Literature DB >> 9799688

13C and 15N-chemical shift anisotropy of ampicillin and penicillin-V studied by 2D-PASS and CP/MAS NMR.

O N Antzutkin1, Y K Lee, M H Levitt.   

Abstract

The principal values of the chemical shift tensors of all 13C and 15N sites in two antibiotics, ampicillin and penicillin-V, were determined by 2-dimensional phase adjusted spinning sideband (2D-PASS) and conventional CP/MAS experiments. The 13C and 15N chemical shift anisotropies (CSA), and their confidence limits, were evaluated using a Mathematica program. The CSA values suggest a revised assignment of the 2-methyl 13C sites in the case of ampicillin. We speculate on a relationship between the chemical shift principal values of many of the 13C and 15N sites and the beta-lactam ring conformation. Copyright 1998 Academic Press.

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Year:  1998        PMID: 9799688     DOI: 10.1006/jmre.1998.1576

Source DB:  PubMed          Journal:  J Magn Reson        ISSN: 1090-7807            Impact factor:   2.229


  2 in total

Review 1.  Chemical shift tensor - the heart of NMR: Insights into biological aspects of proteins.

Authors:  Hazime Saitô; Isao Ando; Ayyalusamy Ramamoorthy
Journal:  Prog Nucl Magn Reson Spectrosc       Date:  2010-05-07       Impact factor: 9.795

2.  15N solid-state NMR provides a sensitive probe of oxidized flavin reactive sites.

Authors:  Ronald L Koder; Joseph D Walsh; Maxim S Pometun; P Leslie Dutton; Richard J Wittebort; Anne-Frances Miller
Journal:  J Am Chem Soc       Date:  2006-11-29       Impact factor: 15.419

  2 in total

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