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| Product | Description | |
|---|---|---|
| Ceftaroline fosamil | Ceftaroline fosamil (TAK-599), a cephalosporin derivative, is an N-phosphono proagent of anti-methicillin-resistant Staphylococcus aureus (MRSA) T-91825. Ceftaroline fosamil can be used for the research of MRSA infection [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TAK-599; PPI0903. CAS No. 400827-46-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14737. |  |
| Ceftaroline Fosamil | Ceftaroline fosamil is a cephalosporin antibacterial indicated for the treatment of adults with acute bacterial skin and soft tissue infections, including those caused by methicillin-resistant Staphylococcus aureus (MRSA). Synonyms: PPI 0903; PPI0903; PPI-0903; T-91825; T 91825; T91825; Teflaro; Zinforo; (6R,7R)-7-[[(2Z)-2-ethoxyimino-2-[5-(phosphonoamino)-1,2,4-thiadiazol-3-yl]acetyl]amino]-3-[[4-(1-methylpyridin-1-ium-4-yl)-1,3-thiazol-2-yl]sulfanyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate. Grades: ≥98%. CAS No. 229016-73-3. Molecular formula: C22H21N8O8PS4. Mole weight: 684.67. |  |
| Ceftaroline fosamil acetate | Ceftaroline fosamil, also known as TAK 599, is a cephalosporin antibiotic with activity against methicillin-resistant Staphylococcus aureus (MRSA) and Gram-positive bacteria. Ceftaroline fosamil is a prodrug of the cephalosporin antibiotic T-91825. Uses: Beta lactam antibiotics. Synonyms: Pyridinium, 4-[2-[[(6R,7R)-2-carboxy-7-[[(2Z)-2-(ethoxyimino)-2-[5-(phosphonoamino)-1,2,4-thiadiazol-3-yl]acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]thio]-4-thiazolyl]-1-methyl-, acetate (1:1); Pyridinium, 4-[2-[[(6R,7R)-2-carboxy-7-[[(2Z)-(ethoxyimino)[5-(phosphonoamino)-1,2,4-thiadiazol-3-yl]acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]thio]-4-thiazolyl]-1-methyl-, acetate; Ceftaroline; Ceftaroline fosamil; PPI 0903; TAK 599; Teflaro; Zinforo. Grades: ≥95%. CAS No. 400827-46-5. Molecular formula: C24H25N8O10PS4. Mole weight: 744.72. | |
| Ceftaroline fosamil (inner) | Ceftaroline fosamil (inner) (TAK-599 free acid), a cephalosporin derivative, is an N-phosphono proagent of anti-methicillin-resistant Staphylococcus aureus (MRSA) T-91825. Ceftaroline fosamil (inner) can be used for the research of MRSA infection [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TAK-599 free acid; PPI0903 free acid. CAS No. 229016-73-3. Pack Sizes: 1 mg. Product ID: HY-14738. | |
| Ceftaroline Impurity4 | Ceftaroline Impurity4. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (7R)-7-((Z)-2-(5-acetamido-1,2,4-thiadiazol-3-yl)-2-(ethoxyimino)acetamido)-3-((4-(1-methylpyridin-1-ium-4-yl)thiazol-2-yl)thio)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate. CAS No. 1240196-56-8. Molecular formula: C24H22N8O6S4. Mole weight: 646.74. Catalog: APB1240196568. |  |
| Avibactam | Avibactam is a novel investigational non-beta-lactam beta-lactamase inhibitor that is being developed for possible use in combination with ceftaroline in the U.S. Avibactam does not have any intrinsic antibacterial activity in its own right, but appears to be capable of inhibiting beta-lactamase enzymes that belong to molecular classes A and C.Avibactam is useful for Antibiotics. Uses: Beta-lactamase inhibitors. Synonyms: Sulfuric acid mono[(1R,2S,5R)-2-(aminocarbonyl)-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl] ester; Avibactam free acid; [(2S,5R)-2-carbamoyl-7-oxo-1,6-diazabicyclo[3.2.1]octan-6-yl] hydrogen sulfate. Grades: >98%. CAS No. 1192500-31-4. Molecular formula: C7H11N3O6S. Mole weight: 265.24. | |
| Avibactam Sodium Salt | Avibactam Sodium Salt, a novel non-?-lactam ?-lactamase inhibitor, binds covalently to Ambler class A ?-lactamases, including KPCs, Ambler class C and some class D b-lactamases. In combination with ceftazidime, Avibactam is a new drug application for avibactam , and was approved by the FDA on February 25, 2015, to treat complicated urinary tract and complicated intra-abdominal Infections caused by antibiotic resistant-pathogens. Avibactam has limited intrinsic antimicrobial activity but restores the in vitro activity of b-lactams including ceftazidime, ceftaroline, the active metabolite of ceftaroline fosamil, and aztreonam against ESBL-producing pathogens. Synonyms: sodium (2S,5R)-2-carbamoyl-7-oxo-1,6-diazabicyclo[321]octan-6-yl sulfate; NXL104; NXL-104; NXL 104; Avibactam; Avibactam sodium. CAS No. 1192491-61-4. Molecular formula: C7H10N3NaO6S. Mole weight: 287.23. | |
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