Weight | 463.556 g/mol |
---|---|
Formula | C22H29N3O6S |
Hydrogen Acceptors | 8 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 6 |
Pivampicillin (33817-20-8)
Pivampicillin Monohydrochloride · Pondocillin · Pivamiser
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- CARNITINE DEFICIENCY INDUCED BY PIVAMPICILLIN AND PIVMECILLINAM THERAPY (The Lancet, 1989)
- Pivampicillin-promoted excretion of pivaloylcarnitine in humans (Biochemical Pharmacology, 1987)
- Pharmacokinetics of ampicillin and its prodrugs bacampicillin and pivampicillin in man (Journal of Pharmacokinetics and Biopharmaceutics, 1979)
- Pharmacokinetics of Bacampicillin Compared with Those of Ampicillin, Pivampicillin, and Amoxycillin (Antimicrobial Agents and Chemotherapy, 1978)
- Bioavailability of oral penicillins in the horse: a comparison of pivampicillin and amoxicillin (Journal of Veterinary Pharmacology and Therapeutics, 1992)
- Pivampicillin, a new orally active ampicillin ester. (Antimicrobial Agents and Chemotherapy, 1970)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Pivampicillin Monohydrochloride
- Pondocillin
- Pivamiser
- Ampicillin Pivaloyl Ester
- Serra Pamies Brand of Pivampicillin Hydrochloride
- Berocillin
- Leo Brand of Pivampicillin
- Pivampicillin Hydrochloride
-
SMILESCC1(C(N2C(S1)C(C2=O)NC(=O)C(C3=CC=CC=C3)N)C(=O)OCOC(=O)C(C)(C)C)C
-
InChIKeyZEMIJUDPLILVNQ-UHFFFAOYSA-N
- Pubchem - Pivampicillin
- Wikipedia - pivampicillin
Pivampicillin is a pivaloyloxymethyl ester of ampicillin. It is a prodrug, which is thought to enhance the oral bioavailability of ampicillin because of its greater lipophilicity compared to that of ampicillin.
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