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| Product | Description | |
|---|---|---|
| Carbenicillin | It is produced by the strain of Semisynthetic penicillin, 6-APA. Carbenicillin is a broad-spectrum semisynthetic penicillin derivative used parenterally. It is a semi-synthetic penicillin antibiotic which interferes with cell wall synthesis of gram-negative bacteria while displaying low toxicity. It is used to treat pseudomonas aeruginosa infection. Synonyms: Carboxybenzylpenicillin; alpha-Carboxybenzylpencillin; Carbenicilina; Carbenicilline; Carbenicillinum; Pyopen; Carboxybenzylpenicillin acid; CBPC; Geopen. Grades: >98%. CAS No. 4697-36-3. Molecular formula: C17H18N2O6S. Mole weight: 378.40. |  |
| Carbenicillin 100mg/ml, in ethanol/water, 0.2um sterile-filtered | Carbenicillin (alpha-carboxybenzyl penicillin) is a synthetic penicillin derivative used as a selection agent for carbenicillin-resistant plasmids (amp). Group: Biochemicals. Alternative Names: a-Carboxybenzyl penicillin disodium salt. Grades: Molecular Biology Grade. CAS No. 4800-94-6. Pack Sizes: 1ml, 5ml. US Biological Life Sciences. |  Worldwide |
| Carbenicillin disodium | Carbenicillin disodium (Sodium carbenicillin) is a broad-spectrum semi-synthetic penicillin antibiotic for gram-negative bacteria. Carbenicillin disodium can interfere the cell wall synthesis while displaying low toxicity to plant tissue [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Sodium carbenicillin. CAS No. 4800-94-6. Pack Sizes: 250 mg; 1 g; 5 g. Product ID: HY-B0525A. |  |
| 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 | 25g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Biochemicals, Research Organics & Inorganics. Formula: C17H16N2Na2O6S. CAS No. 4800-94-6. Prepack ID 32113067-25g. Molecular Weight 422.36. See USA prepack pricing. |  |
| Carbenicillin disodium salt | 5g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Biochemicals, Research Organics & Inorganics. Formula: C17H16N2Na2O6S. CAS No. 4800-94-6. Prepack ID 32113067-5g. Molecular Weight 422.36. See USA prepack pricing. | |
| 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). | |
| 2-Bromo carbenicillin disodium salt | 2-Bromo carbenicillin disodium salt. Group: Biochemicals. Alternative Names: [2S- (2a, 5a, 6b) ]-6-[[ (2-Bromophenyl) carboxyacetyl]amino]-3, 3-dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic acid disodium salt. Grades: Highly Purified. CAS No. 59530-63-1. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C17H15BrN2Na2O6S. US Biological Life Sciences. | Worldwide |
| Ampicillin Beta-Lactamase Modified, 1000X | Ampicillin Beta-Lactamase Modified, is a unique antibiotic that is a stronger inhibitor of b-Lactamase than ampicillin, carbenicillin or methicillin. Ampicillin is modified utilizing a novel method that results in improved transformation efficiencies where higher cell density and longer incubation times traditionally result in the development of ampicillin sensitive satellite colonies. When used at a concentration of 1X, the presence of satellite colonies Identificatis reduced, even after prolonged incubation (2-4 days) and plating of competent cells at 20 fold higher density. Group: Biochemicals. Grades: Molecular Biology Grade. Pack Sizes: 3x1ml. US Biological Life Sciences. | Worldwide |
| Carfecillin sodium | Carfecillin sodium, a phenyl derivative of carbenicillin, is a beta-lactam antibiotic used to treat urinary tract infections. Synonyms: Carbenicillin phenyl sodium; carfecilina sodica; Carfexil; Pencina; Purapen; Carfecillin Sodium Salt; sodium [2S-(2alpha,5alpha,6beta)]-6-[(1,3-dioxo-3-phenoxy-2-phenylpropyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate. Grades: 95%. CAS No. 21649-57-0. Molecular formula: C23H21N2NaO6S. Mole weight: 476.48. | |
| Carfecillin Sodium | Carfecillin Sodium, also known as Carbenicillin Phenyl Sodium and BRL-3475, is the phenyl ester of Carbenicillin that, upon oral administration, is broken down in the intestinal mucosa to the active antibacterial. It is used for urinary tract infections. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Carfecillin Sodium; BRL-3475; BRL 3475; BRL3475; Carbenicillin Phenyl Sodium; Uticillin. Product Category: Others. Appearance: Solid powder. CAS No. 21649-57-0. Molecular formula: C23H21N2NaO6S. Mole weight: 476.48. Purity: >98%. IUPACName: sodium (2S,5R,6R)-3,3-dimethyl-7-oxo-6-(3-oxo-3-phenoxy-2-phenylpropanamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate. Canonical SMILES: O=C([C@@H](C(C)(C)S[C@]1([H])[C@@H]2NC(C(C3=CC=CC=C3)C(OC4=CC=CC=C4)=O)=O)N1C2=O)[O-].[Na+]. Product ID: ACM21649570-1. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Carindacillin sodium | Carindacillin (Carbenicillin indanyl) sodium is an orally active and broad-spectrum antimicrobial agent. Carindacillin sodium can be hydrolyzed to Carbenicillin in vivo. Carindacillin sodium can be used for the research of urinary-tract infection [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Carbenicillin indanyl sodium; CP-15464-2. CAS No. 26605-69-6. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-108880. | |
| Cefpiramide sodium | Cefpiramide sodium is a new Pseudomonas-active cephalosporin with a broad spectrum of antibacterial activity. It was more active against Acinetobacter spp. and Pseudomonas spp. It inhibited many Pseudomonas aeruginosa resistant to carbenicillin, piperacillin, and cefotaxime, but it was less active than ceftazidime and cefsulodin. It also inhibited staphylococci and streptococci and had appreciable activity against Streptococcus faecalis and Listeria moncytogenes. Uses: Anti-bacterial agents. Synonyms: SM-1652; Wy-44635; SM 1652; Wy 44635; SM1652; Wy44635. Grades: >98%. CAS No. 74849-93-7. Molecular formula: C25H23N8NaO7S2. Mole weight: 635.63. | |
| 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. | |
| Sodium Indanylcarbinicillin | Sodium Indanylcarbinicillin. Group: Biochemicals. Alternative Names: (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,6 β )]-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. Grades: Highly Purified. CAS No. 26605-69-6. Pack Sizes: 50mg. Molecular Formula: C26H25N2NaO6S, Molecular Weight: 516.54. US Biological Life Sciences. | Worldwide |
| Timentin (Ticarcillin Disodium/Potassium Clavulanate 15:1) | Timentin is a suitable antibiotic for Agrobacterium counterselection and a mixture of two antibiotics: ticarcillin and clavulanic acid. Most wild Agrobacterium isolates have beta-lactamase activity which clavulanic acid exhibits activity towards. Many Agrobacterium isolates are highly susceptible to Timentin. Agrobacterium strains carrying the standard pBR beta-lactamase gene are also Timentin (clavulanic acid) susceptible. Timentin killing of Agrobacterium wild-type strains is three logs greater than with comparable doses of carbenicillin. In plant transformation experiments, 0.1mg/ml Timentin (15:1) is sufficient to counterselect Agrobacterium.The appropriate dose in tissue culture medium is 0.1 mg/ml (not 0.1 mg/liter) of 15:1 mixture or 0.2 mg/ml of 30:1 mixture. To improve efficacy (of any antimicrobial), solid media are best slightly dried before use. At these concentrations, Timentin exhibits no phytotoxicity toArabidopsis root cultures.Ticarcillin Disodium/Potassium Clavulanate =15:1. 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 disodium/potassium salt. Grades: Highly Purified. CAS No. 4697-14-7,61177-45-5. Pack Sizes: 1g, 10g, 25g. US Biological Life Sciences. | Worldwide |
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