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Sulbactam (CP45899) is a competitive, irreversible beta-lactamase inhibitor. Sulbactam shows antimicrobial activity against multidrug-resistant (MDR) acinetobacter calcoaceticus -- Acinetobacter baumannii (Acb) complex [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CP45899. CAS No. 68373-14-8. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B0334.
Sulbactam
Sulbactam (CP45899) is a competitive, irreversible beta-lactamase inhibitor. Sulbactam shows antimicrobial activity against multidrug-resistant (MDR) acinetobacter calcoaceticus--Acinetobacter baumannii (Acb) complex. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. CAS No. 68373-14-8. Molecular formula: C8H11NO5S. Purity: 0.9971. Product ID: ACM68373148. Alfa Chemistry ISO 9001:2015 Certified.
Sulbactam
Sulbactam. Group: Biochemicals. Grades: Highly Purified. CAS No. 68373-14-8. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences.
Worldwide
Sulbactam
Sulbactam is a β-lactamase inhibitor. This drug is given in combination with β-lactam antibiotics to inhibit β-lactamase, an enzyme produced by bacteria that destroys the antibiotics. Synonyms: RO-1-9213; RO 1-9213; RO1-9213. Grades: >98%. CAS No. 68373-14-8. Molecular formula: C8H11NO5S. Mole weight: 233.24.
Sulbactam
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitespharma & vet compounds & metaboliteseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: CP 45899, Penicillanic acid sulfone, (2S,5R)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-Dioxide, Penicillanic acid dioxide,Sulbactam, (2S-cis)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-Dioxide, Betamaze, Penicillanic acid S,S-dioxide, Sulbactam, Penicillanic acid 1,1-dioxide.
Sulbactam acid
1g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C8H11NO5S. CAS No. 68373-14-8. Prepack ID 69388315-1g. Molecular Weight 233.24. See USA prepack pricing.
Sulbactam Impurity 11
Sulbactam Impurity 11. Uses: For analytical and research use. Group: Impurity standards. CAS No. 15058-64-7. Molecular formula: C8H11NO4S. Mole weight: 217.24. Catalog: APB15058647.
Sulbactam Impurity 19
Sulbactam Impurity 19. Uses: For analytical and research use. Group: Impurity standards. CAS No. 139595-42-9. Molecular formula: C8H9Br2NO3S. Mole weight: 359.03. Catalog: APB139595429.
Sulbactam Impurity A
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 Related Compound A; Valine, 3-sulfino-, D- (8CI); 3-Sulfino-D-valine. Grades: > 95%. CAS No. 23315-18-6. Molecular formula: C5H11NO4S. Mole weight: 181.21.
Sulbactam Impurity C
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: (2S,5R,6R)-6-Bromo-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid 4,4-Dioxide; Sulbactam EP Impurity C; [2S-(2α,5α,6β)]-6-Bromo-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid 4,4-Dioxide; 6β-Bromopenicillanic Acid 1,1-Dioxide; Brobactam S,S-Dioxide. Grades: > 95%. CAS No. 75527-87-6. Molecular formula: C8H10BrNO5S. Mole weight: 312.14.
Sulbactam Impurity D
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. Uses: Beta-lactamase inhibitors. Synonyms: (2S,5R,6R)-6-Bromo-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid; [2S-(2α,5α,6β)]-6-Bromo-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid; 6β-Bromopenicillanic Acid; BRL 25214; Brobactam. Grades: > 95%. CAS No. 26631-90-3. Molecular formula: C8H10BrNO3S. Mole weight: 280.14.
Sulbactam Impurity E
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: (2S,5R)-6,6-dibromo-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid 4,4-Dioxide; Sulbactam EP Impurity E; (2S-cis)-6,6-Dibromo-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid 4,4-Dioxide; 6,6-Dibromopenicillanic Acid 1,1-Dioxide; 6,6-Dibromopenicillanic Acid S,S-Dioxide. Grades: > 95%. CAS No. 76646-91-8. Molecular formula: C8H9Br2NO5S. Mole weight: 391.03.
Sulbactam Impurity F
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: (2S,5R)-6,6-Dibromo-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid; Sulbactam EP Impurity F; (2S-cis)-6,6-dibromo-3,3-dimethyl-7-oxo-4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid; 6,6-Dibromopenicillanic Acid. Grades: > 95%. CAS No. 24158-88-1. Molecular formula: C8H9Br2NO3S. Mole weight: 359.04.
Sulbactam Impurity G
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: (2E)-3-[[(1S)-1-carboxy-2-methyl-2-sulphinopropyl]amino]prop-2-enoic acid. Grades: > 95%. Molecular formula: C8H13NO6S. Mole weight: 251.26.
Sulbactam pivoxil
Sulbactam pivoxil is a proagent of sulbactam. Sulbactam is a β-lactamase inhibitor which poorly adsorbed from gastrointestinal tract. Sulbactam pivoxil has a better absorption than the parent agent and provides high serum levels after oral administration [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CP 47904. CAS No. 69388-79-0. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-108288.
Sulbactam Pivoxil
Sulbactam Pivoxil is a prodrug 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: (2S,5R)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid (2,2-Dimethyl-1-oxopropoxy)methyl Ester 4,4-Dioxide; (Pivaloyloxy)methyl Penicillanate S,S-Dioxide; CP 47904; (2S-cis)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid (2,2-dimethyl-1-oxopropoxy)methyl Ester 4,4-Dioxide. Grades: > 95%. CAS No. 69388-79-0. Molecular formula: C14H21NO7S. Mole weight: 347.38.
Sulbactam Pivoxil
Sulbactam Pivoxil is a prodrug of the semi-synthetic β-lactamase inhibitor Sulbactam. Group: Biochemicals. Alternative Names: (2S, 5R)-3, 3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid (2,2-Dimethyl-1-oxopropoxy)methyl Ester 4,4-Dioxide; (Pivaloyloxy)methyl Penicillanate S,S-Dioxide; CP 47904; (2S-cis)-3, 3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid (2,2-dimethyl-1-oxopropoxy)methyl Ester 4,4-Dioxide. Grades: Highly Purified. CAS No. 69388-79-0. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
Sulbactam Related Compound (6-alfa-Bromopenicillanic acid)
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: (2S,5R,6S)-6-Bromo-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid. Grades: > 95%. CAS No. 24138-28-1. Molecular formula: C8H10BrNO3S. Mole weight: 280.14.
Sulbactam Related Compound A
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Sulbactam Related Compound D
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Sulbactam Related Compound E
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Sulbactam Related Compound F
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Sulbactam sodium
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
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.
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.
3-Sulfino-DL-valine
3-Sulfino-DL-valine. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: Sulbactam EP Impurity A,3-Sulfinovaline. CAS No. 98462-04-5. Pack Sizes: 10MG. IUPAC Name: 2-amino-3-methyl-3-sulfinobutanoic acid. Molecular formula: C5H11NO4S. Mole weight: 181.21. Catalog: APS98462045. SMILES: CC(C)(C(N)C(=O)O)S(=O)O. Format: Neat. Shipping: Room Temperature.
6-Aminopenicillanic acid
It is produced by the strain of Peniclllun chrysogenum and Pleurotus ostreatus. 6-APA is the main raw material for semisynthesis of penicillin, and the key intermediates for semisynthesis of cephalosporin (7-ACA) and 7-amino-deacetylated ceosenoic acid (7-ADCA) can be generated by chemical or enzymatic ring expansion. Synonyms: 6-APA; Sulbactam Impurity B; Amoxicillin Impurity A; Amoxicillin Related Compound A; Amoxicillin EP Impurity A; Ampicillin EP Impurity A; Penicin; Penin; Aminopenicillanic acid; 6-Aps; Phenacyl 6-aminopenicillinate. Grades: > 95%. CAS No. 551-16-6. Molecular formula: C8H12N2O3S. Mole weight: 216.26.
Brobactam
Brobactam is a potent semi-synthetic β-lactamase inhibitor as well as an impurity of Sulbactam. Group: Biochemicals. Alternative Names: (2S, 5R, 6R)-6-Bromo-3, 3-dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid; Sulbactam EP Impurity D; [2S-(2α,5α,6 β )]-6-Bromo-3, 3-dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid; 6 β-Bromopenicillanic Acid; BRL 25214. Grades: Highly Purified. CAS No. 26631-90-3. Pack Sizes: 25mg. US Biological Life Sciences.
Worldwide
Brobactam S,S-Dioxide
Brobactam S,S-Dioxide is an impurity of the semi-synthetic β-lactamase inhibitor Sulbactam. Group: Biochemicals. Alternative Names: (2S, 5R, 6R)-6-Bromo-3, 3-dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid 4,4-Dioxide; Sulbactam EP Impurity C; [2S-(2α,5α,6 β )]-6-Bromo-3, 3-dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid 4,4-Dioxide; 6 β-Bromopenicillanic Acid 1,1-Dioxide. Grades: Highly Purified. CAS No. 75527-87-6. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
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.
Sultamicillin tosylate
Sultamicillin is a compound composed of sulbactam and ampicillin linked as a double ester. Sulbactam is a semisynthetic beta-lactamase inhibitor, which exhibits improved antibacterial activity in combination with ampicillin. Synonyms: Bacimex; Unacim orale. CAS No. 83105-70-8. Molecular formula: C32H38N4O12S3. Mole weight: 766.86.
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