CAS 61177-44-4
:4-Oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3-(2-hydroxyethylidene)-7-oxo-, lithium salt (1:1), (2R,3Z,5R)-
Description:
4-Oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3-(2-hydroxyethylidene)-7-oxo-, lithium salt (1:1), (2R,3Z,5R)- is a complex organic compound characterized by its bicyclic structure, which includes both nitrogen and oxygen heteroatoms. The presence of a carboxylic acid functional group indicates potential acidity and reactivity, while the lithium salt form suggests enhanced solubility and stability in various solvents. The specific stereochemistry denoted by (2R,3Z,5R) implies that the compound has defined spatial arrangements, which can influence its biological activity and interaction with other molecules. This compound may exhibit properties typical of both bicyclic amines and carboxylic acids, potentially making it useful in pharmaceutical applications or as a biochemical probe. Its unique structure could also confer specific binding affinities or catalytic properties, depending on the context of its use. Overall, the compound's characteristics are shaped by its intricate molecular architecture and functional groups, which dictate its chemical behavior and potential applications.
Formula:C8H9NO5·Li
InChI:InChI=1S/C8H9NO5.Li/c10-2-1-4-7(8(12)13)9-5(11)3-6(9)14-4;/h1,6-7,10H,2-3H2,(H,12,13);/b4-1-;/t6-,7-;/m1./s1
InChI key:InChIKey=NFFXIXWEWBDWBZ-JSYANWSFSA-N
SMILES:C(O)(=O)[C@@H]\1N2[C@](O/C1=C\CO)(CC2=O)[H].[Li]
Synonyms:- 4-Oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3-(2-hydroxyethylidene)-7-oxo-, lithium salt (1:1), (2R,3Z,5R)-
- 4-Oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3-(2-hydroxyethylidene)-7-oxo-, monolithium salt, (2R,3Z,5R)-
- 4-Oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3-(2-hydroxyethylidene)-7-oxo-, monolithium salt, [2R-(2α,3Z,5α)]-
- Lithium (2R-(2alpha,3(Z),5alpha))-3-(2-hydroxyethylidene)-4-oxa-7-oxo-1-azabicyclo(3.2.0)heptane-2-carboxylate
- Lithium clavulanate
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Found 10 products.
Clavulanate Lithium
CAS:<p>Nucleic acids and their salts, whether or not chemically defined; other heterocyclic compounds, nesoi</p>Formula:C8H8NO5·LiColor and Shape:White Light Yellow PowderMolecular weight:205.05625lithium [2R-(2α,3(Z),5α)]-3-(2-hydroxyethylidene)-4-oxa-7-oxo-1-azabicyclo[3.2.0]heptane-2-carboxylate
CAS:Formula:C8H8LiNO5Purity:97%Color and Shape:SolidMolecular weight:205.0938Clavulanate lithium
CAS:<p>Clavulanate lithium (Clavulanic acid lithium) is an inhibitor of β-lactamase.</p>Formula:C8H8LiNO5Purity:99.79%Color and Shape:SolidMolecular weight:205.09Clavulanate Lithium
CAS:Formula:C8H8NO5·LiColor and Shape:White To Off-White SolidMolecular weight:198.16 6.94Clavulanate Lithium
CAS:Controlled Product<p>Stability Hygroscopic<br>Applications Clavulanate Lithium is used as an antibacterial compound against a β-lactamase producing strain of Staphylococcus aureus.<br>References Cuffini, A. et al.: Microbios., 87, 31 (1996); Rodriguez, M. et al.: Int. J. Antimicrob. Agents., 29 332 (2007);<br></p>Formula:C8H8NO5·LiColor and Shape:Off-WhiteMolecular weight:205.09Clavulanate Lithium
CAS:<p>Clavulanate lithium is an antibiotic that inhibits the growth of bacteria by binding to penicillin-binding proteins. It is a prodrug that is hydrolyzed in vivo to clavulanic acid, its active form. The inhibitory properties of clavulanate lithium are similar to those of amoxicillin, but it has greater activity against pseudomonas aeruginosa and Staphylococcus aureus. Clavulanate lithium has been shown to increase the plasma concentrations of amoxicillin when used in combination with this drug. It is also effective against a variety of bacterial infections, including Escherichia coli, Proteus mirabilis, Enterobacter cloacae, and Staphylococcus aureus isolates. Clavulanate lithium can be used as an adjunct therapy for the treatment of respiratory tract infections caused by common viruses such as influenza and rhinovirus. Clavulanate</p>Formula:C8H9NO5•LiPurity:Min. 95%Color and Shape:PowderMolecular weight:206.1 g/mol
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