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18 articles for KA Newlander


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

PMID
Cmpds
Data
Article Title
Organization
6
Identification of Potent, Selective, Cell-Active Inhibitors of the Histone Lysine Methyltransferase EZH2.EBI
TBA
47
Discovery of GSK1070916, a potent and selective inhibitor of Aurora B/C kinase.EBI
Glaxosmithkline
17
 
Structure-activity relationships in 3-oxo-1,4-benzodiazepine-2-acetic acid GPIIb/IIIa antagonists. The 2-benzazepine seriesEBI
TBA
17
Discovery of GSK2126458, a Highly Potent Inhibitor of PI3K and the Mammalian Target of Rapamycin.EBI
GlaxoSmithKline
58
Novel ATP-competitive kinesin spindle protein inhibitors.EBI
Glaxosmithkline
7
Discovery of orally active nonpeptide vitronectin receptor antagonists based on a 2-benzazepine Gly-Asp mimetic.EBI
Smithkline Beecham Pharmaceuticals
5
Orally bioavailable nonpeptide vitronectin receptor antagonists with efficacy in an osteoporosis model.EBI
Smithkline Beecham Pharmaceuticals
21
Conformational preferences in a benzodiazepine series of potent nonpeptide fibrinogen receptor antagonists.EBI
Smithkline Beecham Pharmaceuticals
10
Potent, selective, orally active 3-oxo-1,4-benzodiazepine GPIIb/IIIa integrin antagonists.EBI
Smithkline Beecham Pharmaceuticals
5
A novel constrained reduced-amide inhibitor of HIV-1 protease derived from the sequential incorporation of gamma-turn mimetics into a model substrate.EBI
Smithkline Beecham Pharmaceuticals
2
A check on rational drug design: crystal structure of a complex of human immunodeficiency virus type 1 protease with a novel gamma-turn mimetic inhibitor.EBI
Smithkline Beecham Pharmaceuticals
6
Dicarbavasopressin antagonist analogues exhibit reduced in vivo agonist activity.EBI
Smith Kline & French Laboratories
6
A minor modification of residue 1 in potent vasopressin antagonists dramatically reduces agonist activity.EBI
Smith Kline & French Laboratories
6
Guanidine substituted tetrahydroisoquinoline compounds as factor XIa inhibitorsBDB
Bristol-Myers Squibb
11
Spiro-amino-imidazo-fused heterocyclic compounds as beta-secretase modulators and methods of useBDB
Amgen
70
2-Amino-6-arylsulfonylbenzonitriles as non-nucleoside reverse transcriptase inhibitors of HIV-1.BDB
Glaxosmithkline
35
Nonpeptide cyclic cyanoguanidines as HIV-1 protease inhibitors: synthesis, structure-activity relationships, and X-ray crystal structure studies.BDB
Dupont Pharmaceuticals
9
Stereoisomers of cyclic urea HIV-1 protease inhibitors: synthesis and binding affinities.BDB
Dupont Pharmaceuticals