Introduction:Basic information about (2S,5R)-2-(2-acetylhydrazine-1-carbonyl)-7-oxo-1,6-diazabicyclo[3.2.1]octan-6-yl hydrogen sulfate CA, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
(2S,5R)-2-(2-acetylhydrazine-1-carbonyl)-7-oxo-1,6-diazabicyclo[3.2.1]octan-6-yl hydrogen sulfate Basic information
| Product Name: | (2S,5R)-2-(2-acetylhydrazine-1-carbonyl)-7-oxo-1,6-diazabicyclo[3.2.1]octan-6-yl hydrogen sulfate |
| Synonyms: | sodium (2S,5R)-2-(2-acetylhydrazine-1-carbonyl)-7-oxo-1,6-diazabicyclo[3.2.1]octan-6-yl sulfate;FPI-1523 sodium;sodium (2S,5R)-N'-acetyl-7-oxo-6-(sulfooxy)-1,6-diazabicyclo[3.2.1]octane-2-carbohydrazide |
| CAS: | 1452459-52-7 |
| MF: | C9H15N4NaO7S |
| MW: | 346.29 |
| EINECS: | |
| Product Categories: | |
| Mol File: | 1452459-52-7.mol |
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(2S,5R)-2-(2-acetylhydrazine-1-carbonyl)-7-oxo-1,6-diazabicyclo[3.2.1]octan-6-yl hydrogen sulfate Chemical Properties
| form | Solid |
| color | White to off-white |
Safety Information
(2S,5R)-2-(2-acetylhydrazine-1-carbonyl)-7-oxo-1,6-diazabicyclo[3.2.1]octan-6-yl hydrogen sulfate Usage And Synthesis
| Uses | FPI-1523 sodium, a derivative of Avibactam, is a potent β-lactamase inhibitor, with Kds of 4 nM and 34 nM for CTX-M-15 and OXA-48, respectively. FPI-1523 sodium also inhibits PBP2, with an IC50 of 3.2 μM. FPI-1523 sodium exhibits considerable antimicrobial activity[1]. |
| References | [1] King AM, et, al. Structural and Kinetic Characterization of Diazabicyclooctanes as Dual Inhibitors of Both Serine-β-Lactamases and Penicillin-Binding Proteins. ACS Chem Biol. 2016 Apr 15;11(4):864-8. DOI:10.1021/acschembio.5b00944 |
(2S,5R)-2-(2-acetylhydrazine-1-carbonyl)-7-oxo-1,6-diazabicyclo[3.2.1]octan-6-yl hydrogen sulfate Preparation Products And Raw materials