Sulbenicillin disodium

• CAT Number: I016745
• CAS Number: 28002-18-8
• Molecular Formula: C₁₆H₁₆N₂Na₂O₇S₂
• Molecular Weight: 458.42
• Purity: ≥95%
• Target: Bacterial
• IUPAC Name: disodium;(2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenyl-2-sulfonatoacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
• InChI: InChI=1S/C16H18N2O7S2.2Na/c1-16(2)11(15(21)22)18-13(20)9(14(18)26-16)17-12(19)10(27(23,24)25)8-6-4-3-5-7-8;;/h3-7,9-11,14H,1-2H3,(H,17,19)(H,21,22)(H,23,24,25);;/q;2*+1/p-2/t9-,10?,11+,14-;;/m1../s1
• InChIKey: FWRNIJIOFYDBES-HCIBPFAFSA-L
• SMILES: CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)NC(=O)C(C3=CC=CC=C3)S(=O)(=O)[O-])C(=O)[O-])C.[Na+].[Na+]

Sulbenicillin Disodium（Cat No.:I016745）is a broad-spectrum, beta-lactam antibiotic in the penicillin family, effective against both Gram-positive and Gram-negative bacteria. Its unique chemical structure, incorporating a sulfinyl group, enhances its efficacy against Pseudomonas aeruginosa and other challenging pathogens. Sulbenicillin is often used in serious infections, such as respiratory and urinary tract infections, and is typically administered intravenously, allowing for rapid distribution. Known for its synergistic potential with other antibiotics, it is particularly valuable in combination therapies for resistant infections, making it a versatile option in clinical and hospital environments.

Reference

[1]. Eftimiadi C, et al. Antibacterial activity in vitro of sulbenicillin against mucoid and non-mucoid strains of Pseudomonas aeruginosa. Drugs Exp Clin Res. 1985;11(4):241-5.