ChemicalBook > Product Catalog > Organic Chemistry > Hydrazine or hydroxylamine derivatives > (2S,5R)-2-(2-acetylhydrazine-1-carbonyl)-7-oxo-1,6-diazabicyclo[3.2.1]octan-6-yl hydrogen sulfate
(2S,5R)-2-(2-acetylhydrazine-1-carbonyl)-7-oxo-1,6-diazabicyclo[3.2.1]octan-6-yl hydrogen sulfate
(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:
-
- (2S,5R)-2-(2-acetylhydrazine-1-carbonyl)-7-oxo-1,6-diazabicyclo[3.2.1]octan-6-yl hydrogen sulfate
- 1,6-Diazabicyclo[3.2.1]octane-2-carboxylic acid, 7-oxo-6-(sulfooxy)-, 2-(2-acetylhydrazide), (1R,2S,5R)-
- CAS:
- 1452459-50-5
- MF:
- C9H14N4O7S
- MW:
- 322.29
- Mol File:
- 1452459-50-5.mol
More
Less
(2S,5R)-2-(2-acetylhydrazine-1-carbonyl)-7-oxo-1,6-diazabicyclo[3.2.1]octan-6-yl hydrogen sulfate Chemical Properties
- Density
- 1.74±0.1 g/cm3(Predicted)
- pka
- -4.59±0.18(Predicted)
More
Less
(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, 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 also inhibits PBP2, with an IC50 of 3.2 μM. FPI-1523 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 sulfateSupplier
Chunchuang (Wuhan) Technology Co., Ltd
- Tel
- 15727060112
- yutianchun2007@126.com
Hubei Xinyang Medical Technology Co., Ltd
- Tel
- 15347293736
- 2853117764@yongstandards.com
Hebei Weite Medical Technology Co., Ltd
- Tel
- 13180081292 13180081292
- contact@wetogethermed.com