Vancomycin Molecular Interactions: Antibiotic and Enantioselective Mechanisms
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Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-12445-7_8
Reference31 articles.
1. Kerns R et al (2000) The role of hydrophobic substituents in the biological activity of glycopeptide antibiotics. J Am Chem Soc 122:12608–12609
2. O’Brien DP et al (1999) High affinity surface binding of a strongly dimerizing vancomycin-group antibiotic to a model of resistant bacteria. J Am Chem Soc 121:5259–5265
3. Armstrong DW et al (1994) Macrocyclic antibiotics as a new class of chiral selectors for liquid chromatography. Anal Chem 66:1473–1484
4. Kaplan J et al (2001) The role of sugar residues in molecular recognition by vancomycin. J Med Chem 44:1837–1840
5. Jourdan E et al (2003) Use of an amino stationary phase to study the vancomycin dimerization dependence on solute enantioselectivity. J Liq Chromatogr Relat Tech 26:1027–1039
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