Radioiodinated L-703,606 : a potent, selective antagonist to the human NK1 receptor

A new, radioiodinated, NK1 selective radiotracer ([125I]L-703,606) was prepared. L-703,606 is an iodinated analog of the NK1 antagonist CP-96,345 in which the methoxy group has been replaced by an iodine substituent. [125I]L-703,606 was made from the corresponding trimethylsilyl compound by treatmen...

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Veröffentlicht in:Applied radiation and isotopes 1994, Vol.45 (1), p.97-103
Hauptverfasser: FRANCIS, B. E, SWAIN, C, SABIN, V, BURNS, H. D
Format: Artikel
Sprache:eng
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Zusammenfassung:A new, radioiodinated, NK1 selective radiotracer ([125I]L-703,606) was prepared. L-703,606 is an iodinated analog of the NK1 antagonist CP-96,345 in which the methoxy group has been replaced by an iodine substituent. [125I]L-703,606 was made from the corresponding trimethylsilyl compound by treatment with no carrier added Na 125I and an Iodobead in TFA. The tracer was prepared at a specific activity of approx. 1100 Ci/mmol and preliminary binding studies demonstrated that [125I]L-703,606 binds selectively to NK1 receptors with a kd = 0.3 nM. These results suggest that this radioligand will be useful for the biochemical and pharmacological characterization of the human NK1 receptor and, if labeled with I-123, may be useful for non-invasive NK1 receptor imaging via SPECT.
ISSN:0969-8043
1872-9800
DOI:10.1016/0969-8043(94)90154-6