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Automated synthesis of F-18-labelled analogs of metomidate, vorozole and harmine using commercial platform
Three F-18-labelled PET tracers, 2-[F-18]fluoroethyl 1-[(1R)-1-phenylethyl]-1H-imidazole-5-carboxylate ([F-18]FETO), 6-[(S)-(4-chlorophenyl)-(1H)-1,2,4-triazol-1-yl)methyl]-1-(2-[F-18]fluor oethyl)-1H-benzotriazole ([F-18]FVOZ) and 7-[2-(2-[F-18]fluoroethoxy)ethoxy]-1-9H-beta-carboline ([F-18]FHAR)...
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Published in: | Journal of labelled compounds & radiopharmaceuticals 2010-03, Vol.53 (3-4), p.169 |
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container_issue | 3-4 |
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container_title | Journal of labelled compounds & radiopharmaceuticals |
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creator | Rahman, Obaidur Erlandsson, Maria Blom, Elisabeth Långström, Bengt |
description | Three F-18-labelled PET tracers, 2-[F-18]fluoroethyl 1-[(1R)-1-phenylethyl]-1H-imidazole-5-carboxylate ([F-18]FETO), 6-[(S)-(4-chlorophenyl)-(1H)-1,2,4-triazol-1-yl)methyl]-1-(2-[F-18]fluor oethyl)-1H-benzotriazole ([F-18]FVOZ) and 7-[2-(2-[F-18]fluoroethoxy)ethoxy]-1-9H-beta-carboline ([F-18]FHAR) were synthesized by a one-step nucleophilic fluorination using the automated commercial platform TRACERLab FXFN. The labelled products were obtained with 16-20% isolated decay corrected radiochemical yields after 70-75 min synthesis time. The radiochemical and chemical purities were more than 98% in all cases. The synthesis using commercial platform may make these tracers more accessible for clinical research. |
doi_str_mv | 10.1002/jlcr.1742 |
format | article |
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The labelled products were obtained with 16-20% isolated decay corrected radiochemical yields after 70-75 min synthesis time. The radiochemical and chemical purities were more than 98% in all cases. The synthesis using commercial platform may make these tracers more accessible for clinical research.</description><identifier>ISSN: 1099-1344</identifier><identifier>ISSN: 0362-4803</identifier><identifier>DOI: 10.1002/jlcr.1742</identifier><language>eng</language><subject>[F-18]FETO ; [F-18]FHAR ; [F-18]FVOZ ; automated synthesis ; Chemistry ; F-18-labelling ; Kemi ; NATURAL SCIENCES ; NATURVETENSKAP ; PET</subject><ispartof>Journal of labelled compounds & radiopharmaceuticals, 2010-03, Vol.53 (3-4), p.169</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-136437$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Rahman, Obaidur</creatorcontrib><creatorcontrib>Erlandsson, Maria</creatorcontrib><creatorcontrib>Blom, Elisabeth</creatorcontrib><creatorcontrib>Långström, Bengt</creatorcontrib><title>Automated synthesis of F-18-labelled analogs of metomidate, vorozole and harmine using commercial platform</title><title>Journal of labelled compounds & radiopharmaceuticals</title><description>Three F-18-labelled PET tracers, 2-[F-18]fluoroethyl 1-[(1R)-1-phenylethyl]-1H-imidazole-5-carboxylate ([F-18]FETO), 6-[(S)-(4-chlorophenyl)-(1H)-1,2,4-triazol-1-yl)methyl]-1-(2-[F-18]fluor oethyl)-1H-benzotriazole ([F-18]FVOZ) and 7-[2-(2-[F-18]fluoroethoxy)ethoxy]-1-9H-beta-carboline ([F-18]FHAR) were synthesized by a one-step nucleophilic fluorination using the automated commercial platform TRACERLab FXFN. The labelled products were obtained with 16-20% isolated decay corrected radiochemical yields after 70-75 min synthesis time. The radiochemical and chemical purities were more than 98% in all cases. The synthesis using commercial platform may make these tracers more accessible for clinical research.</description><subject>[F-18]FETO</subject><subject>[F-18]FHAR</subject><subject>[F-18]FVOZ</subject><subject>automated synthesis</subject><subject>Chemistry</subject><subject>F-18-labelling</subject><subject>Kemi</subject><subject>NATURAL SCIENCES</subject><subject>NATURVETENSKAP</subject><subject>PET</subject><issn>1099-1344</issn><issn>0362-4803</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNotjEFOwzAURL0AiVJYcAMfoCn-tuM0y6pQQKrEBthGjv3TurLjyk5A5fREwGI0Gr2ZIeQO2BIY4_dHb9ISKskvyAxYXRcgpLwi1zkfGZuylDNyXI9DDHpAS_O5Hw6YXaaxo9sCVoXXLXo_Id1rH_e_IODUd3ZaLOhnTPE7epy4pQedguuRjtn1e2piCJiM056evB66mMINuey0z3j773Pyvn182zwXu9enl816V2TgfCiUMUJz0LVVNTAEA9yU2NXKTgLbMlypSrZCoEWly1q1ugRjLXScY8UrMSeLv9_8haexbU7JBZ3OTdSueXAf6yamfTOODQglRSV-AOwqXMI</recordid><startdate>20100301</startdate><enddate>20100301</enddate><creator>Rahman, Obaidur</creator><creator>Erlandsson, Maria</creator><creator>Blom, Elisabeth</creator><creator>Långström, Bengt</creator><scope>ADTPV</scope><scope>AOWAS</scope><scope>DF2</scope></search><sort><creationdate>20100301</creationdate><title>Automated synthesis of F-18-labelled analogs of metomidate, vorozole and harmine using commercial platform</title><author>Rahman, Obaidur ; Erlandsson, Maria ; Blom, Elisabeth ; Långström, Bengt</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-s122t-6cc3a21a9d6910e1c12c5ef96df961db0e8674b33ede6a596ba51cdd1f22e7273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>[F-18]FETO</topic><topic>[F-18]FHAR</topic><topic>[F-18]FVOZ</topic><topic>automated synthesis</topic><topic>Chemistry</topic><topic>F-18-labelling</topic><topic>Kemi</topic><topic>NATURAL SCIENCES</topic><topic>NATURVETENSKAP</topic><topic>PET</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rahman, Obaidur</creatorcontrib><creatorcontrib>Erlandsson, Maria</creatorcontrib><creatorcontrib>Blom, Elisabeth</creatorcontrib><creatorcontrib>Långström, Bengt</creatorcontrib><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Uppsala universitet</collection><jtitle>Journal of labelled compounds & radiopharmaceuticals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rahman, Obaidur</au><au>Erlandsson, Maria</au><au>Blom, Elisabeth</au><au>Långström, Bengt</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Automated synthesis of F-18-labelled analogs of metomidate, vorozole and harmine using commercial platform</atitle><jtitle>Journal of labelled compounds & radiopharmaceuticals</jtitle><date>2010-03-01</date><risdate>2010</risdate><volume>53</volume><issue>3-4</issue><spage>169</spage><pages>169-</pages><issn>1099-1344</issn><issn>0362-4803</issn><abstract>Three F-18-labelled PET tracers, 2-[F-18]fluoroethyl 1-[(1R)-1-phenylethyl]-1H-imidazole-5-carboxylate ([F-18]FETO), 6-[(S)-(4-chlorophenyl)-(1H)-1,2,4-triazol-1-yl)methyl]-1-(2-[F-18]fluor oethyl)-1H-benzotriazole ([F-18]FVOZ) and 7-[2-(2-[F-18]fluoroethoxy)ethoxy]-1-9H-beta-carboline ([F-18]FHAR) were synthesized by a one-step nucleophilic fluorination using the automated commercial platform TRACERLab FXFN. The labelled products were obtained with 16-20% isolated decay corrected radiochemical yields after 70-75 min synthesis time. The radiochemical and chemical purities were more than 98% in all cases. The synthesis using commercial platform may make these tracers more accessible for clinical research.</abstract><doi>10.1002/jlcr.1742</doi></addata></record> |
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subjects | [F-18]FETO [F-18]FHAR [F-18]FVOZ automated synthesis Chemistry F-18-labelling Kemi NATURAL SCIENCES NATURVETENSKAP PET |
title | Automated synthesis of F-18-labelled analogs of metomidate, vorozole and harmine using commercial platform |
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