Sultamicillin structure
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Common Name | Sultamicillin | ||
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CAS Number | 76497-13-7 | Molecular Weight | 594.657 | |
Density | 1.6±0.1 g/cm3 | Boiling Point | 907.7±65.0 °C at 760 mmHg | |
Molecular Formula | C25H30N4O9S2 | Melting Point | 190° | |
MSDS | N/A | Flash Point | 502.8±34.3 °C |
Use of SultamicillinSultamicillin is an orally active double prodrug of Ampicillin/Sulbactan. Sulbactam is a semisynthetic beta-lactamase inhibitor which, in combination with Ampicillin, extends the antibacterial activity of the latter to include some beta-lactamase-producing strains of bacteria that would otherwise be resistant[1]. |
Name | sultamicillin |
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Synonym | More Synonyms |
Description | Sultamicillin is an orally active double prodrug of Ampicillin/Sulbactan. Sulbactam is a semisynthetic beta-lactamase inhibitor which, in combination with Ampicillin, extends the antibacterial activity of the latter to include some beta-lactamase-producing strains of bacteria that would otherwise be resistant[1]. |
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Related Catalog | |
References |
Density | 1.6±0.1 g/cm3 |
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Boiling Point | 907.7±65.0 °C at 760 mmHg |
Melting Point | 190° |
Molecular Formula | C25H30N4O9S2 |
Molecular Weight | 594.657 |
Flash Point | 502.8±34.3 °C |
Exact Mass | 594.145447 |
PSA | 216.16000 |
LogP | -0.29 |
Vapour Pressure | 0.0±0.3 mmHg at 25°C |
Index of Refraction | 1.668 |
Storage condition | 2-8°C |
Water Solubility | Practically insoluble in water, very slightly soluble in methanol, practically insoluble in ethanol (96 per cent). |
HS Code | 2934999090 |
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Precursor 2 | |
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DownStream 0 |
HS Code | 2934999090 |
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Summary | 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Clinical response at Day 3 of therapy and economic outcomes in hospitalized patients with acute bacterial skin and skin structure infection (ABSSSI).
Curr. Med. Res. Opin. 29(7) , 869-77, (2013) The FDA recently issued guidance for the types of infections that should be included in trials to support an indication for antibacterial treatment. The latest FDA guidance recommends assessing respon... |
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Antibiotic regimens for management of intra-amniotic infection.
Cochrane Database Syst. Rev. 12 , CD010976, (2014) Chorioamnionitis is a common infection that affects both mother and infant. Infant complications associated with chorioamnionitis include early neonatal sepsis, pneumonia, and meningitis. Chorioamnion... |
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Anaerobiospirillum succiniciproducens-induced bacteremia in a healthy man.
Am. J. Emerg. Med. 32(7) , 812.e1-3, (2014) Anaerobiospirillum succiniciproducens is rarely associated with bacteremia but results in significant mortality. Almost all reported bacteremia cases have occurred in immunocompromised hosts, such as ... |
6'-(2-Amino-2-phenylacetamido)penicillanoyloxymethylpenicillanate 1,1-dioxide |
Sultancillin alkali |
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-, [[[(2S,5R,6R)-6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-yl]carbonyl]oxy]methyl ester, 4,4-dioxide, (2S,5R)- |
Unacid PD |
SultaMcillin Base |
VD 1827 |
1,1-Dioxopenicillanoyloxymethyl 6-(D-a-amino-a-phenylacetamido)penicillanate |
({[(2S,5R,6R)-6-{[(2R)-2-Amino-2-phenylacetyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-yl]carbonyl}oxy)methyl (2S,5R)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide |
Sultamicillin |
Bethadl Orale |
Sultamicillin Base |
Baeimex |