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Sulbactam (CP45899) sodium is a competitive, irreversible beta-lactamase inhibitor. Sulbactam sodium shows antimicrobial activity against multidrug-resistant (MDR) acinetobacter calcoaceticus -- Acinetobacter baumannii (Acb) complex [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CP45899 sodium. CAS No. 69388-84-7. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B0334A.
Sulbactam sodium salt
1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C8H10NNaO5S. CAS No. 69388-84-7. Prepack ID 90004872-1g. Molecular Weight 255.22. See USA prepack pricing.
Sulbactam sodium salt
5g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C8H10NNaO5S. CAS No. 69388-84-7. Prepack ID 90004872-5g. Molecular Weight 255.22. See USA prepack pricing.
Sulbactam Sodium Salt
A semi-synthetic β-lactamase inhibitor. It is used in combination with β-lactam antibiotics as antibacterial. Group: Biochemicals. Alternative Names: (2S, 5R)-3, 3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid 4,4-Dioxide Sodium Salt; CP 45899-2; Penicillanic Acid 1,1-Dioxide Sodium Salt; Sodium 1,1-Dioxypenicillanate; Sodium Penicillanate 1,1-Dioxide; Sodium Sulbactam; Sulbactam Sodium; Sulbactam Sodium Salt; Unasyn IM. Grades: Highly Purified. CAS No. 69388-84-7. Pack Sizes: 100mg, 1g, 5g, 10g. US Biological Life Sciences.
Worldwide
Ampicillin Sodium Mixture With Sulbactam Sodium
Ampicillin Sodium Mixture with Sulbactam Sodium is a β-lactamase inhibitor used to enhance the effectiveness of β-lactam antibiotics. Synonyms: Unacyne; Unacid; Unasyn-S; Yucion-S. CAS No. 117060-71-6. Molecular formula: C25H29N3Na2O9S2. Mole weight: 625.62.
Sulbactam (sodium) (Standard)
Sulbactam (sodium) (Standard) is the analytical standard of Sulbactam (sodium). This product is intended for research and analytical applications. Sulbactam (CP45899) sodium is a competitive, irreversible beta-lactamase inhibitor. Sulbactam sodium shows antimicrobial activity against multidrug-resistant (MDR) acinetobacter calcoaceticus--Acinetobacter baumannii (Acb) complex [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 69388-84-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0334AR.
Cefoperazone, Sodium Salt (CP-52640-2, T-1551, Bioperazone, Cefazone, Cefobid)
Cefoperazone is a third generation cephalosporin antibiotic. Cefoperazone exerts its bactericidal effect by inhibiting the bacterial cell wall synthesis, and sulbactam acts as a beta-lactamase inhibitor, to increase the antibacterial activity of cefoperazone against beta-lactamase producing organisms. It is one of few cephalosporin antibiotics effective in treating Pseudomonas bacterial infections which are otherwise resistant to these antibiotics. Group: Biochemicals. Alternative Names: CP-52640-2, T-1551, Bioperazone, Cefazone, Cefobid; (6R, 7R) -7-[[ (2R) -2-[[ (4-Ethyl-2, 3-dioxo-1-piperazinyl) carbonyl]amino]-2- (4-hydroxyphenyl) acetyl]amino]-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. Grades: Highly Purified. CAS No. 62893-20-3. Pack Sizes: 5g, 10g, 25g. US Biological Life Sciences.
Worldwide
Penicillanic Acid Sodium Salt
An impurity of Sulbactam. Sulbactam is an irreversible inhibitor of β-lactamase; it binds to the enzyme and does not allow it to degrade the antibiotic. Synonyms: Sulbactam Impurity 2 Sodium Salt. CAS No. 4027-62-7. Molecular formula: C8H10NO3S.Na. Mole weight: 223.23.
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