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Ceftizoxime alapivoxil hydrochloride is an exceptionally powerful antimicrobial agent, holding significant prominence in the medical research for its notable efficacy in diverse infections stemming from vulnerable bacteria. Synonyms: 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-2-[2-[[(2S)-2-amino-1-oxopropyl]amino]-4-thiazolyl]-2-(methoxyimino)acetyl]amino]-8-oxo-, (2,2-dimethyl-1-oxopropoxy)methyl ester, hydrochloride (1:1), (6R,7R)-; 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-[2-[[(2S)-2-amino-1-oxopropyl]amino]-4-thiazolyl](methoxyimino)acetyl]amino]-8-oxo-, (2,2-dimethyl-1-oxopropoxy)methyl ester, monohydrochloride, (6R,7R)-; 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[[2-[(2-amino-1-oxopropyl)amino]-4-thiazolyl](methoxyimino)acetyl]amino]-8-oxo-, (2,2-dimethyl-1-oxopropoxy)methyl ester, monohydrochloride, [6R-[6α,7β[Z(S*)]]]-; AS 924. Grade: 95%. CAS No. 135767-36-1. Molecular formula: C22H29ClN6O8S2. Mole weight: 605.09.
Ceftizoxime sodium
A semisynthetic cephalosporin antibiotic for the treatment of infections due to susceptible strains of microorganisms. It is third generation cephalosporin effective against Gram-negative and Gram-positive bacteria. Uses: Anti-bacterial agents. Synonyms: Ceftizoxim-Natrium. Grade: ≥98%. CAS No. 68401-82-1. Molecular formula: C13H12N5NaO5S2. Mole weight: 405.38.
Ceftizoxime sodium
Ceftizoxime sodium (SKF-88373) is third generation cephalosporin effective against Gram-negative and Gram-positive bacteria. It binds penicillin-binding proteins (PBPs) and inhibits the bacterial cell wall synthesis. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SKF-88373. CAS No. 68401-82-1. Pack Sizes: 50 mg; 100 mg. Product ID: HY-B1596A.
Ceftizoxime sodium
Ceftizoxime sodium. Group: Biochemicals. Grades: Highly Purified. CAS No. 68401-82-1. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C13H12N5NaO5S2. US Biological Life Sciences.
Worldwide
Ceftizoxime Sodium
A semisynthetic cephalosporin antibiotic which can be administered intravenously or by suppository. The drug is highly resistant to a broad spectrum of beta-lactamases and is active against a wide range of both aerobic and anaerobic gram-positive and gram-negative organisms. It has few side effects and is reported to be safe and effective in aged patients and in patients with hematologic disorders. Alternative Names: Ceftizoxim-natrium. Eposerin. Cefizox. CAS No. 68401-82-1. Product ID: API68401821. Molecular formula: C13H12N5NaO5S2. Mole weight: 405.4. EINECS: 629-729-8. SMILES: CON=C(C1=CSC(=N1)N)C(=O)NC2C3N(C2=O)C(=CCS3)C(=O)[O-].[Na+]. Appearance: White to Light Yellow Crystalline Powder. Standard: USP/JP. Category: Antibiotic APIs.
Ceftizoxime sodium, 850-995ug/mg (HPLC) USP
Ceftizoxime sodium, 850-995ug/mg (HPLC) USP. Group: Biochemicals. Grades: USP. CAS No. 68401-82-1. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences.
Worldwide
Ceftizoxime sodium salt
100mg Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C13H12N5NaO5S2. CAS No. 68401-82-1. Prepack ID 41432628-100mg. Molecular Weight 405.39. See USA prepack pricing.
Ceftizoxime S-Oxide Impurity
an impurity of ceftizoxime. 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]?-8-oxo-, 5-oxide, (6R,?7R)?-. Grade: > 95%. CAS No. 79226-66-7. Molecular formula: C13H13N5O6S2. Mole weight: 399.41.
Ceftobiprole
Ceftobiprole (Ro 63-9141) is a broad-spectrum cephalosporin with high levels of in vitro activity against methicillin- (MRSA) and vancomycin-resistant staphylococci (VRSA) and penicillin-resistant streptococci with a MIC 90 value of 2 μg/mL for MRSA. Ceftobiprole also inhibits gram-positive and gram-negative pathogens. Ceftobiprole can be used for the study of hospital-acquired pneumonia (excluding ventilator-associated pneumonia) and community-acquired pneumonia [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 63-9141; BAL 9141. CAS No. 209467-52-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112579.
Ceftobiprole
Ceftobiprole (Ro 63-9141) is a broad-spectrum cephalosporin with high levels of in vitro activity against methicillin- (MRSA) and vancomycin-resistant staphylococci (VRSA) and penicillin-resistant streptococci with a MIC90 value of 2 μg/mL for MRSA. Ceftobiprole also inhibits gram-positive and gram-negative pathogens. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Ceftobiprole;5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicacid,7-[[(2Z)-2-(5-aMino-1,2,4-thiadiazol-3-yl)-2-(hydroxyiMino)acetyl]aMino]-8-oxo-3-[(E)-[(3R)-2-oxo[1,3-bipyrrolidin]-3-ylidene]Methyl]-,(6R,7R)-. Product Category: Inhibitors. CAS No. 209467-52-7. Molecular formula: C20H22N8O6S2. Mole weight: 534.576. Purity: ≥95.0%. Product ID: ACM209467527. Alfa Chemistry ISO 9001:2015 Certified.
Ceftobiprole medocaril sodium
Ceftobiprole medocaril (BAL5788) sodium is the parenteral proagent of Ceftobiprole (HY-112579). Ceftobiprole is a parenteral pyrrolidinone cephalosporin. Ceftobiprole is a broad-spectrum cephalosporin with high levels of in vitro activity against methicillin- (MRSA) and vancomycin-resistant staphylococci (VRSA) and penicillin-resistant streptococci. Ceftobiprole also inhibits gram-positive and gram-negative pathogens [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAL5788 sodium. CAS No. 252188-71-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-106574A.
Ceftolozane
Ceftolozane (CXA-101 free base; FR264205 free base) is a cephalosporin antibiotic with potent activity against Pseudomonas aeruginosa and strains Enterobacteriaceae, with MIC s of 0.5 and 0.25-0.5 mg/L [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CXA-101 free base; FR264205 free base. CAS No. 689293-68-3. Pack Sizes: 1 mg. Product ID: HY-19806.
Ceftolozane
Ceftolozane is a 5th generation cephalosporin antibiotic. It is a semi-synthetic beta-lactam antibiotic and is used for the treatment of infections with gram-negative bacteria, or gram-positive bacteria that have become resistant to conventional antibiotics. It is also used for the treatment of complicated urinary tract infections and complicated intra abdominal infections combined with the β-lactamase inhibitor tazobactam. Uses: Ceftolozane is used for the treatment of infections with gram-negative bacteria, or gram-positive bacteria that have become resistant to conventional antibiotics. it is also used for the treatment of complicated urinary tract infections and complicated in. Synonyms: 7-{[(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-{[(2-carboxypropan-2-yl)oxy]imino}acetyl]amino}-3-[ (5-amino-4-{[(2-aminoethyl)carbamoyl]amino}-1-methyl-1H-pyrazol-2-ium-2-yl)methyl]-3,4-didehydrocepham-4-carboxylate; CXA-101; CXA101. Grade: 98%. CAS No. 689293-68-3. Molecular formula: C23H30N12O8S2. Mole weight: 666.69.
Ceftolozane sulfate
Ceftolozane (CXA-101) sulfate is an antipseudomonal cephalosporin. Ceftolozane binds to P. aeruginosa essential PBPs (1b, 1c, 2 and 3) with high affinity. Ceftolozane inhibits cell wall synthesis by binding the PBPs. Ceftolozane sulfate inhibits P. aeruginosa and Enterobacteriaceae [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CXA-101; FR264205. CAS No. 936111-69-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-19806A.
Ceftolozane TFA
Ceftolozane TFA is a cephalosporin antibiotic that can be used to inhibit Gram-negative bacterial infections. Ceftolozane TFA can be used to synthesize new antibiotic that are more potent and safer [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1628046-32-1. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-106257A.
Ceftolozane TFA salt
Ceftolozane TFA salt is the salt of Ceftolozane, which is the fifth-generation cephalosporin antibiotic. It is a semi-synthetic β-lactam antibiotic used to treat Gram-negative or Gram-positive bacterial infections that have developed resistance to conventional antibiotics. Synonyms: 5-Amino-2-(((6R,7R)-7-((Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(((2-carboxypropan-2-yl)oxy)imino)acetamido)-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl)methyl)-4-(3-(2-aminoethyl)ureido)-1-methyl-1H-pyrazol-2-ium 2,2,2-trifluoroacetate; 1H-Pyrazolium, 5-amino-4-[[[(2-aminoethyl)amino]carbonyl]amino]-2-[[(6R,7R)-7-[[(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-[(1-carboxy-1-methylethoxy)imino]acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-1-methyl-, 2,2,2-trifluoroacetate (1:1); 5-Amino-4-{[(2-aminoethyl)carbamoyl]amino}-2-{[(6R,7R)-7-{[(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-{[(2-carboxy-2-propanyl)oxy]imino}acetyl]amino}-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl}-1-methyl-1H-pyrazol-2-ium trifluoroacetate; CXA-101 TFA salt; Ceftolozane trifluoroacetate. Grade: ≥95%. CAS No. 1628046-32-1. Molecular formula: C23H30N12O8S2.C2HF3O2. Mole weight: 780.71.
Ceftriaxone
1g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C18H18N8O7S3. CAS No. 73384-59-5. Prepack ID 76468654-1g. Molecular Weight 554.58. See USA prepack pricing.
Ceftriaxone
It is produced by the strain of Semisynthetic third generation cephalosporin for injection. It has the third-generation cephalosporin commonness. It is characterized by a plasma elimination half-life of up to 7.1h, and one dose per day. 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]-8-oxo-3-[[(1,2,5,6-tetrahydro-2-methyl-5,6-dioxo-1,2,4-triazin-3-yl)thio]methyl]-, (6R,7R)-; (6R,7R)-7-[[(2Z)-2-(2-Amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-8-oxo-3-[[(1,2,5,6-tetrahydro-2-methyl-5,6-dioxo-1,2,4-triazin-3-yl)thio]methyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid; 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-8-oxo-3-[[(1,2,5,6-tetrahydro-2-methyl-5,6-dioxo-1,2,4-triazin-3-yl)thio]methyl]-, [6R-[6α,7β(Z)]]-; Biotrakson; Epicephin; Rocefin; Rocephalin; Rophex. Grade: >98%. CAS No. 73384-59-5. Molecular formula: C18H18N8O7S3. Mole weight: 554.58.
Ceftriaxone
Ceftriaxone (Ro 13-9904 free acid) is a broad spectrum β-lactam third-generation cephalosporin antibiotic, which has good antibacterial activity against a variety of gram-negative and positive bacteria. Ceftriaxone is a covalent inhibitor of GSK3β with IC 50 value of 0.78 μM. Ceftriaxone is an inhibitor of Aurora B. Ceftriaxone has anti-inflammatory, antitumor and antioxidant activities. Ceftriaxone can be used in the study of bacterial infections and meningitis [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 13-9904 free acid. CAS No. 73384-59-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-B0712.
Ceftriaxone 3-ene isomer
An impurity of Ceftriaxone, a cephalosporin antibiotic for the treatment of various bacterial infections. Molecular formula: C18H18N8O7S3. Mole weight: 554.57.
An antibacterial. Group: Biochemicals. Alternative Names: Ro-13-9904/001, Rocefin Rocephine. Grades: Highly Purified. CAS No. 104376-79-6. Pack Sizes: 5g, 10g, 25g, 50g, 100g. US Biological Life Sciences.
Worldwide
Ceftriaxone EP Impurity B
An impurity of Cefotaxime sodium. It is also a degradation product for other cephalosporin antibiotics such as: Ceftriaxone , Cefodizime and Ceftiofur. Synonyms: [5aR-[5aα,6β(Z)]]-2-Amino-α-(methoxyimino)-N-(1,4,5a,6-tetrahydro-1,7-dioxo-3H,7H-azeto[2,1-b]furo[3,4-d][1,3]thiazin-6-yl)-4-thiazoleacetamide; 3-Desacetyl Cefotaxime Lactone; Deacetylcefotaxime lactone. Grade: > 95%. CAS No. 66340-33-8. Molecular formula: C14H13N5O5S2. Mole weight: 395.42.
Ceftriaxone EP Impurity C
An impurity of Ceftriaxone, a cephalosporin antibiotic for the treatment of various bacterial infections. Synonyms: Tetrahydro-2-methyl-3-thioxo-1,2,4-triazine-5,6-dione; Ro 11-8390; 2-Methyl-5,6-dioxo-1,2,5,6-tetrahydro-1,2,4-triazine-3-thiol; Ceftriaxone triazine analog. Grade: > 95%. CAS No. 58909-39-0. Molecular formula: C4H5N3O2S. Mole weight: 159.17.
Ceftriaxone EP Impurity D
An impurity of Ceftriaxone, a cephalosporin antibiotic for the treatment of various bacterial infections. Synonyms: S-2-Benzothiazolyl 2-amino-alpha-(methoxyimino)-4-thiazolethiolacetate; (2Z)-2-(2-amino-4-thiazolyl)-2-methoxyiminoethanethioic acid S-(1,3-benzothiazol-2-yl) ester; Ceftriaxone benzothiazolyloxime. Grade: > 95 %. CAS No. 80756-85-0. Molecular formula: C13H10N4O2S3. Mole weight: 350.44.
Ceftriaxone EP Impurity E
An impurity of Ceftriaxone, a cephalosporin antibiotic for the treatment of various bacterial infections. Synonyms: Deacyl ceftriaxone; (6R,7R)-7-Amino-8-oxo-3-[[(1,2,5,6-tetrahydro-2-methyl-5,6-dioxo-1,2,4-triazin-3-yl)thio]methyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid. Grade: > 95%. CAS No. 58909-56-1. Molecular formula: C12H13N5O5S2. Mole weight: 371.4.
Ceftriaxone Impurity 1
Ceftriaxone Impurity 1. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (E)-S-benzo[d]thiazol-2-yl 2-(2-aminothiazol-4-yl)-2-(methoxyimino)ethanethioate. CAS No. 1684396-27-7. Molecular formula: C13H10N4O2S3. Mole weight: 350.44. Catalog: APB1684396277.
Ceftriaxone monosodium salt
Ceftriaxone sodium is a broad-spectrum antibiotic used to treat a variety of bacterial infections. Ceftriaxone belongs to the cephalosporin class of antibiotics and works by interfering with bacterial cell wall synthesis. It binds to and inhibits bacterial penicillin-binding proteins (PBPs), which are enzymes involved in the final step of peptidoglycan synthesis in the bacterial cell wall. This action weakens the cell wall, leading to bacterial cell death. Ceftriaxone is indicated for the treatment of various bacterial infections, including lower respiratory tract infections (such as pneumonia), urinary tract infections (including pyelonephritis), skin and soft tissue infections, intra-abdominal cavity infections, bone and joint infections, septicaemia and meningitis. Synonyms: Ceftriaxone Sodium; 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-8-oxo-3-[[(1,2,5,6-tetrahydro-2-methyl-5,6-dioxo-1,2,4-triazin-3-yl)thio]methyl]-, sodium salt (1:1), (6R,7R)-; Ceftriaxone sodium salt; (6R,7R)-7-[[(2Z)-2-(2-Amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-8-oxo-3-[[(1,2,5,6-tetrahydro-2-methyl-5,6-dioxo-1,2,4-triazin-3-yl)thio]methyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid sodium salt; Biotrakson sodium salt; Epicephin sodium salt; Rocephalin sodium salt. Grade: ≥95%. CAS No. 958633-51-7. Molecular formula: C18H17N8NaO7S3. Mole we
Ceftriaxone sodium
1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C18H18N8Na2O7S3. CAS No. 74578-69-1. Prepack ID 89992119-1g. Molecular Weight 598.55. See USA prepack pricing.
A broad-spectrum cephalosporin antibiotic and cefotaxime derivative with a very long half-life and high penetrability to meninges, eyes and inner ears. Alternative Names: [(2S)-1-(4-amino-2-oxopyrimidin-1-yl)-3-hydroxypropan-2-yl]oxymethylphosphonic acid. Ro-139904. CAS No. 74578-69-1. Product ID: API74578691. Molecular formula: C18H17N8NaO7S3. Mole weight: 576.6. EINECS: 277-930-0. SMILES: CN1C(=NC(=O)C(=O)N1)SCC2=C(N3C(C(C3=O)NC(=O)C(=NOC)C4=CSC(=N4)N)SC2)C(=O)[O-].[Na+]. Appearance: White solid. Category: Antibacterial APIs.
Ceftriaxone Sodium is an antibiotic, a third-generation cephalosporin. It has broad-spectrum activity against Gram-positive bacteria and expanded Gram-negative coverage. lt is useful for the treatment of a number of bacterial infections, includeing ear infections, skin infections, urinary tract infections, pneumonia, gonorrhea, pelvic inflammatory disease, bone and joint infections, intra-abdominal infections, and meningitis and so on. It is used preoperatively to reduce the risk of postoperative infections. It inhibits bacterial cell wall synthesis by means of binding to the penicillin-binding proteins. It is a stimulator of EAAT2 expression with neuroprotective effects in both in vitro and in vivo models, which is based in part on its ability to inhibit neuronal cell death by glutamate excitotoxicity. It may have potential to manipulate glutamate transmission and ameliorate neurotoxicity. It is administered by intravenous or intramuscular injection. Uses: Ceftriaxone sodium is useful for the treatment of a number of bacterial infections. it is used preoperatively to reduce the risk of postoperative infections. it inhibits bacterial cell wall synthesis by means of binding to the penicillin-binding proteins. it is a stimulator of eaat2 expression with neuroprotective effects in both in vitro and in vivo models, which is based in part on its ability t. Synonyms: 2,5,6-tetrahydro-2-methyl-5,6-dioxo-)(methoxyimino)acetyl)
Ceftriaxone sodium 3.5 hydrate
Ceftriaxone sodium 3.5 hydrate. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: sodium (6R,7R)-7-((E)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido)-3-(((2-methyl-6-oxido-5-oxo-2,5-dihydro-1,2,4-triazin-3-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate,disodium salt,hemiseptahydrate. CAS No. 104376-79-6. Molecular formula: C18H16N8Na2O7S3·3·5H2O. Mole weight: 661.60. Catalog: APB104376796.
Ceftriaxone sodium E-isomer
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Ceftriaxone sodium hydrate
Ceftriaxone sodium hydrate (Ro 13-9904 sodium hydrate) is a broad spectrum β-lactam third-generation cephalosporin antibiotic, which has good antibacterial activity against a variety of gram-negative and positive bacteria. Ceftriaxone sodium hydrate is a covalent inhibitor of GSK3β with IC 50 value of 0.78 μM. Ceftriaxone sodium hydrate is an inhibitor of Aurora B. Ceftriaxone sodium hydrate has anti-inflammatory, antitumor and antioxidant activities. Ceftriaxone sodium hydrate can be used in the study of bacterial infections and meningitis [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 13-9904 sodium hydrate. CAS No. 104376-79-6. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B0712A.
Ceftriaxone sodium hydrate (2:4:7)
Ceftriaxone sodium hydrate is a third-generation cephalosporin antibiotic. Synonyms: Ceftriaxone Disodium Salt Hemiheptahydrate; (6R,7R)-7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-8-oxo-3-[[(1,2,5,6-tetrahydro-2-methyl-5,6-dioxo-1,2,4-triazin-3-yl)thio]methyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, disodium salt, hemiheptahydrate; Rocefin; Rocephine. Grade: Assay: ≥ 795 μg/mg. CAS No. 104376-79-6. Molecular formula: C18H16N8O7S3.7/2H2O.2Na. Mole weight: 661.60.
Ceftriaxone sodium salt
1g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C18H16N8Na2O7S3 · 3.5H2O. CAS No. 104376-79-6. Prepack ID 10212773-1g. Molecular Weight 661.6. See USA prepack pricing.
Ceftriaxone sodium salt
Ceftriaxone sodium salt (Ro 13-9904) is a broad spectrum β-lactam third-generation cephalosporin antibiotic, which has good antibacterial activity against a variety of gram-negative and positive bacteria. Ceftriaxone sodium salt is a covalent inhibitor of GSK3β with IC 50 value of 0.78 μM. Ceftriaxone sodium salt is an inhibitor of Aurora B. Ceftriaxone sodium salt has anti-inflammatory, antitumor and antioxidant activities. Ceftriaxone sodium salt can be used in the study of bacterial infections and meningitis [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 13-9904. CAS No. 74578-69-1. Pack Sizes: 100 mg; 500 mg. Product ID: HY-B0712B.
Ceftriaxone Sodium Sterile
Ceftriaxone disodium salt is a third generation semisynthetic cephalosporin antibiotic, which is chemically synthesized form 7-aminocephalosporanic acid (7-ACA). It has a broad spectrum of activity against Gram-positive and Gram-negative aerobic and anaerobic bacteria, and is generally more active against Gram-negative bacteria than the first and second generation cephalosporins. It has increased stability to β-lactamases compared with the first and second generation cephalosporins. Incorporation of the triazine substituted side chain into the 3-position of the cephalosporin nucleus markedly prolong serum half-life. Synonyms: Ceftriaxone sodium, Disodium (6R, 7R)-7-[[ (2Z)- (2-aminothiazol-4-yl) (methoxyimino)acetyl]amino]-3-[[ (2-methyl-6-oxido-5-oxo-2, 5-dihydro-1, 2, 4-triazin-3-yl)sulfanyl]methyl]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylate 3.5 hydrate, 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-8-oxo-3-[[(1,2,5,6-tetrahydro-2-methyl-5,6. CAS No. 104376-79-6. Product ID: PAP-0096. Molecular formula: C18H16N8Na2O7S3·31/2H2O. Mole weight: 661.58. Product Keywords: Antibacterial, Anti-inflammatory and Antiviral Series; PAP-0096; Ceftriaxone Sodium Sterile; 104376-79-6; Ceftriaxone sodium, Disodium (6R, 7R)-7-[[ (2Z)- (2-aminothiazol-4-yl) (methoxyimino)acetyl]amino]-3-[[ (2-methyl-6-oxido-5-oxo-2, 5-dihydro-1, 2, 4-triazin-3-yl)
Cefuracetime
SKF81367 is a cephalosporin antibiotic. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SKF81367. CAS No. 39685-31-9. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-U00154.
It is produced by the strain of Semisynthetic second generation cephalosporin. Cefuroxime is an orally active second-generation cephalosporin antibiotic with increased stability to β-lactamase. Cefuroxime has a broad spectrum activity against Gram-positive and Gram-negative bacteria. Synonyms: Cephuroxime; Cefuroxim; Cefuroximo; Cefuroximum; Sharox; Zinacef; Biofuroksym; Cefuril; (6R,7R)-7-(2-(2-Furyl)glyoxylamido)-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid 7(sup 2)-(Z)-(O-methyloxime) carbamate (ester). Grade: 98%. CAS No. 55268-75-2. Molecular formula: C16H16N4O8S. Mole weight: 424.39.
Cefuroxime
1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H16N4O8S. CAS No. 55268-75-2. Prepack ID 17592387-1g. Molecular Weight 424.39. See USA prepack pricing.
Cefuroxime
Cefuroxime is an orally active second-generation cephalosporin antibiotic with increased stability to β-lactamase. Cefuroxime has a broad spectrum activity against Gram-positive and Gram-negative bacteria [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Kefurox. CAS No. 55268-75-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-B1256A.
Cefuroxime axetil
Cefuroxime is a cephalosporin antibiotic. It is used to treat many kinds of bacterial infections, including severe or life-threatening forms. Cefuroxime axetil is a prodrug of the cephalosporin cefuroxime, which is a second generation oral cephalosporin antibiotic with in vitro antibacterial activity against several gram-positive and gram-negative organisms. Synonyms: Cefuroxime 1-acetoxyethyl ester; Elobact. Grade: ≥97%. CAS No. 64544-07-6. Molecular formula: C20H22N4O10S. Mole weight: 510.47.
Cefuroxime axetil
Cefuroxime Axetil, a proagent of the cephalosporin cefuroxime and an oarl broad spectrum antibiotic, inhibits several gram-positive and gram-negative organisms, including those most frequently associated with various common community-acquired infections [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 64544-07-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B1325.
Cefuroxime Axetil
It is the 1-(acetyloxy) ethyl ester of Cefuroxime , an injectable second generation cephalosporin with an excellent antibacterial activity. This ester has a broader spectrum of activity than cephalexin (first-generation) and is widely used to treat respiratory tract infections. Antibacterial. Group: Biochemicals. Alternative Names: (6R, 7R) -3-[[ (Aminocarbonyl) oxy]methyl]-7-[[ (2Z) -2- (2-furanyl) -2- (methoxyimino) acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid 1-(Acetyloxy)ethyl Ester; Altacef; Bioracef; CCI 15641; Cefaks; Cefazine; Ceftin; Cefurax; Cefuroxime 1-Acetoxyethyl Ester; Elobact; Forcef; Oraxim; Zinat; Zinnat. Grades: Highly Purified. CAS No. 64544-07-6. Pack Sizes: 100mg. US Biological Life Sciences.
Worldwide
Cefuroxime Axetil
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsbritish pharmacopoeiaeuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: (1RS)-1-(acetyloxy)ethyl (6R,7R)-3-[(carbamoyloxy)methyl]-7-[[(Z)-2-(furan-2-yl)-2(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate, CCI 15641,Cefuroxime axetil, Cefuroxime Ester E47.
Cefuroxime Axetil (Amorphous)
Oral antibiotic. Alternative Names: Ceftin. Elobact. Zinnat. Zinat. CAS No. 64544-07-6. Product ID: API64544076. Molecular formula: C20H2N4O10S. Mole weight: 510.48. EINECS: 638-760-6. SMILES: CC(OC(=O)C)OC(=O)C1=C(CSC2N1C(=O)C2NC(=O)C(=NOC)C3=CC=CO3)COC(=O)N. Appearance: White to almost white powder. Standard: EP/USP/BP. Category: Antibacterial APIs.
Cefuroxime Axetil Delta-3
Δ2-Cefuroxime axetil is an oral prodrug of cefuroxime, a second-generation cephalosporin antibiotic. This compound inhibits bacterial cell wall synthesis by targeting penicillin-binding proteins (PBPs), making it effective against a broad spectrum of Gram-positive and Gram-negative bacteria. It is commonly prescribed for respiratory, urinary tract, and skin infections. Synonyms: 1-Acetoxyethyl (6R,7R)-3-((carbamoyloxy)methyl)-7-((Z)-2-(furan-2-yl)-2-(methoxyimino)acetamido)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylate; 5-Thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylic acid, 3-[[(aminocarbonyl)oxy]methyl]-7-[[(2Z)-2-furanyl(methoxyimino)acetyl]amino]-8-oxo-, 1-(acetyloxy)ethyl ester, (6R,7R)-; 5-Thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylic acid, 3-[[(aminocarbonyl)oxy]methyl]-7-[[2-furanyl(methoxyimino)acetyl]amino]-8-oxo-, 1-(acetyloxy)ethyl ester, [6R-[6α,7β(Z)]]-; Cefuroxime Axetil Impurity A (Delta 3-Isomer); Cefuroxime Axetil EP Impurity A; Cefuroxime Axetil Impurity A (EP); Δ2-Cefuroxime axetil; delta3-Cefuroxime axetil. Grade: 95%. CAS No. 123458-61-7. Molecular formula: C20H22N4O10S. Mole weight: 510.47.
Cefuroxime Axetil Delta-3-Isomers
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Cefuroxime Axetil E-isomers
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Cefuroxime axetil Impurity A
Cefuroxime axetil Impurity A. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (6R,7R)-1-acetoxyethyl 3-((carbamoyloxy)methyl)-7-((Z)-2-(furan-2-yl)-2-(methoxyimino)acetamido)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylate. CAS No. 123458-61-7. Molecular formula: C20H22N4O10S. Mole weight: 510.47. Catalog: APB123458617.
Cefuroxime Axetil Impurity E
(αZ)-α-(Methoxyimino)-N-[(5aR,6R)-1,4,5a,6-tetrahydro-1,7-dioxo-3H,7H-azeto[2,1-b]furo[3,4-d][1,3]thiazin-6-yl]-2-furanacetamide is an impurity of Cefuroxime Axetil, the 1-(acetyloxy) ethyl ester of Cefuroxime , an injectable second generation cephalosporin with an excellent antibacterial activity. Synonyms: (αZ)-α-(Methoxyimino)-N-[(5aR,6R)-1,4,5a,6-tetrahydro-1,7-dioxo-3H,7H-azeto[2,1-b]furo[3,4-d][1,3]thiazin-6-yl]-2-furanacetamide. Grade: > 95%. CAS No. 947723-87-7. Molecular formula: C15H13N3O6S. Mole weight: 363.35.
Cefuroxime Axetil Sulfoxide
Cefuroxime axetil sulfoxide is an oxidized derivative of cefuroxime axetil, where the sulfur atom in the dihydrothiazine ring is converted into a sulfoxide group (-S=O). This modification can occur during metabolism or storage due to oxidative processes. While the parent compound, cefuroxime axetil, is a prodrug designed to enhance oral bioavailability of cefuroxime, the sulfoxide derivative may exhibit altered pharmacokinetics and reduced antibacterial activity because the conversion to the active cefuroxime may be compromised. This compound is of interest in stability studies, drug degradation analysis, and understanding the effects of oxidation on the efficacy of β-lactam antibiotics. Synonyms: 1-(Acetyloxy)ethyl (6R,7R)-3-[[(aminocarbonyl)oxy]methyl]-7-[[(2Z)-2-(2-furanyl)-2-(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate 5-oxide; 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[[(aminocarbonyl)oxy]methyl]-7-[[2-furanyl(methoxyimino)acetyl]amino]-8-oxo-, 1-(acetyloxy)ethyl ester, 5-oxide, [6R-[6α,7β(Z)]]-; Cefuroxime axetil Sulfoxide; Cefuroxime Axetil Sulfoxide Mixture. Grade: ≥95%. CAS No. 136235-54-6. Molecular formula: C20H22N4O11S. Mole weight: 526.47.
Cefuroxime-d3
Labeled Cefuroxime. Antibacterial. Group: Biochemicals. Alternative Names: (6R, 7R) -3-[[ (Aminocarbonyl) oxy]methyl]-7-[[ (2Z) -2-furanyl (methoxy-d3-imino) acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Cefuroxime sodium
Cefuroxime sodium is an orally active second-generation cephalosporin antibiotic with increased stability to β-lactamase. Cefuroxime sodium has a broad spectrum activity against Gram-positive and Gram-negative bacteria. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. CAS No. 56238-63-2. Molecular formula: C16H15N4NaO8S. Mole weight: 446.37. Purity: 0.9933. Product ID: ACM56238632. Alfa Chemistry ISO 9001:2015 Certified.
Cefuroxime sodium
Cefuroxime sodium is an orally active second-generation cephalosporin antibiotic with increased stability to β-lactamase. Cefuroxime sodium has a broad spectrum activity against Gram-positive and Gram-negative bacteria [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 56238-63-2. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-B1256.
Cefuroxime sodium
Cefuroxime sodium is a second-generation cephalosporin antibiotic resistant to beta-lactamase. It has a broad-spectrum antimicrobial activity against Gram-positive and Gram-negative bacteria. Uses: Anti-bacterial agents. Synonyms: Anaptivan; Biociclin; Biofurex; (6R,7R)-3-[[(Aminocarbonyl)oxy]methyl]-7-[[(2Z)-2-furanyl(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid Sodium Salt; Cefurin; Duxima; Novocef; Zinacef. Grade: ≥95%. CAS No. 56238-63-2. Molecular formula: C16H15N4NaO8S. Mole weight: 446.36.
Cefuroxime Sodium
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitesstandards for environmental regulatory methodspharma & vet compounds & metabolitesapi standardsbritish pharmacopoeiaeuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: 640/3, 750/2, 640/2,Cefuroxime Axetil Imp. D (EP), 640/1, Cefuroxime sodium, SB, 640/68, Sodium (6R,7R)-3-[(carbamoyloxy)methyl]-7-[[(Z)-(furan-2-yl)(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate, 750/359, GSK682709A, Cefuroxime Sodium (640/359), SD, SC, SA, GSK682708A.
Cefuroxime Sodium
This product is the second generation of cephalosporin for injection. It is stable against the broad spectrum β-lactamase produced by gram-negative bacilli. The stability of β-lactamase is similar to that of the third generation. The activity against gram-positive bacilli was stronger than that of the first generation Chemicalbook cephalosporin, but lower than that of the third generation cephalosporin. The effect on gram-positive bacteria (including zyme-resistant Staphylococcus aureus) was similar to or slightly worse than that of first-generation cephalosporins, but stronger than that of third-generation cephalosporins. CAS No. 56238-63-2. Product ID: PAP-0066. Molecular formula: C16H15N4O8S.Na. Category: Antibiotic. Product Keywords: Antibacterial, Anti-inflammatory and Antiviral Series; Cefuroxime Sodium; PAP-0066; Antibiotic; C16H15N4O8S.Na; 56238-63-2. Appearance: Neat. Standard: USP/EP. Color: White to Pale Beige. EC Number: 260-073-1. Physical State: neat. Solubility: Freely soluble in water, very slightly soluble in ethanol (96 per cent). Storage: Inert atmosphere,2-8°C. Applications: For sensitive bacteria caused by respiratory system, genitourinary system, bone and joint, skin and soft tissue and prevention of surgery and other infections as well as sepsis, meningitis and so on. Melting Point: 240-245°C(dec).
Cefuroxime Sodium Impurity A (Cefuroxime Descarbamoyl)
A degradation product of Cefuroxime, and an intermediate for the synthesis of Cephalosporin antibiotics. Synonyms: (6R,7R)-7-[[(2Z)-2-(2-Furanyl)-2-(methoxyimino)acetyl]amino]-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid; Cefuroxime Sodium Impurity F (EP). Grade: > 95%. CAS No. 56271-94-4. Molecular formula: C15H15N3O7S. Mole weight: 381.37.
1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H15N4NaO8S. CAS No. 56238-63-2. Prepack ID 26234809-1g. Molecular Weight 446.37. See USA prepack pricing.
Antibacterial. Group: Biochemicals. Alternative Names: (6R, 7R) -3-[[ (Aminocarbonyl) oxy]methyl]-7-[[ (2Z) -2-furanyl (methoxyimino) acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid Sodium Salt. Grades: Highly Purified. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
Cefuroxime Sodium (Sterile)
Antibiotic for injection. Alternative Names: Sodium cefuroxime. Anaptivan. Biociclin. Cefuroxime sodium salt. CAS No. 56238-63-2. Product ID: API56238632. Molecular formula: C16H15N4NaO8S. Mole weight: 446.37. EINECS: 260-073-1. SMILES: CON=C(C1=CC=CO1)C(=O)NC2C3N(C2=O)C(=C(CS3)COC(=O)N)C(=O)[O-].[Na+]. Appearance: White to yellowish powder or crystalline powder. Standard: EP/USP/BP. Category: Antibacterial APIs.
Cefuzonam
It is produced by the strain of Semisynthetic third generation cephalosporin for injection. It has the third-generation cephalosporin commonness. It is characterized by stronger anti-gram-positive bacterial activity than other species of the same generation. Synonyms: Cefuzoname; Cefuzonamum; 7beta-{[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetyl]amino}-3-[(1,2,3-thiadiazol-5-ylsulfanyl)methyl]-3,4-didehydrocepham-4-carboxylic acid. Grade: ≥ 95%. CAS No. 82219-78-1. Molecular formula: C16H15N7O5S4. Mole weight: 513.59.