Aspoxicillin structure
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Common Name | Aspoxicillin | ||
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CAS Number | 63358-49-6 | Molecular Weight | 493.533 | |
Density | 1.5±0.1 g/cm3 | Boiling Point | 985.1±65.0 °C at 760 mmHg | |
Molecular Formula | C21H27N5O7S | Melting Point | 195-198° (dec) | |
MSDS | Chinese USA | Flash Point | 549.5±34.3 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of AspoxicillinAspoxicillin is a broad-spectrum antimicrobial agent against 68 isolates of Actinobacillus pleuropneumoniae with an MIC90 value of <= 0.05 μg/ml. Aspoxicillin has a long half-life in mouse serum of 55 minutes[1][2]. |
Name | Aspoxicillin |
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Synonym | More Synonyms |
Description | Aspoxicillin is a broad-spectrum antimicrobial agent against 68 isolates of Actinobacillus pleuropneumoniae with an MIC90 value of <= 0.05 μg/ml. Aspoxicillin has a long half-life in mouse serum of 55 minutes[1][2]. |
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Related Catalog | |
Target |
microbe[1] |
In Vitro | Aspoxicillin is a semisynthetic penicillin derivative[2]Aspoxicillin induces postantibiotic effects (PAEs) against Staphylococcus aureus Smith of 1.7 h in vitro[2]. |
In Vivo | Aspoxicillin induces PAEs against Staphylococcus aureus Smith of 5.2 h in vivo in a thigh infection model in neutropenic mice[2]. |
References |
Density | 1.5±0.1 g/cm3 |
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Boiling Point | 985.1±65.0 °C at 760 mmHg |
Melting Point | 195-198° (dec) |
Molecular Formula | C21H27N5O7S |
Molecular Weight | 493.533 |
Flash Point | 549.5±34.3 °C |
Exact Mass | 493.163116 |
PSA | 215.87000 |
LogP | -0.53 |
Vapour Pressure | 0.0±0.3 mmHg at 25°C |
Index of Refraction | 1.672 |
Storage condition | 2-8°C |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi:Irritant |
Risk Phrases | R36/37/38 |
Safety Phrases | S26 |
RIDADR | NONH for all modes of transport |
RTECS | MB7548000 |
[In vitro study on efficacy of combination use of aspoxicillin and beta-lactam preparations (ceftazidime, cefmetazole and aztreonam) against bacteria isolated from abdominal infections].
Jpn. J. Antibiot. 45(7) , 763-73, (1992) An in vitro study was done to evaluate combination use of aspoxicillin (ASPC) with each of 3 beta-lactam preparations, ceftazidime (CAZ), cefmetazole (CMZ) and aztreonam (AZT). The results obtained ar... |
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[A clinical study of combined therapy of aspoxicillin and ceftazidime on intractable respiratory infections].
Jpn. J. Antibiot. 45(10) , 1282-94, (1992) Both aspoxicillin (ASPC) and ceftazidime (CAZ) were administered together to 55 patients with intractable respiratory tract infections. ASPC and CAZ were administered at daily doses of 4 g and 2 to 4 ... |
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Separation and determination of aspoxicillin in human plasma by micellar electrokinetic chromatography with direct sample injection.
J. Chromatogr. A. 515 , 245-55, (1990) Both the separation and determination of aspoxicillin in human plasma by micellar electrokinetic chromatography (MEKC) were investigated. Selectivity in the separation of seven penicillin antibiotics ... |
glycinamide,n-methyl-d-asparaginyl-n-(2-carboxy-3,3-dimethyl-7-oxo-4-thia-1-a |
(2S,5R,6R)-6-({(2R)-2-(4-Hydroxyphenyl)-2-[(N-methyl-D-asparaginyl)amino]acetyl}amino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid |
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2R)-2-[[(2R)-2-amino-4-(methylamino)-1,4-dioxobutyl]amino]-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-, (2S,5R,6R)- |
ASPOXICILLIN 3-HYDRATE |
n(sup4)-methyl-d-asparagininylamoxicillin |
Aspoxicillin |
[2S-(2a,5a,6b)]-N-Methyl-D-asparaginyl-N-(2-carboxy-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-6-yl)-D-2-(4-hydroxyphenyl)glycinamide |
N4-Methyl-D-asparaginylamoxicillin |
6-[D-2-(D-2-Amino-3-N-methylcarbamoylpropionamido)-2-p-hydroxyphenylacetamido]penicillanic Acid |
Doyle |
Aspoxicilin |
(2S,5R,6R)-6-[(2R)-2-[(2R)-2-Amino-3-(methylcarbamoyl)propionamido]-2-(p-hydroxyphenyl)acetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid |
TA 058 |
ASPC |