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25 articles for thisTarget


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

PMID
Cmpds
Data
Article Title
Organization
39
Recent developments in fragment-based drug discovery.EBI
Astex Therapeutics
15
Fragment-based discovery of mexiletine derivatives as orally bioavailable inhibitors of urokinase-type plasminogen activator.EBI
Astex Therapeutics
29
Fragment-based drug discovery applied to Hsp90. Discovery of two lead series with high ligand efficiency.EBI
Astex Therapeutics
274
Combination of isoindolinone derivatives with SGI-110BDB
Astex Therapeutics
85
Isoindolinone inhibitors of the MDM2-p53 interaction having anticancer activityBDB
Astex Therapeutics
130
Isoindolinone inhibitors of the MDM2-p53 interaction having anticancer activityBDB
Astex Therapeutics
7
Quinoxaline derivatives useful as FGFR kinase modulatorsBDB
Astex Therapeutics
8
Pteridines as FGFR inhibitorsBDB
Astex Therapeutics
7
Quinoxaline derivatives useful as FGFR kinase modulatorsBDB
Astex Therapeutics
71
Naphthyridine derivative compoundsBDB
Astex Therapeutics
24
CompoundsBDB
Astex Therapeutics
44
Bicyclic heterocycle compounds and their uses in therapyBDB
Astex Therapeutics
217
Pharmaceutical compoundsBDB
Astex Therapeutics
217
Bicyclic heterocycle compounds and their uses in therapyBDB
Astex Therapeutics
17
Bicyclic heterocyclic compounds as FGFR inhibitorsBDB
Astex Therapeutics
312
Imidazopyridine derivatives as inhibitors of receptor tyrosine kinasesBDB
Astex Therapeutics
20
Imidazole derivatives and their use as modulators of cyclin dependent kinasesBDB
Astex Therapeutics
13
Fragment-based discovery of the pyrazol-4-yl urea (AT9283), a multitargeted kinase inhibitor with potent aurora kinase activity.BDB
Astex Therapeutics
30
Identification of N-(4-piperidinyl)-4-(2,6-dichlorobenzoylamino)-1H-pyrazole-3-carboxamide (AT7519), a novel cyclin dependent kinase inhibitor using fragment-based X-ray crystallography and structure based drug design.BDB
Astex Therapeutics
12
Rapid Evolution of 6-Phenylpurine Inhibitors of Protein Kinase B through Structure-Based Design.BDB
Astex Therapeutics
12
Identification of Inhibitors of Protein Kinase B Using Fragment-Based Lead Discovery.BDB
Astex Therapeutics
5
Application of fragment screening by X-ray crystallography to beta-secretase.BDB
Astex Therapeutics
11
Application of fragment screening by X-ray crystallography to the discovery of aminopyridines as inhibitors of beta-secretase.BDB
Astex Therapeutics
2
A structural comparison of inhibitor binding to PKB, PKA and PKA-PKB chimera.BDB
Astex Therapeutics
9
Application of Fragment Screening and Fragment Linking to the Discovery of Novel Thrombin Inhibitors.BDB
Astex Therapeutics