CAS 209467-52-7: Ceftobiprole
Formula:C20H22N8O6S2
InChI:InChI=1S/C20H22N8O6S2/c21-20-24-14(26-36-20)11(25-34)15(29)23-12-17(31)28-13(19(32)33)9(7-35-18(12)28)5-8-2-4-27(16(8)30)10-1-3-22-6-10/h5,10,12,18,22,34H,1-4,6-7H2,(H,23,29)(H,32,33)(H2,21,24,26)/b8-5+,25-11-/t10-,12-,18-/m1/s1
InChI key:InChIKey=VOAZJEPQLGBXGO-SDAWRPRTSA-N
SMILES:C(O)(=O)C=1N2[C@@]([C@H](NC(/C(=N\O)/C3=NSC(N)=N3)=O)C2=O)(SCC1/C=C\4/C(=O)N(CC4)[C@@H]5CCNC5)[H]
Synonyms:- (6R,7R)-7-((2Z)-2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-(hydroxyimino)-acetamido)-8-oxo-3-((E)((3'R)-2-oxo-(1,3'-bipyrrolidin)-3-ylidene)-methyl)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid antibiotic
- (6R,7R)-7-[[(2Z)-2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-(hydroxyimino)acetyl]amino]-8-oxo-3-[(E)-[(3′R)-2-oxo[1,3′-bipyrrolidin]-3-ylidene]methyl]-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-(((2Z)-(5-amino-1,2,4-thiadiazol-3-yl)(hydroxyimino)acetyl)amino)-8-oxo-3-((E)-((3'R)-2-oxo(1,3'-bipyrrolidin)-3-ylidene)methyl)-, (6R,7R)-
- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-(5-amino-1,2,4-thiadiazol-3-yl)(hydroxyimino)acetyl]amino]-8-oxo-3-[(E)-[(3′R)-2-oxo[1,3′-bipyrrolidin]-3-ylidene]methyl]-, (6R,7R)-
- 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(hydroxyimino)acetyl]amino]-8-oxo-3-[(E)-[(3′R)-2-oxo[1,3′-bipyrrolidin]-3-ylidene]methyl]-, (6R,7R)-
- Bal 9141
- Bal 9141-000
- Ro 63-9141
- Unii-5T97333Yzk
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Found 5 products.
Ceftobiprole
CAS:Ceftobiprole is a new drug that belongs to the class of beta-lactam antibiotics. It is active against bacteria resistant to penicillin, such as methicillin-resistant Staphylococcus aureus (MRSA), and has shown activity against other bacteria, including multidrug-resistant Enterobacteriaceae. Ceftobiprole has been shown to be effective in treating infections of the skin and soft tissue due to bacterial strains. The mechanism of action for ceftobiprole involves inhibition of cell wall synthesis by binding to penicillin-binding proteins, which prevents cross-linkage of peptidoglycan chains. Ceftobiprole also inhibits protein synthesis by binding to ribosomes and preventing the formation of the initiation complex.Formula:C20H22N8O6S2Purity:Min. 95%Color and Shape:PowderMolecular weight:534.57 g/molCeftobiprole
CAS:Ceftobiprole (Ro 63-9141) is a β-lactam antibacterial agent that exhibits potent bactericidal activity by binding to PBPs.Cost-effective and quality-assured.Formula:C20H22N8O6S2Purity:95%Color and Shape:SolidMolecular weight:534.57
