Abstract
C NMR chemical shifts of vancomycin have been used to obtain the association constants for a number of ligands which bind weakly to the antibiotic. The change in these C chemical shifts upon stepwise addition of ligands provides evidence that the ligands bind in a manner analogous to natural cell-wall precursor analogues. The binding constants obtained are in good agreement with those determined earlier by other methods. Where the ligands are amino acids (glycine or alanine), a potential alkylammonium to amide carbonyl interaction does not promote binding.
| Original language | English |
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| Pages (from-to) | 159-162 |
| Number of pages | 4 |
| Journal | Journal of the Chemical Society, Perkin Transactions 2 |
| Issue number | 1 |
| Publication status | Published - 1 Jan 1995 |