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Cefdinir Impurity 7 is one of Cefdinir impurities. Cefdinir is a semi-synthetic, broad-spectrum antibiotic, used for soft tissue infections and respiratory tract infections. Molecular formula: C17H18N2O4S. Mole weight: 346.40.
Cefdinir Impurity A
(αZ)-2-Amino-α-(hydroxyimino)-4-thiazoleacetamide is an impurity/ degradation product of Cefdinir ; a cephalosporin antibiotic structurally similar to Cefixime. Synonyms: (Z)-2-(2-Aminothiazol-4-yl)-2-(hydroxyimino)acetamide; Cefdinir Impurity A. Grades: > 95%. CAS No. 1450758-21-0. Molecular formula: C5H6N4O2S. Mole weight: 186.19.
Cefdinir Impurity B
Cefdinir Impurity B is one of Cefdinir impurities. Cefdinir is a semi-synthetic, broad-spectrum antibiotic, used for soft tissue infections and respiratory tract infections. Molecular formula: C14H13N5O6S2. Mole weight: 411.41.
Cefdinir Impurity H
Cefdinir Impurity H is one of Cefdinir impurities. Cefdinir is a semi-synthetic, broad-spectrum antibiotic, used for soft tissue infections and respiratory tract infections. Synonyms: Cefdinir impurity H; 178949-04-7; Cefdinir decarboxy open ring lactone; 2O1193FN39; (2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-hydroxyimino-N-[(5-methyl-7-oxo-1,2,4,5-tetrahydrofuro[3,4-d][1,3]thiazin-2-yl)methyl]acetamide; (Z)-2-(2-Aminothiazol-4-yl)-2-(hydroxyimino)-N -(((2RS,5RS)-5-methyl-7-oxo-2,4,5,7-tetrahydro-1H -furo(3,4-d)(1,3)thiazin-2-yl)methyl(acetamide; 2-(2-Aminothiazol-4-yl)-2-(hydroxyimino)-N -(((2RS,5RS)-5-methyl-7-oxo-2,4,5,7-tetrahydro-1H -furo(3,4-d)(1,3)thiazin-2-yl)methyl(acetamide, (Z)-; UNII-2O1193FN39; SCHEMBL23871786; (Z)-2-(2-Aminothiazol-4-yl)-2-(hydroxyimino)-N-{[(2RS,5RS)-5-methyl-7-oxo-2,4,5,7-tetrahydro-1H-furo[3,4-d][1,3]thiazin-2-yl]methyl}acetamide; 4-Thiazoleacetamide, 2-amino-alpha-(hydroxyimino)-N-((1,2,5,7-tetrahydro-5-methyl-7-oxo-4H-furo(3,4-d)(1,3)thiazin-2-yl)methyl)-; 4-THIAZOLEACETAMIDE, 2-AMINO-.ALPHA.-(HYDROXYIMINO)-N-((1,2,5,7-TETRAHYDRO-5-METHYL-7-OXO-4H-FURO(3,4-D)(1,3)THIAZIN-2-YL)METHYL)-. Molecular formula: C14H15N5O6S2. Mole weight: 413.43.
Cefdinir Impurity I
Cefdinir Impurity I is one of Cefdinir impurities. Cefdinir is a semi-synthetic, broad-spectrum antibiotic, used for soft tissue infections and respiratory tract infections. Molecular formula: C14H15N5O6S2. Mole weight: 413.43.
Cefdinir Impurity J
Cefdinir Impurity J is one of Cefdinir impurities. Cefdinir is a semi-synthetic, broad-spectrum antibiotic, used for soft tissue infections and respiratory tract infections. Molecular formula: C14H15N5O6S2. Mole weight: 413.43.
Cefdinir Impurity K
Cefdinir Impurity K is one of Cefdinir impurities. Cefdinir is a semi-synthetic, broad-spectrum antibiotic, used for soft tissue infections and respiratory tract infections. Molecular formula: C14H15N5O6S2. Mole weight: 413.43.
Cefdinir Impurity L
Cefdinir Impurity L is one of Cefdinir impurities. Cefdinir is a semi-synthetic, broad-spectrum antibiotic, used for soft tissue infections and respiratory tract infections. Molecular formula: C14H15N5O6S2. Mole weight: 413.43.
Cefdinir Impurity P
Cefdinir Impurity P is one of Cefdinir impurities. Cefdinir is a semi-synthetic, broad-spectrum antibiotic, used for soft tissue infections and respiratory tract infections. Molecular formula: C14H15N5O6S2. Mole weight: 413.43.
Cefdinir Impurity Q
Cefdinir Impurity Q is one of Cefdinir impurities. Cefdinir is a semi-synthetic, broad-spectrum antibiotic, used for soft tissue infections and respiratory tract infections. Molecular formula: C14H15N5O6S2. Mole weight: 413.43.
Cefdinir Impurity T
Cefdinir Impurity T is one of Cefdinir impurities. Cefdinir is a semi-synthetic, broad-spectrum antibiotic, used for soft tissue infections and respiratory tract infections. Molecular formula: C13H15N5O4S2. Mole weight: 369.42.
Cefdinir Impurity U
Cefdinir Impurity U is one of Cefdinir impurities. Cefdinir is a semi-synthetic, broad-spectrum antibiotic, used for soft tissue infections and respiratory tract infections. Molecular formula: C13H15N5O4S2. Mole weight: 369.42.
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Cefdinir Related Compound B
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Cefdinir Related Compound B
(6R-trans)-7-[[(2-Amino-4-thiazolyl)acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid, is the impurity of Cefdinir , a Cephalosporin antibiotic structurally similar to Cefixime. It can be used to treat infections caused by several Gram-negative and Gram-positive bacteria. Synonyms: (6R-trans)-7-[[(2-Amino-4-thiazolyl)acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid. Grades: > 95%. CAS No. 79350-10-0. Molecular formula: C14H14N4O4S2. Mole weight: 366.42.
Cefdinir Sulfoxide
Cefdinir Sulfoxide is the oxide derivative of Cefdinir; a Cephalosporin antibiotic structurally similar to Cefixime. Synonyms: (6R,7R)-7-[[(2Z)-2-(2-Amino-4-thiazolyl)-2-(hydroxyimino)acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid 5-Oxide. Grades: > 95%. CAS No. 934986-48-8. Molecular formula: C14H13N5O6S2. Mole weight: 411.42.
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. Grades: 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 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
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 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)?-. Grades: > 95%. CAS No. 104145-95-1. Molecular formula: C19H18N6O5S3. Mole weight: 506.58.
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.
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. Grades: ≥ 98%. CAS No. 117467-28-4. Molecular formula: C25H28N6O7S3. Mole weight: 620.72.
Cefditoren pivoxil
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
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 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. Grades: >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. Grades: ≥ 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-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
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
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 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 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·HCl
Cefepime·HCl. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences.
Worldwide
Cefepime hydrochloride
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Anticefepime is an impurity of Cefepime, an fourth generation cephalosporin antibiotic. Synonyms: 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-pyrrolidinium inner salt; Cefepime Impurity A. Grades: > 95%. CAS No. 97164-57-3. Molecular formula: C19H24N6O5S2. Mole weight: 480.57.
Cefepime Impurity C
A metabolite of Cefditorin , a new oral cephem. Synonyms: (Z)-2-Amino-α-(methoxyimino)-N-(2-oxoethyl)-4-thiazoleacetamide; THR 221V; Cefepime Impurity. Grades: > 95%. CAS No. 104301-63-5. Molecular formula: C8H10N4O3S. Mole weight: 242.26.
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 D
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Cefepime Related Compound E
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
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. Grades: > 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.
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. Grades: > 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 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
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
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. Grades: 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
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. Grades: 98%. CAS No. 1225208-94-5. Molecular formula: C30H34ClN7O10S2. Mole weight: 752.22.
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.
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 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.