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.
It is produced by the strain of Penicillium notatum NRRL 1209, Pen. chrysogenum NRRL 1951. It has strong activity of anti-gram-positive bacteria and spirochetes, and has weak anti-gram-negative bacteria activity. It is widely used in clinical practice. Uses: Anti-bacterial agents. Synonyms: (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium Salt; 3,3-Dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Monosodium Salt; American Penicillin; Benzylpenicillin Sodium; Benzylpenicillin Sodium Salt; Benzylpenicillinic Acid Sodium Salt; Crystapen; Ethacillin; Monocillin; Monosodium Benzylpenicillin; Mycofarm; Nalpen G; Nobak; Novocillin; Pen-A-Brasive; Penicillin G Sodium; Penilaryn; Sodium 6-(Phenylacetamido)penicillanate; Sodium Benzylpenicillin; Sodium Benzylpenicillin G; Sodium Penicillin; Sodium Penicillin G; NSC 69877; NSC-69877; NSC69877; 7-NO2-ICA. Grades: 98%. CAS No. 69-57-8. Molecular formula: C16H17N2NaO4S. Mole weight: 356.37.
Penicillin G sodium salt
Penicillin G sodium salt is a typical β-lactam antibiotic. Uses: Scientific research. Group: Natural products. Alternative Names: Benzylpenicillin sodium salt. CAS No. 69-57-8. Pack Sizes: 100 mg. Product ID: HY-B1463.
Penicillin G sodium salt (Benzylpenicillin sodium salt)
25g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17N2NaSO4. CAS No. 69-57-8. Prepack ID 47080913-25g. Molecular Weight 356.37. See USA prepack pricing.
Penicillin G sodium salt (Benzylpenicillin sodium salt)
5g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17N2NaSO4. CAS No. 69-57-8. Prepack ID 47080913-5g. Molecular Weight 356.37. See USA prepack pricing.
Penicillin G, Sodium Salt USP
Penicillin G is a broad based antibiotic used in mammalian cell culture. Penicillin G blocks the formation of bacterial cell walls, rendering bacteria unable to multiply and spread. The spectrum of activity of Penicillin G includes many aerobic and anaerobic gram-positive organisms. Aerobes susceptible to Penicillin G include most beta-hemolytic streptococci, beta-lactamase-negative staphylococci, Actinomyces species, some Bacillus anthracis, Corynebacterium species, and Erysipelothrix rhusiopathiae. Most species of anaerobes, including Clostridium species, but excluding beta-lactamase-producing Bacteroides species, are also susceptible to Penicillin G. Penicillin G is easily ...id Monosodium Salt; (2S, 5R, 6R)-3, 3-dimethyl-7-oxo-6-[(phenylacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Monosodium Salt; American Penicillin; Benzylpenicillin Sodium; Benzylpenicillin Sodium Salt; Benzylpenicillinic Acid Sodium Salt; Crystapen; Ethacillin; Monocillin; Monosodium Benzylpenicillin; Mycofarm; Nalpen G; Nobak; Novocillin; Pen-A-Brasive; Penicillin G Sodium; Penilaryn; Sodium 6- (Phenylacetamido) penicillanate; Sodium Benzylpenicillin; Sodium Benzylpenicillin G; Sodium Benzylpenicillinate. Grades: USP. CAS No. 69-57-8. Pack Sizes: 50g, 100g, 500g, 1Kg. Molecular Formula: C16H17N2O4NaS, Molecular Weight: 356.37. US Biological Life Sciences.
Worldwide
5R,6R-Benzylpenicilloate Disodium Salt
5R,6R-Benzylpenicilloate Disodium Salt is the β-lactamase cleavage product/metabolite of antibiotic Penicillin G. Synonyms: [2R-[2α(R*),4β]]-4-carboxy-5,5-dimethyl-α-[(phenylacetyl)amino]-2-thiazolidineacetic Acid Disodium Salt; (αR,2R,4S)-4-Carboxy-5,5-dimethyl-α-[(2-phenylacetyl)amino]-2-Thiazolidineacetic Acid Sodium Salt. CAS No. 63448-72-6. Molecular formula: C16H18N2Na2O5S. Mole weight: 396.37.
Carbenicillin Disodium
Carbenicillin is a semi-synthetic penicillin antibiotic which interferes with cell wall synthesis of gram-negative bacteria while displaying low toxicity. The carboxypenicillins are susceptible to degradation by beta-lactamase enzymes, although they are more resistant than ampicillin to degradation. Carbenicillin is also more stable at lower pH than ampicillin. Synonyms: (2S,5R,6R)-6-[(2-Carboxy-2-phenylacetyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium Salt; N-(2-Carboxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-6-yl)-2-phenylmalonamic Acid Disodium Salt; Anabactyl; Carbapen; Carbecin; Carbenicilline Disodium; Carboxybenzylpenicillin Sodium; Fugacillin; Geocillin; Geopen; Gripenin; Hyoper; Microcillin; NSC 111071; Piopen; Pyopen; α-Carboxybenzylpenicillin Sodium Salt; BRL-2064; BRL 2064; BRL2064. Grades: ≥90%. CAS No. 4800-94-6. Molecular formula: C17H16N2Na2O6S. Mole weight: 422.36.
Carbenicillin Disodium Salt
Carbenicillin (alpha-carboxybenzyl penicillin) is a synthetic penicillin derivative used as a selection agent for carbenicillin-resistant plasmids (amp). Group: Biochemicals. Alternative Names: (2S, 5R, 6R)-6-[(2-Carboxy-2-phenylacetyl)amino]-3, 3-dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Sodium Salt; N-(2-Carboxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-6-yl)-2-phenylmalonamic Acid Disodium Salt; Anabactyl; BRL 2064; Carbapen; Carbecin; Carbenicillin Sodium; Carbenicilline Disodium; Carboxybenzyl penicillin Sodium; Disodium (α -Carboxybenzyl) penicillin; Disodium Carbenicillin; Fugacillin; Geocillin; Geopen; Gripenin; Hyoper; Microcillin; NSC 111071; Piopen; Pyopen; Pyopene; Sodium carbenicillin; α -Carboxybenzyl penicillin Sodium Salt. Grades: Molecular Biology Grade. CAS No. 4800-94-6. Pack Sizes: 5g, 10g, 25g, 100g. Molecular Formula: C17H16N2O6SNa2, Molecular Weight: 422.4. US Biological Life Sciences.
Worldwide
Carbenicillin Sodium Monohydrate
Carbenicillin is a semi-synthetic penicillin antibiotic which interferes with cell wall synthesis of gram-negative bacteria while displaying low toxicity. Synonyms: (2S,5R,6R)-6-[(2-Carboxy-2-phenylacetyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium Salt hydrate (1:x:1); Carbenicilline sodium monohydrate; Carboxybenzylpenicillin Sodium monohydrate; α-Carboxybenzylpenicillin Sodium Salt monohydrate. Grades: 79%. Molecular formula: C17H18N2O6S.xNa.H2O. Mole weight: 378.40 (free acid).
Cefmetazole
It is produced by the strain of Semisynthetic second generation cephalosporin for injection. It belongs to the cephalomycin-type compound. and its sodium salt is used in preparations. Cefmeazole is an antibiotic with broad spectrum activity against gram-positive and Gram-negative bacteria. It binds to a penicillin-binding protein (PBPs) responsible for the cross-linking of peptidoglycan. Uses: Cefmetazole has antibacterial activity. Synonyms: Cefmetazolo; Cefmetazolum; U-72791A; U72791A; Zefazone; CS-1170; CS 1170; CS1170; (6R, 7S)-7- ({[ (cyanomethyl)sulfanyl]acetyl}amino)-7-methoxy-3-{[ (1-methyl-1H-tetrazol-5-yl)sulfanyl]methyl}-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic acid. Grades: 95%. CAS No. 56796-20-4. Molecular formula: C15H17N7O5S3. Mole weight: 471.53.
Cefminox sodium
Cefminox is a broad-spectrum, bactericidal cephalosporin antibiotic. It is especially effective against Gram-negative and anaerobic bacteria. Cefminox Sodium is the sodium salt form of cefminox, which is a semi-synthetic, second-generation and beta-lactamase-stable cephalosporin with antibacterial activity. It is also known as Meicelin and MT-141, which is a penicillin binding protein inhibitor used to treat bacterial infection. Synonyms: MT-141; MT 141; Meicelin. Grades: ≥98%. CAS No. 75498-96-3. Molecular formula: C16H20N7O7S3Na. Mole weight: 541.56.
Cefotetan disodium
Cefotetan is a second-generation cephalosporin. It can bind to penicillin-binding proteins and disrupts the cell wall synthesis. Cefotetan is active against some strains of β-lactamase producing bacteria. Cefotetan shows anti-microbial activity against Gram-positive and Gram-negative bacteria and it is more efficacious against Gram-negative and anaerobic bacteria. Uses: Antibacterial. Synonyms: ICI156834; ICI 156834; ICI-156834; YM 09330; YM09330; YM-09330; Yamatetan; Cefotan; Apatef; 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[[4-(2-amino-1-carboxy-2-oxoethylidene)-1,3-dithietan-2-yl]carbonyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, sodium salt (1:2), (6R,7S)-; 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[[4-(2-amino-1-carboxy-2-oxoethylidene)-1,3-dithietan-2-yl]carbonyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, disodium salt, (6R,7S)-; 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[[4-(2-amino-1-carboxy-2-oxoethylidene)-1,3-dithietan-2-yl]carbonyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, disodium salt, [6R-(6α,7α)]-; Cefotetan sodium; Ceftenon; Cepan Darvilen. Grades: 98%. CAS No. 74356-00-6. Molecular formula: C17H15N7Na2O8S4. Mole weight: 619.59.
Cefpiramide
It is produced by the strain of Semisynthetic third generation cephalosporin for injection. Its sodium salt is used in preparations. Cefpiramide binds to penicillin-binding proteins (PBPs), transpeptidases that are responsible for crosslinking of peptidoglycan. By preventing crosslinking of peptidoglycan, cell wall integrity is lost and cell wall synthesis is halted. Synonyms: Cefpiramide acid; Cefpiramido; Cefpiramidum; (6R,7R)-7-((R)-2-(4-Hydroxy-6-methylnicotinamido)-2-(4-hydroxyphenyl)acetamido)-3-(((1-methyl-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. Grades: 95%. CAS No. 70797-11-4. Molecular formula: C25H24N8O7S2. Mole weight: 612.64.
Ceftriaxone Sodium
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 ... 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. Synonyms: 2,5,6-tetrahydro-2-methyl-5,6-dioxo-)(methoxyimino)acetyl)amino)-8-oxo-3-(((4-triazin-3-yl)thio)methyl)-,sodiumsalt,hydrate(2:4:7)(6r-(6-alpha,7-2;beta(z)))-; [6R-[6alpha, 7beta (Z)]]-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]-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic acid sodium salt. Grades: 98%. CAS No. 74578-69-1. Molecular formula: C18H16N8Na2O7S3. Mole weight: 598.54.
Clavulanate Potassium, Streptomyces sp.
Clavulanic acid is a beta-lactam antibiotic produced by several species of the genus Streptomyces. The free acid degrades and is isolated and maintained as either the sodium or potassium salt. Clavulanate is a weak antibiotic but is a potent inhibitor of beta- lactamases. In combination with penicillin and cephalosporins it shows potent synergistic activity. Clavulanic acid is a suicide inhibitor, covalently binding to a serine residue in the active site of the beta-lactamase. Group: Biochemicals. Alternative Names: Timentin; Ticarcillin; MM 14151; [2R-(2α, 3Z, 5α)]-3-(2-hydroxyethylidene)-7-oxo-4-oxa- 1-azabicyclo[3. 2. 0]heptane-2-carboxylate potassium salt. Grades: Highly Purified. CAS No. 61177-45-5. Pack Sizes: 5mg. US Biological Life Sciences.
Worldwide
Clavulanic Acid, Potassium Salt (MM 14151, Potassium Clavulanate)
Clavulanic acid is a beta-lactam antibiotic produced by several species of the genus Streptomyces. The free acid degrades and is isolated and maintained as either the sodium or potassium salt. Clavulanate is a weak antibiotic but is a potent inhibitor of beta- lactamases. In combination with penicillin and cephalosporins it shows potent synergistic activity. Clavulanic acid is a suicide inhibitor, covalently binding to a serine residue in the active site of the beta-lactamase. Group: Biochemicals. Alternative Names: Timentin; Ticarcillin; MM 14151; [2R-(2α, 3Z, 5α)]-3-(2-hydroxyethylidene)-7-oxo-4-oxa- 1-azabicyclo[3. 2. 0]heptane-2-carboxylate potassium salt. Grades: Highly Purified. CAS No. 61177-45-5. Pack Sizes: 10mg, 50mg, 100mg, 1g. US Biological Life Sciences.
Worldwide
Cloxacillin Sodium Monohydrate
Cloxacillin Sodium Monohydrate is a sodium salt of cloxacillin that is a penicillinase-resistant, acid resistant, semi-synthetic penicillin. Uses: Anti-bacterial agents. Synonyms: Cloxapen. Grades: >98%. CAS No. 7081-44-9. Molecular formula: C19H19ClN3NaO6S. Mole weight: 475.88.
Desmethyl Nafcillin Sodium Salt
Desmethyl Nafcillin Sodium Salt is an impurity of Nafcillin, a semi-synthetic penicillin antibiotic that is particularly effective against Gram-positive bacteria. Synonyms: 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2-methoxy-1-naphthalenyl)carbonyl]amino]-3,3-dimethyl-7-oxo-, sodium salt (1:1), (2S,5R,6R)-; 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2-methoxy-1-naphthalenyl)carbonyl]amino]-3,3-dimethyl-7-oxo-, monosodium salt, (2S,5R,6R)-; 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2-methoxy-1-naphthalenyl)carbonyl]amino]-3,3-dimethyl-7-oxo-, monosodium salt, [2S-(2α,5α,6β)]-; BRL 1336; Nafcillin Desmethyl Impurity. Grades: 98%. CAS No. 1104-49-0. Molecular formula: C20H19N2NaO5S. Mole weight: 422.43.
Dicloxacillin-13C4 Sodium Salt Monohydrate
Labeled Dicloxacillin. A semi-synthetic antibiotic related to Penicillin. Antibacterial. Group: Biochemicals. Alternative Names: (2S, 5R, 6R) -6- [ [ [3- (2, 6-Dichlorophenyl) -5-methyl-4-isoxazolyl] carbonyl] amino] -3, 3-dimethyl-7-oxo-4-thia-1-azabicyclo [3. 2. 0] heptane-2-carboxylic Acid-13C4 Sodium Salt Hydrate. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Dicloxacillin Sodium hydrate
Dicloxacillin Sodium hydrate (Dicloxacillin sodium salt monohydrate) is a narrow-spectrum β-Lactam antibiotic of the penicillin class, is used to treat infections caused by susceptible Gram-positive bacteria, active against beta-lactamase-producing organisms such as Staphylococcus aureus [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Dicloxacillin sodium salt monohydrate. CAS No. 13412-64-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg. Product ID: HY-B0977.
Dicloxacillin Sodium Salt Monohydrate
The sodium monohydrate salt form of Dicloxacillin, a β-Lactam compound, could be used as an antibiotic especially against Gram-positive bacteria and also be significant in biological studies. Synonyms: (2S,5R,6R)-6-[[[3-(2,6-Dichlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium Salt Hydrate; 3-(2,6-Dichlorophenyl)-5-methyl-4-isoxazolyl Penicillin Sodium Salt Monohydrate; Dichlorstapenor Sodium; Dicloxacillin Sodium Hydrate; P1011; Sodium Dicloxacillin Monohydrate; BRL1702; BRL 1702; BRL-1702; P 1011; P-1011; P1011; 3-(2,6-DICHLOROPHENYL)-5-METHYL-4-ISOXAZOLYL PENICILLIN; DICLOXACILLIN SODIUM SALT HYDRATE VETRAN; DICLOXACILLIN SODIUM EPD(CRM STANDARD); DICLOXACILLIN SODIUM USP(CRM STANDARD); DICLOXACILLIN SODIUM WHO(CRM STANDARD); 4-Thia-1-azabicyclo3.2.0heptane-2-carbox. Grades: 97%. CAS No. 13412-64-1. Molecular formula: C19H16Cl2N3NaO5S.H2O. Mole weight: 510.32.
Ertapenem Disodium
It is a long-acting, broad-spectrum antibiotic that is in the β-lactam subclass known as carbapenems. It inhibits the synthesis of bacterial cell walls by attaching to penicillin-binding proteins. It has activity against Gram-positive and Gram-negative bacteria. Synonyms: Ertapenem sodium; 1-Azabicyclo(3.2.0)hept-2-ene-2-carboxylic acid, 3-((5-(((3-carboxyphenyl)amino)carbonyl)-3-pyrrolidinyl)thio)-6-(1-hydroxyethyl)-4-methyl-7-oxo-, disodium salt, (4R-(3(3S*,5S*),4alpha,5beta,6beta(R*)))-; L 749. Grades: ≥97%. CAS No. 153832-38-3. Molecular formula: C22H23N3Na2O7S. Mole weight: 519.48.
Ertapenem Sodium
Ertapenem Sodium is the sodium salt of ertapenem. Ertapenem has in vitro activity against gram-positive and gram-negative aerobic and anaerobic bacteria. The bactericidal activity of ertapenem results from the inhibition of cell wall synthesis and is mediated through ertapenem binding to penicillin binding proteins (PBPs). In Escherichia coli, it has strong affinity toward PBPs 1a, 1b, 2, 3, 4 and 5 with preference for PBPs 2 and 3. Ertapenem is stable against hydrolysis by a variety of beta-lactamases, including penicillinases, and cephalosporinases and extended spectrum beta-lactamases. Ertapenem is hydrolyzed by metallo-beta-lactamases. Ertapenem has been shown to be active against most isolates of the following microorganisms in vitro and in clinical infections. Synonyms: Invanz; Ertapenem sodium salt; MK-0826. Grades: 98%. CAS No. 153773-82-1. Molecular formula: C22H24N3NaO7S. Mole weight: 497.50.
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.
β--lactamase inactivates β-lactam antibiotics by breaking open the β-lactam ring. Protein determined by biuret. Applications: Β-lactamase is used to inactivate β-lactam antibiotics by breaking open the β-lactam ring. β-lactamase is used to study antibiotic resistance and resistance suppression1. this product is produced from enterobacter cloacae. Group: Enzymes. Synonyms: β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC . Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Activity: 6-18 units/mg protein (using benzylpenicillin); 0.2-0.6 units/mg protein (using benzylpenicillin). Storage: 2-8°C. Form: Lyophilized powder containing sodium phosphate and sodium Citrate buffer salts. Source: Enterobacter cloacae. β-lactamase; penicillinase; cephalosporinase; neutrapen; penicillin β-lactamase; exopenicillinase; ampicillinase; penicillin amido-β-lactamhydrolase; penicillinase I, II; β-lactamase I-III; β-lactamase A, B, C; β-lactamase AME I; cephalosporin-β-lactamase; EC 3.5.2.6; 9073-60-3. Cat No: NATE-0774.
N-Oxacilloilyl (+)-6-Aminopenicillanic Acid Disodium Salt
N-Oxacilloilyl (+)-6-Aminopenicillanic Acid Disodium Salt is a derivative of Oxacillin, which is used as an antibiotic related to Penicillin. Synonyms: 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[ (R) -2-[ (2R, 4S) -4-carboxy-5, 5-dimethyl-2-thiazolidinyl]-2-[[ (5-methyl-3-phenyl-4-isoxazolyl) carbonyl]amino]acetyl]amino]-3, 3-dimethyl-7-oxo-, sodium salt, (2S,5R,6R)- (1:2); Disodium (2S,5R,6R)-6-[([(2R,4S)-4-carboxylato-5,5-dimethyl-1,3-thiazolidin-2-yl]{[(5-methyl-3-phenyl-1,2-oxazol-4-yl)carbonyl]amino}acetyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate. Grades: 97%. Molecular formula: C27H29N5Na2O8S2. Mole weight: 661.66.
Oxacillin Penillic Acid Disodium Salt (Mixture of Diastereomers)
Oxacillin Penillic Acid Disodium Salt is a derivative of Oxacillin, which is used as an antibiotic related to Penicillin. Synonyms: 2,3,7,7a-Tetrahydro-2,2-dimethyl-5-(5-methyl-3-phenyl-4-isoxazolyl)-Imidazo[5,1-b]thiazole-3,7-dicarboxylic Acid Disodium Salt; Disodium 2,2-dimethyl-5-(5-methyl-3-phenyl-1,2-oxazol-4-yl)-2,3,7,7a-tetrahydroimidazo[5,1-b][1,3]thiazole-3,7-dicarboxylate; Imidazo[5,1-b]thiazole-3,7-dicarboxylic acid, 2,3,7,7a-tetrahydro-2,2-dimethyl-5-(5-methyl-3-phenyl-4-isoxazolyl)-, sodium salt (1:2). Grades: 80%. Molecular formula: C19H17N3Na2O5S. Mole weight: 445.40.
Oxacillin sodium salt
Oxacillin sodium salt is an orally active synthetic penicillin with good bactericidal activity against staphylococci and other gram-positive pathogens [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1173-88-2. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B0925.
Oxacillin Sodium Salt
The sodium salt form of Oxacillin which is a narrow-spectrum antibiotic and commonly used for studying the mechanisms of penicillinase resistance. It can be used for penicillin-resistant Staphylococcus infections. Uses: The sodium salt form of oxacillin which is a narrow-spectrum antibiotic and commonly used for studying the mechanisms of penicillinase resistance. Synonyms: 3,3-Dimethyl-6-(5-methyl-3-phenyl-4-isoxazolecarboxamido)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Monosodium 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 monosodium salt; [2S-(2α,5α,6β)]-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 Monosodium Salt; 5-Methyl-3-phenyl-4-isoxazolyl Penicillin Sodium Salt; BRL 1400; Bactocil; Bactocil Sodium; Bristopen; Cryptocillin; Micropenin; Monosodium Oxacillin; NSC 527712; Oxabel; Oxacillin Sodium Salt; Penicillin P12; Penstapho; Penstaphocid; Prostaphlin; SQ 16423; 4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylicacid,3,3-dimethyl-6-(5-methyl-3;5-methyl-3-phenyl-4-isoxazolylpenicillin,sodium; bactocill; bristopen; brl1400. Grades: > 90%. CAS No. 1173-88-2. Molecular formula: C19H18N3NaO5S. Mole weight: 423.42.
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
Oxacillin Sodium Salt Monohydrate
Oxacillin sodium monohydrate is a semi-synthetic antibacterial agent and is a narrow spectrum beta-lactam antibiotic of the penicillin class. Synonyms: (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 Hydrate; Penicillin P-12 Hydrate; Sodium Oxacillin Hydrate; BRL-1400 Hydrate; Bactocill Hydrate; Bristopen Hydrate; Stapenor Hydrate; Oxacillin sodium hydrate; Cryptocillin; Prostaphlin; Stapenor; BAY-M-1099; BAY M 1099. Grades: 96%. CAS No. 7240-38-2. Molecular formula: C19H18N3NaO5S.H2O. Mole weight: 441.43.
Oxacillin Sodium Salt Monohydrate
Semi-synthetic antibiotic related to Penicillin. Antibacterial. 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 Hydrate; Penicillin P-12 Hydrate; Sodium Oxacillin Hydrate; BRL-1400 Hydrate; Bactocill Hydrate; Bristopen Hydrate; Stapenor Hydrate. Grades: Highly Purified. CAS No. 7240-38-21. Pack Sizes: 1g. US Biological Life Sciences.
Clavulanic acid is a beta-lactam antibiotic produced by several species of the genus Streptomyces. The free acid degrades and is isolated and maintained as either the sodium or potassium salt. Clavulanate is a weak antibiotic but is a potent inhibitor of beta- lactamases. In combination with penicillin and cephalosporins it shows potent synergistic activity. Clavulanic acid is a suicide inhibitor, covalently binding to a serine residue in the active site of the beta-lactamase. Group: Biochemicals. Alternative Names: Timentin; Ticarcillin; MM 14151; [2R-(2α, 3Z, 5α)]-3-(2-hydroxyethylidene)-7-oxo-4-oxa- 1-azabicyclo[3. 2. 0]heptane-2-carboxylate potassium salt. Grades: Highly Purified. CAS No. 61177-45-5. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C8H8NO5·K. US Biological Life Sciences.
Worldwide
Potassium clavulanate, 1:1 mixture with silicon dioxide
Clavulanic acid is a beta-lactam antibiotic produced by several species of the genus Streptomyces. The free acid degrades and is isolated and maintained as either the sodium or potassium salt. Clavulanate is a weak antibiotic but is a potent inhibitor of beta- lactamases. In combination with penicillin and cephalosporins it shows potent synergistic activity. Clavulanic acid is a suicide inhibitor, covalently binding to a serine residue in the active site of the beta-lactamase. Group: Biochemicals. Alternative Names: Timentin; Ticarcillin; MM 14151; [2R-(2α, 3Z, 5α)]-3-(2-hydroxyethylidene)-7-oxo-4-oxa- 1-azabicyclo[3. 2. 0]heptane-2-carboxylate potassium salt. Grades: Highly Purified. CAS No. 61177-45-5. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C8H8NO5·K. US Biological Life Sciences.
Worldwide
Sodium Indanylcarbinicillin
Sodium Indanylcarbinicillin, a penicillin-derived, has been used as a β-lactam antibiotic which inhibits the synthesis of peptidoglycan, a key component of the bacterial cell wall. It also has been shown to reduce blood pressure in mammals. Uses: Anti-bacterial agents. Synonyms: (2S,5R,6R)-6-[[3-[(2,3-Dihydro-1H-inden-5-yl)oxy]-1,3-dioxo-2-phenylpropyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium Salt; (2S,5R,6R)-6-[[3-[(2,3-dihydro-1H-inden-5-yl)oxy]-1,3-dioxo-2-phenylpropyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Monosodium Salt; [2S-(2α,5α,6β)]-6-[[3-[(2,3-Dihydro-1H-inden-5-yl)oxy]-1,3-dioxo-2-phenylpropyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Monosodium Salt; CP 15464-2; Carbenicillin Indanyl Sodium; Carindacillin Sodium; Carindapen; GU-Pen; Geocillin; Indanyl Carbenicillin Sodium Salt; Monosodium Indanyl Carbenicillin; Sodium 5-indanylcarbenicillin; Sodium Indanylcarbenicillin; 4800-94-6 (Carbenicillin Disodium). Grades: >98%. CAS No. 26605-69-6. Molecular formula: C26H25N2NaO6S. Mole weight: 516.54.
Temocillin disodium salt
Temocillin disodium salt is the salt of Temocillin. Temocillin is a β-lactamase-resistant penicillin that is effective against Gram-negative bacteria. Uses: Anti-bacterial agents. Synonyms: disodium [2S-(2alpha,5alpha,6alpha)]-6-(carboxylato-3-thienylacetamido)-6-methoxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate; (6S)-6-[(Sodiooxycarbonyl-3-thienylacetyl)amino]-6-methoxypenicillanic acid sodium salt; Temocillin sodium; temocillin disodium. Grades: ≥90%. CAS No. 61545-06-0. Molecular formula: C16H18N2Na2O7S2. Mole weight: 458.42.
Azlocillin sodium salt
Azlocillin is an acylampicillin antibiotic with an extended spectrum of activity and greater in vitro potency than the carboxy penicillins. Azlocillin is similar to mezlocillin and piperacillin. It demonstrates antibacterial activity against a broad spectrum of bacteria, including Pseudomonas aeruginosa and, in contrast to most cephalosporins, exhibits activity against enterococci. Uses: Anti-bacterial agents. Synonyms: Bayer Brand of Azlocillin; Sodium Azlocillin; Securopen; Bay-e 6905; Baye 6905; Bay e 6905; Azlocillin; Azlocillin Bayer Brand. Grades: >98%. CAS No. 37091-65-9. Molecular formula: C20H23N5O6SNa. Mole weight: 484.48.
Benzyl Penicilloic Acid Mono-Sodium Salt (Mixture of Diastereomers)
An impurity of Penicilloic Acid which is a thiazolidinedicarboxylic acid obtained from the penicillins by the hydrolytic opening of the lactam ring. Grades: > 95%. Molecular formula: C16H19N2O5S.Na. Mole weight: 374.39.
Would you like to list your products on USA Chemical Suppliers?
Our database is helping our users find suppliers everyday.