Synthesis and receptor binding properties of 2β-alkynyl and 2β-(1,2,3-triazol)substituted 3β-(substituted phenyl)tropane derivatives
摘要:
A series of 2b-alkynyl and 2b-(1,2,3-triazol) substituted 3b-(substituted phenyl) tropanes were synthesized and evaluated for affinities at dopamine, serotonin, and norepinephrine membrane transporters using competitive radioligand binding assays. All tested compounds were found to exhibit nanomolar or subnanomolar affinity for the dopamine transporter (DAT). One of the most potent and selective compounds in the series was 3b-(4-chlorophenyl)-2b-(4-nitrophenylethynyl) tropane (10c) that possessed an IC50 value of 0.9 nM at the DAT and K-i values of 230 nM and 620 nM at the norepinephrine transporter ( NET) and serotonin transporter (5-HTT), respectively. (C) 2008 Elsevier Ltd. All rights reserved.
Synthesis and receptor binding properties of 2β-alkynyl and 2β-(1,2,3-triazol)substituted 3β-(substituted phenyl)tropane derivatives
摘要:
A series of 2b-alkynyl and 2b-(1,2,3-triazol) substituted 3b-(substituted phenyl) tropanes were synthesized and evaluated for affinities at dopamine, serotonin, and norepinephrine membrane transporters using competitive radioligand binding assays. All tested compounds were found to exhibit nanomolar or subnanomolar affinity for the dopamine transporter (DAT). One of the most potent and selective compounds in the series was 3b-(4-chlorophenyl)-2b-(4-nitrophenylethynyl) tropane (10c) that possessed an IC50 value of 0.9 nM at the DAT and K-i values of 230 nM and 620 nM at the norepinephrine transporter ( NET) and serotonin transporter (5-HTT), respectively. (C) 2008 Elsevier Ltd. All rights reserved.
Synthesis and receptor binding properties of 2β-alkynyl and 2β-(1,2,3-triazol)substituted 3β-(substituted phenyl)tropane derivatives
作者:Chunyang Jin、Hernán A. Navarro、F. Ivy Carroll
DOI:10.1016/j.bmc.2008.04.008
日期:2008.5
A series of 2b-alkynyl and 2b-(1,2,3-triazol) substituted 3b-(substituted phenyl) tropanes were synthesized and evaluated for affinities at dopamine, serotonin, and norepinephrine membrane transporters using competitive radioligand binding assays. All tested compounds were found to exhibit nanomolar or subnanomolar affinity for the dopamine transporter (DAT). One of the most potent and selective compounds in the series was 3b-(4-chlorophenyl)-2b-(4-nitrophenylethynyl) tropane (10c) that possessed an IC50 value of 0.9 nM at the DAT and K-i values of 230 nM and 620 nM at the norepinephrine transporter ( NET) and serotonin transporter (5-HTT), respectively. (C) 2008 Elsevier Ltd. All rights reserved.