42 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Brain penetrant liver X receptor (LXR) modulators based on a 2,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole core.

Vitae Pharmaceuticals
Discovery of a Novel, Orally Efficacious Liver X Receptor (LXR)ß Agonist.

Vitae Pharmaceuticals
Identification of spirooxindole and dibenzoxazepine motifs as potent mineralocorticoid receptor antagonists.

Vitae Pharmaceuticals
Structure-based design and synthesis of 1,3-oxazinan-2-one inhibitors of 11ß-hydroxysteroid dehydrogenase type 1.

Vitae Pharmaceuticals
Biphenyl/diphenyl ether renin inhibitors: filling the S1 pocket of renin via the S3 pocket.

Vitae Pharmaceuticals
Discovery and optimization of adamantyl carbamate inhibitors of 11ß-HSD1.

Vitae Pharmaceuticals
Spirocyclic ureas: orally bioavailable 11beta-HSD1 inhibitors identified by computer-aided drug design.

Vitae Pharmaceuticals
Structure-based design of β-site APP cleaving enzyme 1 (BACE1) inhibitors for the treatment of Alzheimer's disease.

Vitae Pharmaceuticals
Discovery of BI 135585, an in vivo efficacious oxazinanone-based 11β hydroxysteroid dehydrogenase type 1 inhibitor.

Vitae Pharmaceuticals
Methylamine derivatives as lysysl oxidase inhibitors for the treatment of cancer

The Institute of Cancer Research: Royal Cancer Hospital
SALT AND CRYSTAL FORM OF DIHYDROPYRIDO[2,3-d]PYRIMIDINE DERIVATE

Nanjing Chia Tai Tianqing Pharmaceutical
Pyrrolone or pyrrolidinone melanin concentrating hormone receptor-1 antagonists

Bristol-Myers Squibb
Tricyclic substituted thiadiazine dioxide compounds as BACE inhibitors, compositions and their use

Merck Sharp & Dohme
New insights into homopiperazine-based 5-HT1A/5-HT7R ligands: synthesis and biological evaluation.

University of Orleans
Structure of the Acinetobacter baumannii dithiol oxidase DsbA bound to elongation factor EF-Tu reveals a novel protein interaction site.

University of Queensland
Capzimin is a potent and specific inhibitor of proteasome isopeptidase Rpn11.

California Institute of Technology
Orvinol and thevinol derivatives useful in the treatment of depression

The University of Bath
Indoline scaffold SHP-2 inhibitors and cancer treatment method

University of South Florida
Synthesis and biological activities of potent peptidomimetics selective for somatostatin receptor subtype 2.

Merck Research Laboratories
The identification of a novel natural activator of p300 histone acetyltranferase provides new insights into the modulation mechanism of this enzyme.

Universitá
In vivo receptor occupancy of the angiotensin II receptor by nonpeptide antagonists: relationship to in vitro affinities and in vivo pharmacologic potency.

Merck Research Laboratories
Effects of remoxipride and some related new substituted salicylamides on rat brain receptors.

Astra LÄKemedel