16 articles for D Marcotte
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.

Biogen
Discovery of biaryl carboxylamides as potent ROR¿ inverse agonists.

Biogen Idec
Discovery of novel pyrazole-containing benzamides as potent ROR¿ inverse agonists.

Biogen
Structure-based design of low-nanomolar PIM kinase inhibitors.

Biogen Idec
2,4-Diaminopyrimidine MK2 inhibitors. Part I: Observation of an unexpected inhibitor binding mode.

Abbott Laboratories
Design, synthesis, and biological evaluation of pyrazolopyrimidine-sulfonamides as potent multiple-mitotic kinase (MMK) inhibitors (part I).

Biogen Idec
Discovery of structural diverse reversible BTK inhibitors utilized to develop a novel in vivo CD69 and CD86 PK/PD mouse model.

Amgen
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.

Biogen
Discovery of Potent Selective Nonzinc Binding Autotaxin Inhibitor BIO-32546.

Biogen
Discovery of BIIB068: A Selective, Potent, Reversible Bruton's Tyrosine Kinase Inhibitor as an Orally Efficacious Agent for Autoimmune Diseases.

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.

Biogen
Design, synthesis and identification of novel, orally bioavailable non-covalent Nrf2 activators.

Biogen
Optimization of novel reversible Bruton's tyrosine kinase inhibitors identified using Tethering-fragment-based screens.

Biogen
Small molecules inhibit the interaction of Nrf2 and the Keap1 Kelch domain through a non-covalent mechanism.

Biogen Idec
4-oxo-3,4-dihydro-1,2,3-benzotriazine modulators of GPR139

Takeda Pharmaceutical
Design, synthesis, and anticonvulsant activity of some derivatives of xanthone with aminoalkanol moieties.

Jagiellonian University Medical College