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Phenyl thiazolyl urea and carbamate derivatives as new inhibitors of bacterial cell-wall biosynthesis
Abstract
Over 50 phenyl thiazolyl urea and carbamate derivatives were synthesized for evaluation as new inhibitors of bacterial cell-wall biosynthesis. Many of them demonstrated good activity against MurA and MurB and gram-positive bacteria including MRSA, VRE and PRSP. 3,4-Difluorophenyl 5-cyanothiazolylurea (3p) with clog P of 2.64 demonstrated antibacterial activity against both gram-positive and gram-negative bacteria.
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Some similarities exist between our molecules and known inhibitors of bacterial cell wall biosynthesis and lipid biosynthesis.
“Some similarities exist between our molecules and known inhibitors of bacterial cell wall biosynthesis (Li et al., 2003; Francisco et al., 2004) and lipid biosynthesis (Russell, 2004).”
From Small Molecule Fluoride Toxicity Agonists (2015) · cites this paper as Francisco et al., 2004
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Cited by
Sorted by citations
Small Molecule Fluoride Toxicity Agonists
Nelson, J. W., Plummer, M. S., Blount, K. F., Ames, T. D., & Breaker, R. R. (2015) · Chemistry & Biology · doi:10.1016/j.chembiol.2015.03.016 · Cited by 30
Metadata
- Authors
- Francisco, G. D., Li, Z., Albright, J. D., Eudy, N. H., Katz, A. H., Petersen, P. J., Labthavikul, P., Singh, G., Yang, Y., Rasmussen, B. A., Lin, Y.-I., & Mansour, T. S.
- Venue
- Bioorganic & Medicinal Chemistry Letters
- Publisher
- Elsevier BV
- Published
- 2004-01
- Volume
- 14
- Issue
- 1
- Pages
- 235-238
- ISSN
- 0960-894X
- Cited by
- 74
- References
- 0
- Language
- en
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