Literature DB >> 10637361

Studies and syntheses of siderophores, microbial iron chelators, and analogs as potential drug delivery agents.

J M Roosenberg1, Y M Lin, Y Lu, M J Miller.   

Abstract

Siderophores (microbial iron chelators) play an extremely important role in microbial pathogenicity. Microbial uptake of siderophore-iron complexes through active transport systems allow microbes to survive and proliferate even under iron deficient environments during invasion of a host. Due to their structural complexity, unique iron (III) chelation, acquisition properties, and their therapeutic potential, siderophores have attracted much attention in a broad range of disciplines. Tremendous progress has been made in siderophore syntheses, in determination of the structures and functions of outer membrane receptors (e.g. FhuA and FepA), and in the mechanistic insight into siderophore-iron-mediated active transport processes. One of the important practical applications of this active transport system is development of species-selective active drug transport (the Trojan Horse approach) to potentially treat infections due to drug resistant strains of microbes. Siderophore-drug conjugates have shown great potential in active drug delivery to target pathogenic microbes.

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Year:  2000        PMID: 10637361     DOI: 10.2174/0929867003375353

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  39 in total

1.  Design, synthesis, and study of a mycobactin-artemisinin conjugate that has selective and potent activity against tuberculosis and malaria.

Authors:  Marvin J Miller; Andrew J Walz; Helen Zhu; Chunrui Wu; Garrett Moraski; Ute Möllmann; Esther M Tristani; Alvin L Crumbliss; Michael T Ferdig; Lisa Checkley; Rachel L Edwards; Helena I Boshoff
Journal:  J Am Chem Soc       Date:  2011-01-28       Impact factor: 15.419

Review 2.  Interactions among strategies associated with bacterial infection: pathogenicity, epidemicity, and antibiotic resistance.

Authors:  José L Martínez; Fernando Baquero
Journal:  Clin Microbiol Rev       Date:  2002-10       Impact factor: 26.132

3.  Structure-activity relationship of new anti-tuberculosis agents derived from oxazoline and oxazole benzyl esters.

Authors:  Garrett C Moraski; Mayland Chang; Adriel Villegas-Estrada; Scott G Franzblau; Ute Möllmann; Marvin J Miller
Journal:  Eur J Med Chem       Date:  2010-01-14       Impact factor: 6.514

4.  Accessorizing natural products: adding to nature's toolbox.

Authors:  Sherry S Lamb; Gerard D Wright
Journal:  Proc Natl Acad Sci U S A       Date:  2005-01-12       Impact factor: 11.205

5.  Desketoneoenactin-siderophore conjugates for Candida: evidence of iron transport-dependent species selectivity.

Authors:  Geneviève Bernier; Vinay Girijavallabhan; Aaron Murray; Noormohamed Niyaz; Pingyu Ding; Marvin J Miller; François Malouin
Journal:  Antimicrob Agents Chemother       Date:  2005-01       Impact factor: 5.191

6.  Design and synthesis of a siderophore conjugate as a potent PSMA inhibitor and potential diagnostic agent for prostate cancer.

Authors:  Pingyu Ding; Paul Helquist; Marvin J Miller
Journal:  Bioorg Med Chem       Date:  2007-11-17       Impact factor: 3.641

Review 7.  Siderophore-based iron acquisition and pathogen control.

Authors:  Marcus Miethke; Mohamed A Marahiel
Journal:  Microbiol Mol Biol Rev       Date:  2007-09       Impact factor: 11.056

8.  Characterization of the Aspergillus nidulans transporters for the siderophores enterobactin and triacetylfusarinine C.

Authors:  Hubertus Haas; Michelle Schoeser; Emmanuel Lesuisse; Joachim F Ernst; Walther Parson; Beate Abt; Günther Winkelmann; Harald Oberegger
Journal:  Biochem J       Date:  2003-04-15       Impact factor: 3.857

9.  Design and synthesis of a novel protected mixed ligand siderophore.

Authors:  Pingyu Ding; Clara E Schous; Marvin J Miller
Journal:  Tetrahedron Lett       Date:  2008-03-31       Impact factor: 2.415

10.  Novel antisense oligonucleotides containing hydroxamate linkages: targeted iron-triggered chemical nucleases.

Authors:  Marvin J Miller; Hui Li; Catherine A Foss
Journal:  Biometals       Date:  2009-01-28       Impact factor: 2.949

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