17 articles for MF Boehm
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
EC144 is a potent inhibitor of the heat shock protein 90.

Biogen Idec
Synthesis and biological evaluation of a new class of geldanamycin derivatives as potent inhibitors of Hsp90.

Conforma Therapeutics
Design and synthesis of benzofused heterocyclic RXR modulators.

Eli Lilly
Design, synthesis and structure-activity relationship of novel RXR-selective modulators.

Ligand Pharmaceuticals
Design and synthesis of novel RXR-selective modulators with improved pharmacological profile.

Ligand Pharmaceuticals
Design, synthesis, and structure-activity relationship studies of novel 6,7-locked-[7-(2-alkoxy-3,5-dialkylbenzene)-3-methylocta]-2,4,6-trienoic acids.

Ligand Pharmaceuticals
Novel (2E,4E,6Z)-7-(2-alkoxy-3,5-dialkylbenzene)-3-methylocta-2,4,6-trienoic acid retinoid X receptor modulators are active in models of type 2 diabetes.

Ligand Pharmaceuticals
Synthesis of retinoid X receptor-specific ligands that are potent inducers of adipogenesis in 3T3-L1 cells.

Ligand Pharmaceuticals
Synthesis and characterization of heteroarotinoids demonstrate structure specificity relationships.

University of Oklahoma Health Sciences Center
Discovery of novel retinoic acid receptor agonists having potent antiproliferative activity in cervical cancer cells.

Ligand Pharmaceuticals
Synthesis of high specific activity [3H]-9-cis-retinoic acid and its application for identifying retinoids with unusual binding properties.

Ligand Pharmaceuticals
Synthesis and structure-activity relationships of novel retinoid X receptor-selective retinoids.

Ligand Pharmaceuticals
Design and synthesis of potent retinoid X receptor selective ligands that induce apoptosis in leukemia cells.

Ligand Pharmaceuticals
Naphthyridine derivative compounds

Astex Therapeutics
Benzimidazol-2-amines as MIDH1 inhibitors

Bayer Pharma Aktiengesellschaft
Substituted benzamides as RIPK2 inhibitors

Boehringer Ingelheim International
N-Phenyl-4-pyrazolo[1,5-b]pyridazin-3-ylpyrimidin-2-amines as potent and selective inhibitors of glycogen synthase kinase 3 with good cellular efficacy.

Glaxosmithkline