Analogs of Eu3+ DOTAM-Gly-Phe-OH and Tm3+ DOTAM-Gly-Lys-OH : Synthesis and magnetic properties of potential PARACEST MRI contrast agents

Chelated lanthanide ions, especially gadolinium, have found wide use as contrast agents in magnetic resonance imaging. A new paradigm for generating contrast, termed PARACEST, was recently described that requires the slow exchange of water or other exchangeable protons present in the ligand framewor...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Bioorganic & medicinal chemistry 2008-06, Vol.16 (11), p.6156-6166
Hauptverfasser: SUCHY, Mojmir, LI, Alex X, BARTHA, Robert, HUDSON, Robert H. E
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 6166
container_issue 11
container_start_page 6156
container_title Bioorganic & medicinal chemistry
container_volume 16
creator SUCHY, Mojmir
LI, Alex X
BARTHA, Robert
HUDSON, Robert H. E
description Chelated lanthanide ions, especially gadolinium, have found wide use as contrast agents in magnetic resonance imaging. A new paradigm for generating contrast, termed PARACEST, was recently described that requires the slow exchange of water or other exchangeable protons present in the ligand framework. In previous work, we have described a synthetic method for the preparation of dipeptide conjugates of DOTAM for use as PARACEST agents. Two compounds possessed interesting magnetic properties: the Eu(3+) complex of DOTAM-Gly-Phe-OH and the Tm(3+) complex of DOTAM-Gly-Lys-OH. To understand the relationship between the structure of these complexes and their magnetic properties, we have expanded our synthetic methodology and prepared several new complexes. Ligands have been prepared in which the terminal phenylalanine moieties have been replaced with tryptophan or tyrosine, the distance to the amino acid residue possessing an alpha-substituent has been changed, or phenylalanine and lysine have been combined in the peptide sequence. The preparation of lanthanide(III) complexes of these ligands has been achieved and their PARACEST properties have been determined.
doi_str_mv 10.1016/j.bmc.2008.04.038
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71640389</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>71640389</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1745-d42ed94919432fa7a75592e2028505c54ec1fa8cbd98ac64a51532f3dc90470b3</originalsourceid><addsrcrecordid>eNpVkL1OwzAUhS0EgvLzACzICywo4dqxk5gtKqUgFRVBma1bxymp8lPidOgb8Ni4UIGYPJzvHF1_hJwzCBmw-GYZzmsTcoA0BBFClO6RAROxCKJIsX0yABWnAaQqPiLHzi0BgAvFDskRS4VMlJQD8pk1WLULR9uCjtbRNb2bzrKnYFxtgud3G0wfKDY5ndX_ksnGbZNb-rpp-nfrSvdN1bhobF8auurale360n7PrtreNn2JFX3OXrLh6HVGn14eqWmbvkPXU1z42J2SgwIrZ8927wl5ux_Nhg_BZDp-HGaTwLBEyCAX3ObK_0KJiBeYYCKl4pYDTyVII4U1rMDUzHOVookFSiY9GOVGgUhgHp2Qq59df-TH2rpe16Uztqqwse3a6YTFwptUHmQ_oOla5zpb6FVX1thtNAO91a-X2uvXW_0ahPYl37nYja_ntc3_GjvfHrjcAegMVkWHjSndL8dBcCWEir4ALp6LEQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>71640389</pqid></control><display><type>article</type><title>Analogs of Eu3+ DOTAM-Gly-Phe-OH and Tm3+ DOTAM-Gly-Lys-OH : Synthesis and magnetic properties of potential PARACEST MRI contrast agents</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Collection</source><creator>SUCHY, Mojmir ; LI, Alex X ; BARTHA, Robert ; HUDSON, Robert H. E</creator><creatorcontrib>SUCHY, Mojmir ; LI, Alex X ; BARTHA, Robert ; HUDSON, Robert H. E</creatorcontrib><description>Chelated lanthanide ions, especially gadolinium, have found wide use as contrast agents in magnetic resonance imaging. A new paradigm for generating contrast, termed PARACEST, was recently described that requires the slow exchange of water or other exchangeable protons present in the ligand framework. In previous work, we have described a synthetic method for the preparation of dipeptide conjugates of DOTAM for use as PARACEST agents. Two compounds possessed interesting magnetic properties: the Eu(3+) complex of DOTAM-Gly-Phe-OH and the Tm(3+) complex of DOTAM-Gly-Lys-OH. To understand the relationship between the structure of these complexes and their magnetic properties, we have expanded our synthetic methodology and prepared several new complexes. Ligands have been prepared in which the terminal phenylalanine moieties have been replaced with tryptophan or tyrosine, the distance to the amino acid residue possessing an alpha-substituent has been changed, or phenylalanine and lysine have been combined in the peptide sequence. The preparation of lanthanide(III) complexes of these ligands has been achieved and their PARACEST properties have been determined.</description><identifier>ISSN: 0968-0896</identifier><identifier>EISSN: 1464-3391</identifier><identifier>DOI: 10.1016/j.bmc.2008.04.038</identifier><identifier>PMID: 18457955</identifier><language>eng</language><publisher>Oxford: Elsevier Science</publisher><subject>Acetamides - chemical synthesis ; Biological and medical sciences ; Contrast Media - chemical synthesis ; Contrast media. Radiopharmaceuticals ; Dipeptides - chemical synthesis ; Europium ; Glycine - chemistry ; Heterocyclic Compounds - chemical synthesis ; Heterocyclic Compounds, 1-Ring - chemical synthesis ; Ligands ; Lysine - chemistry ; Magnetic Resonance Imaging ; Magnetic Resonance Spectroscopy ; Medical sciences ; Pharmacology. Drug treatments ; Phenylalanine - chemistry ; Spectrometry, Mass, Electrospray Ionization ; Thulium</subject><ispartof>Bioorganic &amp; medicinal chemistry, 2008-06, Vol.16 (11), p.6156-6166</ispartof><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1745-d42ed94919432fa7a75592e2028505c54ec1fa8cbd98ac64a51532f3dc90470b3</citedby><cites>FETCH-LOGICAL-c1745-d42ed94919432fa7a75592e2028505c54ec1fa8cbd98ac64a51532f3dc90470b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=20429449$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18457955$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SUCHY, Mojmir</creatorcontrib><creatorcontrib>LI, Alex X</creatorcontrib><creatorcontrib>BARTHA, Robert</creatorcontrib><creatorcontrib>HUDSON, Robert H. E</creatorcontrib><title>Analogs of Eu3+ DOTAM-Gly-Phe-OH and Tm3+ DOTAM-Gly-Lys-OH : Synthesis and magnetic properties of potential PARACEST MRI contrast agents</title><title>Bioorganic &amp; medicinal chemistry</title><addtitle>Bioorg Med Chem</addtitle><description>Chelated lanthanide ions, especially gadolinium, have found wide use as contrast agents in magnetic resonance imaging. A new paradigm for generating contrast, termed PARACEST, was recently described that requires the slow exchange of water or other exchangeable protons present in the ligand framework. In previous work, we have described a synthetic method for the preparation of dipeptide conjugates of DOTAM for use as PARACEST agents. Two compounds possessed interesting magnetic properties: the Eu(3+) complex of DOTAM-Gly-Phe-OH and the Tm(3+) complex of DOTAM-Gly-Lys-OH. To understand the relationship between the structure of these complexes and their magnetic properties, we have expanded our synthetic methodology and prepared several new complexes. Ligands have been prepared in which the terminal phenylalanine moieties have been replaced with tryptophan or tyrosine, the distance to the amino acid residue possessing an alpha-substituent has been changed, or phenylalanine and lysine have been combined in the peptide sequence. The preparation of lanthanide(III) complexes of these ligands has been achieved and their PARACEST properties have been determined.</description><subject>Acetamides - chemical synthesis</subject><subject>Biological and medical sciences</subject><subject>Contrast Media - chemical synthesis</subject><subject>Contrast media. Radiopharmaceuticals</subject><subject>Dipeptides - chemical synthesis</subject><subject>Europium</subject><subject>Glycine - chemistry</subject><subject>Heterocyclic Compounds - chemical synthesis</subject><subject>Heterocyclic Compounds, 1-Ring - chemical synthesis</subject><subject>Ligands</subject><subject>Lysine - chemistry</subject><subject>Magnetic Resonance Imaging</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Medical sciences</subject><subject>Pharmacology. Drug treatments</subject><subject>Phenylalanine - chemistry</subject><subject>Spectrometry, Mass, Electrospray Ionization</subject><subject>Thulium</subject><issn>0968-0896</issn><issn>1464-3391</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkL1OwzAUhS0EgvLzACzICywo4dqxk5gtKqUgFRVBma1bxymp8lPidOgb8Ni4UIGYPJzvHF1_hJwzCBmw-GYZzmsTcoA0BBFClO6RAROxCKJIsX0yABWnAaQqPiLHzi0BgAvFDskRS4VMlJQD8pk1WLULR9uCjtbRNb2bzrKnYFxtgud3G0wfKDY5ndX_ksnGbZNb-rpp-nfrSvdN1bhobF8auurale360n7PrtreNn2JFX3OXrLh6HVGn14eqWmbvkPXU1z42J2SgwIrZ8927wl5ux_Nhg_BZDp-HGaTwLBEyCAX3ObK_0KJiBeYYCKl4pYDTyVII4U1rMDUzHOVookFSiY9GOVGgUhgHp2Qq59df-TH2rpe16Uztqqwse3a6YTFwptUHmQ_oOla5zpb6FVX1thtNAO91a-X2uvXW_0ahPYl37nYja_ntc3_GjvfHrjcAegMVkWHjSndL8dBcCWEir4ALp6LEQ</recordid><startdate>20080601</startdate><enddate>20080601</enddate><creator>SUCHY, Mojmir</creator><creator>LI, Alex X</creator><creator>BARTHA, Robert</creator><creator>HUDSON, Robert H. E</creator><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20080601</creationdate><title>Analogs of Eu3+ DOTAM-Gly-Phe-OH and Tm3+ DOTAM-Gly-Lys-OH : Synthesis and magnetic properties of potential PARACEST MRI contrast agents</title><author>SUCHY, Mojmir ; LI, Alex X ; BARTHA, Robert ; HUDSON, Robert H. E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1745-d42ed94919432fa7a75592e2028505c54ec1fa8cbd98ac64a51532f3dc90470b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Acetamides - chemical synthesis</topic><topic>Biological and medical sciences</topic><topic>Contrast Media - chemical synthesis</topic><topic>Contrast media. Radiopharmaceuticals</topic><topic>Dipeptides - chemical synthesis</topic><topic>Europium</topic><topic>Glycine - chemistry</topic><topic>Heterocyclic Compounds - chemical synthesis</topic><topic>Heterocyclic Compounds, 1-Ring - chemical synthesis</topic><topic>Ligands</topic><topic>Lysine - chemistry</topic><topic>Magnetic Resonance Imaging</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Medical sciences</topic><topic>Pharmacology. Drug treatments</topic><topic>Phenylalanine - chemistry</topic><topic>Spectrometry, Mass, Electrospray Ionization</topic><topic>Thulium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SUCHY, Mojmir</creatorcontrib><creatorcontrib>LI, Alex X</creatorcontrib><creatorcontrib>BARTHA, Robert</creatorcontrib><creatorcontrib>HUDSON, Robert H. E</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bioorganic &amp; medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SUCHY, Mojmir</au><au>LI, Alex X</au><au>BARTHA, Robert</au><au>HUDSON, Robert H. E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analogs of Eu3+ DOTAM-Gly-Phe-OH and Tm3+ DOTAM-Gly-Lys-OH : Synthesis and magnetic properties of potential PARACEST MRI contrast agents</atitle><jtitle>Bioorganic &amp; medicinal chemistry</jtitle><addtitle>Bioorg Med Chem</addtitle><date>2008-06-01</date><risdate>2008</risdate><volume>16</volume><issue>11</issue><spage>6156</spage><epage>6166</epage><pages>6156-6166</pages><issn>0968-0896</issn><eissn>1464-3391</eissn><abstract>Chelated lanthanide ions, especially gadolinium, have found wide use as contrast agents in magnetic resonance imaging. A new paradigm for generating contrast, termed PARACEST, was recently described that requires the slow exchange of water or other exchangeable protons present in the ligand framework. In previous work, we have described a synthetic method for the preparation of dipeptide conjugates of DOTAM for use as PARACEST agents. Two compounds possessed interesting magnetic properties: the Eu(3+) complex of DOTAM-Gly-Phe-OH and the Tm(3+) complex of DOTAM-Gly-Lys-OH. To understand the relationship between the structure of these complexes and their magnetic properties, we have expanded our synthetic methodology and prepared several new complexes. Ligands have been prepared in which the terminal phenylalanine moieties have been replaced with tryptophan or tyrosine, the distance to the amino acid residue possessing an alpha-substituent has been changed, or phenylalanine and lysine have been combined in the peptide sequence. The preparation of lanthanide(III) complexes of these ligands has been achieved and their PARACEST properties have been determined.</abstract><cop>Oxford</cop><pub>Elsevier Science</pub><pmid>18457955</pmid><doi>10.1016/j.bmc.2008.04.038</doi><tpages>11</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0968-0896
ispartof Bioorganic & medicinal chemistry, 2008-06, Vol.16 (11), p.6156-6166
issn 0968-0896
1464-3391
language eng
recordid cdi_proquest_miscellaneous_71640389
source MEDLINE; Elsevier ScienceDirect Journals Collection
subjects Acetamides - chemical synthesis
Biological and medical sciences
Contrast Media - chemical synthesis
Contrast media. Radiopharmaceuticals
Dipeptides - chemical synthesis
Europium
Glycine - chemistry
Heterocyclic Compounds - chemical synthesis
Heterocyclic Compounds, 1-Ring - chemical synthesis
Ligands
Lysine - chemistry
Magnetic Resonance Imaging
Magnetic Resonance Spectroscopy
Medical sciences
Pharmacology. Drug treatments
Phenylalanine - chemistry
Spectrometry, Mass, Electrospray Ionization
Thulium
title Analogs of Eu3+ DOTAM-Gly-Phe-OH and Tm3+ DOTAM-Gly-Lys-OH : Synthesis and magnetic properties of potential PARACEST MRI contrast agents
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T16%3A01%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Analogs%20of%20Eu3+%20DOTAM-Gly-Phe-OH%20and%20Tm3+%20DOTAM-Gly-Lys-OH%20:%20Synthesis%20and%20magnetic%20properties%20of%20potential%20PARACEST%20MRI%20contrast%20agents&rft.jtitle=Bioorganic%20&%20medicinal%20chemistry&rft.au=SUCHY,%20Mojmir&rft.date=2008-06-01&rft.volume=16&rft.issue=11&rft.spage=6156&rft.epage=6166&rft.pages=6156-6166&rft.issn=0968-0896&rft.eissn=1464-3391&rft_id=info:doi/10.1016/j.bmc.2008.04.038&rft_dat=%3Cproquest_cross%3E71640389%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=71640389&rft_id=info:pmid/18457955&rfr_iscdi=true