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J Cardiovasc Pharmacol. 2000 Nov;36(5 Suppl 1):S58-60.

Syntheses of the first endothelin-A- and -B-selective radioligands for positron emission tomography.

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  • 1Clinical Pharmacology Unit, University of Cambridge, Addenbrooke's Hospital, UK. pjj20@medschl.cam.ac.uk

Abstract

We have synthesized two potential positron emission tomography (PET) radioligands for the endothelin (ET) receptor. [11C]-PD156707 was produced by O-methylation of PD169390 using [11C]iodomethane. Radiochemical conversions of the order of 74 +/- 3.2% (n = 8) were obtained. The radiochemical purity of the isolated [11C]-PD156707 was 99% and the specific activity was 538 mCi/micromol. [18F]-BQ3020 was produced from [18F]fluoride in a total radiochemical yield of 2.7 +/- 0.4% (n = 10) in 238 +/- 5 min. The radiochemical purity was 95% and specific activities of the order of 670-930 mCi/micromol were obtained.

PMID:
11078336
[PubMed - indexed for MEDLINE]
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