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Zhang Q, Jin B, Shi Z, et al. Novel enterobactin analogues as potential therapeutic chelating agents: Synthesis, thermodynamic and antioxidant studies. Sci Rep. 2016;6:34024doi: 10.1038/srep34024.
Zhang, Q., Jin, B., Shi, Z., Wang, X., Liu, Q., Lei, S., & Peng, R. (2016). Novel enterobactin analogues as potential therapeutic chelating agents: Synthesis, thermodynamic and antioxidant studies. Scientific reports, 634024. https://doi.org/10.1038/srep34024
Zhang, Qingchun, et al. "Novel enterobactin analogues as potential therapeutic chelating agents: Synthesis, thermodynamic and antioxidant studies." Scientific reports vol. 6 (2016): 34024. doi: https://doi.org/10.1038/srep34024
Zhang Q, Jin B, Shi Z, Wang X, Liu Q, Lei S, Peng R. Novel enterobactin analogues as potential therapeutic chelating agents: Synthesis, thermodynamic and antioxidant studies. Sci Rep. 2016 Sep 27;6:34024. doi: 10.1038/srep34024. PMID: 27671769; PMCID: PMC5037427.
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Sci Rep. 2016 Sep 27;6:34024. doi: 10.1038/srep34024.

Novel enterobactin analogues as potential therapeutic chelating agents: Synthesis, thermodynamic and antioxidant studies.

Scientific reports

Qingchun Zhang, Bo Jin, Zhaotao Shi, Xiaofang Wang, Qiangqiang Liu, Shan Lei, Rufang Peng

Affiliations

  1. State Key Laboratory Cultivation Base for Nonmetal Composites and Functional Materials, Southwest University of Science and Technology, Mianyang 621010, China.
  2. Department of Chemistry, School of Materials Science and Engineering, Southwest University of Science and Technology, Mianyang 621010, China.
  3. Research Center of Laser Fusion, China Academy of Engineering Physics, Mianyang 621010, China.

PMID: 27671769 PMCID: PMC5037427 DOI: 10.1038/srep34024

Abstract

A series of novel hexadentate enterobactin analogues, which contain three catechol chelating moieties attached to different molecular scaffolds with flexible alkyl chain lengths, were prepared. The solution thermodynamic stabilities of the complexes with uranyl, ferric(III), and zinc(II) ions were then investigated. The hexadentate ligands demonstrate effective binding ability to uranyl ion, and the average uranyl affinities are two orders of magnitude higher than 2,3-dihydroxy-N

References

  1. Inorg Chem. 2002 Dec 16;41(25):6731-42 - PubMed
  2. Dalton Trans. 2008 Jan 28;(4):539-50 - PubMed
  3. Crit Rev Food Sci Nutr. 1992;32(1):67-103 - PubMed
  4. Inorg Chem. 2001 Jun 4;40(12):2835-41 - PubMed
  5. Inorg Chem. 2010 Jul 19;49(14):6755-65 - PubMed
  6. Inorg Chem. 2001 Jul 30;40(16):3922-35 - PubMed
  7. J Org Chem. 2004 May 14;69(10):3530-7 - PubMed
  8. Hum Exp Toxicol. 1991 May;10(3):195-8 - PubMed
  9. J Am Chem Soc. 2011 May 25;133(20):7942-56 - PubMed
  10. J Am Chem Soc. 1976 Mar 31;98(7):1763-7 - PubMed
  11. Neurotoxicology. 1999 Oct;20(5):785-92 - PubMed
  12. Inorg Chem. 2008 Mar 17;47(6):2000-10 - PubMed
  13. Chem Commun (Camb). 2013 Jul 21;49(57):6379-81 - PubMed
  14. Arch Toxicol. 2007 Jun;81(6):389-95 - PubMed
  15. Dalton Trans. 2004 Nov 7;(21):3772-81 - PubMed
  16. Rev Environ Health. 2005 Jul-Sep;20(3):177-93 - PubMed
  17. J Inorg Biochem. 2002 Apr 10;89(1-2):123-30 - PubMed
  18. Chemistry. 2011 Feb 7;17(6):1818-27 - PubMed
  19. Res Commun Chem Pathol Pharmacol. 1989 Apr;64(1):161-4 - PubMed
  20. J Med Chem. 1995 Jul 7;38(14):2606-14 - PubMed

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