| Product Unit Size | Cost | Quantity | Stock |
|---|
Penicillin V is a hydrophobic β-lactam antibiotic that displays antibacterial efficacy against gram positive bacteria. Penicillin V is less active than penicillin G against gram negative bacteria but exhibits better oral absorption kinetics. Penicillin V inhibits cell wall synthesis and does not display effective inhibition of β-lactamase-producing bacteria.
| Cas No. | 132-98-9 |
|---|---|
| Purity | ≥98% |
| Formula | C16H17KN2O5S |
| Formula Wt. | 388.48 |
| Chemical Name | (2S,5R,6R)-3,3-Dimethyl-7-oxo-6-[( phenoxyacetyl)- amino]-4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid monopotassium salt |
| IUPAC Name | potassium;(2S,5R,6R)-3, 3-dimethyl-7-oxo-6-[(2-phenoxyacetyl)amino]-4-thia-1-azabicyclo[3.2.0] heptane-2-carboxylate |
| Synonym | Penicillin V Potassium salt, Antibiocin, Beromycin, Cliacil, Milcopen, Stabicilline, Phenoxymethylpenicillin potassium. |
| Melting Point | 197-202°C |
| Solubility | Soluble in water. |
| Appearance | White to off white powder |
| Store Temp | Ambient |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
|---|---|
| Info Sheet |
Demain AL. Production of beta-lactam antibiotics and its regulation. Proc Natl Sci Counc Repub China B. 1991 Oct;15(4):251-65. PMID: 1815263.
Bär H, Zarnack J. Molecular-biological bases of the mechanism of action of penicillins and cephasporins. Pharmazie. 1970 Jan 1;25(1):10-22. PMID: 4987180.