Cefoselis

CAS: 122841-10-5

Rif. 3D-FC44042

Informazioni sul prodotto

• Nome: Cefoselis
• Sinonimi: (-)-5-Amino-2-[[(6R,7R)-7-[2-(2-amino-4-thiazolyl)glyoxylamido]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-1-(2-hydroxyethyl)pyrazolium hydroxide, inner salt, 7²-(Z)-(O-methyloxime), (6R,7R)-3-{[5-amino-1-(2-hydroxyethyl)-1H-pyrazol-2-ium-2-yl]methyl}-7-{[(2E)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetyl]amino}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate, (6R,7R)-7-[[(2Z)-2-(2-Amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-3-[[2,3-dihydro-2-(2-hydroxyethyl)-3-imino-1H-pyrazol-1-yl]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-3-[[2,3-dihydro-2-(2-hydroxyethyl)-3-imino-1H-pyrazol-1-yl]methyl]-8-oxo-, [6R-[6α,7β(Z)]]-, 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-3-[[2,3-dihydro-2-(2-hydroxyethyl)-3-imino-1H-pyrazol-1-yl]methyl]-8-oxo-, (6R,7R)-, 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-3-[[2,3-dihydro-2-(2-hydroxyethyl)-3-imino-1H-pyrazol-1-yl]methyl]-8-oxo-, (6R,7R)-, 5-amino-2-{[(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}-1-(2-hydroxyethyl)-1H-pyrazol-2-ium, Cefoselis main-ring, Wincef

Descrizione

Cefoselis is a cephalosporin antibiotic that has been shown to be effective against bacterial infections. It is the only oral cephalosporin that has been approved for the treatment of community-acquired pneumonia. Cefoselis is administered in low doses in order to minimize the risk of developing bacterial resistance. Cefoselis binds to bacterial 16S ribosomal RNA and inhibits protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division. The reaction mechanism of cefoselis involves the formation of an acylsulfate intermediate, which reacts with nucleophilic sulfur atoms in cysteine residues on the bacterial cell wall. This leads to lysis of the bacterial cell membrane and cell death.
Cefoselis sulfate is a salt form of cefoselis that is stable at high temperatures and can be dissolved in water or human serum without precipitation. It also has a chemical stability that enables it to

• Marchio: Biosynth

Proprietà chimiche

• Purezza: Min. 95%