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Cited by 256

The DOI matches its Crossref record; 35 of the 35 references it cites were found in a registry or an index.

Boron-containing inhibitors of synthetases

Baker, Stephen J., Tomsho, John W., Benkovic, Stephen J.·2011·Chemical Society Reviews

Abstract

The use of boron in small-molecule pharmaceuticals is increasing. Boron's ubiquitous occurrence in nature and the recent success of a boronic acid drug (Velcade®) in the clinic have alleviated many concerns over its use in pharmaceuticals. In addition, the unique physicochemical properties of boronic acids make them an attractive addition to the medicinal chemists toolbox. This tutorial review will discuss these properties and potential benefits for anyone interested in finding novel enzyme inhibitors. An exceptional class of boronic acids, the oxaboroles, will be highlighted and their properties and uses will be discussed in detail. Finally, the current paradigm for the reaction of boronic acids with enzyme nucleophiles will be summarized.

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Crossref · 10.1039/c0cs00131g

Cites

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Metadata

Authors
Baker, S. J., Tomsho, J. W., & Benkovic, S. J.
Venue
Chemical Society Reviews
Published
2011
Volume
40
Issue
8
Pages
4279
ISSN
  • 0306-0012 (ISSN-L)
  • 1460-4744
OpenAlex
W2107529999
Cited by
256
References
35
FWCI
0.47
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Boron-containing inhibitors of synthetases. https://app.cochat.ai/papers/10.1039/c0cs00131g
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Baker, S. J., Tomsho, J. W., & Benkovic, S. J. (2011). Boron-containing inhibitors of synthetases. Chemical Society Reviews. https://doi.org/10.1039/c0cs00131g

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.