1989
DOI: 10.1039/c39890000792
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Towards tumour targeting with copper-radiolabelled macrocycle–antibody conjugates

Abstract: Tetra-aza-macrocycles covalently attached to a monoclonal anti body may be efficiently radiolabelled with 64Cu or 67Cu at pH 4, minimising non-specific binding to the protein, giving a kinetically stable conjugate in vivo.

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Cited by 36 publications
(41 citation statements)
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“…These features have been harnessed to develop macrocycles able to transport radioisotopic agents to a tumour site ( 64 Cu and 67 Cu for example). [2] Moreover, changes in the nitrogen (or carbon) substitution can determine their potential applications. In particular, functionalisation of cyclen by substituents such as acetate binding arms has led to a new class of ligands which are able to coordinate lanthanide cations especially Gd III .…”
Section: Introductionmentioning
confidence: 99%
“…These features have been harnessed to develop macrocycles able to transport radioisotopic agents to a tumour site ( 64 Cu and 67 Cu for example). [2] Moreover, changes in the nitrogen (or carbon) substitution can determine their potential applications. In particular, functionalisation of cyclen by substituents such as acetate binding arms has led to a new class of ligands which are able to coordinate lanthanide cations especially Gd III .…”
Section: Introductionmentioning
confidence: 99%
“…Mouse antibody 7-6C1 against TIMP-1 was purchased from Oncogene Science. The metalloprotease inhibitor CT1847 (20) was kindly provided by A. Docherty (Celltech, Slough, U.K.).…”
Section: Methodsmentioning
confidence: 99%
“…[40b] viewed as good chelating agent which may have utility in NMR imaging, [33] and in biological screenings. [34] The α-Furthermore, benzaldehyde reacts differently with phosaminophosphonate analogs have been recently de-phane (PH 3 ) in alcoholic solution and affords bis(α-ethoxyscribed.…”
Section: Synthesis Of α-Hydroxyalkylphosphinic Acidsmentioning
confidence: 99%