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Synthesis, Biological Activity, and Mechanism of Action of Mono-Substituted 5-Halouracil Salts

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Pharmaceutical Chemistry Journal Aims and scope

Mono-substituted sodium salts of 5-fluoro-, 5-chloro-, 5-bromo-, and 5-iodouracil were synthesized. The toxicity and effect of the synthesized compounds on the DNA-binding activity of transcription factors CREB, NFAT, NF-κB, p53, STAT1, GAS, VDR, HSF1, and HIF1á were studied. It was found that the sodium salts of 5-chloro-, 5-bromo-, and 5-iodouracil did not exhibit cytotoxicity comparable with that of the sodium salt of 5-fluorouracil.

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Correspondence to S. P. Ivanov.

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Translated from Khimiko-Farmatsevticheskii Zhurnal, Vol. 48, No. 4, pp. 14 – 16, April, 2014.

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Salimgareeva, M.K., Farafontova, E.I., Abdrakhimova, G.S. et al. Synthesis, Biological Activity, and Mechanism of Action of Mono-Substituted 5-Halouracil Salts. Pharm Chem J 48, 235–237 (2014). https://doi.org/10.1007/s11094-014-1084-9

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  • DOI: https://doi.org/10.1007/s11094-014-1084-9

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