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| Product | Description | |
|---|---|---|
| Cefdinir Thiazine Analog Lactone Form (Mixture of Diastereomers) | Cefdinir Thiazine Analog Lactone Form (Mixture of Diastereomers) is one of Cefdinir impurities. Cefdinir is a semi-synthetic, broad-spectrum antibiotic, used for soft tissue infections and respiratory tract infections. Synonyms: α-[[(2-Amino-4-thiazolyl)(hydroxyimino)acetyl]amino]-1,2,5,7-tetrahydro-5-methyl-7-oxo-4H-Furo[3,4-d][1,3]thiazine-2-acetic Acid Sodium Salt; USP Cefdinir Related Compound A Sodium Salt. Grade: 95%. Molecular formula: C14H14N5NaO6S2. Mole weight: 435.41. |  |
| Cefdinir Thiazine Analog Lactone Form (Mixture of Diastereomers) | Cefdinir Thiazine Analog Lactone Form (Mixture of Diastereomers). Uses: For analytical and research use. Group: Impurity standards. Pack Sizes: 5MG. Catalog: APS006578. Format: Neat. Shipping: Room Temperature. |  |
| Cefditoren | Cefditoren is a third-generation cephalosporin antibiotic for oral use. It is commonly marketed under the trade name Spectracef by Vansen Pharma Inc. Uses: Anti-bacterial agents. Synonyms: 5-Thia-1-azabicyclo[4.2.0]?oct-2-ene-2-carboxylic acid, 7-[[(2Z)?-2-(2-amino-4-thiazolyl)?-2-(methoxyimino)?acetyl]?amino]?-3-[(1Z)?-2-(4-methyl-5-thiazolyl)?ethenyl]?-8-oxo-, (6R,?7R)?-. Grade: > 95%. CAS No. 104145-95-1. Molecular formula: C19H18N6O5S3. Mole weight: 506.58. | |
| Cefditoren | Cefditoren. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (6R,7R)-7-((Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido)-3-((Z)-2-(4-methylthiazol-5-yl)vinyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. CAS No. 104145-95-1. Molecular formula: C19H18N6O5S3. Mole weight: 506.05. Catalog: APB104145951. | |
| Cefditoren | Cefditoren is an orally active antibiotic with broad-spectrum antibacterial activity, capable of inhibiting both Gram-negative and Gram-positive bacteria. It has a MIC 50 of 0.25-0.5 mg/L against Streptococcus pneumoniae strains. Cefditoren is effective against respiratory tract infections and skin infections [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 104145-95-1. Pack Sizes: 5 mg; 10 mg. Product ID: HY-159688. |  |
| Cefditoren-[13C,d3] | Cefditoren-[13C,d3] is the labelled analogue of Cefditoren. Cefditoren is the third-generation cephalosporin antibiotic for oral use. Synonyms: Cefditoren-13C,D3; (6R,7R)-7-[[(2Z)-(2-Amino-4-thiazolyl)methoxyimino)acetyl]amino]-3-[(1Z)-2-(4-methyl-5-thiazolyl)ethenyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid-13C,d3; (6R-(3(Z),6alpha,7beta(Z)))-7-((2-Amino-4-thiazolyl)(methoxyimino)acetyl)amino-3-(2-(4-methyl-5-thiazolyl)ethenyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid-13C,d3. Grade: 95% by HPLC; 98% atom 13C; 98% atom D. Molecular formula: C18[13C]H15D3N6O5S3. Mole weight: 510.60. | |
| Cefditoren acid sodium salt | Cefditoren acid sodium salt. Group: Biochemicals. Alternative Names: (6R, 7R) -7-[[ (2Z) - (2-Amino-4-thiazolyl) methoxyimino) acetyl]amino]-3-[ (1Z) -2- (4-methyl-5-thiazolyl) ethenyl]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic acid sodium salt; ME 1206. Grades: Highly Purified. CAS No. 104146-53-4. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C19H17N6NaO5S3, Molecular Weight: 528.56. US Biological Life Sciences. |  Worldwide |
| Cefditoren pivoxil | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Cefditoren pivoxil | Cefditoren pivoxil. Group: Biochemicals. Alternative Names: (6R, 7R) -7-[[ (2Z) - (2-Amino-4-thiazolyl) methoxyimino) acetyl]amino]-3-[ (1Z) -2- (4-methyl-5-thiazolyl) ethenyl]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic acid pivaloyloxymethyl ester; Cefditoren. Grades: Highly Purified. CAS No. 117467-28-4. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C25H28N6O7S3. US Biological Life Sciences. | Worldwide |
| Cefditoren pivoxil | It is produced by the strain of Semisynthetic third generation oral cephalosporin. Cefditoren Pivoxil possesses a broad-spectrum of antibacterial activity against both Gram-positive and Gram-negative species with stability to many beta-lactamases of clinical importance. Uses: Anti-bacterial agents. Synonyms: Spectracef; Cefditoren pivaloyloxymethyl ester; CDTR-PI; Cefditorin; Meiact; Cefditoren PI voxil; (-)-(6R,7R)-2,2-dimethylpropionyloxymethyl 7-((Z)-2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido)-3-((Z)-2-(4-methylthiazol-5-yl)ethenyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylate; ME-1207; ME 1207; ME1207. Grade: ≥ 98%. CAS No. 117467-28-4. Molecular formula: C25H28N6O7S3. Mole weight: 620.72. | |
| Cefditoren Pivoxil | Cefditoren Pivoxil (ME 1207) is a broad-spectrum, third-generation, oral cephalosporin antibacterial with enhanced stability against many common β lactamases. Cefditoren Pivoxil has activity against Gram-negative organisms and Gram-positive organisms. Cefditoren Pivoxil can be used in the research of infection diseases such as acute exacerbations of chronic bronchitis, community-acquired pneumonia (CAP), streptococcal pharyngitis/tonsillitis, or uncomplicated skin and skin structure infections [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefditoren pivoxyl; Cefditoren pivaloyloxymethyl ester; ME 1207. CAS No. 117467-28-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-17452A. | |
| Cefditoren (Pivoxil) | Cefditoren Pivoxil (ME 1207) is a broad-spectrum. third-generation, oral cephalosporin. antibacterial with enhanced stability against. many common β lactamases. Cefditoren Pivoxil. has activity against Gram-negative organisms and. Gram-positive organisms. Alternative Names: (6R,7R)-7-[[(2Z)-(2-Amino-4-thiazolyl)methoxyimino)acetyl]amino]-3-[(1Z)-2-(4-methyl-5-thiazolyl)ethenyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicAcidPivaloyloxymethylEster;Meiac;5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicacid,7-[[(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-3-[2-Chemicalbook(4-methyl-5-thiazolyl)ethenyl]-8-oxo-,(2,2-dimethyl-1-oxopropoxy)methylester,[6R-[3(Z),6α,7β(Z)]]-;5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicacid,7-[[(2Z)-(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-3-[(1Z)-2-(4-methyl-5-thiazolyl)ethenyl]-8-oxo-,(2,2-dimethyl-1-oxopropoxy)methylester,(6R,7R)-. CAS No. 117467-28-4. Product ID: API117467284. Molecular formula: C25H28N6O7S3. Mole weight: 620.72. EINECS: 688-157-7. Appearance: Solid. Category: Antibiotic APIs. |  |
| Cefditoren Pivoxil Impurity 50 | Cefditoren Pivoxil Impurity 50. Uses: For analytical and research use. Group: Impurity standards. CAS No. 104146-11-4. Molecular formula: C29H27N3O5S2. Mole weight: 561.67. Catalog: APB104146114. | |
| Cefditoren sodium | Cefditoren sodium. Uses: For analytical and research use. Group: Impurity standards. CAS No. 104146-53-4. Molecular formula: C19H17N6NaO5S3. Mole weight: 528.55. Catalog: APB104146534. | |
| Cefditoren sodium | Cefditoren sodium (ME 1206) is a broad-spectrum, third-generation, oral cephalosporin antibacterial with enhanced stability against many common β lactamases. Cefditoren sodium has activity against Gram-negative organisms and Gram-positive organisms. Cefditoren sodium can be used in the research of infection diseases such as acute exacerbations of chronic bronchitis, community-acquired pneumonia (CAP), streptococcal pharyngitis/tonsillitis, or uncomplicated skin and skin structure infections [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ME 1206. CAS No. 104146-53-4. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-17452. | |
| Cefditoren Sodium Salt | Cefditoren sodium is a third generation cephalosporin antibiotic potentially for the treatment of bacterial infection. Synonyms: (6R,7R)-7-[[(2Z)-(2-Amino-4-thiazolyl)methoxyimino)acetyl]amino]-3-[(1Z)-2-(4-methyl-5-thiazolyl)ethenyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid Sodium Salt; ME 1206. Grade: >95%. CAS No. 104146-53-4. Molecular formula: C19H17N6NaO5S3. Mole weight: 528.56. | |
| Cefepime | Cefepime (BMY-28142) is a broad-spectrum and cross the blood-brain barrier cephalosporin. Cefepime shows antibacterial effects against both Gram-positive and Gram-negative aerobic bacteria. Cefepime induces neurotoxicity [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BMY-28142. CAS No. 88040-23-7. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 500 mg. Product ID: HY-B0692. | |
| Cefepime | It is produced by the strain of Semisynthetic fourth generation cephalosporin for injection. Uses: Anti-bacterial agents. Synonyms: Maxipime; Cefepima; Cefepimum; Axepim; BMY 28142; BMY-28142; E-Cefepime; CFPM. Grade: ≥ 95%. CAS No. 88040-23-7. Molecular formula: C19H24N6O5S2. Mole weight: 480.56. | |
| Cefepime | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C19H24N6O5S2. CAS No. 88040-23-7. Prepack ID 12850730-1g. Molecular Weight 480.56. See USA prepack pricing. |  |
| Cefepime-13C-d3 | Cefepime-D3,13C is a labelled analogue of Cefepine, a cephalosporin that has antibacterial effects against Gram-positive and Gram-negative bacteria. Synonyms: 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-, [6R-[6α,?7β(Z)?]?]?- (9CI). Grade: > 95%. Molecular formula: C19H22N6O5S2D3. Mole weight: 485.58. | |
| Cefepime-d3 Sulfate | Cefepime-d3 Sulfate. Group: Biochemicals. Alternative Names: [6R-[6α,7 β (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-d3) -pyrrolidinium sulfate (1:1). Grades: Highly Purified. CAS No. 131857-28-8. Pack Sizes: 1mg. Molecular Formula: C19H23D3N6O9S3, Molecular Weight: 581.66. US Biological Life Sciences. | Worldwide |
| Cefepime dihydrochloride | 1g Pack Size. Group: Bioactive Small Molecules, Aroma Chemicals. Formula: C19H24N6O5S2.2ClH. CAS No. 107648-80-6. Prepack ID 89966856-1g. Molecular Weight 553.489. See USA prepack pricing. | |
| Cefepime Dihydrochloride | 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: Maxipime. Cefepime HCl. Cefepime hydrochloride. cefepime dihydrochloride monohydrate. CAS No. 123171-59-5. Product ID: API123171595. Molecular formula: C19H28Cl2N6O6S2. Mole weight: 571.5. EINECS: 642-959-3. SMILES: C[N+]1(CCCC1)CC2=C(N3C(C(C3=O)NC(=O)C(=NOC)C4=CSC(=N4)N)SC2)C(=O)O.O.Cl.[Cl-]. Standard: EP/USP. Category: Antibacterial APIs. | |
| Cefepime Dihydrochloride | Cefepime Dihydrochloride. Uses: For analytical and research use. Group: Impurity standards. CAS No. 107648-80-6. Molecular formula: C19H26Cl2N6O5S2. Mole weight: 553.47. Catalog: APB107648806. | |
| Cefepime dihydrochloride monohydrate | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C19H28Cl2N6O6S2. CAS No. 123171-59-5. Prepack ID 90018543-1g. Molecular Weight 571.5. See USA prepack pricing. | |
| Cefepime Dihydrochloride Monohydrate | Semisynthetic, fourth generation cephalosporin antibiotic. Antibacterial. Group: Biochemicals. Alternative Names: 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-methylpyrrolidinium Inner Salt Dihydrochloride Monohydrate; Axepim; Cepimex; Maxipime. Grades: Highly Purified. CAS No. 123171-59-5. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Cefepime Dihydrochloride Monohydrate | Cefepime Dihydrochloride Monohydrate is a broad-spectrum cephalosporin with enhanced coverage against Gram-positive and Gram-negative bacteria [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 123171-59-5. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0616. | |
| Cefepime dioxime | 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: Cefepime Impurity B; (6R,7R)-7-[[(2Z)-[2-[[(2Z)-(2-Aminothiazol-4-yl)(methoxyimino)acetyl]amino]thiazol-4-yl](methoxyimino)acetyl]amino]-3-[(1-methylpyrrolidinio)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate; Pyrrolidinium, 1-[[(6R,7R)-7-[[(2Z)-2-[2-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]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-, inner salt; (6R,7R)-7-((Z)-2-(2-((Z)-2-(2-Aminothiazol-4-yl)-2-(methoxyimino)acetamido)thiazol-4-yl)-2-(methoxyimino)acetamido)-3-((1-methylpyrrolidin-1-ium-1-yl)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate; Cefepime EP Impurity B; Cefepime dihydrochloride monohydrate EP Impurity B. Grade: ≥95%. CAS No. 2923899-40-3. Molecular formula: C25H29N9O7S3. Mole weight: 663.75. | |
| Cefepime EP Impurity C | A metabolite 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: Cefepime Impurity C; Cefepime dihydrochloride monohydrate EP Impurity C; (2Z)-2-(2-Aminothiazol-4-yl)-N-(formylmethyl)-2-(methoxyimino)acetamide; (Z)-2-(2-Aminothiazol-4-yl)-2-(methoxyimino)-N-(2-oxoethyl)acetamide; T 2588G; THR 221V; (Z)-2-Amino-α-(methoxyimino)-N-(2-oxoethyl)-4-thiazoleacetamide; Thiazolyloxime. acetaldehyde; USP Cefepime Related Compound C; Cefepime USP Related Compound C; Cefepime Related Compound C. Grade: >95%. CAS No. 104301-63-5. Molecular formula: C8H10N4O3S. Mole weight: 242.26. | |
| Cefepime EP Impurity C | Cefepime EP Impurity C. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)-N-(2-oxoethyl)acetamide. CAS No. 104301-63-5. Molecular formula: C8H10N4O3S. Mole weight: 242.26. Catalog: APB104301635. | |
| Cefepime EP Impurity E | Cefepime EP Impurity E. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (6R,7R)-7-amino-3-((1-methylpyrrolidin-1-ium-1-yl)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate. CAS No. 103296-32-8. Molecular formula: C13H19N3O3S. Mole weight: 297.37. Catalog: APB103296328. | |
| Cefepime EP Impurity 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: Cefepime Impurity F; Cefepime dihydrochloride monohydrate EP Impurity F; (6R,7R)-7-[[[(6R,7R)-7-[[(2Z)-(2-Aminothiazol-4-yl)-(methoxyimino)acetyl]amino]-3-[(1-methylpyrrolidinio)-methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-2-yl]-carbonyl]amino]-3-[(1-methylpyrrolidinio)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate; Cefepime NMP-ACA Impurity; Cefepime EP Impurity F; (6R,7R)-7-((6R,7R)-7-((Z)-2-(2-Aminothiazol-4-yl)-2-(methoxyimino)acetamido)-3-((1-methylpyrrolidin-1-ium-1-yl)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxamido)-3-((1-methylpyrrolidin-1-ium-1-yl)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate; Cefepime dimer. Grade: ≥95%. Molecular formula: C32H42N9O7S3+. Mole weight: 760.92. | |
| Cefepime·HCl | Cefepime·HCl. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Cefepime hydrochloride | Pharmaceutical Secondary Standard; Certified Reference Material. Group: Pharmacopeia & metrological institutes standards. | |
| Cefepime hydrochloride | United States Pharmacopeia (USP) Reference Standard. 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. 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 | 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-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 | 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 | 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 | 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 | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| 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 | 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. | |
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