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Calculations of Geometric Parameters and Physicochemical Properties of Complexes Formed of FE(II)-Reactive 1,2,4-Trioxolane Ring and Some Anti-Malaria Drugs Via Traceless Linker

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Pharmaceutical Chemistry Journal Aims and scope

There is a method to employ aberrant levels of mobile ferrous iron (Fe(II)) for selective drug delivery in vivo. This approach makes use of a 1,2,4-trioxolane moiety, which serves as an Fe(II)- sensitive “trigger,” making drug release contingent on Fe(II)-promoted trioxolane fragmentation. In this study we focused on the prototype drug conjugate of 1,2,4-trioxolane ring joined via a traceless linker to drug species, which is conjugated to the linker via a free amine or alcohol function to form a complex.We studied four complexes formed of different drugs with various linkers. The structure and physicochemical properties of complexes were studied using the Hartree – Fock method with 6-311++G** basis set. The influence of the oxalan ring and various drugs on the properties of complexes has been studied. Geometric parameter, energies, nuclear chemical shielding constants, direction of dipole moment vector, partition coefficients, electric polarizabilities, and other physicochemical properties of these compounds have been calculated.

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References

  1. R. Karaman and H. Hallak, Chem. Biol. Drug Des., 76(4), 350 – 360 (2010).

    Article  CAS  PubMed  Google Scholar 

  2. A. T. Peterson, BMC Infect. Dis., 9, 59 (2009).

    Article  PubMed  PubMed Central  Google Scholar 

  3. A. Hitani, T. Nakamura, H. Ohtomo, et al., J. Infect. Chemother., 12(5),277 – 282 (2006).

    Article  CAS  PubMed  Google Scholar 

  4. www.cdc.gov/malaria/about/disease.htm

  5. H. J. Vial, S.Wein, C. Farenc, et al., Proc. Natl. Acad. Sci. USA, 101(43), 15458 – 15463 (2004).

    Article  CAS  PubMed  Google Scholar 

  6. M. W. Hentze, M. U. Muckenthaler, B. Galy, and C. Camaschella, Cell, 142(1), 24 – 38 (2010).

    Article  CAS  PubMed  Google Scholar 

  7. J. L. Vennerstrom et al., Nature, 430(7002), 900 – 904 (2004).

    Article  CAS  PubMed  Google Scholar 

  8. N. Valecha et al., Clin. Infect. Dis., 51(6), 684 – 691 (2010).

    Article  CAS  PubMed  Google Scholar 

  9. J. J. Moehrle et al., Brit. J. Clin. Pharmacol., 75(2), 524 – 537 (2013).

    Article  CAS  Google Scholar 

  10. C. L. Hartwig et al., J. Med. Chem., 54(23), 8207 – 8213 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. C. L. Hartwig et al., Biochem. Pharmacol. 77(3), 322 – 336 (2009).

    Article  CAS  PubMed  Google Scholar 

  12. M. A. Fügi, S. Wittlin, Y. Dong, and J. L. Vennerstrom, Antimicrob. Agents Chemother., 54(3), 1042 – 1046 (2010).

    Article  CAS  PubMed  Google Scholar 

  13. D. J. Creek et al., Antimicrob. Agents Chemother., 52(4), 1291 – 1296 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. A. E. Mercer et al., J. Biol. Chem., 282(13), 9372 – 9382 (2007).

    Article  CAS  PubMed  Google Scholar 

  15. U. Eckstein-Ludwig et al., Nature, 424(6951), 957 – 961 (2003).

    Article  CAS  PubMed  Google Scholar 

  16. R. K. Haynes et al., Chem. Med. Chem., 7(12), 2204 – 2226 (2012).

    Article  CAS  PubMed  Google Scholar 

  17. P. M. O’Neill, et al., Angew. Chem. Int. Ed. (Engl.), 43(32), 4193 – 4197 (2004).

    Article  CAS  Google Scholar 

  18. M. Klemba, I. Gluzman, and D. E. Goldberg, J. Biol. Chem., 279(41), 43000 – 43007 (2004).

    Article  CAS  PubMed  Google Scholar 

  19. E. Deu et al., Chem. Biol., 17(8), 808 – 819 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. S. Arastu-Kapur et al., Nat. Chem. Biol., 4(3), 203 – 213 (2008).

    Article  CAS  PubMed  Google Scholar 

  21. E. Deu et al., Proc. Natl. Acad. Sci. USA, 110(45), 18244 – 18249 (2013).

    Article  PubMed  Google Scholar 

  22. B. Spangler et al., J. Med. Chem., 59, 11161 – 11170 (2016).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Bayat, Z., Gholizadeh, A. Calculations of Geometric Parameters and Physicochemical Properties of Complexes Formed of FE(II)-Reactive 1,2,4-Trioxolane Ring and Some Anti-Malaria Drugs Via Traceless Linker. Pharm Chem J 53, 411–418 (2019). https://doi.org/10.1007/s11094-019-02012-0

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  • DOI: https://doi.org/10.1007/s11094-019-02012-0

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