5'-Noraristeromycin Repurposing: Well-known S-Adenosyl-L-homocysteine Hydrolase Inhibitor As a Potential Drug Against Leukemia

5'-Noraristeromycin as a racemic mixture of enantiomers was found to exhibit a pronounced cytotoxic effect on leukemia cells; IC<sub>50</sub> for the Jurkat, K562, and THP-1 cell lines was 7.3, 1.3, and 3.7 μM, respectively. The general toxicity of 5'-noraristeromycin was studied in experiments on white mice upon single-dose intragastric administration; toxicometric parameters were determined, and the clinical and pathomorphological presentation of acute intoxication was studied. LD<sub>50</sub> of the substance was shown to be 63.2 (52.7÷75.8) mg/kg; LD16, 44.7 mg/kg, and LD84, 89.4 mg/kg. Administration of the substance at a dose within the studied dose range is accompanied by systemic damage to the internal organs and tissues of the experimental animals.

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Journal
Acta Naturae
Published
2024-11-12
DOI
https://doi.org/10.32607/actanaturae.27443
Primary Topic
Cancer therapeutics and mechanisms
Type
article
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article

5'-Noraristeromycin Repurposing: Well-known S-Adenosyl-L-homocysteine Hydrolase Inhibitor As a Potential Drug Against Leukemia

Pavel Spirin, Valeria Vedernikova, Sergey N. Kochetkov, Yu. I. Velikorodnaya et al.
Acta Naturae
Cancer therapeutics and mechanisms
article

5'-Noraristeromycin Repurposing: Well-known S-Adenosyl-L-homocysteine Hydrolase Inhibitor As a Potential Drug Against Leukemia

Pavel Spirin, Valeria Vedernikova, Sergey N. Kochetkov, Yu. I. Velikorodnaya, Anastasia L. Khandazhinskaya, Elena S. Matyugina, В. С. Прасолов, Aleksandr Vladimirovich Gorshenin, O. N. Novikova, M. D. Krengauz
article en

Abstract

5'-Noraristeromycin as a racemic mixture of enantiomers was found to exhibit a pronounced cytotoxic effect on leukemia cells; IC<sub>50</sub> for the Jurkat, K562, and THP-1 cell lines was 7.3, 1.3, and 3.7 μM, respectively. The general toxicity of 5'-noraristeromycin was studied in experiments on white mice upon single-dose intragastric administration; toxicometric parameters were determined, and the clinical and pathomorphological presentation of acute intoxication was studied. LD<sub>50</sub> of the substance was shown to be 63.2 (52.7÷75.8) mg/kg; LD16, 44.7 mg/kg, and LD84, 89.4 mg/kg. Administration of the substance at a dose within the studied dose range is accompanied by systemic damage to the internal organs and tissues of the experimental animals.

Acta NaturaeVol. 16(3)
Engelhardt Institute of Molecular Biology (RU), Moscow Institute of Physics and Technology (RU), Moscow Power Engineering Institute (RU), Genetic Technologies (Australia) (AU), Moscow Aviation Institute (RU), Federal Medical-Biological Agency (RU)
Good health and well-being
Openalex Percentile: Top 82%
Cancer therapeutics and mechanisms
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