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| Product | Description | |
|---|---|---|
| Penicillin G sodium salt | 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. Grade: 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 |
| 2-Bromo Carbenicillin Disodium Salt | 2-Bromo Carbenicillin Disodium Salt is an analogue of Carbenicillin, which is a semi-synthetic penicillin antibiotic. Uses: Carbenicillin analogue, an antibacterial. Synonyms: [2S-(2α,5α,6β)]-6-[[(2-Bromophenyl)carboxyacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Disodium Salt; Disodium (2S,5R,6R)-6-{[(2-bromophenyl)(carboxylato)acetyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate; 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[2-(2-bromophenyl)-2-carboxyacetyl]amino]-3,3-dimethyl-7-oxo-, sodium salt, (2S,5R,6R)- (1:2). Grade: ≥95%. CAS No. 59530-63-1. Molecular formula: C17H15BrN2Na2O6S. Mole weight: 501.26. | |
| 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. | |
| Azidocillin | Azidocillin is produced by the strain of 6-APA and Ampicillin. The activity of anti-hemolytic Streptococcus, Streptococcus pneumoniae and enterococcus is slightly better than penicillin, while staphylococcus aureus, which is sensitive to penicillin, is slightly better than penicillin, and is less stable to penicillinase than amamicillin to influenza bacilli. Stable to acid, oral. The preparation is its sodium salt or potassium salt (melting point 194°C decomposition), used as an antibacterial agent and feed additive. Synonyms: AZIDOCILLIN; GLOBACILLIN; 6α-(2-Azido-2-phenylacetylamino)penicillanic acid; BRL 2534; SPC 297 D. Grade: 95%. CAS No. 17243-38-8. Molecular formula: C16H17N5O4S. Mole weight: 375.41. | |
| 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 |
| 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. Grade: 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. Grade: ≥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. Grade: 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. Grade: 95%. CAS No. 70797-11-4. Molecular formula: C25H24N8O7S2. Mole weight: 612.64. | |
| 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 | |
| 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 | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsbritish pharmacopoeiaeuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: 3-(o-Chlorophenyl)-5-methyl-4-isoxazolyl penicillin sodium salt monohydrate, Sodium cloxacillin monohydrate, Oxacillin Imp. E (EP), 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, monosodium salt, monohydrate, (2S,5R,6R)- (9CI),Oxacillin Sodium Imp. E (EP), Cloxacillin Sodium Monohydrate, Oxacillin Sodium Imp. E (EP) as Sodium Salt Monohydrate, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[3-(o-chlorophenyl)-5-methyl-4-isoxazolecarboxamido]-3,3-dimethyl-7-oxo-, monosodium salt, monohydrate (8CI), 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, monosodium salt, monohydrate, [2S-(2alpha,5alpha,6beta)]-, Sodium 6-[3-(o-Chlorophenyl)-5-methyl-4-isoxazolecarboxamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate hydrate. |  |
| 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. Grade: >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. Grade: 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. Grade: 97%. CAS No. 13412-64-1. Molecular formula: C19H16Cl2N3NaO5S.H2O. Mole weight: 510.32. | |
| Doripenem-d4 sodium salt | Doripenem-d4 is used as an internal standard for the quantification of doripenem by GC- or LC-MS. Doripenem is a broad-spectrum antibiotic in the β-lactam subclass known as carbapenems. It is active against Gram-negative and Gram-positive bacteria, including S. aureus, S. pneumoniae, E. coli, and K. pneumoniae. It inhibits bacterial cell wall synthesis via forming stable acyl enzymes with penicillin-binding proteins, thereby inactivating them. Synonyms: 3-[[(3S,5S)-5S-[[(aminosulfonyl)amino]methyl]-3-pyrrolidinyl]thio]-6S-[(1R)-1-hydroxyethyl]-4R-(methyl-d3)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-4-d1-2-carboxylic acid, monosodium salt. Grade: ≥99% atom D. Molecular formula: C15H19D4N4O6S2·Na. Mole weight: 446.51. | |
| 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. Grade: ≥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. Grade: 95% by HPLC. CAS No. 153773-82-1. Molecular formula: C22H24N3NaO7S. Mole weight: 497.50. | |
| Flucloxacillin Sodium | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopypesticides & metabolitespharma & vet compounds & metabolitespesticides & metabolitespharma & vet compounds & metabolitesbritish pharmacopoeiaeuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: Flucloxacillin sodium, NSC 277175, Monosodium flucloxacillin,4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, monosodium salt, (2S,5R,6R)- (9CI), Sodium [3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]penicillin, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolecarboxamido]-3,3-dimethyl-7-oxo-, sodium salt (7CI), Floxapen, Floxapen sodium, Sodium flucloxacillin, Staphylex, Flucloxacillin sodium salt, 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, monosodium salt, [2S-(2?,5?,6?)]-, Floxacillin sodium, BRL-2039. | |
| 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 |
| Nafcillin-[d5] sodium salt | Nafcillin-[d5] sodium salt is the labelled salt of Nafcillin. Nafcillin, a semi-synthetic β-lactamase-resistant penicillin analogue, has been found to be an antibiotic that could be effective especially against Gram-positive bacteria. Synonyms: Nafcillin-D5 sodium salt; (2S,5R,6R)-6-[[(2-(Ethoxy-d5)-1-naphthalenyl)carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium Salt; Naftopen-d5; Naphthicillin-d5; Nafcil-d5; Sodium 6-(2-(ethoxy-d5)-1-naphthamido)penicillanate; 6-(2-(Ethoxy-d5)-1-naphthamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium Salt; 6-(2-(Ethoxy-d5)-1-naphthamido)penicillin Sodium Salt; Sodium Nafcillin-d5. Grade: ≥97% by HPLC; ≥99% atom D. CAS No. 1356354-25-0. Molecular formula: C21H16D5N2NaO5S. Mole weight: 441.49. | |
| Native Enterobacter cloacae β-Lactamase | 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. |  |
| 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 ( (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 |
| 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. Grade: 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. | Worldwide |
| Penicillin X Sodium | It is produced by the strain of Penicillium notatum NRRL 1209, Pen. chrysogenum NRRL 1951. It is an antibiotic. Synonyms: (2S,5β)-6α-[[(4-Hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2β-carboxylic acid sodium salt; 6α-[(4-Hydroxyphenylacetyl)amino]penicillani cacid sodium salt; Penicillin III sodium; p-Hydroxybenzylpenicillin sodium; Benzylpenicillin Impurity C. Grade: > 95%. CAS No. 5985-13-7. Molecular formula: C16H17N2O5SNa. Mole weight: 372.37. | |
| Phenethicillin-d5 Sodium Salt | Phenethicillin-d5 Sodium Salt. Group: Biochemicals. Alternative Names: Pheneticillin-d5 Sodium Salt; Phenoxy PC-d5 Sodium Salt; Phenoxyethylpenicillin-d5 Sodium Salt; Synthepen-d5 Sodium Salt; α-Phenoxyethylpenicillin-d5 Sodium Salt; 1-Phenoxyethylpenicillin-d5 Sodium Salt; Alfacilin-d5 Sodium Salt; Feneticillin-d5 Sodium Salt; NSC 117548-d5 Sodium Salt; Optipen-d5 Sodium Salt; Penicillin-d5 152 Sodium Salt; Penicillin MV Sodium Salt; Peniplus Sodium Salt; Penorale-d5 Sodium Salt; Penova-d5 Sodium Salt; (2S, 5R, 6R)-3, 3-Dimethyl-7-oxo-6-[(1-oxo-2-phenoxypropyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid-d5 Sodium Salt. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C17H14D5N2NaO5S, Molecular Weight: 391.43. US Biological Life Sciences. | Worldwide |
| Phenethicillin Sodium Salt | Phenethicillin Sodium Salt. Group: Biochemicals. Alternative Names: Pheneticillin Sodium Salt; Phenoxy PC Sodium Salt; Phenoxyethylpenicillin Sodium Salt; Synthepen Sodium Salt; α-Phenoxyethylpenicillin Sodium Salt; 1-Phenoxyethylpenicillin Sodium Salt; Alfacilin Sodium Salt; Feneticillin Sodium Salt; NSC 117548 Sodium Salt; Optipen Sodium Salt; Penicillin 152 Sodium Salt; Penicillin MV Sodium Salt; Peniplus Sodium Salt; Penorale Sodium Salt; Penova Sodium Salt; (2S, 5R, 6R)-3, 3-Dimethyl-7-oxo-6-[(1-oxo-2-phenoxypropyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Sodium Salt. Grades: Highly Purified. CAS No. 30302-52-4. Pack Sizes: 1mg. Molecular Formula: C17H29N2NaO5S, Molecular Weight: 386.4. US Biological Life Sciences. | Worldwide |
| Potassium clavulanate, 1:1 mixture with cellulose | 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 |
| Tazobactam acid | Tazobactam acid is a pharmaceutical drug that inhibits the action of bacterial β-lactamases, especially those belonging to the SHV-1 and TEM groups. It is commonly used as the sodium salt. It is derived from the penicillin nucleus and is a penicillinic acid sulfone. It is used with β-lactam antibiotics to enhance their effect. It has antibacterial activity. Uses: Anti-bacterial agents. Synonyms: Tazobactam acid; Tazobactamum; Zosyn; CL-298741; YTR-830H. Grade: >98%. CAS No. 89786-04-9. Molecular formula: C10H12N4O5S. Mole weight: 300.29. | |
| 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. Grade: >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. Grade: > 95%. Molecular formula: C16H19N2O5S.Na. Mole weight: 374.39. | |
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