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| Product | Description | |
|---|---|---|
| Cefazolin | Cefazolin (Cephazolin) is a first-generation cephalosporin antibiotic and can be used in varieties of bacterial infections research [1]. Cefazolin has anti-inflammatory effect and can attenuate post-operative cognitive dysfunction (POCD) [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cephazolin. CAS No. 25953-19-9. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B1892. |  |
| Cefazolin | It is produced by the strain of Semisynthetic first generation cephalosporin for injection. The activity of Cefazolin to gram-positive bacteria was similar to Cefazolin and Cefazolin, but the activity of gram-negative bacteria was slightly stronger. After intramuscular injection, blood drug concentration increased (blood peak concentration is equivalent to 3-4 times of cefthiophene), and serum elimination half-life was 1.8h, mainly discharged in urine. It may also be used before and during certain surgeries to help prevent infection. Synonyms: Cephazolin; Cephamezine; Cefazoline; Cefamezin; Cephazoline; Cephazolidin; Cefazolina; Cefazolinum; Cefazolin acid; Elzogram; Kefzol; (6R-trans)-3-(((5-Methyl-1,3,4-thiadiazol-2-yl)thio)methyl)-8-oxo-7-(((1H-tetrazol-1-yl)acetyl)-amino)-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid; 7-(1-(1H-)-Tetrazolylacetamido)-3-(2-(5-methyl-1,3,4-thiadiazolyl)thiomethyl)delta3-cephem-4-carboxylic acid. Grades: 98%. CAS No. 25953-19-9. Molecular formula: C14H14N8O4S3. Mole weight: 454.51. |  |
| Cefazolin | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Cefazolin, (6R,7R)-3-[[(5-Methyl-1,3,4-thiadiazol-2-yl)sulfanyl]methyl]-8-oxo-7-[(1H-tetrazol-1-ylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid, (6R,7R)-3-[[(5-Methyl-1,3,4-thiadiazol-2-yl)thio]methyl]-8-oxo-7-[[2-(1H-tetrazol-1-yl)acetyl]amino]-5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. |  |
| Cefazolin 3-Hydroxymethyl Impurity | Des[(5-Methyl-1,3,4-thiadiazol-2-yl)thio] Cefazolin-3-methanol is an impurity of Cefazolin. Synonyms: (6R,7R)-3-(Hydroxymethyl)-8-oxo-7-[[2-(1H-tetrazol-1-yl)acetyl]amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid. Grades: > 95%. CAS No. 478494-71-2. Molecular formula: C11H12N6O5S. Mole weight: 340.32. | |
| Cefazolin EP Impurity G | An impurity of Cefazolin, an antibiotic used for the treatment of bacterial infections. Synonyms: Cefazolin Lactone; Cefazolin Sodium Impurity G. CAS No. 1172998-53-6. Molecular formula: C11H10N6O4S. Mole weight: 322.3. | |
| Cefazolin EP Impurity I | Cefazolin EP Impurity I. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1675244-99-1. Molecular formula: C14H16N8O5S3. Mole weight: 472.51. Catalog: APB1675244991. | |
| Cefazolin Impurity 23 | Cefazolin Impurity 23. Uses: For analytical and research use. Group: Impurity standards. CAS No. 152541-04-3. Molecular formula: C8H12N2OS2. Mole weight: 216.32. Catalog: APB152541043. | |
| Cefazolin Impurity 7 | Cefazolin Impurity 7. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1072000-00-0. Molecular formula: C17H22N8O4S3Si. Mole weight: 526.68. Catalog: APB1072000000. | |
| Cefazolin Impurity 9 | Cefazolin Impurity 9. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1322626-65-2. Molecular formula: C14H15N9O3S3. Mole weight: 453.51. Catalog: APB1322626652. | |
| Cefazolin Impurity A | 7-Amino-3-[(5-methyl-1,3,4-thiadiazol-2-ylthio)methyl]-3-cephem-4-carboxylic Acid is a substrate used in the assessment of immobilized PGA orientation and in the synthesis of beta lactam antibiotics. Synonyms: 7-Amino-3-[(2-methyl-1,3,4-thiadiazol-5-ylthio)methyl]-3-cephem-4-carboxylic Acid; (6R-trans)-7-Amino-3-[[(5-methyl-1,3,4-thiadiazol-2-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid; 7-ZACA. Grades: > 95%. CAS No. 30246-33-4. Molecular formula: C11H12N4O3S3. Mole weight: 344.44. | |
| Cefazolin Impurity C | an impurity of Cefazolin. Synonyms: (6R,7R)-3-Methyl-8-oxo-7-[(1H-tetrazol-1-ylacetyl)amino]-5-thia-1-azabicyclo [4.2.0]oct-2-ene-2-carboxylic acid. Grades: > 95%. CAS No. 56842-77-4. Molecular formula: C11H12N6O4S. Mole weight: 324.32. | |
| Cefazolin Impurity D | An impurity of Cefazolin, an antibiotic used for the treatment of bacterial infections. Synonyms: 5-Thia-1-azabicyclo[4.2.0]?oct-2-ene-2-carboxylic acid, 3-[(acetyloxy)?methyl]?-8-oxo-7-[[2-(1H-tetrazol-1-yl)?acetyl]?amino]?-, (6R,?7R)?-. Grades: > 95%. CAS No. 32510-61-5. Molecular formula: C13H14N6O6S. Mole weight: 382.36. | |
| Cefazolin Impurity E | 5-Methyl-1,3,4-thiadiazol-2-thiol, is a new potent nitrification inhibitors. It is also an intermediate in the synthesis of Thiazolylacetylglycine Oxime. Synonyms: 5-Methyl-1,3,4-Thiadiazole-2(3H)-thione; 2-Methyl-Δ2-1,3,4-thiadiazoline-5-thione; 2-Mercapto-5-methyl-1,3,4-thiadiazole; 2-Methyl-1,3,4-thiadiazol-5-thiol; 5-Methyl-2-sulfanyl-1,3,4-thiadiazole; 5-Methyl-3H-1,3,4-thiadiazole-2-thione; 5-Methyl-2-mercapto. Grades: > 95%. CAS No. 29490-19-5. Molecular formula: C3H4N2S2. Mole weight: 132.21. | |
| CefazolinImpurityEP-J | CefazolinImpurityEP-J. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 2-((2-(1H-tetrazol-1-yl)acetamido)(carboxy)methyl)-5-methylene-5,6-dihydro-2H-1,3-thiazine-4-carboxylic acid. CAS No. 1675245-00-7. Molecular formula: C11H12N6O5S. Mole weight: 340.32. Catalog: APB1675245007. | |
| Cefazolin sodium | Cefazolin sodium, derived from 7-amino-cephalosporanic acid, is a semi-synthetic, first-generation cephalosporin antibiotic. Uses: Antibacterial. Synonyms: sodium;(6R,7R)-3-[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanylmethyl]-8-oxo-7-[[2-(tetrazol-1-yl)acetyl]amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate Ancef Cefamedin Cefamezine Cefazolin Cefazolin Sodium Cephamezine Cephazolin Cephazolin Sodium Cep. Grades: >97%. CAS No. 27164-46-1. Molecular formula: C14H13N8NaO4S3. Mole weight: 476.48. | |
| Cefazolin sodium | Cefazolin sodium is a first-generation cephalosporin antibiotic and can be used in varieties of bacterial infections research [1]. Cefazolin sodium has anti-inflammatory effect and can attenuate post-operative cognitive dysfunction (POCD) [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cephazolin sodium. CAS No. 27164-46-1. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B1078. | |
| Cefazolin Sodium | Cefazolin Sodium. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 1g, 5g, 25g. US Biological Life Sciences. |  Worldwide |
| Cefazolin sodium salt | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C14H13N8NaO4S3. CAS No. 27164-46-1. Prepack ID 39760978-1g. Molecular Weight 476.49. See USA prepack pricing. |  |
| Cefazolin sodium salt | Cefazolin sodium salt. Group: Biochemicals. Alternative Names: (6R,7R)-3-[[(5-Methyl-1,3,4-thiadiazol-2-yl)thio]methyl]-8-oxo-7-[(1H-tetrazol-1-ylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid sodium salt; Atirin; Azolin. Grades: Highly Purified. CAS No. 27164-46-1. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C14H13N8NaO4S3. US Biological Life Sciences. | Worldwide |
| Cefazolin, Sodium Salt (SKF-41558, Cefamedin) | An antibacterial. Group: Biochemicals. Alternative Names: SKF-41558, Cefamedin. Grades: Highly Purified. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Cefazolin USP Impurity B | Cefazolin USP Impurity B. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: N-(2,2-dihydroxyethyl)-2-(1H-tetrazol-1-yl)acetamide. CAS No. 1675245-47-2. Molecular formula: C5H9N5O3. Mole weight: 187.16. Catalog: APB1675245472. | |
| 7-Amino-3 chloromethyl-3-cephem-4-carboxylic Acid p-Methoxybenzyl Ester Hydrochloride | Cefazolin intermediate as antibacterials. Group: Biochemicals. Alternative Names: (6R,7R)-7-Amino-3-(chloromethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid (4-Methoxyphenyl)methyl Ester Hydrochloride. Grades: Highly Purified. CAS No. 113479-65-5. Pack Sizes: 25mg, 50mg, 100mg, 250mg, 500mg. Molecular Formula: C??H??Cl?N?O?S, Molecular Weight: 405.3. US Biological Life Sciences. | Worldwide |
| Cefathiamidine | It is produced by the strain of Semisynthetic first generation cephalosporin for injection. Cefathiamidin has better antibacterial activity than cefazolin, cefuroxime and cefamidin against Streptococcus pneumoniae, Streptococcus pyogenes, MSSA, MSSE and Moraxella mucosa inflammation, and it showed strong activity against enterococcus. Its MIC90 (2.0 ?/mL)is slightly weaker than vancomycin (1.0?/mL). It also has some activity to MRSA and MRSE. Synonyms: (6R-trans) -3-[ (Acetyloxy) methyl]-7-[[[[[ (1-methylethyl) amino][ (1-methylethyl) imino]methyl]thio]acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid; 7-[2-[(N,N'-diisopropylamidino)thio]acetamido]-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid; Cephathiamidine. Grades: > 95%. CAS No. 33075-00-2. Molecular formula: C19H28N4O6S2. Mole weight: 472.58. | |
| Cefazaflur sodium | Cefazaflur sodium is a semi-synthetic cephalosporin with broad antibiotic spectrum. Its activity against gram-negative bacteria is similar to Cephalothin and stronger than Cefazolin. Synonyms: SKF-59962. CAS No. 52123-49-6. Molecular formula: C13H12F3N6NaO4S3. Mole weight: 492.5. | |
| Ceftezole | It is produced by the strain of Semisynthetic first generation cephalosporin for injection. Ceftezole was similar to cefazolin in antibacterial activity, pharmacokinetics and safety. Uses: Anti-bacterial agents. Synonyms: CG-B 3Q; CTZ; Ceftezol; FR 10123; (6R,7R)-3-(((1,3,4-thiadiazol-2-yl)thio)methyl)-7-(2-(1H-tetrazol-1-yl)acetamido)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid; (6R,7R)-8-Oxo-7-[(1H-tetrazol-1-ylacetyl)amino]-3-[(1,3,4-thiadiazol-2-ylthio)methyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid; (6R-trans)-8-Oxo-7-[(1H-tetrazol-1-ylacetyl)amino]-3-[(1,3,4-thiadiazol-2-ylthio)methyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid. Grades: > 95%. CAS No. 26973-24-0. Molecular formula: C13H12N8O4S3. Mole weight: 440.48. | |
| Cephalexin | Cefalexin, also spelled cephalexin, is an antibiotic that can treat a number of bacterial infections. It kills gram-positive and some gram-negative bacteria by disrupting the growth of the bacterial cell wall. Cefalexin is a beta-lactam antibiotic within the class of first-generation cephalosporins. It works similarly to other agents within this class, including intravenous cefazolin, but can be taken by mouth.Cefalexin can treat certain bacterial infections, including those of the middle ear, bone and joint, skin, and urinary tract. It may also be used for certain types of pneumonia, strep throat, and to prevent bacterial endocarditis. Cefalexin is not effective against infections caused by methicillin-resistant Staphylococcus aureus (MRSA), Enterococcus, or Pseudomonas. Like other antibiotics, cefalexin cannot treat viral infections, such as the flu, common cold or acute bronchitis. Cefalexin can be used in those who have mild or moderate allergies to penicillin. However, it is not recommended in those with severe penicillin allergies.Common side effects include upset stomach and diarrhea. An allergic reaction and infection with Clostridium difficile, a type of diarrhea, is also possible. To date, no evidence of harm to the baby has been found when used during pregnancy or breast feeding. It can be used in children and those over 65 years of age. Those with kidney problems may require a decrease in dose.In 2012, cefalexin wa |  |
| Cephalexin hydrochloride | Cefalexin hydrochloride is a cephalosporin antibiotic. It is a first-generation cephalosporin antibiotic introduced in 1967 by Eli Lilly and Company. It is an orally administered agent with a similar antimicrobial spectrum to the intravenous agents cefalotin and cefazolin. Uses: Anti-bacterial agents. Synonyms: Keflex hydrochloride. Grades: >98%. CAS No. 59695-59-9. Molecular formula: C16H18ClN3O4S. Mole weight: 383.85. | |
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