity for a novel series of 2,4,8,22-tetraazatetracyclo[14.3.1.1³,¿?¿.1¿?¿,¹³]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaene macrocycles.EBI
Cephalon
 
Structure-activity relationships in 3-oxo-1,4-benzodiazepine-2-acetic acid GPIIb/IIIa antagonists. The 2-benzazepine seriesEBI
TBA
Phenylbutyrates as potent, orally bioavailable vitronectin receptor (integrin alphavbeta3) antagonists.EBI
Glaxosmithkline
Azepanone-based inhibitors of human and rat cathepsin K.EBI
Glaxosmithkline
Synthetic analogues of SB-219383. Novel C-glycosyl peptides as inhibitors of tyrosyl tRNA synthetase.EBI
Glaxosmithkline
Discovery of orally active nonpeptide vitronectin receptor antagonists based on a 2-benzazepine Gly-Asp mimetic.EBI
Smithkline Beecham Pharmaceuticals
Orally bioavailable nonpeptide vitronectin receptor antagonists with efficacy in an osteoporosis model.EBI
Smithkline Beecham Pharmaceuticals
Conformational preferences in a benzodiazepine series of potent nonpeptide fibrinogen receptor antagonists.EBI
Smithkline Beecham Pharmaceuticals
ATP-Citrate lyase as a target for hypolipidemic intervention. 2. Synthesis and evaluation of (3R,5S)-omega-substituted-3-carboxy-3, 5-dihydroxyalkanoic acids and their gamma-lactone prodrugs as inhibitors of the enzyme in vitro and in vivo.EBI
Smithkline Beecham Pharmaceuticals
(E)-3-[[[[6-(2-carboxyethenyl)-5-[[8-(4- methoxyphenyl)octyl]oxy]-2-pyridinyl]-methyl]thio]methyl]benzoic acid and related compounds: high affinity leukotriene B4 receptor antagonists.EBI
Smithkline Beecham Pharmaceuticals
1,4-Cyclohexanecarboxylates: potent and selective inhibitors of phosophodiesterase 4 for the treatment of asthma.EBI
Smithkline Beecham Pharmaceuticals
Substituted tricyclic compounds as FGFR inhibitorsBDB
Incyte