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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.
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Penicillin G potassium salt (Benzylpenicillin potassium salt)
25g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17KN2O4S. CAS No. 113-98-4. Prepack ID 23531529-25g. Molecular Weight 372.48. See USA prepack pricing.
Phenoxy methyl penicillinic acid potassium salt, Potency ≥1500U/mg. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100MU. US Biological Life Sciences.
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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.
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.
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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.
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Dihydropenicillin F Potassium Salt
An impurity of Penicillin Potassium which is an antibacterial drug and acts through the inhibition of biosynthesis of cell-wall mucopeptide. Synonyms: potassium salt of 6-pentylpenicillin; Pennicillin G potassium; 6-pentylpenicillin. Grade: > 95%. CAS No. 31447-86-6. Molecular formula: C14H21N2O4S.K. Mole weight: 352.5.
Penicillin g
Penicillin g. Uses: Designed for use in research and industrial production. Additional or Alternative Names: PENICILLIN G K-SALT;PENICILLIN G POTASSIUM;PENICILLIN G POTASSIUM SALT;(5r,6r)-benzylpenicillin;(phenylmethyl)-penicilli;(phenylmethyl)penicillin;(phenylmethyl)-penicillinicaci;(phenylmethyl)penicillinicacid. Appearance: powder. CAS No. 61-33-6. Molecular formula: C16H18N2O4S. Mole weight: 334.39. Purity: 95%+. IUPACName: (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid. Canonical SMILES: CC1(C(N2C(S1)C(C2=O)NC(=O)CC3=CC=CC=C3)C(=O)O)C. Density: 1.42g/cm³. ECNumber: 200-506-3. Product ID: ACM61336. Alfa Chemistry ISO 9001:2015 Certified.
Penicillin V-d5 potassium
Penicillin V-d 5 (potassium) is the deuterium labeled Penicillin V Potassium[1]. Penicillin V Potassium (Phenoxymethylpenicillin potassium salt) is an orally active antibiotic. Penicillin V Potassium inhibits the growth of Streptococci, C. difficile and S. aureus. Penicillin V Potassium can be used for the research of otitis, sinusitis, pharyngitis and tonsillitis[2][3][4][5]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: Phenoxymethylpenicillin-d5 potassium salt. CAS No. 2699607-22-0. Pack Sizes: 1 mg. Product ID: HY-B0975S1.
Penicillin V Potassium
Penicillin V Potassium (Phenoxymethylpenicillin potassium salt) is an orally active antibiotic. Penicillin V Potassium inhibits the growth of Streptococci , C. difficile and S. aureus. Penicillin V Potassium can be used for the research of otitis, sinusitis, pharyngitis and tonsillitis [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: Phenoxymethylpenicillin potassium salt. CAS No. 132-98-9. Pack Sizes: 5 g; 10 g. Product ID: HY-B0975.
Penicillin V Potassium Salt
The Potassium Salt form of Penicillin V is an orally active penicillin that has been found to be an effective antibiotic against sorts of bacteria. Uses: Penicillins. Synonyms: (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-[(2-phenoxyacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Potassium; 6-(Phenoxyacetamido)penicillanic Acid Potassium; Antibiocin; Calciopen K; Cilacil; Fenoxypen; Vepicombin; 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-(2-phenoxyacetamido)-, (2S,5R,6R)-, Potassium salt. Grade: 96%. CAS No. 132-98-9. Molecular formula: C16H17KN2O5S. Mole weight: 388.48.
Potassium benzylpenicillin
Penicillin G potassium is a fast-acting antibiotic, used to treat bacterial infections that affect the blood, heart, lungs, joints, and genital areas. 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 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 Benzylpenicillinate; Potassium Penicillin G; Scotcil; Tabilin; Penicillin G potassium salt; Potassium benzylpenicillin. Grade: 98%. CAS No. 113-98-4. Molecular formula: C16H17KN2O4S. Mole weight: 372.48.
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
Benzylpenicillinate-d7, Potassium Salt
Benzylpennicillin (penicillin G) is a widely used antibiotic in veterinary medicine. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
Penicillin V potassium salt
100g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17KN2O5S. CAS No. 132-98-9. Prepack ID 55440700-100g. Molecular Weight 388.48. See USA prepack pricing.
Penicillin V potassium salt
25g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17KN2O5S. CAS No. 132-98-9. Prepack ID 55440700-25g. Molecular Weight 388.48. See USA prepack pricing.
Penicillin V potassium salt
analytical standard. Group: Application areas.
Penicillin V Potassium Salt
Antibacterial. Group: Biochemicals. Alternative Names: (2S, 5R, 6R)-3, 3-Dimethyl-7-oxo-6-[(2-phenoxyacetyl)amino]-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Potassium; 6- (Phenoxyacetamido) penicillanic Acid Potassium; Antibiocin. Grades: Highly Purified. CAS No. 132-98-9. Pack Sizes: 100mg. US Biological Life Sciences.
Worldwide
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