12 articles for I van Wijngaarden
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Opiate receptor interaction of compounds derived from or structurally related to fentanyl.

TBA
Functional characteristics of a series of N4-substituted 1-(2,3-dihydro-1,4-benzodioxin-5-yl)piperazines as 5-HT1A receptor ligands. Structure-activity relationships.

Solvay Pharma
Structure-affinity relationship studies on 5-HT1A receptor ligands. 2. Heterobicyclic phenylpiperazines with N4-aralkyl substituents.

Solvay Duphar Research Laboratories
1H-imidazo[4,5-c]quinolin-4-amines: novel non-xanthine adenosine antagonists.

Center For Bio-Pharmaceutical Sciences
2-Phenylpyrroles as conformationally restricted benzamide analogues. A new class of potential antipsychotics. 1.

Duphar Research Laboratories
5-HT1A-versus D2-receptor selectivity of flesinoxan and analogous N4-substituted N1-arylpiperazines.

Solvay Pharma
Structure-affinity relationship studies on 5-HT1A receptor ligands. 1. Heterobicyclic phenylpiperazines with N4-alkyl substituents.

Solvay Duphar Research Laboratories
Development of high-affinity 5-HT3 receptor antagonists. Structure-affinity relationships of novel 1,7-annelated indole derivatives.

Solvay Duphar
N4-unsubstituted N1-arylpiperazines as high-affinity 5-HT1A receptor ligands.

Solvay Duphar Research Laboratories
A series of N4-imidoethyl derivatives of 1-(2,3-dihydro-1,4-benzodioxin-5-yl)piperazine as 5-HT1A receptor ligands: synthesis and structure-affinity relationships.

Solvay Duphar Research Laboratories
2-Phenylpyrroles as conformationally restricted benzamide analogues. A new class of potential antipsychotics. 2.

Duphar Research Laboratories
Hybrid cholecystokinin-A antagonists based on molecular modeling of lorglumide and L-364,718.

Center For Bio-Pharmaceutical Sciences