𝔖 Bobbio Scriptorium

✦ LIBER ✦

Design, Synthesis and Biological Activity of Novel Dimethyl-{2-[6-substituted-indol-1-yl]-ethyl}-amine as Potent, Selective, and Orally-Bioavailable 5-HT1D Agonists.

✍ Scribed by Methvin Isaac; et al. et al.

Publisher: John Wiley and Sons
Year: 2004
Weight: 102 KB
Volume: 35
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200412132

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Design and Synthesi

ChemInform Abstract: Design and Synthesis of a Series of 6-Substituted-2-pyridinylmethylamine Derivatives as Novel, High-Affinity, Selective Agonists at 5-HT1A Receptors.

✍ Bernard Vacher; Bernard Bonnaud; Philippe Funes; Nathalie Jubault; Wouter Koek; 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 38 KB 👁 2 views

ChemInform Abstract: Design and Synthesi

ChemInform Abstract: Design and Synthesis of trans-N-[4- [2-(6-Cyano-1,2,3,4-tetrahydroisoquinolin-2-yl)ethyl]cyclohexyl] -4-quinolinecarboxamide (SB-277011): A Potent and Selective Dopamine D3 Receptor Antagonist with High Oral Bioavailability and CNS Penetration in the Rat.

✍ Geoffrey Stemp; et al. et al. 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB