Molecular structure of Moxalactam sodium salt, CAS Number: 64953-12-4
Moxalactam sodium salt (CAS 64953-12-4)
See product citations (8)
Alternate Names:
(6R,7R)-7-[[2-Carboxy(4-hydroxyphenyl)acetyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-oxa-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid disodium salt
Application:
Moxalactam sodium salt is an antibiotic effective against E. coli and P. aeruginosa
CAS Number:
64953-12-4
Purity:
≥85%
Molecular Weight:
564.44
Molecular Formula:
C20H18N6O9S•2Na
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Moxalactam sodium salt (MOXA) is an antibiotic compound more effective against Escherichia coli and Pseudomonas aeruginosa than cephalosporins. It belongs to the group of β-lactam antibiotics and is effective against Gram-positive and Gram-negative bacteria. It has been found to possess a wide range of biological activities, including anti-inflammatory, anti-fibrotic, anti-fungal, and anti-bacterial properties.
Moxalactam sodium salt (CAS 64953-12-4) References
- Phenotypic library-based microbial source tracking methods: efficacy in the California collaborative study. | Harwood, VJ., et al. 2003. J Water Health. 1: 153-66. PMID: 15382721
- Filamentous Fungi (Magnaporthe grisea and Fusarium oxysporum). | Khang, CH., et al. 2006. Methods Mol Biol. 344: 403-20. PMID: 17033082
- In Vitro Activity of the New β-Lactamase Inhibitors Relebactam and Vaborbactam in Combination with β-Lactams against Mycobacterium abscessus Complex Clinical Isolates. | Kaushik, A., et al. 2019. Antimicrob Agents Chemother. 63: PMID: 30642943
- Protein Stability Effects in Aggregate-Based Enzyme Inhibition. | Torosyan, H. and Shoichet, BK. 2019. J Med Chem. 62: 9593-9599. PMID: 31589047
- Multigene Engineering by GoldenBraid Cloning: From Plants to Filamentous Fungi and Beyond. | Vazquez-Vilar, M., et al. 2020. Curr Protoc Mol Biol. 130: e116. PMID: 32150346
- Screening of an FDA-Approved Library for Novel Drugs against Y. pestis. | Gur, D., et al. 2021. Antibiotics (Basel). 10: PMID: 33401634
- An Efficient Strategy for Obtaining Mutants by Targeted Gene Deletion in Ophiostoma novo-ulmi. | Sarmiento-Villamil, JL., et al. 2021. Front Microbiol. 12: 699783. PMID: 34335533
- beta-Lactam drug allergens: fine structural recognition patterns of cephalosporin-reactive IgE antibodies. | Pham, NH. and Baldo, BA. 1996. J Mol Recognit. 9: 287-96. PMID: 9131470
- Meropenem and moxalactam: Novel β-lactam antibiotics for efficient Agrobacterium-mediated transformation | Y Ogawa, M Mii. 2007. Plant Science. 172: 564-572.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Moxalactam sodium salt, 1 g | sc-250419 | 1 g | $195.00 | |||
Moxalactam sodium salt, 5 g | sc-250419A | 5 g | $632.00 |