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Design, Synthesis and Testing of Transition State Analogues of Alanine Racemase as Antibacterials

Design, Synthesis and Testing of Transition State Analogues of Alanine Racemase as Antibacterials <jats:p>Transition state analogues have been designed for alanine racemase , an important enzyme target for the development of bacterial cell wall inhibitors. These analogues are based on the transition state structure obtained from MINDO/3 calculations on the reaction pathway of a model alanine racemization . A number of analogues have been synthesized and are shown to have weak anti-bacterial activity, but results from microbiological assays indicate that their antibacterial activity is not due to inhibition of alanine racemase . Subsequent n.m.r .studies have shown that they are unstable in aqueous environments. Formaldehyde has been identified as one of the degradation products, and the likely source of antibacterial activity. </jats:p> http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Australian Journal of Chemistry CrossRef

Design, Synthesis and Testing of Transition State Analogues of Alanine Racemase as Antibacterials

Australian Journal of Chemistry , Volume 38 (2): 297 – Jan 1, 1985

Design, Synthesis and Testing of Transition State Analogues of Alanine Racemase as Antibacterials


Abstract

<jats:p>Transition state analogues have been designed for alanine racemase , an important enzyme target for the development of bacterial cell wall inhibitors. These analogues are based on the transition state structure obtained from MINDO/3 calculations on the reaction pathway of a model alanine racemization . A number of analogues have been synthesized and are shown to have weak anti-bacterial activity, but results from microbiological assays indicate that their antibacterial activity is not due to inhibition of alanine racemase . Subsequent n.m.r .studies have shown that they are unstable in aqueous environments. Formaldehyde has been identified as one of the degradation products, and the likely source of antibacterial activity. </jats:p>

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Publisher
CrossRef
ISSN
0004-9425
DOI
10.1071/ch9850297
Publisher site
See Article on Publisher Site

Abstract

<jats:p>Transition state analogues have been designed for alanine racemase , an important enzyme target for the development of bacterial cell wall inhibitors. These analogues are based on the transition state structure obtained from MINDO/3 calculations on the reaction pathway of a model alanine racemization . A number of analogues have been synthesized and are shown to have weak anti-bacterial activity, but results from microbiological assays indicate that their antibacterial activity is not due to inhibition of alanine racemase . Subsequent n.m.r .studies have shown that they are unstable in aqueous environments. Formaldehyde has been identified as one of the degradation products, and the likely source of antibacterial activity. </jats:p>

Journal

Australian Journal of ChemistryCrossRef

Published: Jan 1, 1985

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