CAS 98753-19-6
:Cefpirome sulfate
Description:
Cefpirome sulfate is a broad-spectrum cephalosporin antibiotic, classified under the fourth generation of cephalosporins. It is primarily used to treat a variety of bacterial infections, particularly those caused by Gram-negative bacteria, including Pseudomonas aeruginosa. Cefpirome exhibits a high degree of stability against beta-lactamases, enzymes produced by some bacteria that can inactivate many antibiotics. The compound is typically administered via injection and is known for its favorable pharmacokinetic properties, including good tissue penetration and a relatively long half-life, which allows for less frequent dosing. Its mechanism of action involves inhibiting bacterial cell wall synthesis, leading to cell lysis and death. Cefpirome sulfate is generally well-tolerated, but like all antibiotics, it may cause side effects, including allergic reactions and gastrointestinal disturbances. It is important to use this antibiotic judiciously to minimize the risk of developing antibiotic resistance. As with any medication, its use should be guided by susceptibility testing and clinical judgment.
Formula:C22H23N6O5S2·HO4S
InChI:InChI=1S/C22H22N6O5S2.H2O4S/c1-33-26-15(13-10-35-22(23)24-13)18(29)25-16-19(30)28-17(21(31)32)12(9-34-20(16)28)8-27-7-3-5-11-4-2-6-14(11)27;1-5(2,3)4/h3,5,7,10,16,20H,2,4,6,8-9H2,1H3,(H3-,23,24,25,29,31,32);(H2,1,2,3,4)/b26-15-;/t16-,20-;/m1./s1
InChI key:InChIKey=RKTNPKZEPLCLSF-QHBKFCFHSA-N
SMILES:C(O)(=O)C=1N2[C@@]([C@H](NC(/C(=N\OC)/C3=CSC(N)=N3)=O)C2=O)(SCC1C[N+]4=C5C(CCC5)=CC=C4)[H].S(=O)(=O)([O-])O
Synonyms:- 1-[[(6R,7R)-7-[[(2Z)-(2-Amino-4-thiazolyl)(methoxyimino)acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-6,7-dihydro-5H-cyclopenta[b]pyridinium sulfate
- 1-{[(6R,7R)-7-{[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetyl]amino}-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl}-6,7-dihydro-5H-cyclopenta[b]pyridinium hydrogen sulfate
- 5H-Cyclopenta[b]pyridinium, 1-[[(6R,7R)-7-[[(2Z)-(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-6,7-dihydro-, sulfate (1:1)
- Broact
- Cefpirome sulphate
- HR 810 sulfate
- Keiten
- Cefpirome sulfate
- Cefpirome Sulfate
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Found 11 products.
Cefpirome Sulfate
CAS:Formula:C22H22N6O5S2·H2SO4Purity:>95.0%(HPLC)(N)Color and Shape:White to Almost white powder to crystalMolecular weight:612.65Cefpirome sulfate, 95%
CAS:<p>A fourth generation cephalosporin antibiotic</p>Formula:C22H22N6O5S2•H2SO4Purity:95%Molecular weight:612.665H-Cyclopenta[b]pyridinium,1-[[(6R,7R)-7-[[(2Z)-(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-6,7-dihydro-, sulfate (1:1)
CAS:Formula:C22H24N6O9S3Purity:82%Color and Shape:SolidMolecular weight:612.6558Cefpirome sulfate
CAS:Formula:C22H24N6O9S3Purity:≥ 760μg/mg (Cefpirome on dry basis)Color and Shape:White to pale yellow crystalline powderMolecular weight:612.66Cefpirome sulfate
CAS:Controlled ProductFormula:C22H22N6O5S2·H2O4SColor and Shape:NeatMolecular weight:612.66Cefpirome sulfate
CAS:<p>Cefpirome sulfate (HR-810 sulfate) is a fourth generation cephalosporin antibiotic.</p>Formula:C22H24N6O9S3Purity:97.52%Color and Shape:White Or Off White Crystalline PowderMolecular weight:612.66Cefpirome Sulfate
CAS:Controlled Product<p>Applications Fourth generation cephalosporin antibiotic.<br>References Kavi, J., et al.: J. Antimicrob. Chemother., 22, 911 (1988), Horstmann, G., et al.: Arzneim.-Forsch., 40, 1250 (1990),<br></p>Formula:C22H22N6O5S2·H2O4SColor and Shape:Yellowish CrystallineMolecular weight:612.66Cefpirome sulfate
CAS:<p>Cefpirome sulfate is a cephalosporin antibiotic that has been used in the treatment of infectious diseases. It is active against a wide range of microorganisms, including Gram-positive and Gram-negative bacteria and mycoplasma. Cefpirome sulfate is given for intravenous injection as an alternative to glucose. The drug binds to the cell wall of bacteria, causing lysis and cell death. Cefpirome sulfate also inhibits bacterial growth by inhibiting protein synthesis at the level of the ribosome, where it binds to the 50S subunit. This binding prevents peptide chain elongation and affects RNA synthesis by impairing translocation of tRNA from the A site on the ribosome to the P site on the ribosome. Thermodynamic data show that cefpirome sulfate has a high degree of stability in human serum compared with vancomycin hydrochloride (another cephalosporin antibiotic).</p>Formula:C22H24N6O9S3Purity:Min. 95 Area-%Color and Shape:White Off-White PowderMolecular weight:612.66 g/mol









