Synthesis of acyclic nucleoside phosphonates targeting flavin-dependent thymidylate synthase in Mycobacterium tuberculosis

[Display omitted] Flavin-Dependent Thymidylate Synthase (FDTS) encoded by ThyX gene was discovered as a new class of thymidylate synthase involved in the de novo synthesis of dTMP named only in 30 % of human pathogenic bacteria. This target was pursed for the development of new antibacterial agents...

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Veröffentlicht in:Bioorganic & medicinal chemistry 2021-09, Vol.46, p.116351-116351, Article 116351
Hauptverfasser: Biteau, Nicolas G., Roy, Vincent, Lambry, Jean-Christophe, Becker, Hubert F., Myllykallio, Hannu, Agrofoglio, Luigi A.
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Sprache:eng
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Zusammenfassung:[Display omitted] Flavin-Dependent Thymidylate Synthase (FDTS) encoded by ThyX gene was discovered as a new class of thymidylate synthase involved in the de novo synthesis of dTMP named only in 30 % of human pathogenic bacteria. This target was pursed for the development of new antibacterial agents against multiresistant pathogens. We have developed a new class of ANPs based on the mimic of two natural’s cofactors (dUMP and FAD) as inhibitors against Mycobacterium tuberculosis ThyX. Several synthetic efforts were performed to optimize regioselective N1-alkylation, cross-coupling metathesis and Sonogashira cross-coupling. Compound 19c showed a poor 31.8% inhibitory effect on ThyX at 200 μM.
ISSN:0968-0896
0960-894X
1464-3391
DOI:10.1016/j.bmc.2021.116351