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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.
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.
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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.
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.
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