Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the American suppliers website for prices, SDS or more information. You can also view suppliers in Australia, NZ or the UK.
| Product | Description | |
|---|---|---|
| Methicillin sodium | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. |  |
| Methicillin Sodium | The sodium salt of Meticillin, a β-lactam antibiotic, could be obtained through semi-synthetic and used as an antibacterial agent especially against Gram-positive bacteria. Synonyms: Azapen; BRL 1241; Belfacillin; Celbenin; Sodium 6-(2',6'-dimethoxybenzamido)penicillanate; Penaureus; Sodium Methicillin; Staficyn; Staphcillin; Synticillin; 2-carboxylic acid sodium salt; Belfacillin; Penaureus. Grade: 96%. CAS No. 132-92-3. Molecular formula: C17H19N2NaO6S. Mole weight: 402.40. |  |
| Methicillin sodium salt | Methicillin sodium salt (Meticillin sodium) is a ?-lactam, semi-synthetic antibiotic related to penicillin antibiotic. Methicillin sodium salt inhibits penicillin-binding proteins involved in the synthesis of peptidoglycan. Methicillin sodium salt inhibits S. aureus with a MIC value of 2.1 ?g/mL. Methicillin sodium salt can be used for the research of inflammation[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Meticillin sodium. CAS No. 132-92-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0974. |  |
| Methicillin Sodium, USP | Methicillin sodium is a narrow spectrum β-lactam antibiotic related to Penicillin. β-lactams interfere with PBP (penicillin binding protein) activity involved in the final phase of peptidoglycan synthesis. PBPs are enzymes which catalyze a pentaglycine crosslink between alanine and lysine residues providing additional strength to the cell wall. Without a pentaglycine crosslink, the integrity of the cell wall is severely compromised and ultimately leads to cell lysis and death. Resistance to β-lactams is commonly due to cells containing plasmid encoded β-lactamases. Methicillin is mostly resistant to β-lactamases. Methicillin targets primarily the cell wall of Gram positive organisms especially Staphylococcus aureus. Group: Biochemicals. Alternative Names: Sodium (2, 6-dimethoxyphenyl) penicillin; (2S, 5R, 6R) -6-[ (2, 6-Dimethoxybenzoyl) amino]-3, 3-dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Sodium Salt; Meticillin; Staphcillin. Grades: USP. CAS No. 132-92-3. Pack Sizes: 50mg, 250mg, 500mg. US Biological Life Sciences. |  Worldwide |
| 24-Bromo-fusidic acid sodium salt | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: 29-Nordammara-17(20),24-dien-21-oic acid, 16-(acetyloxy)-24-bromo-3,11-dihydroxy-, sodium salt (1:1), (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-; (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-16-(Acetyloxy)-24-bromo-3,11-dihydroxy-29-nordammara-17(20),24-dien-21-oic acid sodium salt; 24-Bromofusidic acid sodium salt; Zibrofusidic acid sodium salt. Grade: ≥95%. CAS No. 827603-99-6. Molecular formula: C31H46BrNaO6. Mole weight: 617.60. | |
| 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid,6-[(2,6-dimethoxybenzoyl)amino]-3,3-dimethyl-7-oxo-,sodium salt(1:1),(2S,5R,6R)- | 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid,6-[(2,6-dimethoxybenzoyl)amino]-3,3-dimethyl-7-oxo-,sodium salt(1:1),(2S,5R,6R)-. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (2S,5R,6R)-6-[(2,6-Dimethoxybenzoyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo [3.2.0]heptane-2-carboxylic Acid Sodium Salt. Product Category: Heterocyclic Organic Compound. CAS No. 132-92-3. Molecular formula: C17H20N2O6S.Na. Mole weight: 402.39733. Density: g/cm³. Product ID: ACM132923. Alfa Chemistry ISO 9001:2015 Certified. Categories: METHICILLIN SODIUM. |  |
| BO3482 | BO3482, a dithiocarbamate carbapenem, inhibits the growth of methicillin-resistant Staphylococci (MRS) (MIC90= 6.25 mg/mL) and has a dithiocarbamate chain at the C-2 position of 1beta-methyl-carbapenem. Synonyms: BO3482; BO 3482; BO-3482; (4R,5S,6S)-6-[(1R)-1-hydroxyethyl]-3-[2-hydroxyethyl(methyl)carbamothioyl]sulfanyl-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid; sodium. CAS No. 198013-53-5. Molecular formula: C14H20N2NaO5S2. Mole weight: 383.44. | |
| 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. | |
| Fusidic Acid EP Impurity A | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(24SR,17Z)-16α-(Acetyloxy)-3β,11β,24,25-tetrahydroxy-4β,8,14-trimethyl-18-nor-5β,10αcholest-17(20)-en-21-oic acid; 24,25-Dihydro-24,25-dihydroxyfusidic acid; Fusidic Acid Impurity A; Sodium Fusidate EP Impurity A. Grade: ≥95%. Molecular formula: C31H50O8. Mole weight: 550.73. | |
| Fusidic Acid EP Impurity B | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z)-3β,11β-Dihydroxy-17-[(6SR)-6-hydroxy-7,7-dimethyl-2-oxooxepan-3-ylidene]-4β,8,14-trimethyl-18-nor-5β,10α-androstan-16α-yl acetate; 24,25-Dihydro-24,25-dihydroxyfusidic acid 21,25-lactone; Fusidic Acid Impurity B; Sodium Fusidate EP Impurity B; (3R,4S,5S,8S,9S,10S,11R,13R,14S,16S,Z)-3,11-dihydroxy-17-((SR)-6-hydroxy-7,7-dimethyl-2-oxooxepan-3-ylidene)-4,8,10,14-tetramethylhexadecahydro-1H-cyclopenta[a]phenanthren-16-yl acetate. Grade: ≥95%. Molecular formula: C31H48O7. Mole weight: 532.72. | |
| Fusidic Acid EP Impurity C | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z)-3β,11β-Dihydroxy-17-[(6S)-6-(1-hydroxy-1-methylethyl)-2-oxodihydro-2H-pyran-3(4H)-ylidene]-4β,8,14-trimethyl-18-nor-5β,10α-androstan-16α-yl acetate; (24R)-24,25-Dihydro-24,25-dihydroxyfusidic acid 21,24-lactone; Fusidic Acid Impurity C; (3R,4S,5S,8S,9S,10S,11R,13R,14S,16S,Z)-3,11-Dihydroxy-17-((R)-6-(2-hydroxypropan-2-yl)-2-oxodihydro-2H-pyran-3(4H)-ylidene)-4,8,10,14-tetramethylhexadecahydro-1H-cyclopenta[a]phenanthren-16-yl acetate; Sodium Fusidate EP Impurity C. Grade: ≥95%. CAS No. 3054708-75-4. Molecular formula: C31H48O7. Mole weight: 532.72. | |
| Fusidic Acid EP Impurity D | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z)-3β,11β-Dihydroxy-17-[(6R)-6-(1-hydroxy-1-methylethyl)-2-oxodihydro-2H-pyran-3(4H)-ylidene]-4β,8,14-trimethyl-18-nor-5β,10α-androstan-16α-yl acetate; (24S)-24,25-Dihydro-24,25-dihydroxyfusidic acid 21,24-lactone; Fusidic Acid Impurity D; (3R,4S,5S,8S,9S,10S,11R,13R,14S,16S,Z)-3,11-Dihydroxy-17-((S)-6-(2-hydroxypropan-2-yl)-2-oxodihydro-2H-pyran-3(4H)-ylidene)-4,8,10,14-tetramethylhexadecahydro-1H-cyclopenta[a]phenanthren-16-yl acetate; Sodium Fusidate EP Impurity D. Grade: ≥95%. CAS No. 3054708-76-5. Molecular formula: C31H48O7. Mole weight: 532.72. | |
| Fusidic Acid EP Impurity E | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z,24EZ)-16α-(Acetyloxy)-3β,11β,26-trihydroxy-4β,8,14-trimethyl-18-nor-5β,10α-cholesta-17(20),24-dien-21-oic acid; 26-Hydroxyfusidic acid; Sodium Fusidate EP Impurity E; Fusidic Acid Impurity E; (3α,4α,5α,11α,16β,17Z)-16-(Acetyloxy)-3,11,26-trihydroxy-4,8,14-trimethyl-18-norcholesta-17(20),24-dien-21-oic acid; 26-Hydroxy Fusidic Acid; (2Z)-2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-Acetoxy-3,11-dihydroxy-4,8,10,14-tetramethylhexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)-7-hydroxy-6-methylhept-5-enoic acid. Grade: ≥95%. CAS No. 2802408-15-5. Molecular formula: C31H48O7. Mole weight: 532.71. | |
| Fusidic Acid EP Impurity F | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z,24EZ)-16α-(Acetyloxy)-3β,11β-dihydroxy-4β,8,14-trimethyl-26-oxo-18-nor-5β,10α-cholesta-17(20),24-dien-21-oic acid; 26-Oxofusidic acid; 27-oxo-Fusidic Acid; (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-16-(Acetyloxy)-3,11-dihydroxy-26-oxo-29-nordammara-17(20),24-dien-21-oic acid; Sodium Fusidate EP Impurity F; Fusidic Acid Impurity F; (2Z)-2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-Acetoxy-3,11-dihydroxy-4,8,10,14-tetramethylhexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)-6-methyl-7-oxohept-5-enoic acid. Grade: ≥95%. CAS No. 1415035-94-7. Molecular formula: C31H46O7. Mole weight: 530.70. | |
| Fusidic Acid EP Impurity G | A metabolite of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Uses: A metabolite of fusidic acid. Synonyms: (Z)-2-((4S,5S,8S,9S,10S,11R,13R,14S,16S)-16-Acetoxy-11-hydroxy-4,8,10,14-tetramethyl-3-oxohexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)-6-methylhept-5-enoic acid; 3-Ketofusidic acid; ent-(17Z)-16α-(Acetyloxy)-11β-hydroxy-4β,8,14-trimethyl-3-oxo-18-nor-5β,10α-cholesta-17(20),24-dien-21-oic acid; 3-Didehydrofusidic acid; (4α,8α,9β,11α,13α,14β,16β,17Z)-16-(Acetyloxy)-11-hydroxy-3-oxo-29-nordammara-17(20),24-dien-21-oic acid; 29-Nor-8α,9β,13α,14β-dammara-17(20),24-dien-21-oic acid, 11α,16β-dihydroxy-3-oxo-, 16-acetate, (Z)-; 3-Oxofusidic acid; 3-Keto Fusidic Acid; Fusidic Acid Impurity G; Sodium Fusidate EP Impurity G. Grade: ≥95%. CAS No. 4680-37-9. Molecular formula: C31H46O6. Mole weight: 514.69. | |
| Fusidic Acid EP Impurity H | A metabolite of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Uses: A metabolite of fusidic acid. Synonyms: ent-(17Z)-16α-(Acetyloxy)-3β-hydroxy-4β,8,14-trimethyl-11-oxo-18-nor-5β,10α-cholesta-17(20),24-dien-21-oic acid; 11-Didehydrofusidic acid; 11-Keto fusidic acid; 11-Monoketofusidic acid; (3α,4α,8α,9β,13α,14β,16β,17Z)-16-(Acetyloxy)-3-hydroxy-11-oxo-29-nordammara-17(20),24-dien-21-oic acid; 29-Nor-8α,9β,13α,14β-dammara-17(20),24-dien-21-oic acid, 3α,16β-dihydroxy-11-oxo-, 16-acetate, (Z)-; 11-Ketofusidic acid; 11-Oxofusidic acid; Fusidic Acid Impurity H; (Z)-2-((3R,4S,5S,8S,9S,10S,13R,14S,16S)-16-Acetoxy-3-hydroxy-4,8,10,14-tetramethyl-11-oxohexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)-6-methylhept-5-enoic acid; Sodium Fusidate EP Impurity H. Grade: ≥95%. CAS No. 16711-91-4. Molecular formula: C31H46O6. Mole weight: 514.69. | |
| Fusidic Acid EP Impurity I | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z)-3β,11β,16β-Trihydroxy-4β,8,14-trimethyl-18-nor-5β,10α-cholesta-17(20),24-dien-21-oic acid; 16-epi-Deacetylfusidic acid; (3α,4α,8α,9β,11α,13α,14β,16α,17Z)-3,11,16-Trihydroxy-29-nordammara-17(20),24-dien-21-oic acid; Deacetyl-16-epifusidic acid; 29-Nor-8α,9β,13α,14β-dammara-17(20),24-dien-21-oic acid, 3α,11α,16α-trihydroxy-, (Z)-; 16-Epideacetylfusidic acid; NSC 319631; Fusidic Acid Impurity I; (Z)-6-Methyl-2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16R)-3,11,16-trihydroxy-4,8,10,14-tetramethylhexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)hept-5-enoic acid; Sodium Fusidate EP Impurity I. Grade: ≥95%. CAS No. 5951-83-7. Molecular formula: C29H46O5. Mole weight: 474.68. | |
| Fusidic Acid EP Impurity J | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z)-3β,11β-Dihydroxy-4β,8,14-trimethyl-18-nor-5β,10α-cholesta-17(20),24-dieno-21(16β)-lactone; 16-epi-Deacetylfusidic acid 21,16-lactone; 29-Nor-8α,9β,13α,14β-dammara-17(20),24-dien-21-oic acid, 3α,11α,16α-trihydroxy-, γ-lactone; Deacetyl-16-epifusidic acid γ-lactone; (3α,4α,8α,9β,11α,13α,14β,16α)-3,11,16-Trihydroxy-29-nordammara-17(20),24-dien-21-oic acid, γ-lactone; Fusidic Acid Impurity J; (2aS,3S,4R,6aS,6bS,7R,8aR,11aR,12aS,12bS)-4,7-Dihydroxy-3,6a,12a,12b-tetramethyl-9-(4-methylpent-3-en-1-yl)-1,2,2a,3,4,5,6,6a,6b,7,8,8a,11a,12,12a,12b-hexadecahydro-10H-naphtho[2',1':4,5]indeno[2,1-b]furan-10-one; Sodium Fusidate EP Impurity J. Grade: ≥95%. CAS No. 13011-12-6. Molecular formula: C29H44O4. Mole weight: 456.66. | |
| Fusidic Acid EP Impurity K | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: 29-Nor-8α,9β,13α,14β-dammara-17(20),24-dien-21-oic acid, 3α,11α,16β-trihydroxy-, γ-lactone; 16-Deacetylfusidic acid γ-lactone; ent-(17Z)-3β,11β-dihydroxy-4β,8,14-trimethyl-18-nor-5β,10α-cholesta-17(20),24-dieno-21(16α)-lactone; Deacetylfusidic acid 21,16-lactone; 16-O-Deacetylfusidic acid lactone; (3α,4α,8α,9β,11α,13α,14β,16β)-3,11,16-Trihydroxy-29-nordammara-17(20),24-dien-21-oic acid, γ-lactone; (2aS,3S,4R,6aS,6bS,7R,8aR,11aS,12aS,12bS)-4,7-Dihydroxy-3,6a,12a,12b-tetramethyl-9-(4-methylpent-3-en-1-yl)-1,2,2a,3,4,5,6,6a,6b,7,8,8a,11a,12,12a,12b-hexadecahydro-10H-naphtho[2',1':4,5]indeno[2,1-b]furan-10-one; Sodium Fusidate EP Impurity K; Fusidic Acid Impurity K. Grade: ≥95%. CAS No. 4701-54-6. Molecular formula: C29H44O4. Mole weight: 456.66. | |
| Fusidic Acid EP Impurity L | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z)-16α-(Acetyloxy)-3β-hydroxy-4β,8,14-trimethyl-18-nor-5β,10α-cholesta-9(11),17(20),24-trien-21-oic acid; 9,11-Anhydrofusidic acid; (3α,4α,8α,13α,14β,16β,17Z)-16-(Acetyloxy)-3-hydroxy-29-nordammara-9(11),17(20),24-trien-21-oic acid; (Z)-2-((3R,4S,5S,8R,10S,13R,14S,16S)-16-Acetoxy-3-hydroxy-4,8,10,14-tetramethyl-1,2,3,4,5,6,7,8,10,12,13,14,15,16-tetradecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)-6-methylhept-5-enoic acid; 9,11-Anhydro Fusidic Acid; Fusidic Acid Impurity L; Sodium Fusidate EP Impurity L. Grade: ≥95%. CAS No. 74048-41-2. Molecular formula: C31H46O5. Mole weight: 498.70. | |
| Fusidic Acid EP Impurity M | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z)-16α-(Acetyloxy)-3β-hydroxy-4β,8,14-trimethyl-18-nor-5β,10α-cholesta-17(20),24-dien-21-oic acid; 11-Deoxyfusidic acid; (3α,4α,8α,9β,13α,14β,16β,17Z)-16-(Acetyloxy)-3-hydroxy-29-nordammara-17(20),24-dien-21-oic acid; 11-Deoxy Fusidic Acid; Fusidic Acid Impurity M; (Z)-2-((3R,4S,5S,8S,9S,10S,13R,14S,16S)-16-Acetoxy-3-hydroxy-4,8,10,14-tetramethylhexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)-6-methylhept-5-enoic acid; Sodium Fusidate EP Impurity M. Grade: ≥95%. CAS No. 1013937-16-0. Molecular formula: C31H48O5. Mole weight: 500.71. | |
| Fusidic Acid EP Impurity O | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Synonyms: ent-(17Z)-3β,11β,16α-Trihydroxy-4β,8,14-trimethyl-18-nor-5β,10α-cholesta-17(20),24-dien-21-oic acid; Deacetylfusidic acid; 16-O-Deacetylfusidic acid; Fusidic Acid Impurity O; Sodium Fusidate EP Impurity O; (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-3,11,16-Trihydroxy-29-nordammara-17(20),24-dien-21-oic acid; 29-Nor-8α,9β,13α,14β-dammara-17(20),24-dien-21-oic acid, 3α,11α,16β-trihydroxy-, (Z)-; 16-Desacetylfusidic acid; (Z)-6-Methyl-2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-3,11,16-trihydroxy-4,8,10,14-tetramethylhexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)hept-5-enoic acid. Grade: ≥95%. CAS No. 13090-91-0. Molecular formula: C29H46O5. Mole weight: 474.67. | |
| Fusidic Acid EP Impurity O sodium salt | An impurity of Fusidic acid, which is a steroidal antibiotic belonging to the fusidane class, derived from Fusidium coccineum. Fusidic acid is primarily effective against Gram-positive bacteria, including Staphylococcus aureus (particularly methicillin-resistant strains, MRSA). It is used to treat skin and soft tissue infections. Uses: An impurity of fusidic acid. Synonyms: 29-Nordammara-17(20),24-dien-21-oic acid, 3,11,16-trihydroxy-, monosodium salt, (3α,4α,8α,9β,11α,13α,14β,16β,17Z)-; 16-Deacetyl fusidic acid sodium salt; Sodium Fusidate EP Impurity O; Fusidic Acid EP Impurity O sodium salt; Sodium (Z)-6-methyl-2-((3R,4S,5S,8S,9S,10S,11R,13R,14S,16S)-3,11,16-trihydroxy-4,8,10,14-tetramethylhexadecahydro-17H-cyclopenta[a]phenanthren-17-ylidene)hept-5-enoate; ent-(17Z)-3β,11β,16α-Trihydroxy-4β,8,14-trimethyl-18-nor-5β,10α-cholesta-17(20),24-dien-21-oic acid sodium salt; Deacetylfusidic acid sodium salt; 16-O-Deacetylfusidic acid sodium salt. Grade: ≥95%. CAS No. 55601-53-1. Molecular formula: C29H45NaO5. Mole weight: 496.65. | |
| Meropenem Sodium Carbonate | Meropenem with sodium carbonate is a salt form of Meropenem, a β-lactam antibiotic of the carbapenem subclass that has been shown to inhibit penicillinase-negative, -positive and methicillin-susceptible staphylococci. This compound demonstrates the ability to also affect strains of 11 species of streptococci. Mechanistic studies suggest that Meropenem's antimicrobial activity is based on its high affinity for the majority of penicillin-binding proteins, which are cell wall-synthesizing enzymes. Meropenem is very effective because it resists inactivation by the majority of microbial LACTB (β-lactamases) as well as kidney dehydropeptidase I. Experiments have shown Meropenem to have a low toxicity profile and, in contrast to similar compounds, no central nervous system toxicity. Synonyms: (4R, 5S, 6S)-3-[[(3S, 5S)5-[(Dimethylamino)carbonyl]-3-pyrrolidinyl]thio]-6-((1R)-1-hydroxyethyl)-4-methyl-7-oxo-1-azabicyclo[3, 2, 0]hept-2-ene-2-carboxyloc acid. CAS No. 96036-03-2 free acid. Product ID: PAP-0097. Molecular formula: C17H25N3O5S xNa2CO3. Mole weight: 383.46 (free acid). Product Keywords: Antibacterial, Anti-inflammatory and Antiviral Series; PAP-0097; Meropenem Sodium Carbonate; 96036-03-2 free acid; (4R, 5S, 6S)-3-[[(3S, 5S)5-[(Dimethylamino)carbonyl]-3-pyrrolidinyl]thio]-6-((1R)-1-hydroxyethyl)-4-methyl-7-oxo-1-azabicyclo[3, 2, 0]hept-2-ene-2-carboxyloc acid. Chemical Name: Meropenem with sodium carbona |  |
| Oxacillin Sodium Salt ( (2S, 5R, 6R) -3, 3-Dimethyl-6-[[ (5-methyl-3-phenyl-4-isoxazolyl) carbonyl]amino]-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Sodium Salt, Penicillin P-12, Sodium Oxacillin, BRL-1400, Bactocill, Bristopen, Stapenor) | Oxacillin is a penicillinase-resistant β-lactam. It is similar to methicillin, and has replaced methicillin in clinical use. Another related compound is nafcillin. Since it is resistant to penicillinase enzymes, such as that produced by Staphylococcus aureus, it is widely used clinically in the US to treat penicillin-resistant Staphylococcus aureus. However, with the introduction and widespread use of both oxacillin and methicillin, antibiotic-resistant strains called oxacillin-resistant Staphylococcus aureus (MRSA/ORSA) have become increasingly prevalent worldwide. MRSA/ORSA is treated using vancomycin. Group: Biochemicals. Alternative Names: (2S, 5R, 6R) -3, 3-Dimethyl-6-[[ (5-methyl-3-phenyl-4-isoxazolyl) carbonyl]amino]-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Sodium Salt; Penicillin P-12; Sodium Oxacillin; BRL-1400; Bactocill; Bristopen; Stapenor. Grades: Highly Purified. CAS No. 1173-88-2. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| Teicoplanin | Teicoplanin is a glycopeptide antibiotic indicated for use in serious infections caused by Gram-positive bacteria, including Methicillin-resistant Staphylococcus aureus and Enterococcus aureus.Teicoplanin shows antiviral activity for HIV-1, SARS-CoV1 and SARS-CoV2. Teicoplanin sodium shows anti-MRSA activity [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Antibiotic MDL-507; MDL-507. CAS No. 61036-62-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-A0097. | |
Our database is helping our users find suppliers everyday.
