Helsel ME, Franz KJ. Pharmacological activity of metal binding agents that alter copper bioavailability. Dalton Trans. 2015;44:8760–70.
Hider RC, Kong X. Chemistry and biology of siderophores. Nat Prod Rep. 2010;27:637–57.
Miethke M. Molecular strategies of microbial iron assimilation: from high-affinity complexes to cofactor assembly systems. Metallomics. 2013;5:15–28.
Snow GA. Isolation and Structure of Mycobactin T, a Growth Factor from Mycobacterium tuberculosis. Biochem J. 1965;97:166–75.
Sontag B, Gerlitz M, Paululat T, Rasser HF, Grün-Wollny I, Hansske FG. Oxachelin, a Novel Iron Chelator and Antifungal Agent from Streptomyces sp. GW9/1258. J Antibiot. 2006;59:659–63.
Fox Ramos AE, Evanno L, Poupon E, Champy P, Beniddir MA. Natural products targeting strategies involving molecular networking: different manners, one goal. Nat Prod Rep. 2019;36:960–80.
Harada K, Tomita K, Fujii K, Masuda K, Mikami Y, Yazawa K, Komaki H. Isolation and Structural Characterization of Siderophores, Madurastatins, Produced by a Pathogenic Actinomadura madurae. J Antibiot. 2004;57:125–35.
Mazzei E, Iorio M, Maffioli SI, Sosio M, Donadio S. Characterization of madurastatin C1, a novel siderophore from Actinomadura sp. J Antibiot. 2012;65:267–9.
Yan J-X, Chevrette MG, Braun DR, Harper MK, Currie CR, Bugni TS. Madurastatin D1 and D2, Oxazoline Containing Siderophores Isolated from an Actinomadura sp. Org Lett. 2019;21:6275–9.
Wu C, Miller PA, Miller MJ. Syntheses and studies of amamistatin B analogs reveals that anticancer activity is relatively independent of stereochemistry, ester or amide linkage and select replacement of one of the metal chelating groups. Bioorg Med Chem Lett. 2011;21:2611–5.
Ikeda Y, Nonaka H, Furumai T, Onaka H, Igarashi Y. Nocardimicins A, B, C, D, E, and F, Siderophores with Muscarinic M3 Receptor Inhibiting Activity from Nocardia sp. TP-A0674. J Nat Prod. 2005;68:1061–5.
Kessler H. Cis‐trans‐Isomerie bei N‐monosubstituierten Amiden. Angew Chem. 1968;80:201.
Bhushan R, Brückner H. Use of Marfey’s reagent and analogs for chiral amino acid analysis: assessment and applications to natural products and biological systems. J Chromatogr B. 2011;879:3148–61.
Marfey P. Determination of d-amino acids. II. Use of a bifunctional reagent, 1,5-difluoro-2,4-dinitrobenzene. Carlsberg Res Commun. 1984;49:591–96.
Zhang X, He H, Ma R, Ji Z, Wei Q, Dai H, et al. Madurastatin B3, a rare aziridine derivative from actinomycete Nocardiopsis sp. LS150010 with potent anti-tuberculosis activity. J Ind Microbiol Biotechnol. 2017;44:589–94.
Shaaban KA, Saunders MA, Zhang Y, Tran T, Elshahawi SI, Ponomareva LV, et al. Spoxazomicin D and Oxachelin C, Potent Neuroprotective Carboxamides from the Appalachian Coal Fire-Associated Isolate Streptomyces sp. RM-14-6. J Nat Prod. 2017;80:2–11.
Tyler AR, Mosaei H, Morton S, Waddell PG, Wills C, McFarlane W, et al. Structural Reassignment and Absolute Stereochemistry of Madurastatin C1 (MBJ-0034) and the Related Aziridine Siderophores: Madurastatins A1, B1, and MBJ-0035. J Nat Prod. 2017;80:1558–62.
Marner M, Patras MA, Kurz M, Zubeil F, Förster F, Schuler S, et al. Molecular Networking-Guided Discovery and Characterization of Stechlisins, a Group of Cyclic Lipopeptides from a Pseudomonas sp. J Nat Prod. 2020;83:2607–17.
留言 (0)