Syntheses and binding affinities of 6-nitroquipazine analogues for serotonin transporter. Part 1

Bioorganic & Medicinal Chemistry Letters
2000.0

Abstract

6-Nitroquipazine has been known as one of the most potent and selective inhibitors of serotonin transporter in vitro and in vivo. Nine derivatives of 6-nitroquipazine were synthesized and tested for their potential abilities to displace [3H]citalopram binding to the rat cortical membranes.

Knowledge Graph

Similar Paper

Syntheses and binding affinities of 6-nitroquipazine analogues for serotonin transporter. Part 1
Bioorganic & Medicinal Chemistry Letters 2000.0
Syntheses and binding affinities of 6-nitroquipazine analogues for serotonin transporter. part 2: 4-Substituted 6-nitroquipazines
Bioorganic & Medicinal Chemistry Letters 2002.0
Syntheses and binding affinities of 6-nitroquipazine analogues for serotonin transporter. Part 5: 2′-Substituted 6-nitroquipazines
Bioorganic & Medicinal Chemistry 2007.0
Design and Synthesis of 1-(3-(Dimethylamino)propyl)-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile (Citalopram) Analogues as Novel Probes for the Serotonin Transporter S1 and S2 Binding Sites
Journal of Medicinal Chemistry 2013.0
Thiophene derivatives: a new series of potent norepinephrine and serotonin reuptake inhibitors
Bioorganic & Medicinal Chemistry Letters 2002.0
Synthesis and receptor binding properties of 2β-alkynyl and 2β-(1,2,3-triazol)substituted 3β-(substituted phenyl)tropane derivatives
Bioorganic & Medicinal Chemistry 2008.0
A rhodamine-labeled citalopram analogue as a high-affinity fluorescent probe for the serotonin transporter
Bioorganic & Medicinal Chemistry Letters 2013.0
Pyrroloisoquinoline antidepressants. 3. A focus on serotonin
Journal of Medicinal Chemistry 1990.0
Synthesis and Biological Evaluation of Meperidine Analogues at Monoamine Transporters
Journal of Medicinal Chemistry 2005.0
Synthesis, molecular docking and binding studies of selective serotonin transporter inhibitors
European Journal of Medicinal Chemistry 2011.0