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| Product | Description | |
|---|---|---|
| Cefepime hydrochloride | Pharmaceutical Secondary Standard; Certified Reference Material. Group: Pharmacopeia & metrological institutes standards. |  |
| Cefepime Hydrochloride | It is an anti-bacterial drug and a non-competitive inhibitor. It is a semi-synthetic, fourth generation cephalosporin antibiotic. Uses: Anti-bacterial agents. Synonyms: Cefepime dihydrochloride; Cepimex; Axepim; Cepimax; Cefepime HCl; BMY 28142 Hydrochloride; Maxcef; Maxipime; Novapime; [6R-[6α,7β(Z)]]-1-[[7-[[(2-Amino-4-thiazolyl)(methoxyimino)acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-1-methyl-pyrrolidinium hydrochloride; Pyrrolidinium, 1-[[(6R,7R)-7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-1-methyl-, chloride, hydrochloride (1:1:1); Pyrrolidinium, 1-[[(6R,7R)-7-[[(2Z)-(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-1-methyl-, chloride, monohydrochloride; Pyrrolidinium, 1-[[7-[[(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-1-methyl-, chloride, monohydrochloride, [6R-[6α,7β(Z)]]-. Grade: 95%. CAS No. 107648-80-6. Molecular formula: C19H26Cl2N6O5S2. Mole weight: 553.48. |  |
| Cefepime hydrochloride hydrate | Cefepime is an extended-spectrum parenteral cephalosporin antibiotic active in vitro against a broad spectrum of gram-positive and gram-negative aerobic bacteria. Cefepime dosing was 1-4 g/day (0.5-2.0 g twice daily) for adults; ceftazidime dosing was 1-6 g/day (0.5 g every 12 hours to 2.0 g every 8 hours). A limited number of cefepime-treated patients received 2 g every 8 hours. The median length of dosing for both cefepime and ceftazidime was 7 days. Cefepime has a decreased propensity to induce beta-lactamases compared with other beta-lactam antibiotics. Cefepime has a pharmacokinetic disposition similar to that of other renally eliminated cephalosporins, with a half-life of approximately 2 hours. Cefepime has demonstrated clinical efficacy against a variety of infections, including urinary tract infections, pneumonia, and skin structure infections. Cefepime is generally well tolerated. Synonyms: Maxipime. Grade: >98%. CAS No. 123171-59-5. Molecular formula: C19H28Cl2N6O6S2. Mole weight: 571.50. | |
| Cefepime Hydrochloride with Arginine | A fourth-generation cephalosporin antibacterial agent that is used in the treatment of infections, including those of the abdomen, urinary tract, respiratory tract, and skin. It is effective against PSEUDOMONAS AERUGINOSA and may also be used in the empiric treatment of FEBRILE NEUTROPENIA. Alternative Names: Axepim. Cepimex. Maxipime. CAS No. 107648-80-6. Product ID: API107648806. Molecular formula: C19H26Cl2N6O5S2. Mole weight: 553.5. EINECS: 827-945-9. SMILES: C[N+]1(CCCC1)CC2=C(N3C(C(C3=O)NC(=O)C(=NOC)C4=CSC(=N4)N)SC2)C(=O)O.Cl.[Cl-]. Appearance: Solid. Standard: USP/ IP. Category: Antibiotic APIs. |  |
| Cefepime parent nucleus | Cefepime parent nucleus. Uses: For analytical and research use. Group: Impurity standards. CAS No. 103121-85-3. Molecular formula: C13H20ClN3O3S. Mole weight: 333.38. Catalog: APB103121853. | |
| Cefepime Related Compound A | An impurity of Cefepime. Cefepime is a fourth-generation cephalosporin antibiotic known for its broad-spectrum activity against a wide range of Gram-positive and Gram-negative bacteria. It is particularly effective against many organisms that are resistant to other antibiotics, including some beta-lactamase-producing strains. Cefepime is often used to treat severe infections such as pneumonia, urinary tract infections, and bloodstream infections. Synonyms: 1-({(6R,7R)-7-[(E)-2-(2-Aminothiazol-4-yl)-2-(methoxyimino)acetamido]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl}methyl)-1-methylpyrrolidinium chloride; USP Cefepime Related Compound A; Cefepime USP Related Compound A; E-Cefepime chloride salt; (E)-Cefepime chloride; Pyrrolidinium, 1-[[(6R,7R)-7-[[(2E)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-1-methyl-, chloride (1:1); Pyrrolidinium, 1-[[7-[[(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-1-methyl-, chloride, [6R-[6α,7β(E)]]-; 1-(((6R,7R)-7-((E)-2-(2-Aminothiazol-4-yl)-2-(methoxyimino)acetamido)-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl)methyl)-1-methylpyrrolidin-1-ium chloride. Grade: ≥95%. Molecular formula: C19H25ClN6O5S2. Mole weight: 517.02. | |
| Cefepime Related Compound B | An impurity of Cefepime. Cefepime is a fourth-generation cephalosporin antibiotic known for its broad-spectrum activity against a wide range of Gram-positive and Gram-negative bacteria. It is particularly effective against many organisms that are resistant to other antibiotics, including some beta-lactamase-producing strains. Cefepime is often used to treat severe infections such as pneumonia, urinary tract infections, and bloodstream infections. Synonyms: 1-({(6R,7R)-7-[(Z)-2-{2-[(Z)-2-(2-Aminothiazol-4-yl)-2-(methoxyimino)acetamido]thiazol-4-yl}-2-(methoxyimino)acetamido]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl}methyl)-1-methylpyrrolidinium chloride; USP Cefepime Related Compound B; Cefepime USP Related Compound B; Cefepime dioxime chloride salt. Grade: ≥95%. Molecular formula: C25H30ClN9O7S3. Mole weight: 700.20. | |
| Cefepime Related Compound D | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Cefepime Related Compound E | An impurity of Cefepime. Cefepime is a fourth-generation cephalosporin antibiotic known for its broad-spectrum activity against a wide range of Gram-positive and Gram-negative bacteria. It is particularly effective against many organisms that are resistant to other antibiotics, including some beta-lactamase-producing strains. Cefepime is often used to treat severe infections such as pneumonia, urinary tract infections, and bloodstream infections. Synonyms: 1-{[(6R,7R)-7-Amino-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl}-1-methylpyrrolidin-1-ium chloride; 7-Amino-3-[(1-methylpyrrolidin-1-ium-1-yl)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate hydrochloride; Pyrrolidinium, 1-[[(6R,7R)-7-amino-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-1-methyl-, chloride; Pyrrolidinium, 1-[(7-amino-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl)methyl]-1-methyl-, hydroxide, inner salt, monohydrochloride, (6R-trans)-; USP Cefepime Related Compound E; Cefepime USP Related Compound E; Cefepime amine derivative; (6R,7R)-7-Amino-3-[(1-methylpyrrolidinium-1-yl)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate chloride. Grade: ≥95%. CAS No. 103121-85-3. Molecular formula: C13H20ClN3O3S. Mole weight: 333.83. | |
| Cefepime Related Compound E | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Cefepime Related Compound F | An impurity of Cefepime. Cefepime is a fourth-generation cephalosporin antibiotic known for its broad-spectrum activity against a wide range of Gram-positive and Gram-negative bacteria. It is particularly effective against many organisms that are resistant to other antibiotics, including some beta-lactamase-producing strains. Cefepime is often used to treat severe infections such as pneumonia, urinary tract infections, and bloodstream infections. Synonyms: 1-{[(6R,7R)-7-[(Z)-2-(2-Aminothiazol-4-yl)-2-(methoxyimino)acetamido]-2-{(6R,7R)-2-carboxy-3-[(1-methylpyrrolidinium-1-yl)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-7-ylcarbamoyl}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl}-1-methylpyrrolidinium chloride; Cefepime dimer; USP Cefepime Related Compound F; Cefepime USP Related Compound F; Cefepime Related Compound F. Grade: ≥95%. Molecular formula: C32H43Cl2N9O7S3. Mole weight: 832.83. | |
| Cefetamet | Cefetamet is a third-generation cephalosporin antibiotic and the active agent of Cefeamet pivoxil after hydrolysis. Uses: Anti-bacterial agents. Synonyms: Cepime O; Deacetoxycefotaxime; FR 13300; LY 97964; Ro 15-8074; Ro 15-8074/005; Ultipime O; Altamet; Antibiotic Ro 15-8074; (6R,7R)-7-[[(2Z)-(2-Amino-4-thiazolyl)(methoxyimino)acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Ac. Grade: > 95%. CAS No. 65052-63-3. Molecular formula: C14H15N5O5S2. Mole weight: 397.43. | |
| Cefetamet | Cefetamet is a cephalosporin antibiotic. Cefetamet has the potential for the research of both upper and lower community-acquired respiratory tract infections [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 15-8074; Deacetoxycefotaxime. CAS No. 65052-63-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-A0111. |  |
| Cefetamet | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Cefetamet | Cefetamet. Group: Biochemicals. Alternative Names: Cepime O; Deacetoxycefotaxime; FR 13300; LY 97964; Ro 15-8074; Ro 15-8074/005; Ultipime O; Altamet; Antibiotic Ro 15-8074; (6R, 7R) -7-[[ (2Z) - (2-Amino-4-thiazolyl) (methoxyimino) acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid; [6R-[6α,7 β (Z) ]]-7-[[ (2-amino-4-thiazolyl) (methoxyimino) acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid; (6R, 7R) -7-[[ (2Z) -2- (2-Amino-4-thiazolyl) -2- (methoxyimino) acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid. Grades: Highly Purified. CAS No. 65052-63-3. Pack Sizes: 500mg. Molecular Formula: C14H15N5O5S2, Molecular Weight: 397.43. US Biological Life Sciences. |  Worldwide |
| Cefetamet-d3 | Labelled Cefetamet is a third-generation cephalosporin antibiotic and the active agent of Cefeamet pivoxil after hydrolysis. Group: Biochemicals. Alternative Names: Cepime O-d3; Deacetoxycefotaxime-d3; FR 13300-d3; LY 97964-d3; Ro 15-8074-d3; Ro 15-8074/005-d3; Ultipime O-d3; Altamet-d3; Antibiotic Ro 15-8074-d3; (6R, 7R) -7-[[ (2Z) - (2-Amino-4-thiazolyl) (methoxyimino) acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid-d3; [6R-[6α,7 β (Z) ]]-7-[[ (2-amino-4-thiazolyl) (methoxyimino) acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid-d3; (6R, 7R) -7-[[ (2Z) -2- (2-Amino-4-thiazolyl) -2- (methoxyimino) acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid-d3. Grades: Highly Purified. CAS No. 65243-33-6 (unlabeled). Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Cefetamet pivoxil | It is produced by the strain of Semisynthetic third generation oral cephalosporin. Cefetamet Pivoxil, a presomatic drug, is a t-pentanoxy methyl ester of Cefetamet. Uses: Anti-bacterial agents. Synonyms: Cefetamet pivoxyl; Globocef; Cefetamet pivaloyloxymethyl ester; 7-(2-(2-Aminothiazol-4-yl)-2-(methoxyimino)acetamido)-3-desacetoxyceph-3-em-4-carboxylic acid pivaloyloxymethyl ester; Cefetamet Pivoxil; Cefetamet (Pivaloyloxy)methyl Ester; Cefyl. Grade: > 95%. CAS No. 65243-33-6. Molecular formula: C20H25N5O7S2. Mole weight: 511.57. | |
| Cefetamet Pivoxil | Third generation cephalosporin antibiotics. Antibacterial. Group: Biochemicals. Alternative Names: (6R, 7R) -7-[[ (2Z) -2- (2-Amino-4-thiazolyl) -2- (methoxyimino) acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid (2,2-Dimethyl-1-oxopropoxy)methyl Ester; Cefetamet (Pivaloyloxy)methyl Ester; Ceftamet Pivoxil; Cefyl; Ro 15-8075. Grades: Highly Purified. CAS No. 65243-33-6. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| Cefetamet pivoxil hydrochloride | Cefetamet pivoxil hydrochloride. Group: Biochemicals. Grades: Highly Purified. CAS No. 111696-23-2. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| Cefetamet pivoxil hydrochloride | Cefetamet pivoxil hydrochloride is an oral third generation cephalosporin antibiotic. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 15-8075. CAS No. 111696-23-2. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-B1894A. | |
| Cefetamet Pivoxil Hydrochloride | The hydrochloride salt form of Cefetamet pivoxil, one of the third generation cephalosporin antibiotics, could be effective in the treatment for sorts of infections caused by sensitive bacteria. Uses: The hydrochloride salt form of cefetamet pivoxil could be effective in the treatment for sorts of infections caused by sensitive bacteria. Synonyms: Cefetamet pivoxil hydrochloride; CS-O-14591. Grade: 95%. CAS No. 111696-23-2. Molecular formula: C20H26ClN5O7S2. Mole weight: 548.03. | |
| Cefetamet pivoxyl | Cefetamet pivoxyl is a cephalosporin antibiotic. Cefetamet pivoxyl inhibits 355 enteropathogens Keime, Gram-negative bacteria (ausgenommen Pseudomonas aeruginosa ) and Legionella pneumophila [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 15-8075 free base. CAS No. 65243-33-6. Pack Sizes: 50 mg; 100 mg. Product ID: HY-B1894. | |
| Cefiderocol | Cefiderocol (S-649266) is a siderophore cephalosporin which has a potent activity against a broad range of aerobic Gram-negative bacterial species with MIC 50 s of 2 μg/mL or less. Uses: Scientific research. Group: Signaling pathways. Alternative Names: S-649266. CAS No. 1225208-94-5. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17628. | |
| Cefiderocol | This active molecular is a potent cephalosporin antibiotic with a catechol moiety on the 3-position side chain under the development of Shionogi. Cefiderocol exhibits potent activity against the non-fermenting Gram-negative bacteria in vitro including Acinetobacter baumannii, Pseudomonas aeruginosa and Stenotrophomonas maltophilia. Now Cefiderocol is in clinical Phase III for treatment of severe infections caused by Carbapenem-resistant Gram-negative pathogens. Uses: Gram-negative infections. Synonyms: S-649266; S 649266; S649266; Cefiderocol; (6R,7R)-7-[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-{[(2-carboxypropan-2-yl)oxy]imino}acetamido]-3-({1-[2-(2-chloro-3,4-dihydroxybenzamido)ethyl]pyrrolidin-1-ium-1-yl}methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate; S649266. Grade: 95%. CAS No. 1225208-94-5. Molecular formula: C30H34ClN7O10S2. Mole weight: 752.22. | |
| Cefixim | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H15N5O7S2. CAS No. 79350-37-1. Prepack ID 18918748-1g. Molecular Weight 453.45. See USA prepack pricing. |  |
| Cefixime | It is produced by the strain of Semisynthetic third generation oral cephalosporin. Cefixime is an antibiotic useful for the treatment of a number of bacterial infections. Uses: Cefixime is useful for the treatment of a number of bacterial infections, such as in acute otitis media, respiratory tract infections, and urinary tract infections and so on. it is effective against a variety of gram-negative bacteria, including e. coli, k. pneumoniae, and h. influenzae. Synonyms: FK-027; FR-17027; CL-284635; Cefixoral; Cefspan; Cephoral; Unixime; Cefixima; Cefiximum; 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 7-(((2-amino-4-thiazolyl)((carboxymethoxy)imino)acetyl)amino)-3-ethenyl-8-oxo-, trihydrate, (6R-(6alpha,7beta(Z)))-. Grade: > 95%. CAS No. 79350-37-1. Molecular formula: C16H15N5O7S2. Mole weight: 453.45. | |
| Cefixime | Orally active, third generation cephalosporin antibiotic. Group: Biochemicals. Alternative Names: (6R, 7R) -7-[[ (2Z) -2- (2-Amino-4-thiazolyl) -2-[ (carboxymethoxy) imino]acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid; FK-027; FR- 17027; CL-284635;Cefixoral; Cefspan; Cephoral; Unixime. Grades: Highly Purified. CAS No. 79350-37-1. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Cefixime | Cefixime is an antibiotic and a third generation cephalosporin antibiotic, useful for the treatment of a number of bacterial infections. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. CAS No. 79350-37-1. Purity: 0.9944. Product ID: ACM79350371. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Cefixime | Cefixime (FR-17027) is an orally active antibiotic and a third generation cephalosporin antibiotic, useful for the treatment of a number of bacterial infections [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: FR-17027; FK-027; CL-284635. CAS No. 79350-37-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-B1381. | |
| Cefixime | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Cefixime | Oral antibiotic. Alternative Names: Cephoral. Cefixima. Cefiximum. CAS No. 79350-37-1. Product ID: API79350371. Molecular formula: C16H15N5O7S2-3H2O. Mole weight: 507.5. EINECS: 616-684-4. SMILES: C=CC1=C(N2C(C(C2=O)NC(=O)C(=NOCC(=O)O)C3=CSC(=N3)N)SC1)C(=O)O. Appearance: White to almost yellowish crystalline powder. Standard: EP/USP. Category: Antibacterial APIs. | |
| Cefixime EP Impurity A (Technical Grade) (Mixture of Diastereomers) | Cefixime EP Impurity A (Technical Grade) (Mixture of Diastereomers). Uses: For analytical and research use. Group: Impurity standards. Alternative Names: Cefixime Imp. A (EP). CAS No. 1614255-90-1. Pack Sizes: 5MG. IUPAC Name: 2-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(carboxymethoxyimino)acetyl]amino]-2-[(2R)-5-methyl-7-oxo-1,2,4,5-tetrahydrofuro[3,4-d][1,3]thiazin-2-yl]acetic acid. Molecular formula: C16H17N5O8S2. Mole weight: 471.46. Catalog: APS1614255901. SMILES: CC1OC(=O)C2=C1CS[C@@H](N2)C(NC(=O)\C(=N/OCC(=O)O)\c3csc(N)n3)C(=O)O. Format: Neat. Shipping: Dry ice. | |
| Cefixime EP Impurity B | Cefixime EP Impurity B. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1335475-19-8. Molecular formula: C15H17N5O6S2. Mole weight: 427.45. Catalog: APB1335475198. | |
| Cefixime EP Impurity B | Cefixime EP Impurity B. Group: Biochemicals. Alternative Names: 2- [ [ (Z) - [1- (2-amino-4-thiazolyl) -2- [ [ [ (2R, 5RS) -5-methyl-7-oxo-1, 2, 5, 7-tetrahydro-4H-furo [3, 4-d] [1, 3] thiazin-2-yl] methyl] amino] -2-oxoethylidene] amino] oxy] acetic Acid. Grades: Highly Purified. CAS No. 1335475-19-8. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Cefixime EP Impurity C | Cefixime EP Impurity C. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (6R,7S)-7-((Z)-2-(2-aminothiazol-4-yl)-2-((carboxymethoxy)imino)acetamido)-8-oxo-3-vinyl-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. CAS No. 108691-83-4. Molecular formula: C16H15N5O7S2. Mole weight: 453.45. Catalog: APB108691834. | |
| Cefixime EP Impurity C (Cefixime 7-epimer) | Cefixime EP Impurity C is an impurity of the third generation cephalosporin antibiotic, Cefixime. Synonyms: 108691-83-4; 7-epi-Cefixime (Cefixime EP Impurity C); (6R,7S)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(carboxymethoxyimino)acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid; Cefixime EP Impurity C (Cefixime 7-epimer); DTXSID20747309. Grade: > 95%. CAS No. 108691-83-4. Molecular formula: C16H15N5O7S2. Mole weight: 453.46. | |
| Cefixime EP Impurity D | Cefixime EP Impurity D is an impurity of cefixime which is a semi-synthetic third-generation oral cephalosporin antibiotic used to treat a variety of bacterial infections. Synonyms: (E)-Cefixime; [6R-[6α,7β(E)]]-7-[[(2-Amino-4-thiazolyl)[(carboxymethoxy)imino]acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid. Grade: 95%. CAS No. 97164-56-2. Molecular formula: C16H15N5O7S2. Mole weight: 453.45. | |
| Cefixime Ethyl Ester Sodium Salt (Cefixime EP Impurity F) | Cefixime Ethyl Ester Sodium Salt (Cefixime EP Impurity F). Uses: For analytical and research use. Group: Impurity standards. Catalog: APS001212. Format: Neat. | |
| Cefixime Impurity 11 | Cefixime Impurity 11. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (6R,7R)-7-((Z)-2-(2-aminothiazol-4-yl)-2-((carboxymethoxy)imino)acetamido)-8-oxo-3-vinyl-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid 5-oxide. CAS No. 1335555-87-7. Molecular formula: C16H15N5O8S2. Mole weight: 469.45. Catalog: APB1335555877. | |
| Cefixime Impurity (7-AVCA) | A key intermediate in the manufacturing of Cephalosporin compounds. Synonyms: (6R,7R)-7-Amino-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid; (6R-trans)-7-Amino-3-ethenyl-8-oxo-5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid; 7-AVCA. Grade: > 95%. CAS No. 79349-82-9. Molecular formula: C9H10N2O3S. Mole weight: 226.26. | |
| Cefixime impurity A | Cefixime EP Impurity A is an impurity of the third generation cephalosporin antibiotic, Cefixime. Synonyms: α-[[(Z)-2-(2-amino-4-thiazolyl)-2-[(carboxymethoxy)imino]acetyl]amino]-2-[(2R)-5-methyl-7-oxo-1,2,5,7-tetrahydro-4H-furo[3,4-d][1,3]thiazin-2-yl]acetic Acid. Grade: > 95%. CAS No. 1335475-08-5. Molecular formula: C16H17N5O8S2. Mole weight: 471.47. | |
| Cefixime Impurity B (Mixture of Diastereomers) | Cefixime EP Impurity B is an impurity of the third generation cephalosporin antibiotic, Cefixime. Synonyms: Acetic acid, 2-[[(Z)?-[1-(2-amino-4-thiazolyl)?-2-oxo-2-[[(1,?2,?5,?7-tetrahydro-5-methyl-7-oxo-4H-furo[3,?4-d]?[1,?3]?thiazin-2-yl)?methyl]?amino]?ethylidene]?amino]?oxy]?-. Grade: > 95%. CAS No. 1335475-19-8. Molecular formula: C15H17N5O6S2. Mole weight: 427.46. | |
| Cefixime Impurity E | Cefixime EP Impurity E is an impurity of the third generation cephalosporin antibiotic, Cefixime. Synonyms: Cefixime Impurity E; 72701-01-0; (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(carboxymethoxyimino)acetyl]amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid; (6R,7R)-7-({(2Z)-2-(2-Amino-1,3-thiazol-4-yl)-2-[(carboxymethoxy)imino]acetyl}amino)-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid; DTXSID00747524; (6R,7R)-7-[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-[(carboxymethoxy)imino]acetamido]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. Grade: > 95%. CAS No. 72701-01-0. Molecular formula: C15H15N5O7S2. Mole weight: 441.44. | |
| Cefixime Impurity F | Cefixime EP Impurity F is an impurity of the third generation cephalosporin antibiotic, Cefixime. Synonyms: Cefixime Ethyl Ester Sodium Salt; (6R,7R)-7-[[(Z)-2-(2-aminothiazol-4-yl)-2-[(2-ethoxy-2- oxoethoxy)imino]acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2- ene-2-carboxylic acid. Grade: > 95%. CAS No. 79368-95-9. Molecular formula: C18H19N5O7S2. Mole weight: 481.51. | |
| Cefixime methyl ester | Cefixime Methyl Ester is an ester impurity of the third generation cephalosporin antibiotic, Cefixime. Synonyms: (6R,7R)-7-[[(2Z)-2-(2-Amino-4-thiazolyl)-2-[(2-methoxy-2-oxoethoxy)imino]acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid; [6R-[6α,7β(Z)]]-7-[[(2-Amino-4-thiazolyl)[(2-methoxy-2-oxoethoxy)imino]acetyl]amino]-3-ethenyl-8-. Grade: > 95%. CAS No. 88621-01-6. Molecular formula: C17H17N5O7S2. Mole weight: 467.48. | |
| Cefixime trihydrate | Cefixime trihydrate (FR-17027 trihydrate) is an antibiotic and a third generation cephalosporin antibiotic, useful for the treatment of a number of bacterial infections [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: FR-17027 trihydrate; FK-027 trihydrate; CL-284635 trihydrate. CAS No. 125110-14-7. Pack Sizes: 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B1381A. | |
| Cefixime trihydrate | A broad spectrum third generation cephalosporin targeting a wide range of gram-positive and gram-negative organisms. It is especially useful against pathogens responsible for causing ear, nose, and throat infections such as haemophilus influenzae and moraxella. Synonyms: [6R-[6α,7β(Z)]]-7-[[(2-Amino-4-thiazolyl)[(carboxymethoxy)imino]acetyl]amino]-3-ethenyl-8-oxo-5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid Trihydrate; (E)-cefixime trihydrate; Ytterbium(III) Ionophore I. Grade: ≥97%. CAS No. 125110-14-7. Molecular formula: C16H15N5O7S2.3H2O. Mole weight: 507.50. | |
| Cefixime Trihydrate, 950-1030ug/mg | Cefixime Trihydrate, 950-1030ug/mg. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| Cefmenoxime | It is produced by the strain of Semisynthetic third generation cephalosporin for injection. Synonyms: Cefmenoximum; Cefmenoxima; (6R,7R)-(2-(2-Amino-4-thiazolyl)glyoxylamido)-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-en-2-carbonsaeure-7-(Z)-(O-methyloxim); AB 50912; SCE 1365; 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid,7-[[(2Z)-(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-,(6R,7R)-. Grade: ≥ 97%. CAS No. 65085-01-0. Molecular formula: C16H17N9O5S3. Mole weight: 511.56. | |
| Cefmenoxime hydrochloride | Cefmenoxime hydrochloride. Group: Biochemicals. Alternative Names: (6R, 7R) -7-[[ (2Z) - (2-Amino-4-thiazolyl) (methoxyimino) 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 hemihydrochloride; Abbott 50192; Bestcall. Grades: Highly Purified. CAS No. 75738-58-8. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C16H17N9O5S3·½HCl. US Biological Life Sciences. | Worldwide |
| Cefmenoxime hydrochloride | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C16H18ClN9O5S3. CAS No. 75738-58-8. Prepack ID 70933063-1g. Molecular Weight 548.02. See USA prepack pricing. | |
| Cefmenoxime hydrochloride | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Cefmenoxime hydrochloride | Cefmenoxime hydrochloride is a third-generation cephalosporin antibiotic with strong antimicrobial activities against Streptococcus pneumoniae, Haemophilus influenzae and Moraxella subgenus Branhamella catarrhalis that were 3 major aerobic bacteria from sinusitis. It is administered intravenously or intramuscularly. It is active against most common gram-positive and gram-negative microorganisms, It is a potent inhibitor of Enterobacteriaceae and is highly resistant to hydrolysis by beta-lactamases. It has a high rate of efficacy in many types of infection and to date no severe side effects have been noted. Uses: Cefmenoxime hydrochloride is active against most common gram-positive and gram-negative microorganisms, it is a potent inhibitor of enterobacteriaceae and is highly resistant to hydrolysis by beta-lactamases. Synonyms: Cefmenoxime Hydrochloride; SCE 1365 hydrochloride; AB 50912 hemihydrochloride; EINECS 278-299-4; Cefmenoxime hemihydrochloride; Cefmenoxime HCl; SCE1365; Hydrochloride, Cefmenoxime; SCE 1365; SCE-1365; VA10523; A838501; 7-[[2-(2-amino-4-thiazolyl)-2-methoxyimino-1-oxoethyl]amino]-3-[[(1-methyl-5-tetrazolyl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid hydrochloride; 8-[2. Grade: 98%. CAS No. 75738-58-8. Molecular formula: C32H35ClN18O10S6. Mole weight: 1059.58. | |
| Cefmenoxime hydrochloride | Cefmenoxime (SCE-1365) hydrochloride is a new semisynthetic cephalosporin antibiotic. Cefmenoxime has antibacterial activity against a wide variety of gram-positive and gram-negative bacteria [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SCE-1365 hydrochloride. CAS No. 75738-58-8. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-B0875. | |
| Cefmetazole | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardschiral molecules. Alternative Names: 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[[(cyanomethyl)thio]acetyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, (6R,7S)- (9CI), SKF 83088, Cefmetazole, U 72791a, 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[[(cyanomethyl)thio]acetyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, (6R-cis)-,5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[2-[(cyanomethyl)thio]acetyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, (6R,7S)-, (6R,7S)-7-[[2-[(Cyanomethyl)thio]acetyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, CS 1170, U 72791. | |
| Cefmetazole | Semi-synthetic antibiotic derived from Cephamycin. Antibacterial. Group: Biochemicals. Alternative Names: (6R, 7S) -7-[[2-[ (Cyanomethyl) thio]acetyl]amino]-7-methoxy-3-[[ (1-methyl-1H-tetrazol-5-yl) thio]methyl]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid; SKF 83088; U 72791; U 72791a. Grades: Highly Purified. CAS No. 56796-20-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Cefmetazole | It is produced by the strain of Semisynthetic second generation cephalosporin for injection. It belongs to the cephalomycin-type compound. and its sodium salt is used in preparations. Cefmeazole is an antibiotic with broad spectrum activity against gram-positive and Gram-negative bacteria. It binds to a penicillin-binding protein (PBPs) responsible for the cross-linking of peptidoglycan. Uses: Cefmetazole has antibacterial activity. Synonyms: Cefmetazolo; Cefmetazolum; U-72791A; U72791A; Zefazone; CS-1170; CS 1170; CS1170; (6R,7S)-7-({[(cyanomethyl)sulfanyl]acetyl}amino)-7-methoxy-3-{[(1-methyl-1H-tetrazol-5-yl)sulfanyl]methyl}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. Grade: 95%. CAS No. 56796-20-4. Molecular formula: C15H17N7O5S3. Mole weight: 471.53. | |
| Cefmetazole Impurity 16 | Cefmetazole Impurity 16. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 1-methyl-1H-tetrazole-5-thiol. CAS No. 13183-79-4. Molecular formula: C2H4N4S. Mole weight: 116.14. Catalog: APB13183794. | |
| Cefmetazole Impurity 8 | 7-[[[(cyanomethyl)thio]acetyl]amino]-7-Methoxy Cephalosporanic Acid is an metabolite of Cefmetazole, an semi-synthetic antibiotic derived from Cephamycin. 7-[[[(cyanomethyl)thio]acetyl]amino]-7-Methoxy Cephalosporanic Acid have also shown bactericidal activity in various studies. Synonyms: (6R-cis)-3-[(Acetyloxy)methyl]-7-[[[(cyanomethyl)thio]acetyl]amino]-7-methoxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid. Grade: > 95%. CAS No. 56796-16-8. Molecular formula: C15H17N3O7S2. Mole weight: 415.45. | |
| Cefmetazole Oxidation Impurity 2 | Cefmetazole Oxidation Impurity 2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 105974-42-3. Molecular formula: C11H22O3. Mole weight: 202.29. Catalog: APB105974423. | |
| Cefmetazole sodium | Cefmetazole sodium, containing N-methyl thiotetrazole side chains, is a semi-synthetic, second-generation cephalosporin antibiotic with broad spectrum activity. Uses: Anti-bacterial agents. Synonyms: (6R,7S)-7-(2-(cyanomethylthio)acetamido)-7-methoxy-3-((1-methyl-1H-tetrazol-5-ylthio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid Sodium Salt; CS-1170 Sodium Salt; Cefmetazon Sodium; Metafar; Metazol; Sodium Cefmetazole; Zefazone; CMZ sodium. Grade: ≥95%. CAS No. 56796-39-5. Molecular formula: C15H16N7O5S3.Na. Mole weight: 493.52. | |
| Cefmetazole sodium | Cefmetazole sodium (Sodium cefmetazole) is a semisynthetic cephamycin antibiotic with broad-spectrum antibacterial activity, covering gram-positive, gram-negative, and anaerobic bacteria. Cefmetazole sodium binds to penicillin binding proteins (PBPs), resulting in interfering bacterial cell wall biosynthesis. Cefmetazole sodium is used for the research of gynecologic, intraabdominal, urinary tract, respiratory tract and skin and soft tissue infections [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Sodium cefmetazole. CAS No. 56796-39-5. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-B1257. | |
| Cefmetazole sodium | Cefmetazole sodium. Group: Biochemicals. Grades: Highly Purified. CAS No. 56796-39-5. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C15H16N7NaO5S3. US Biological Life Sciences. | Worldwide |
| Cefmetazole Sodium | A semisynthetic cephamycin antibiotic with a broad spectrum of activity against both gram-positive and gram-negative microorganisms. It has a high rate of efficacy in many types of infection and to date no severe side effects have been noted. Alternative Names: Zefazone. CEFMETAZOLE SODIUM SALT. Cefmetazon. CAS No. 56796-39-5. Product ID: API56796395. Molecular formula: C15H16N7NaO5S3. Mole weight: 493.5. EINECS: 627-393-7. SMILES: CN1C(=NN=N1)SCC2=C(N3C(C(C3=O)(NC(=O)CSCC#N)OC)SC2)C(=O)[O-].[Na+]. Appearance: White to Off-white Solid. Standard: EP/USP. Category: Antibacterial APIs. | |
| Cefmetazole sodium salt, 860-1003ug/mg | Cefmetazole sodium salt, 860-1003ug/mg. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences. | Worldwide |
| Cefminox | It is produced by the strain of Semisynthetic third generation cephalosporin for injection. It belongs to the cephalomycin-type compound. and its sodium salt containing 7 molecules of crystalline water is used in preparations. Synonyms: 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[[(2-amino-2-carboxyethyl)thio]acetyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, [6R-[6α,7α,7(S*)]]-; CMNX. Grade: ≥ 95%. CAS No. 84305-41-9. Molecular formula: C16H21N7O7S3. Mole weight: 519.58. | |
| Cefminox sodium | Cefminox is a broad-spectrum, bactericidal cephalosporin antibiotic. It is especially effective against Gram-negative and anaerobic bacteria. Cefminox Sodium is the sodium salt form of cefminox, which is a semi-synthetic, second-generation and beta-lactamase-stable cephalosporin with antibacterial activity. It is also known as Meicelin and MT-141, which is a penicillin binding protein inhibitor used to treat bacterial infection. Synonyms: MT-141; MT 141; Meicelin. Grade: ≥98%. CAS No. 75498-96-3. Molecular formula: C16H20N7O7S3Na. Mole weight: 541.56. | |
| Cefminox sodium | Cefminox sodium (MT-141) is a semisynthetic cephamycin, which exhibits a broad spectrum of antibacterial activity [1]. Cefminox sodium (MT-141) also acts as a dual agonist of prostacyclin receptor (IP) and PPARγ , upregulates cAMP production and PTEN expression and inhibits Akt/mTOR signaling. Cefminox sodium (MT-141) also prevents pulmonary arterial hypertension [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MT-141. CAS No. 75498-96-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-128932. | |
| Cefminox sodium heptahydrate | Cefminox sodium heptahydrate is a salt form of Cefminox, which is a second generation cephalosporin antibiotic. Uses: Anti-bacterial agents. Synonyms: Cefminox sodium hydrate. CAS No. 92636-39-0. Molecular formula: C16H21N7O7S3Na.7H2O. Mole weight: 668.68. | |
| Cefminox Sodium Heptahydrate | Cefminox is a semisynthetic broad spectrum cephamycin antibiotic. Antibacterial. Group: Biochemicals. Alternative Names: (6R, 7S) -7- [ [2- [ [ (2S) -2-Amino-2-carboxyethyl] thio] acetyl] amino] -7-methoxy-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 Heptahydrate; Cefminox Sodium Salt Heptahydrate; Meicelin Heptahydrate. Grades: Highly Purified. CAS No. 75498-96-3. Pack Sizes: 500mg. US Biological Life Sciences. | Worldwide |
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