Cloxacillin Sodium structure
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Common Name | Cloxacillin Sodium | ||
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CAS Number | 642-78-4 | Molecular Weight | 475.878 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C19H17ClN3NaO5S | Melting Point | 170ºC | |
MSDS | N/A | Flash Point | N/A |
Use of Cloxacillin SodiumCloxacillin sodium exhibits antibiotic efficacy, with a MIC of 256 mg/L for Staphylococcus aureus 25923[1][2][3]. |
Name | cloxacillin sodium |
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Synonym | More Synonyms |
Description | Cloxacillin sodium exhibits antibiotic efficacy, with a MIC of 256 mg/L for Staphylococcus aureus 25923[1][2][3]. |
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Related Catalog | |
In Vitro | Cloxacillin is an antibiotic useful for the study of a number of bacterial infections[1]. Cell Viability Assay[1] Cell Line: Strains M12 and M60. Concentration: 0.5 μg/mL. Incubation Time: 4-24 h. Result: Significantly reduced the bacterial numbers. |
In Vivo | Cloxacillin sodium (50 mg/kg, Subcutaneously) results a significant antibiotic efficacy against S. aureus[3] Animal Model: Mice[2]. Dosage: 10 mg/kg (Pharmacological Analysis). Administration: Given subcutaneously. Result: Reached a maximal concentration in plasma of 8.4 μg/mL at 10 min and had a half-life of approximately 15 min. Animal Model: Mice injected with approximately 2 × 106 CFU of bacteria in 0.1 mL saline were aseptically injected into the right thigh muscle[3]. Dosage: 0–500 mg/kg. Administration: Subcutaneously in the nuchal region at 1 h after infection. Result: Resulted in a significant decrease in the number of viable S. aureus measured 18 h thereafter. |
References |
Melting Point | 170ºC |
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Molecular Formula | C19H17ClN3NaO5S |
Molecular Weight | 475.878 |
Exact Mass | 475.058075 |
PSA | 140.87000 |
LogP | 1.54280 |
Storage condition | 2-8°C |
Stability | Stable. Incompatible with strong oxidizing agents. Refrigerate. |
Water Solubility | H2O: 50 mg/mL, clear, colorless |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Hazard Codes | Xn |
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Risk Phrases | 36/37/38-42/43 |
Safety Phrases | S22 |
WGK Germany | 2 |
RTECS | XH8920000 |
HS Code | 2941109900 |
~% Cloxacillin Sodium CAS#:642-78-4 |
Literature: WO2012/164355 A1, ; Page/Page column 9-10 ; |
~% Cloxacillin Sodium CAS#:642-78-4 |
Literature: WO2012/164355 A1, ; |
~% Cloxacillin Sodium CAS#:642-78-4 |
Literature: WO2012/164355 A1, ; |
HS Code | 2941109900 |
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Tegopen |
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[[3-(2-chlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-, sodium salt, (2S,5R,6R)-, hydrate (1:1:1) |
Staphybiotic |
Sodium cloxacillin |
cloxacillin sodium hydrate |
Ankerbin |
Cloxapen |
Austrastaph |
(2S,5R,6R)-6-[[[3-(2-Chlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium Salt Monohydrate |
Prevencilina P |
Cloxacillin sodium salt hydrate |
Sodium cloxacillin monohydrate |
cloxacillin sodium monohydrate |
Orbenin |
Sodium (2S,5R,6R)-6-({[3-(2-chlorophenyl)-5-methyl-1,2-oxazol-4-yl]carbonyl}amino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate hydrate (1:1:1) |
MFCD00150735 |
Prostaphilin A |
Ekvacillin |
[(2S,5R,6R)-6-({[3-(2-Chlorophenyl)-5-methyl-1,2-oxazol-4-yl]carbonyl}amino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylato-κO]sodium hydrate (1:1) |
sodium, [(2S,5R,6R)-6-[[[3-(2-chlorophenyl)-5-methyl-4-isoxazolyl]carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylato-κO]-, hydrate (1:1) |
Cloxacillin Sodium Salt |
EINECS 211-390-9 |
Gelstaph |
Monosodium (2S,5R,6R)-6-(3-(o-Chlorophenyl)-5-methyl-4-isoxazolecarboxamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate Monohydrate |
Cloxacillin Sodium |