Synthesis and binding affinities of 2 beta-(3-iodoallyloxycarbonyl)3 beta-(4-substituted-aryl)tropane analogues as ligands for the dopamine transporter studies

Authors
Chung, KHLim, CHLee, DRJin, CBChi, DY
Issue Date
2001-12-03
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.11, no.23, pp.3077 - 3080
Abstract
Tropane analogues from cocaine, which is known to be one of the most reinforcing and addictive compounds, were designed, synthesized, and characterized for inhibition of presynaptic uptake of dopamine (DA) in brain. Eight new derivatives of 3 beta -aryl-2 beta-(3-iodoallyloxycarbonyl)tropanes were synthesized and tested for their potential abilities to displace [H-3]2 beta -carbomethoxy-3 beta-(4-fluorophenyl)tropane (WIN 35,428) binding to the rat striatal membranes. (C) 2001 Elsevier Science Ltd. All rights reserved.
Keywords
POSITRON EMISSION TOMOGRAPHY; CENTRAL NERVOUS-SYSTEM; PARKINSONS-DISEASE; IMAGING AGENTS; COCAINE; ESTERS; <TC-99M>TRODAT-1; INHIBITION; CHEMISTRY; PROVIDES; POSITRON EMISSION TOMOGRAPHY; CENTRAL NERVOUS-SYSTEM; PARKINSONS-DISEASE; IMAGING AGENTS; COCAINE; ESTERS; <TC-99M>TRODAT-1; INHIBITION; CHEMISTRY; PROVIDES; tropane analogues
ISSN
0960-894X
URI
https://pubs.kist.re.kr/handle/201004/139919
DOI
10.1016/S0960-894X(01)00625-4
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KIST Article > 2001
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