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14 articles for L Silvian


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

PMID
Data
Article Title
Organization
Discovery of biaryls as ROR¿ inverse agonists by using structure-based design.EBI
Biogen
Discovery of biaryl carboxylamides as potent ROR¿ inverse agonists.EBI
Biogen Idec
Structure-based design of low-nanomolar PIM kinase inhibitors.EBI
Biogen Idec
Structure-based design of 2,6,7-trisubstituted-7H-pyrrolo[2,3-d]pyrimidines as Aurora kinases inhibitors.EBI
Biogen Idec
Synthesis, SAR and biological evaluation of 1,6-disubstituted-1H-pyrazolo[3,4-d]pyrimidines as dual inhibitors of Aurora kinases and CDK1.EBI
Biogen Idec
Design, synthesis, and biological evaluation of pyrazolopyrimidine-sulfonamides as potent multiple-mitotic kinase (MMK) inhibitors (part I).EBI
Biogen Idec
Structure-activity relationship of ortho- and meta-phenol based LFA-1 ICAM inhibitors.EBI
Biogen Idec
Design and synthesis of a series of meta aniline-based LFA-1 ICAM inhibitors.EBI
Biogen Idec
Utilizing structure based drug design and metabolic soft spot identification to optimize the in vitro potency and in vivo pharmacokinetic properties leading to the discovery of novel reversible Bruton's tyrosine kinase inhibitors.EBI
Biogen
Investigating small molecules to inhibit germinal center kinase-like kinase (GLK/MAP4K3) upstream of PKCθ phosphorylation: Potential therapy to modulate T cell dependent immunity.EBI
Biogen
Optimization of novel reversible Bruton's tyrosine kinase inhibitors identified using Tethering-fragment-based screens.EBI
Biogen
Small molecules inhibit the interaction of Nrf2 and the Keap1 Kelch domain through a non-covalent mechanism.EBI
Biogen Idec
4-oxo-3,4-dihydro-1,2,3-benzotriazine modulators of GPR139BDB
Takeda Pharmaceutical
Design, synthesis, and anticonvulsant activity of some derivatives of xanthone with aminoalkanol moieties.BDB
Jagiellonian University Medical College