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dc.contributor.authorSonopo, Molahlehi S.
dc.contributor.authorZeevaart, Jan R.
dc.contributor.authorVenter, Kobus
dc.contributor.authorWinks, Susan
dc.contributor.authorMarjanovic-Painter, Biljana
dc.date.accessioned2017-04-07T11:31:20Z
dc.date.available2017-04-07T11:31:20Z
dc.date.issued2016
dc.identifier.citationSonopo, M.S. et al. 2016. Carbon-14 radiolabelling and tissue distribution evaluation of a potential anti-TB compound. Journal of labelled compounds and radiopharmaceuticals, 59:264-269. [https://doi.org/10.1002/jlcr.3391]en_US
dc.identifier.issn0362-4803
dc.identifier.issn1099-1344 (Online)
dc.identifier.urihttp://hdl.handle.net/10394/21226
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/abs/10.1002/jlcr.3391
dc.identifier.urihttps://doi.org/10.1002/jlcr.3391
dc.description.abstractThis paper describes a five-step synthesis of a carbon-14-labelled pyrazole compound (11). A total of 2.96 MBq of 11 was obtained with the specific activity of 2242.4 MBq/mmol. The radiochemical purity was >99%, and the overall radiochemical yield was 60% based on the [14C6] 4-bromoaniline starting material. Biodistribution results showed that the radiotracer (administrated orally) has a high accumulation in the small intestine, large intestine and liver of both non-infected and tuberculosis (TB)-infected mice. Therefore, this suggests that compound 11 undergoes hepatobiliary clearance. The compound under investigation has been found to be slowly released from the liver between 2 and 8 h. The study revealed that 11 has no affinity for TB cellsen_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.titleCarbon-14 radiolabelling and tissue distribution evaluation of a potential anti-TB compounden_US
dc.typeArticleen_US
dc.contributor.researchID16951484 - Zeevaart, Jan Rijn


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