ACS Infectious Diseases, volume 4, issue 5, pages 715-735
Developments in Glycopeptide Antibiotics
Blaskovich Mark AT
1, 2
,
Hansford Karl A
1, 2
,
Butler Mark D.
1, 2
,
Jia Zhiguang
1, 2
,
Mark Alan E.
1, 2
,
Cooper Matthew A.
1, 2
1
Institute for Molecular Bioscience, The University of Queensland, 306 Carmody Road, Brisbane, Queensland 4072, Australia
|
2
School of Chemistry and Molecular Biosciences, The University of Queensland, Chemistry Building 68, Cooper Road, Brisbane, Queensland 4072, Australia
|
Publication type: Journal Article
Publication date: 2018-01-24
Journal:
ACS Infectious Diseases
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 5.3
ISSN: 23738227
PubMed ID:
29363950
Infectious Diseases
Abstract
Glycopeptide antibiotics (GPAs) are a key weapon in the fight against drug resistant bacteria, with vancomycin still a mainstream therapy against serious Gram-positive infections more than 50 years after it was first introduced. New, more potent semisynthetic derivatives that have entered the clinic, such as dalbavancin and oritavancin, have superior pharmacokinetic and target engagement profiles that enable successful treatment of vancomycin-resistant infections. In the face of resistance development, with multidrug resistant (MDR) S. pneumoniae and methicillin-resistant Staphylococcus aureus (MRSA) together causing 20-fold more infections than all MDR Gram-negative infections combined, further improvements are desirable to ensure the Gram-positive armamentarium is adequately maintained for future generations. A range of modified glycopeptides has been generated in the past decade via total syntheses, semisynthetic modifications of natural products, or biological engineering. Several of these have undergone extensive characterization with demonstrated in vivo efficacy, good PK/PD profiles, and no reported preclinical toxicity; some may be suitable for formal preclinical development. The natural product monobactam, cephalosporin, and β-lactam antibiotics all spawned multiple generations of commercially and clinically successful semisynthetic derivatives. Similarly, next-generation glycopeptides are now technically well positioned to advance to the clinic, if sufficient funding and market support returns to antibiotic development.
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Citations by publishers
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35
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1 publication, 0.56%
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1 publication, 0.56%
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1 publication, 0.56%
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1 publication, 0.56%
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5
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- We do not take into account publications that without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
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GOST
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Blaskovich M. A. et al. Developments in Glycopeptide Antibiotics // ACS Infectious Diseases. 2018. Vol. 4. No. 5. pp. 715-735.
GOST all authors (up to 50)
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Blaskovich M. A., Hansford K. A., Butler M. D., Jia Z., Mark A. E., Cooper M. A. Developments in Glycopeptide Antibiotics // ACS Infectious Diseases. 2018. Vol. 4. No. 5. pp. 715-735.
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RIS
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TY - JOUR
DO - 10.1021/acsinfecdis.7b00258
UR - https://doi.org/10.1021%2Facsinfecdis.7b00258
TI - Developments in Glycopeptide Antibiotics
T2 - ACS Infectious Diseases
AU - Blaskovich, Mark AT
AU - Hansford, Karl A
AU - Butler, Mark D.
AU - Mark, Alan E.
AU - Cooper, Matthew A.
AU - Jia, Zhiguang
PY - 2018
DA - 2018/01/24 00:00:00
PB - American Chemical Society (ACS)
SP - 715-735
IS - 5
VL - 4
PMID - 29363950
SN - 2373-8227
ER -
Cite this
BibTex
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@article{2018_Blaskovich,
author = {Mark AT Blaskovich and Karl A Hansford and Mark D. Butler and Alan E. Mark and Matthew A. Cooper and Zhiguang Jia},
title = {Developments in Glycopeptide Antibiotics},
journal = {ACS Infectious Diseases},
year = {2018},
volume = {4},
publisher = {American Chemical Society (ACS)},
month = {jan},
url = {https://doi.org/10.1021%2Facsinfecdis.7b00258},
number = {5},
pages = {715--735},
doi = {10.1021/acsinfecdis.7b00258}
}
Cite this
MLA
Copy
Blaskovich, Mark AT, et al. “Developments in Glycopeptide Antibiotics.” ACS Infectious Diseases, vol. 4, no. 5, Jan. 2018, pp. 715-735. https://doi.org/10.1021%2Facsinfecdis.7b00258.