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37661-08-8CCOC(=O)OC(C)OC(=O)C1N2C(=O)C(NC(=O)[C@H](N)c3ccccc3)C2SC1(C)C.Cl37661-08-8White or almost white powder or granules, hygroscopic.
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개요Bacampicillin was synthesized by Ekstrom¨ et al. of Astra Lakemedel in 1975. It is ¨ more stable against acid than ampicillin and more rapidly absorbed orally; its absorption is less affected by a patient’s most recent meal than is the case for ampicillin. Bacampicillin is hydrolyzed by intestinal esterase after oral administration and then behaves the same as ampicillin. In double-blind comparison studies, bacampicillin was shown to be as effective as ampicillin when administered at half the dose.
용도Bacampicillin is a penicillin class of antibiotic. Bacampicillin is a prodrug of ampicillin (A634300) with improved oral bioavailability.
정의ChEBI: The hydrochloride salt of bacampicillin.
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