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| Product | Description | |
|---|---|---|
| Penicillinase | Penicillinase is a beta-lactamase. beta-lactamase enzymes inactivate beta-lactam antibiotics by hydrolyzing the peptide bond of the characteristic four-membered beta-lactam ring rendering the antibiotic ineffective [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 9001-74-5. Pack Sizes: 5 mL. Product ID: HY-E70012. |  |
| Native Bacillus cereus Penicillinase | Penicillinase specifically catalyzes the hydrolysis of β-lactam ring of penicillin. Applications: Used in the production of penicillin. Group: Enzymes. Synonyms: EC 3.5.2.6; 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; 9073-60-3. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. Mole weight: Mr ~30 kDa. Storage: -20°C. Source: Bacillus cereus. EC 3.5.2.6; 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; 9073-60-3. Pack: Bottomless glass bottle. Contents are inside inserted fused cone. Cat No: NATE-0542. |  |
| β-lactamase | A group of enzymes of varying specificity hydrolysing β-lactams; some act more rapidly on penicillins, some more rapidly on cephalosporins. The latter were formerly listed as EC 3.5.2.8, cephalosporinase. Group: Enzymes. Synonyms: 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. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4508; β-lactamase; EC 3.5.2.6; 9073-60-3; 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. Cat No: EXWM-4508. | |
| β-Lactamase Blend, Recombinant | β--lactamase inactivates β-lactam antibiotics by breaking open the β-lactam ring. 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 3.5.2.6; 9073-60-3. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Activity: 600-1500 IU beta-lactamase I per vial; 60-100 IU beta-lactamase II per vial. Storage: 2-8°C. Form: Lyophilized powder containing sodium chloride, potassium phosphate and sorbitol. Source: E. coli. 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-0776. | |
| β-Lactamase from Pseudomonas aeruginosa, Recombinant | β--lactamase inactivates β-lactam antibiotics by breaking open the β-lactam ring. 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 suppression. product is produced from pseudomonas aeruginosa and is expressed in e. coli. 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 3.5.2.6; 907. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Activity: > 20 U/mg (with cephalosporin C); > 400 U/mg (with benzylpenicilin). Storage: 2-8°C. Form: Lyophilized powder containing sodium chloride and potassium phosphate. Source: E. coli. Species: Pseudomonas aeruginosa. 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-0777. | |
| Cephalosporin C | It is produced by the strain of Cephalosporium aceemonium C.M.I 49137. Cephalosporin C has weak resistance to gram-positive and negative bacteria, is stable to penicillinase, and can be broken down by cephalosporin enzyme. Hydrolysis and removal of side chains to obtain 7-amino-cefenoic acid (7-ACA) is an important raw material for the preparation of semi-synthetic cephalosporin. Synonyms: 7-(5-Amino-5-carboxyvaleramido)cephalosporanic acid; 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 3-((acetyloxy)methyl)-7-((5-amino-5-carboxy-1-oxopentyl)amino)-8-oxo-, (6R-(6alpha,7beta(R*)))-; Centpropazine; Cephalosporin; Cephalosporn C. Grades: 95%. CAS No. 61-24-5. Molecular formula: C16H21N3O8S. Mole weight: 415.42. |  |
| Cephradine | Cephradine (Cefradine) is a broad-spectrum and orally active cephalosporin. Cephradine is active against both gram-positive and gram-negative pathogens. Cephradine is effective in eradicating most penicillinase-producing organisms. Cephradine has been used in the research of genitourinary, gastrointestinal and respiratory tract infections, and in infections of the skin and soft tissues. Cephradine blocks solar-ultraviolet induced skin inflammation through direct inhibition of TOPK [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefradine; SQ-11436. CAS No. 38821-53-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-B1156. | |
| Cephradine monohydrate | Cephradine (Cefradine) monohydrate is a broad-spectrum and orally active cephalosporin. Cephradine monohydrate is active against both grampositive and gram-negative pathogens and effective in eradicating most penicillinase-producing organisms known to be resistant to penicillin G, penicillin V, and ampicillin. Cephradine monohydrate has been used in the research of genitourinary, gastrointestinal and respiratory tract infections, and in infections of the skin and soft tissues. Cephradine monohydrate blocks solar-ultraviolet induced skin inflammation through direct inhibition of TOPK [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefradine monohydrate. CAS No. 75975-70-1. Pack Sizes: 100 mg; 500 mg. Product ID: HY-128449. | |
| 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. | |
| 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: (1R,5S,6S,8R,2'S,4'S)-2-(2-(3-carboxyphenylcarbamoyl)pyrrolidin-4-ylthio)-6-(1-hydroxyethyl)-1-methylcarbapenem-3-carboxylic acid; 1-Azabicyclo(3.2.0)hept-2-ene-2-carboxylic acid, 3-(((3S,5S)-5-(((3-carboxyphenyl)amino)carbonyl)-3-pyrrolidinyl)thio)-6-((1R)-1-hydroxyethyl-4-methyl-7-oxo-, (4R,5S,6S)-; 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-, (4R-(3(3S*, 5S*), 4α, 5β, 6β(R*)))-. Grades: 95%. CAS No. 153832-46-3. Molecular formula: C22H25N3O7S. Mole weight: 475.52. | |
| 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. | |
| Flucloxacillin | Flucloxacillin is a semi-synthetic isoxazole penicillin. The antibacterial effect is stronger than oxacillin, the antibacterial activity against penicillinase-producing Staphylococcus aureus is slightly higher than cloxacillin, and the oral absorption rate is twice as high as cloxacillin. Uses: Flucloxacillin is used to treat infections caused by susceptible gram-positive bacteria and has activity against beta-lactamase-producing organisms. Synonyms: Floxapen; flucloxacilina; Flucloxacillinum; 3-(2-Chloro-6-fluorophenyl)-5-methyl-4-isoxazolylpenicillin; BRL 2039. Grades: >98%. CAS No. 5250-39-5. Molecular formula: C19H17ClFN3O5S. Mole weight: 453.87. | |
| Lactamase (Crude Enzyme) | Penicillinase from Bacillus cereushas been shown to contain three distinct species when purified and examined for homogeneity by sedimentation analysis, amino-terminal analysis, and vertical acrylamide gel electrophoresis. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Synthesis; medicine; biotechnology; pharmacology. Group: Enzymes. Synonyms: 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. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. 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. Pack: 100ml. Cat No: NATE-1839. | |
| 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 |  |
| Native Bacillus cereus β-lactamase Blend | β--lactamase inactivates β-lactam antibiotics by breaking open the β-lactam ring. Applications: Useful for assaying penicillins and cephalosporins. 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 3.5.2.6; 9073-60-3. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Storage: at -20°C. Ok to freeze. Form: Lyophilized Powder. Source: Bacillus cereus 569/H9. 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-1628. | |
| 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. | |
| Native Pseudomonas fluorescens β-Lactamase | β--lactamase inactivates β-lactam antibiotics by breaking open the β-lactam ring. 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 3.5.2.6; 9073-60-3. Enzyme Commission Number: EC 3.5.2.6. CAS No. 9073-60-3. β-Lactamase. Storage: 2-8°C. Form: Lyophilized powder containing potassium phosphate and sodium bicarbonate. Source: Pseudomonas fluorescens. 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-0775. | |
| Oxacillin | Oxacillin is a semisynthetic penicillinase-resistant and acid-stable penicillin with an antimicrobial activity. It is a narrow-spectrum beta-lactam antibiotic of the penicillin class. It is widely used in resistant staphylococci infections. It binds to penicillin-binding proteins in the bacterial cell wall, thus blocking the synthesis of peptidoglycan, which leads to inhibition of cell growth and causes cell lysis. It was developed by Beecham and has been listed. Uses: Oxacillin is widely used in resistant staphylococci infections. Synonyms: [2S-(2,5,6)]-3,3-dimethyl-6-(methyl-3-phenylisoxaz-4-ole-carboxamide-7-oxy-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid; 5-Methyl-3-phenyl-4-isoxazolyl-penicillin. Grades: 98%. CAS No. 66-79-5. Molecular formula: C19H19N3O5S. Mole weight: 401.44. | |
| 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 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 |
| Penicillin | It is produced by the strain of Cephalosporium aceemonium, C. salmosynnematum, Emericellopsis salmosynnemata. It has weak anti-gram-positive bacteria (activity against Staphylococcus aureus is only 1% of penicillin G) and anti-gram-negative bacteria activity, and can be broken down by penicillinase and cross-resistant to penicillin G. Synonyms: Penicillin N; Synnematin B; Cephalosporin N; Adicillin; Salmotin; SYNNEMATINB; Adicillinum; Synnematin N; (2S,5R,6R)-6-(5-Amino-5-carboxyvaleramido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptan-2-carbonsaeure; Cephalosphorin R; 6-N- ( (5-Amino-5-carboxy) pentanoyl) aminopenicillansaeure; (4-Amino-4-carboxybutyl)penicillin; NSC 113137; (D-4-Amino-4-carboxybutyl) penicillinic acid. Grades: 95%. CAS No. 525-94-0. Molecular formula: C14H21N3O6S. Mole weight: 359.40. | |
| Penicillin G Potassium Salt | Penicillin G is a narrow spectrum antibiotic derived from Streptococcus pneumoniae. It is the drug of choice for groups A, B, C and G streptococci, nonenterococcal group D streptococci, viridians group streptococci, and non-penicillinase producing staphylococcus. The potassium salt has been used to study murosomes of staphylococci and the penicillin-induced lysis of Streptococcus mutans. Group: Biochemicals. Alternative Names: (2S, 5R, 6R)-3, 3-Dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Potassium Salt; Penicillin G Potassium Salt; Benzylpenicillin Potassium; Cosmopen; Cristapen; Crytapen; Eskacillin; Falapen; Forpen; Hipercilina; Hyasorb; Hylenta; M-Cillin; Monopen; NSC 131815; Notaral; Pentid; Pentids; Potassium 6- (Phenylacetamido) penicillanate; Potassium Benzylpenicillin; Potassium Benzylpenicillinate; Potassium Penicillin G; Scotcil; Tabilin. Grades: Cell Culture Grade. CAS No. 113-98-4. Pack Sizes: 100g, 500g, 1Kg. US Biological Life Sciences. | Worldwide |
| Phenoxymethylpenilloic Acid (Penilloic Acid V) | A reversible competitive inhibitor of Penicillinase, ß-Lactamase 1. Group: Biochemicals. Alternative Names: Penilloic Acid V. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Pipacycline | A semi-synthetic tetracycline formed by a mannich condensation of formaldehyde and 4-hydroxyethylpiperazine with tetracyclin. It inhibits the formation of penicillinase, the enzyme that inactivates penicillin in bacteria. It is used in salt form with penicillin V for parenteral use. Synonyms: Mepicycline; Pipacyclinum. Grades: >98% by HPLC. CAS No. 1110-80-1. Molecular formula: C29H38N4O9. Mole weight: 586.63. | |
| Quinacillin | It is produced by the strain of Semisynthetic penicillin. It is also effective against gram-positive and gram-negative bacteria and penicillinase producing bacteria. Synonyms: Quinacilina; Quinacilline; Quinacillinum; (3-Carboxy-2-quinoxalinyl)penicillin; 3-Carboxy-2-quinoxalinylpenicillic acid; chinacillin; 7-chloro-2-ethyl-1,2,3,4-tetrahydro-4-oxo-6-quinazolinesulfonamide; 3-{[(2S,5R,6R)-2-Carboxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-6-yl]carbamoyl}-2-quinoxalinecarboxylic acid. CAS No. 1596-63-0. Molecular formula: C18H16N4O6S. Mole weight: 416.41. | |
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