O-Aryloxycarbonyl Hydroxamates: New β-Lactamase Inhibitors That Cross-Link the Active Site-Reference-Cited by-同舟云学术

O-Aryloxycarbonyl Hydroxamates: New β-Lactamase Inhibitors That Cross-Link the Active Site

Published:2007-07-12 Issue:31 Volume:129 Page:9548-9549
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Wyrembak Pauline N.¹,Babaoglu Kerim¹,Pelto Ryan B.¹,Shoichet Brian K.¹,Pratt R. F.¹

Affiliation:

1. Department of Chemistry, Wesleyan University, Middletown, Connecticut 06459, and Department of Pharmaceutical Chemistry, University of California, San Francisco, 1700 4th Street, San Francisco, California 94158-2330

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja072370u

Reference12 articles.

1. β-Lactamase inhibitors: evolving compounds for evolving resistance targets

2. Understanding the longevity of the β-lactam antibiotics and of antibiotic/β-lactamase inhibitor combinations

3. beta-Lactamase-catalyzed hydrolysis of acyclic depsipeptides and acyl transfer to specific amino acid acceptors.

4. Kinetics and mechanism of the serine .beta.-lactamase catalyzed hydrolysis of depsipeptides

5. Synthesis, Hydrolysis, and Evaluation of 3-Acylamino-3,4-dihydro-2-oxo-2H-1,3-benzoxazinecarboxylic Acids and Linear Azadepsipeptides as Potential Substrates/Inhibitors of β-Lactam-Recognizing Enzymes

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