19 articles for A Gobbi
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Identification of N-sulfonyl-tetrahydroquinolines as RORc inverse agonists.

Genentech
Discovery of imidazo[1,5-a]pyridines and -pyrimidines as potent and selective RORc inverse agonists.

Genentech
Minor Structural Change to Tertiary Sulfonamide RORc Ligands Led to Opposite Mechanisms of Action.

Genentech
Reduction in lipophilicity improved the solubility, plasma-protein binding, and permeability of tertiary sulfonamide RORc inverse agonists.

Genentech
A reversed sulfonamide series of selective RORc inverse agonists.

Argenta Discovery
Identification of tertiary sulfonamides as RORc inverse agonists.

Genentech
Structure-based design of substituted hexafluoroisopropanol-arylsulfonamides as modulators of RORc.

Genentech
Targeting KRAS Mutant Cancers via Combination Treatment: Discovery of a 5-Fluoro-4-(3

Genentech
Discovery of oxa-sultams as RORc inverse agonists showing reduced lipophilicity, improved selectivity and favorable ADME properties.

Genentech
Development of Potent and Selective Pyrazolopyrimidine IRAK4 Inhibitors.

Genentech
Discovery of Potent Benzolactam IRAK4 Inhibitors with Robust in Vivo Activity.

Genentech
Therapeutic compounds and methods of use thereof

Genentech
Compound useful for the treatment of degenerative and inflammatory diseases

Galapagos
Isoindolinone inhibitors of the MDM2-p53 interaction having anticancer activity

Astex Therapeutics
Heteroarylbenzimidazole compounds

Bayer Pharma Aktiengesellschaft
Substituted 7-azabicycles and their use as orexin receptor modulators

Janssen Pharmaceutica
Substituted pyrrolopyrimidines as HDM2 inhibitors

Merck Sharp & Dohme
The antiparasitic clioquinol induces apoptosis in leukemia and myeloma cells by inhibiting histone deacetylase activity.

Soochow University
Compounds and methods useful for directing stem cell differentiation

Vanderbilt University