کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1356139 | 981091 | 2011 | 8 صفحه PDF | دانلود رایگان |
Synthesis of [11C]celecoxib, a selective COX-2 inhibitor, and [11C]SC-62807, a major metabolite of celecoxib, were achieved and the potential of these PET probes for assessing the function of drug transporter in biliary excretion was evaluated. The synthesis of [11C]celecoxib was achieved in one-pot by reacting [11C]methyl iodide with an excess of the corresponding pinacol borate precursor using Pd2(dba)3, P(o-tolyl)3, and K2CO3 (1:4:9) in DMF. The radiochemical yield of [11C]celecoxib was 63 ± 23% (decay-corrected, based on [11C]CH3I) (n = 7) with a specific radioactivity of 83 ± 23 GBq/μmol (n = 7). The average time of synthesis from end of bombardment including formulation was 30 min with >99% radiochemical purity. [11C]SC-62807 was synthesized from [11C]celecoxib by further rapid oxidation in the presence of excess KMnO4 with microwave irradiation. The radiochemical yield of [11C]SC-62807 was 55 ± 9% (n = 3) (decay-corrected, based on [11C]celecoxib) with a specific radioactivity of 39 ± 4 GBq/μmol (n = 3). The average time of synthesis from [11C]celecoxib including formulation was 20 min and the radiochemical purity was >99%. PET studies in rats and the metabolite analyzes of [11C]celecoxib and [11C]SC-62807 showed largely different excretion processes, and consequently, [11C]SC-62807 was rapidly excreted via hepatobiliary excretion without further metabolism. [11C]SC-62807 was shown to have a high potential as a PET probe for evaluating drug transporter function in biliary excretion.
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Journal: Bioorganic & Medicinal Chemistry - Volume 19, Issue 9, 1 May 2011, Pages 2997–3004