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Synthesis of [11C] N-(2-chloro-5-thiomethylphenyl)-N′-(3-methoxyphenyl)-N′-methylguanidine ([11C]GMOM): a candidate PET tracer for imaging the PCP site of the NMDA ion channel
The N‐methyl‐D‐aspartate (NMDA) ion channel plays an important role in a number of neurodegenerative disorders including stroke, Parkinson's disease, Huntington's Chorea, Alzheimer's disease, schizophrenia and epilepsy. To provide effective radioligands for imaging the PCP binding sit...
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Published in: | Journal of labelled compounds & radiopharmaceuticals 2002-10, Vol.45 (11), p.955-964 |
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container_issue | 11 |
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container_title | Journal of labelled compounds & radiopharmaceuticals |
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creator | Waterhouse, Rikki N. Dumont, Filip Sultana, Abida Simpson, Norman Laruelle, Marc |
description | The N‐methyl‐D‐aspartate (NMDA) ion channel plays an important role in a number of neurodegenerative disorders including stroke, Parkinson's disease, Huntington's Chorea, Alzheimer's disease, schizophrenia and epilepsy. To provide effective radioligands for imaging the PCP binding site of the NMDA ion channel, we synthesized and characterized in vitro the candidate PCP site ligand N‐(2‐chloro‐5‐thiomethylphenyl)‐N′‐(3‐methoxyphenyl)‐N′‐methylguanidine (GMOM: Ki = 5.2 ± 0.3 nM, log P = 2.34). The corresponding PET radiotracer [11C]GMOM was synthesized with a radiochemical yield of 8.4 ± 3.2% EOS and with a specific activity of 1.23 ± 0.25 Ci/μmol EOS (n = 5). The average time required for synthesis, purification and formulation was 52 ± 5 min. The final product was prepared in a sterile saline solution suitable for in vivo use. Copyright © 2002 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/jlcr.622 |
format | article |
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To provide effective radioligands for imaging the PCP binding site of the NMDA ion channel, we synthesized and characterized in vitro the candidate PCP site ligand N‐(2‐chloro‐5‐thiomethylphenyl)‐N′‐(3‐methoxyphenyl)‐N′‐methylguanidine (GMOM: Ki = 5.2 ± 0.3 nM, log P = 2.34). The corresponding PET radiotracer [11C]GMOM was synthesized with a radiochemical yield of 8.4 ± 3.2% EOS and with a specific activity of 1.23 ± 0.25 Ci/μmol EOS (n = 5). The average time required for synthesis, purification and formulation was 52 ± 5 min. The final product was prepared in a sterile saline solution suitable for in vivo use. Copyright © 2002 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0362-4803</identifier><identifier>EISSN: 1099-1344</identifier><identifier>DOI: 10.1002/jlcr.622</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Biological and medical sciences ; Contrast media. Radiopharmaceuticals ; glutamate ; Medical sciences ; NMDA ; PET ; Pharmacology. Drug treatments ; phencyclidine ; radiotracer</subject><ispartof>Journal of labelled compounds & radiopharmaceuticals, 2002-10, Vol.45 (11), p.955-964</ispartof><rights>Copyright © 2002 John Wiley & Sons, Ltd.</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3312-3296d4421fb70750290082ae642384508e6587208ae8aa74509b8ebe13975e473</citedby><cites>FETCH-LOGICAL-c3312-3296d4421fb70750290082ae642384508e6587208ae8aa74509b8ebe13975e473</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13986709$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Waterhouse, Rikki N.</creatorcontrib><creatorcontrib>Dumont, Filip</creatorcontrib><creatorcontrib>Sultana, Abida</creatorcontrib><creatorcontrib>Simpson, Norman</creatorcontrib><creatorcontrib>Laruelle, Marc</creatorcontrib><title>Synthesis of [11C] N-(2-chloro-5-thiomethylphenyl)-N′-(3-methoxyphenyl)-N′-methylguanidine ([11C]GMOM): a candidate PET tracer for imaging the PCP site of the NMDA ion channel</title><title>Journal of labelled compounds & radiopharmaceuticals</title><addtitle>J Label Compd Radiopharm</addtitle><description>The N‐methyl‐D‐aspartate (NMDA) ion channel plays an important role in a number of neurodegenerative disorders including stroke, Parkinson's disease, Huntington's Chorea, Alzheimer's disease, schizophrenia and epilepsy. To provide effective radioligands for imaging the PCP binding site of the NMDA ion channel, we synthesized and characterized in vitro the candidate PCP site ligand N‐(2‐chloro‐5‐thiomethylphenyl)‐N′‐(3‐methoxyphenyl)‐N′‐methylguanidine (GMOM: Ki = 5.2 ± 0.3 nM, log P = 2.34). The corresponding PET radiotracer [11C]GMOM was synthesized with a radiochemical yield of 8.4 ± 3.2% EOS and with a specific activity of 1.23 ± 0.25 Ci/μmol EOS (n = 5). The average time required for synthesis, purification and formulation was 52 ± 5 min. The final product was prepared in a sterile saline solution suitable for in vivo use. Copyright © 2002 John Wiley & Sons, Ltd.</description><subject>Biological and medical sciences</subject><subject>Contrast media. Radiopharmaceuticals</subject><subject>glutamate</subject><subject>Medical sciences</subject><subject>NMDA</subject><subject>PET</subject><subject>Pharmacology. Drug treatments</subject><subject>phencyclidine</subject><subject>radiotracer</subject><issn>0362-4803</issn><issn>1099-1344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNp1kM1u1DAYRS1EJYYWiUfwBmm6cPFfYoddFdrhZzIdQREIhCyPx5m4TZ2RnarNjmeib9QnwUMqEAtWlu93dHR1AXhO8BHBmL68aE04yil9BCYEFwUijPPHYIJZThGXmD0BT2O8wDjdOJ-Au4-D7xsbXYRdDb8RUn6HCzSlyDRtFzqUob5x3ZXtm6HdNtYP7SFa3P_4iaYM7dLudvgnHsnNtfZu7byF09_KWXVWHb6CGhrt126tewuXJ-ewD9rYAOsuQHelN85vYOoCl-USRpeY1Gj3X1Svj6HrPDSN9t62B2Cv1m20zx7effDp9OS8fIPmZ7O35fEcGcYIRYwW-ZpzSuqVwCLDtMBYUm1zTpnkGZY2z6SgWGortRYpKVbSrixhhcgsF2wfTEevCV2MwdZqG1LPMCiC1W5stRtbpbET-mJEtzoa3dZBe-PiX54VMhe4SBwauRvX2uG_PvVuXn4YvQ-8i729_cPrcKlywUSmPi9m6utp9UXy6r2q2C_1wZxv</recordid><startdate>20021015</startdate><enddate>20021015</enddate><creator>Waterhouse, Rikki N.</creator><creator>Dumont, Filip</creator><creator>Sultana, Abida</creator><creator>Simpson, Norman</creator><creator>Laruelle, Marc</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20021015</creationdate><title>Synthesis of [11C] N-(2-chloro-5-thiomethylphenyl)-N′-(3-methoxyphenyl)-N′-methylguanidine ([11C]GMOM): a candidate PET tracer for imaging the PCP site of the NMDA ion channel</title><author>Waterhouse, Rikki N. ; Dumont, Filip ; Sultana, Abida ; Simpson, Norman ; Laruelle, Marc</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3312-3296d4421fb70750290082ae642384508e6587208ae8aa74509b8ebe13975e473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Biological and medical sciences</topic><topic>Contrast media. Radiopharmaceuticals</topic><topic>glutamate</topic><topic>Medical sciences</topic><topic>NMDA</topic><topic>PET</topic><topic>Pharmacology. Drug treatments</topic><topic>phencyclidine</topic><topic>radiotracer</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Waterhouse, Rikki N.</creatorcontrib><creatorcontrib>Dumont, Filip</creatorcontrib><creatorcontrib>Sultana, Abida</creatorcontrib><creatorcontrib>Simpson, Norman</creatorcontrib><creatorcontrib>Laruelle, Marc</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Journal of labelled compounds & radiopharmaceuticals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Waterhouse, Rikki N.</au><au>Dumont, Filip</au><au>Sultana, Abida</au><au>Simpson, Norman</au><au>Laruelle, Marc</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of [11C] N-(2-chloro-5-thiomethylphenyl)-N′-(3-methoxyphenyl)-N′-methylguanidine ([11C]GMOM): a candidate PET tracer for imaging the PCP site of the NMDA ion channel</atitle><jtitle>Journal of labelled compounds & radiopharmaceuticals</jtitle><addtitle>J Label Compd Radiopharm</addtitle><date>2002-10-15</date><risdate>2002</risdate><volume>45</volume><issue>11</issue><spage>955</spage><epage>964</epage><pages>955-964</pages><issn>0362-4803</issn><eissn>1099-1344</eissn><abstract>The N‐methyl‐D‐aspartate (NMDA) ion channel plays an important role in a number of neurodegenerative disorders including stroke, Parkinson's disease, Huntington's Chorea, Alzheimer's disease, schizophrenia and epilepsy. 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subjects | Biological and medical sciences Contrast media. Radiopharmaceuticals glutamate Medical sciences NMDA PET Pharmacology. Drug treatments phencyclidine radiotracer |
title | Synthesis of [11C] N-(2-chloro-5-thiomethylphenyl)-N′-(3-methoxyphenyl)-N′-methylguanidine ([11C]GMOM): a candidate PET tracer for imaging the PCP site of the NMDA ion channel |
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