CAS 75498-96-3
:Cefminox sodium
Description:
Cefminox sodium is a semisynthetic cephalosporin antibiotic, classified under the broader category of beta-lactam antibiotics. It is primarily used for its antibacterial properties, effective against a range of Gram-positive and Gram-negative bacteria. Cefminox sodium works by inhibiting bacterial cell wall synthesis, leading to cell lysis and death. This compound is typically administered via injection and is often utilized in clinical settings for treating various infections, including those of the respiratory tract, skin, and soft tissues. Its pharmacokinetic profile includes good tissue penetration and a relatively short half-life, necessitating multiple doses for sustained therapeutic effect. Cefminox sodium is generally well-tolerated, but like other antibiotics, it may cause side effects such as allergic reactions or gastrointestinal disturbances. It is important to use this antibiotic judiciously to prevent the development of antibiotic resistance. As with all medications, its use should be guided by susceptibility testing and clinical judgment.
Formula:C16H21N7O7S3·Na
InChI:InChI=1S/C16H21N7O7S3.Na/c1-22-15(19-20-21-22)33-4-7-3-32-14-16(30-2,13(29)23(14)10(7)12(27)28)18-9(24)6-31-5-8(17)11(25)26;/h8,14H,3-6,17H2,1-2H3,(H,18,24)(H,25,26)(H,27,28);/t8-,14-,16+;/m1./s1
InChI key:InChIKey=PCFNCVRMULUNFA-YNJMIPHHSA-N
SMILES:N(C(CSC[C@H](C(O)=O)N)=O)[C@@]1(OC)[C@@]2(N(C1=O)C(C(O)=O)=C(CSC=3N(C)N=NN3)CS2)[H].[Na]
Synonyms:- (6R,7S)-7-[[[[(2S)-2-Amino-2-carboxyethyl]thio]acetyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid sodium salt
- (6R-(6Alpha,7Alpha))-7-((((2-Amino-2-Carboxyethyl)Thio)Acetyl)Amino)-7-Methoxy-3-(((1-Methyl-1H-Tetrazol-5-Yl)Thio)Methyl)-8-Oxo-5-Thia-1-Azabicyclo(4.2.0)Oct-2-Ene-2-Carboxylic Acid Monosodium Salt
- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[2-[[(2S)-2-amino-2-carboxyethyl]thio]acetyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, sodium salt (1:1), (6R,7S)-
- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[[(2-amino-2-carboxyethyl)thio]acetyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, monosodium salt, [6R-[6α,7α,7(S*)]]-
- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[[[(2S)-2-amino-2-carboxyethyl]thio]acetyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, monosodium salt, (6R,7S)-
- 5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[2-[[(2S)-2-amino-2-carboxyethyl]thio]acetyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, sodium salt, (6R,7S)- (1:1)
- 7beta-[2-[2(S)-Amino-2-carboxyethylthio]acetamido]-7alpha-methoxy-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid sodium salt
- Alteporina
- Cefminox sodium
- Cefminox sodium salt
- Meicelin
- Mt-141
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid,7-[[[(2-amino-2-carboxyethyl)thio]acetyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, sodium salt, [6R-[6a,7a,7(S*)]]-
CAS:Formula:C16H21N7NaO7S3Purity:97%Color and Shape:SolidMolecular weight:542.5654Cefminox Sodium Salt
CAS:Formula:C16H20N7O7S3·NaColor and Shape:Off-White SolidMolecular weight:518.57 22.99Cefminox Sodium Heptahydrate
CAS:<p>Applications Cefminox is a semisynthetic broad spectrum cephamycin antibiotic. Antibacterial.<br>References Inouye, S., et al.: Antimicrob. Agents Chemother., 26, 722 (1984), Watanabe, T., et al.: Drugs Exp. Clin. Res., 10, 293 (1984), Tsuruoka, T., et al.: Eur. J. Biochem., 151, 209 (1985),<br></p>Formula:C16H34N7NaO14S3Color and Shape:NeatMolecular weight:667.66Cefminox Sodium
CAS:<p>Cefminox Sodium is a beta-lactam antibiotic, which is synthesized through chemical modification of naturally occurring compounds. This product is classified as a second-generation cephalosporin, derived from cephalosporin C obtained from the fungus Acremonium. It exerts its mode of action by inhibiting bacterial cell wall synthesis. This occurs through the binding to penicillin-binding proteins, ultimately disrupting the cross-linking of peptidoglycan chains which are essential for bacterial cell wall integrity.</p>Formula:C16H20N7O7S3·NaPurity:Min. 95%Molecular weight:541.56 g/mol




