Sulbactam 68373-14-8 C8H11NO5S
Sulbactam Basic information |
Product Name: | Sulbactam |
Synonyms: | (2S,5R)-3,3-DIMETHYL-4,4,7-TRIOXO-4LAMBDA6-THIA-1-AZA-BICYCLO[3.2.0]HEPTANE-2-CARBOXYLIC ACID;(2S-CIS)-3,3-DIMETHYL-7-OXO-4-THIA-1-AZABICYCLO[3,2,0]HEPTANE-2-CARBOXYLIC ACID 4,4-DIOXIDE;3,3-DIMETHYL-4,4,7-TRIOXO-4LAMBDA6-THIA-1-AZA-BICYCLO[3.2.0]HEPTANE-2-CARBOXYLIC ACID;SULBACTAM;SULBACTAM ACID;sulbactam acid (base);PENICILLANIC ACID SULFONE;(2S,5R)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide |
CAS: | 68373-14-8 |
MF: | C8H11NO5S |
MW: | 233.24 |
EINECS: | 269-878-2 |
Product Categories: | Peptide Synthesis/Antibiotics;MERITAL |
Mol File: | 68373-14-8.mol |
Sulbactam Chemical Properties |
storage temp. | −20°C |
form | lyophilized powder |
MSDS Information |
Provider | Language |
---|---|
Sulbactam | English |
Sulbactam Usage And Synthesis |
Usage | antidepressant, dopamine uptake inhibitor |
Usage | Sulbactam sodium is a semi-synthetic penem antibiotic formed by the oxidation of penicillanic acid to its sulfone and was invented by Barth at Pfizer in 1978. Sulbactam sodium is a weak antibiotic but its action as an irreversible inhibitor of β-lactamase is exploited to block the degradation of other penicillin derivatives. Sulbactam acts as a synergist with cephalosporins and penicillins against Gram positive bacteria and is used commercially in combination with ampicillin. |
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