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
Optimization of orally bioavailable alkyl amine renin inhibitors.

Vitae Pharmaceuticals
Non-canonical modulators of nuclear receptors.

Vitae Pharmaceuticals
The use of spirocyclic scaffolds in drug discovery.

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
Cyclic polypeptides for PCSK9 inhibition

Merck Sharp & Dohme
Methylamine derivatives as lysysl oxidase inhibitors for the treatment of cancer

The Institute of Cancer Research: Royal Cancer Hospital
Compounds that inhibit Mcl-1 protein

Amgen
SALT AND CRYSTAL FORM OF DIHYDROPYRIDO[2,3-d]PYRIMIDINE DERIVATE

Nanjing Chia Tai Tianqing Pharmaceutical
CDK2/4/6 inhibitors

Pfizer
Methods for treating pulmonary hypertension

Reviva Pharmaceuticals
Tetrahydronaphthyl urea derivative

Mochida 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
Therapeutic pyrazolyl thienopyridines

Thesan Pharmaceuticals
Orvinol and thevinol derivatives useful in the treatment of depression

The University of Bath
Inhibitors of c-fms kinase

Janssen Pharmaceutica
Indoline scaffold SHP-2 inhibitors and cancer treatment method

University of South Florida
GABA(C) receptors as drug targets.

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

Merck Research Laboratories
Pharmacology and functions of metabotropic glutamate receptors.

Emory University
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
Aminomethylpyrimidines as novel DPP-IV inhibitors: a 10(5)-fold activity increase by optimization of aromatic substituents.

Hoffmann-La Roche