Name | cefpiramide |
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Synonyms |
CEFPIRAMIDE
Cefpiramide acid |
Description | Cefpiramide (SM-1652) free acid is a semisynthetic cephalosporin with broad-spectrum antibacterial activity. Cefpiramide free acid shows strong antibacterial effect on both gram-positive bacteria and gram-negative bacteria. Cefpiramide free acid is moderately susceptible to β-lactamase[1][2]. |
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Related Catalog | |
Target |
Bacterial[1][2] |
In Vitro | Cefpiramide (0-2048 µg/mL; 16-18 hours) shows good activity to against most non-fermentative Gram-negative bacilli and Enterococci (32 µg/mL with 97% inhibition)[1]. Cefpiramide (0-2048 µg/mL; 16-18 hours) exhibits high effective to against Pseudomonas aeruginosa with MIC[50] and MIC[90] values of 4 µg/mL and 16 µg/mL separately[1]. Cell Viability Assay[1] Cell Line: 761 bacterial isolates (35 different species of common bacterial pathogens) Concentration: 0-2048 µg/mL Incubation Time: 16-18 hours Result: Showed broad-spectrum antibacterial activity. |
In Vivo | Cefpiramide (25 mg/kg; i.v.; once) shows anti-Streptococcus pneumoniae activity in experimental pneumococcal meningitis[2]. Cefpiramide (25 mg/kg; i.v.; once) reduces bacteria in CSF more than 10[4] CFU/ml[2]. Animal Model: New Zealand white male rabbits(2-3 kg)[2]. Dosage: 25 mg/kg Administration: Intravenous injection; once. Result: Anti-Streptococcus pneumoniae. |
References |
Density | 1.75 g/cm3 |
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Melting Point | 213-215° (dec) |
Molecular Formula | C25H24N8O7S2 |
Molecular Weight | 612.63700 |
Exact Mass | 612.12100 |
PSA | 263.36000 |
LogP | 1.04640 |
Index of Refraction | 1.821 |
RIDADR | NONH for all modes of transport |
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HS Code | 3003201900 |
HS Code | 3003201900 |
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