Source:http://linkedlifedata.com/resource/pubmed/id/17514336
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
21
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pubmed:dateCreated |
2007-5-21
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pubmed:abstractText |
A cross-bridged cyclam ligand bearing two N-carboxymethyl pendant arms (1) has been found to form a copper(II) complex that exhibits significantly improved biological behavior in recent research towards (64)Cu-based radiopharmaceuticals. Both the kinetic inertness and resistance to reduction of Cu-1 are believed to be relevant to its enhanced performance. To explore the influence of pendant arm length on these properties, new cross-bridged cyclam and cyclen ligands with longer N-carboxyethyl pendant arms, 2 and 4, and their respective copper(II) complexes have been synthesized. Both mono- as well as di-O-protonated forms of Cu-2 have also been isolated and structurally characterized. The spectral and structural properties of Cu-2 and Cu-4, their kinetic inertness in 5 M HCl, and electrochemical behavior have been obtained and compared to those of their N-carboxymethyl-armed homologs, Cu-1 and Cu-3. Only the cyclam-based Cu-1 and Cu-2 showed unusually high kinetic inertness towards acid decomplexation. While both of these complexes also exhibited quasi-reversible Cu(II)/Cu(I) reductions, Cu-2 is easier to reduce by a substantial margin of +400 mV, bringing it within the realm of physiological reductants. Similarly, of the cyclen-based complexes, Cu-4 is also easier to reduce than Cu-3 though both reductions are irreversible. Biodistribution studies of (64)Cu-labeled 2 and 4 were performed in Sprague Dawley rats. Despite comparable acid inertness to their shorter-armed congeners, both longer-armed ligand complexes have poorer bio-clearance properties. This inferior in vivo behavior may be a consequence of their higher reduction potentials.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Amines,
http://linkedlifedata.com/resource/pubmed/chemical/Copper,
http://linkedlifedata.com/resource/pubmed/chemical/Ligands,
http://linkedlifedata.com/resource/pubmed/chemical/Macrocyclic Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Organometallic Compounds
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1477-9226
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pubmed:author |
pubmed-author:AndersonCarolyn JCJ,
pubmed-author:GolenJames AJA,
pubmed-author:HerouxKatie JKJ,
pubmed-author:KasselScottS,
pubmed-author:RheingoldArnold LAL,
pubmed-author:SouthwickEvanE,
pubmed-author:TomelliniSterling ASA,
pubmed-author:TranchemontagneDavid JDJ,
pubmed-author:WadasThaddeus JTJ,
pubmed-author:WeismanGary RGR,
pubmed-author:WidgerPeter C BPC,
pubmed-author:WongEdward HEH,
pubmed-author:WoodinKatrina SKS
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pubmed:issnType |
Print
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pubmed:day |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2150-62
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pubmed:dateRevised |
2007-12-3
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pubmed:meshHeading |
pubmed-meshheading:17514336-Amines,
pubmed-meshheading:17514336-Animals,
pubmed-meshheading:17514336-Copper,
pubmed-meshheading:17514336-Crystallography, X-Ray,
pubmed-meshheading:17514336-Electrochemistry,
pubmed-meshheading:17514336-Female,
pubmed-meshheading:17514336-Kidney,
pubmed-meshheading:17514336-Ligands,
pubmed-meshheading:17514336-Liver,
pubmed-meshheading:17514336-Macrocyclic Compounds,
pubmed-meshheading:17514336-Molecular Structure,
pubmed-meshheading:17514336-Organometallic Compounds,
pubmed-meshheading:17514336-Rats,
pubmed-meshheading:17514336-Rats, Sprague-Dawley,
pubmed-meshheading:17514336-Tissue Distribution
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pubmed:year |
2007
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pubmed:articleTitle |
The long and short of it: the influence of N-carboxyethyl versusN-carboxymethyl pendant arms on in vitro and in vivo behavior of copper complexes of cross-bridged tetraamine macrocycles.
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pubmed:affiliation |
Department of Chemistry, University of New Hampshire, Durham, New Hampshire 03824, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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