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QuickView for penicillin G (compound)


PubChem
Name: Penicillin G
PubChem Compound ID: 2349
Description: A penicillin derivative commonly used in the form of its sodium or potassium salts in the treatment of a variety of infections. It is effective against most gram-positive bacteria and against gram-negative cocci. It has also been used as an experimental convulsant because of its actions on GAMMA-AMINOBUTYRIC ACID mediated synaptic transmission.
Molecular formula: C16H18N2O4S
Molecular weight: 334.391 g/mol
Synonyms:
Sodium penicillin G; Cosmopen; Specilline G; Free benzylpenicillin; Megacillin tablets; Pen-A-Brasive; Falapen; Abbocillin; Benzylpenicillinic acid; Penalev.
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DrugBank
Identification
Name: Penicillin G
Name (isomeric): DB01053
Drug Type: small molecule
Description: A penicillin derivative commonly used in the form of its sodium or potassium salts in the treatment of a variety of infections. It is effective against most gram-positive bacteria and against gram-negative cocci. It has also been used as an experimental convulsant because of its actions on GAMMA-AMINOBUTYRIC ACID mediated synaptic transmission.
Brand: Pentids, Galofak, Cillora, Specilline G, Abbocillin, Pharmacillin, Pradupen, Penicillinic Acid, Benzyl-, Bicillin L-A, Benzylpenicillin G, Ursopen, Cosmopen, Pencillin G, Penicillin G Potassium, Bicillin, Dropcillin, Penicillin G Sodium, Pfizerpen, Compocillin G, Gelacillin, Cilopen, Wycillin, Pfizerpen G, Penicillin G Potassium in Plastic Container, Penicillin-G Potassium, Benzylpenicillinic Acid, Penicillin, Pentids '200', Benzylpenicillin, Crysticillin 300 A.S., Ayercillin, Cilloral, Permapen, Free Benzylpenicillin, Free Penicillin Ii, Megacillin, Phenylacetamidopenicillanic Acid, Benzopenicillin, Liquacillin, Free Penicillin G
Category: Anti-Bacterial Agents, Penicillins
CAS number: 61-33-6
Pharmacology
Indication: For use in the treatment of severe infections caused by penicillin G-susceptible microorganisms when rapid and high penicillin levels are required such as in the treatment of septicemia, meningitis, pericarditis, endocarditis and severe pneumonia.
Pharmacology:
Penicillin G is a penicillin beta-lactam antibiotic used in the treatment of bacterial infections caused by susceptible, usually gram-positive, organisms. The name "penicillin" can either refer to several variants of penicillin available, or to the group of antibiotics derived from the penicillins. Penicillin G has in vitro activity against ...
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Mechanism of Action: By binding to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall, penicillin G inhibits the third and last stage of bacterial cell wall synthesis. Cell lysis is then mediated by bacterial cell wall autolytic enzymes such as autolysins; it is possible that penicillin G interferes with an autolysin inhibitor.
Absorption: Rapidly absorbed following both intramuscular and subcutaneous injection. Initial blood levels following parenteral administration are high but transient. Oral absorption in fasting, healthy humans is only about 15-30% as it is very susceptible to acid-catalyzed hydrolysis.
Protein binding: Bind to serum proteins (45-68%), mainly albumin.
Biotransformation: About 16-30% of an intramuscular dose is metabolized to penicilloic acid, an inactive metabolite. Small amounts of 6-aminopenicillanic acid have been recovered in the urine of patients on penicillin G. A small percentage of the drug appears to be hydroxylated into one or more active metabolites, which are also excreted via urine.
Route of elimination: Penicillin G is eliminated by the kidneys. Nonrenal clearance includes hepatic metabolism and, to a lesser extent, biliary excretion.
Half Life: In adults with normal renal function is reportedly 0.4–0.9 hours
Clearance: 560ml/min in healthy humans
Toxicity: Oral LD50 in rat is 8900 mk/kg. Neurological adverse reactions, including convulsions, may occur with the attainment of high CSF levels of beta-lactams. Neutropenia can occur if high doses are administered consistently for over 2 weeks.
Affected organisms: Enteric bacteria and other eubacteria
Interactions
Drug interaction:
OxytetracyclinePossible antagonism of action
ThioridazineIncreased risk of cardiotoxicity and arrhythmias
MethacyclinePossible antagonism of action
DoxycyclinePossible antagonism of action
DemeclocyclinePossible antagonism of action
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Targets


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