Aromatic ring functionalization of benzolactam derivatives: New potent dopamine D3 receptor ligands
✍ Scribed by Raquel Ortega; Harald Hübner; Peter Gmeiner; Christian F. Masaguer
- Publisher
- Elsevier Science
- Year
- 2011
- Tongue
- English
- Weight
- 398 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0960-894X
No coin nor oath required. For personal study only.
✦ Synopsis
Since the discovery of the dopamine D(3) receptor, an intensive effort has been directed toward the development of potent and selective ligands in order to elucidate the function and potential therapeutic advantages of targeting D(3) receptors. As a part of our efforts, a novel series of substituted benzolactams derivatives was synthesized mostly through palladium-catalyzed reactions. Their affinities on D(1)-D(4) receptors were evaluated and the data led us to highly potent D(3) ligands, some of them highly selective for D(3) receptor, compared to the related dopamine receptor subtypes. Functional D(3) activity assays of the most relevant compounds have been carried out revealing antagonist as well as partial agonist activity.
📜 SIMILAR VOLUMES
## Abstract magnified image A series of pyrrolo[2,3‐__d__]pyrimidine Mannich bases of type **9, 12, 15** and **16** have been prepared as potential dopamine D4 receptor ligands. The syntheses start from 4‐aminopyrimidin‐6‐one **3** with pyrrole annulations and Mannich reactions with formaldehyde a
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.