18 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Three-dimensional quantitative structure-activity relationships from molecular similarity matrices and genetic neural networks. 2. Applications.

Harvard University
Receptor surface models. 2. Application to quantitative structure-activity relationships studies.

Molecular Simulations
1-(substituted-benzyl)imidazole-2(3H)-thione inhibitors of dopamine beta-hydroxylase.

University of Illinois
Synthesis of indane derivatives as mechanism-based inhibitors of dopamine β-hydroxylase

TBA
NVP-BHG712: Effects of Regioisomers on the Affinity and Selectivity toward the EPHrin Family.

Johann Wolfgang Goethe University
Soluble Guanylate Cyclase Inhibitors Discovered among Natural Compounds.

Inserm U1182 - Cnrs Umr7645
Pyridine alkaloids with activity in the central nervous system.

University of Auckland
The biology and synthesis of α-hydroxytropolones.

City University of New York
Unsaturated heterocyclic amines as potent time-dependent inhibitors of dopamine beta-hydroxylase.

TBA
Multisubstrate inhibitors of dopamine beta-hydroxylase. 2. Structure-activity relationships at the phenethylamine binding site.

TBA
Multisubstrate inhibitors of dopamine beta-hydroxylase. 1. Some 1-phenyl and 1-phenyl-bridged derivatives of imidazole-2-thione.

TBA
Substituted 1-benzylimidazole-2-thiols as potent and orally active inhibitors of dopamine beta-hydroxylase.

TBA
Inhibitors of dopamine beta-hydroxylase. 3. Some 1-(pyridylmethyl)imidazole-2-thiones.

TBA
Beta-substituted phenethylamines as high-affinity mechanism-based inhibitors of dopamine beta-hydroxylase.

Smith Kline & French Laboratories
Synthesis of some novel potent and selective catechol O-methyltransferase inhibitors.

Orion
Benzofurans as mechanism-based inhibitors of dopamine beta-hydroxylase.

Pennsylvania State University
1-(Thienylalkyl)imidazole-2(3H)-thiones as potent competitive inhibitors of dopamine beta-hydroxylase.

Merrell Dow Research Institute
Some benzyl-substituted imidazoles, triazoles, tetrazoles, pyridinethiones, and structural relatives as multisubstrate inhibitors of dopamine beta-hydroxylase. 4. Structure-activity relationships at the copper binding site.

Smith Kline & French Laboratories