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Synthesis and evaluation of radiolabeled AGI-5198 analogues as candidate radiotracers for imaging mutant IDH1 expression in tumors

Mutations in the metabolic enzyme isocitrate dehydrogenase 1 (IDH1) are commonly found in gliomas. AGI-5198, a potent and selective inhibitor of the mutant IDH1 enzyme, was radiolabeled with radioiodine and fluorine-18. These radiotracers were evaluated as potential probes for imaging mutant IDH1 ex...

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Pubblicato in:Bioorg Med Chem Lett
Autori principali: Chitneni, Satish K., Reitman, Zachary J., Spicehandler, Rebecca, Gooden, David M., Yan, Hai, Zalutsky, Michael R.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2018
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5817038/
https://ncbi.nlm.nih.gov/pubmed/29366652
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bmcl.2018.01.015
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