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Synthesis of 7-amino-3a,4-dihydro-3H-[1]benzopyrano[4,3-c]isoxazole derivatives displaying combined alpha2-adrenoceptor antagonistic and 5-HT reuptake inhibiting activities.
- Source :
-
Bioorganic & medicinal chemistry [Bioorg Med Chem] 2006 Jul 01; Vol. 14 (13), pp. 4361-72. Date of Electronic Publication: 2006 Mar 15. - Publication Year :
- 2006
-
Abstract
- Following a program searching for dual 5-HT reuptake inhibitors and alpha(2)-adrenoceptor antagonists started at Johnson & Johnson Pharmaceutical Research & Development, we now report on the synthesis of a series of 7-amino-3a,4-dihydro-3H-[1]benzopyrano[4,3-c]isoxazole derivatives, some of which proved to be the most potent alpha(2)-adrenoceptor blockers within this chemical class of tricyclic isoxazolines, while keeping potent 5-HT reuptake inhibiting activity.
- Subjects :
- Adrenergic alpha-Antagonists chemical synthesis
Adrenergic alpha-Antagonists pharmacology
Animals
Male
Rats
Rats, Wistar
Selective Serotonin Reuptake Inhibitors chemical synthesis
Selective Serotonin Reuptake Inhibitors pharmacology
Adrenergic alpha-2 Receptor Antagonists
Adrenergic alpha-Antagonists chemistry
Isoxazoles chemistry
Pyrans chemistry
Selective Serotonin Reuptake Inhibitors chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 0968-0896
- Volume :
- 14
- Issue :
- 13
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 16540335
- Full Text :
- https://doi.org/10.1016/j.bmc.2006.02.043