Literature DB >> 35106813

Synthesis of carbon-14 and stable isotope labeled Censavudine.

Richard C Burrell1, Samuel J Bonacorsi1, Adrian Ortiz2, Tamas Benkovics2, Zhongping Shi2.   

Abstract

Censavudine is a nucleoside reverse transcriptase inhibitor (NRTI) explored clinically by Bristol Myers Squibb for the treatment of human immunodeficiency virus-1 (HIV-1). As part of the development process, a carbon-14 labeled analog was synthesized for use in a human absorption, distribution, metabolism, and excretion (ADME) study. A stable isotope labeled analog was also synthesized for use as a mass spectrum internal standard in bioanalytical assays to accurately quantify the concentration of the drug in biological samples. Carbon-14 labeled Censavudine was synthesized in 10 steps in a 9% overall yield from carbon-14 labeled trimethylsilylacetylene. A total of 4.44 mCi of material was prepared with a specific activity of 0.25 μCi/mg. The radiochemical and UV purities were 99% and it met all of the specifications for use in a human clinical study. Deuterium labeled Censavudine was synthesized in two steps in a 68% overall yield from [D4 ]-thymine. A total of 237 mg were prepared with a UV purity of 99%.
© 2022 John Wiley & Sons, Ltd.

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Keywords:  Censavudine; carbon-14 labeling; human immunodeficiency virus-1 (HIV-1); nucleoside reverse transcriptase inhibitors (NRTIs); stable isotope labeling

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Year:  2022        PMID: 35106813     DOI: 10.1002/jlcr.3964

Source DB:  PubMed          Journal:  J Labelled Comp Radiopharm        ISSN: 0362-4803            Impact factor:   1.921


  1 in total

1.  Synthesis of [2 H5 ]baricitinib via [2 H5 ]ethanesulfonyl chloride.

Authors:  Ross D Jansen-van Vuuren; Rahul Vohra
Journal:  J Labelled Comp Radiopharm       Date:  2022-03-24       Impact factor: 1.949

  1 in total

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