26 articles for thisTarget
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Cholinergic activity of acetylenic imidazoles and related compounds.

Upjohn
Synthesis and hypocholesterolemic activity of 6,7-dihydro-4H-pyrazolo[1,5-a]pyrrolo[3,4-d]pyrimidine-5,8-diones, novel inhibitors of acylCoA:cholesterol O-acyltransferase.

Upjohn
Peptidomimetic HIV protease inhibitors: phosphate prodrugs with improved biological activities.

Upjohn
Inhibitors of the protease from human immunodeficiency virus: design and modeling of a compound containing a dihydroxyethylene isostere insert with high binding affinity and effective antiviral activity.

Upjohn
Renin inhibitory peptides. A beta-aspartyl residue as a replacement for the histidyl residue at the P-2 site.

Upjohn
Synthesis and renin inhibitory activity of angiotensinogen analogues having dehydrostatine, Leu psi [CH2S]Val, or Leu psi [CH2SO]Val at the P1-P1' cleavage site.

Upjohn
Conformationally constrained renin inhibitory peptides: gamma-lactam-bridged dipeptide isostere as conformational restriction.

Upjohn
Design, structure-activity, and molecular modeling studies of potent renin inhibitory peptides having N-terminal Nin-For-Trp (Ftr): angiotensinogen congeners modified by P1-P1' Phe-Phe, Sta, Leu psi[CH(OH)CH2]Val or leu psi[CH2NH]Val substitutions.

Upjohn
alpha,alpha-Difluoro-beta-aminodeoxystatine-containing renin inhibitory peptides.

Upjohn
Renin inhibitors containing psi[CH2O] pseudopeptide inserts.

Upjohn
Potent renin inhibitory peptides containing hydrophilic end groups.

Upjohn
Thermodynamics of the interaction of inhibitors with the binding site of recombinant human renin.

Upjohn
Renin inhibitory peptides. Incorporation of polar, hydrophilic end groups into an active renin inhibitory peptide template and their evaluation in a human renin infused rat model and in conscious sodium-depleted monkeys.

Upjohn
Studies on (H(+)-K+)-ATPase inhibitors of gastric acid secretion. Prodrugs of 2-[(2-pyridinylmethyl)sulfinyl]benzimidazole proton-pump inhibitors.

Upjohn
Novel indolodioxanes with antihypertensive effects: potent ligands for the 5-HT1A receptor.

Upjohn
Pyridyl-and pyrimidinyl-substituted pyrrole-, thiophene- and furane-derivatives as kinase inhibitors

Nerviano Medical Sciences
Substituted 6,7-dialkoxy-3-isoquinolinol derivatives as inhibitors of phosphodiesterase 10 (PDE 10A)

Allergan
Substituted biaryl compound

Ube Industries
Lactam compounds as EP4 receptor-selective agonists for use in the treatment of EP4-mediated diseases and conditions

Cayman Chemical
Imidazothiadiazole and imidazopyrazine derivatives as protease activated receptor 4 (PAR4) inhibitors for treating platelet aggregation

Bristol-Myers Squibb
3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant IDH

Novartis
Arylpyrrolopyridine derived compounds as LRRK2 inhibitors

H. Lundbeck
Amino-substituted isothiazoles

Bayer Pharma Aktiengesellschaft
BMP inhibitors and methods of use thereof

The Brigham and Women'S Hospital
Protein kinase C inhibitors and uses thereof

Rigel Pharmaceuticals
Combination of kinase inhibitors and uses thereof

Intellikine