Penicillin G: Difference between revisions

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== Chemistry ==
== Chemistry ==
Penicillin G is stable against degradation (hydrolysis)  by  beta-[[lactamase]]s, including[[ penicillinase]]s, and [[cephalosporinase]]s.  Its IUPAC chemical name is (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0] heptane-2-carboxylic acid and it has chemical formula C<sub>16</sub>H<sub>18</sub>N<sub>2</sub>O<sub>4</sub>S (MW = 334.3901 g/mol).
Penicillin G is degraded by (hydrolysis)  by  beta-[[lactamase]]s, including[[ penicillinase]]s, and [[cephalosporinase]]s.  Its IUPAC chemical name is (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0] heptane-2-carboxylic acid and it has chemical formula C<sub>16</sub>H<sub>18</sub>N<sub>2</sub>O<sub>4</sub>S (MW = 334.3901 g/mol).


== Mechanism of action ==
== Mechanism of action ==
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== External links ==
== External links ==
* {{DailyMed}}
{{CZMed}}
* Drug Bank [http://www.drugbank.ca/cgi-bin/getCard.cgi?CARD=DB01053.txt]
* Drug Bank [http://www.drugbank.ca/cgi-bin/getCard.cgi?CARD=DB01053.txt][[Category:Suggestion Bot Tag]]

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(CC) Image: David E. Volk
penicillin G
IUPAC name: see chemistry section
Synonyms: benzopenicillin, benzylpenicillin
Formula: C16H18N2O4S

 Uses: antibiotic drug

 Properties: beta-lactam

 Hazards: see drug interactions

Mass (g/mol): CAS #:
334.3901 61-33-6



Penicillin G, also called benzopenicillin or benzylpenicillin, a penicillin derivative, is a beta-lactam-based antibiotic drug used to treat severe infections from most Gram-positive and some Gram-negative cocci. It is also an experimental drug for the treatment of convulsions due to it effects on synaptic transmission mediated by gamma-aminobutyric acid.

Chemistry

Penicillin G is degraded by (hydrolysis) by beta-lactamases, includingpenicillinases, and cephalosporinases. Its IUPAC chemical name is (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenylacetyl)amino]-4-thia-1-azabicyclo[3.2.0] heptane-2-carboxylic acid and it has chemical formula C16H18N2O4S (MW = 334.3901 g/mol).

Mechanism of action

Penicillins work by binding to specific penicillin-binding proteins (PBPs) in the bacterial cell wall and inhibiting the final stage of bacterial cell wall synthesis, resulting in autolysis of the bacterial cells by autolysin enzymes.

Drug interactions

Penicillins increase the effects of anticoagulant drugs including acenocoumarol, anisindione, dicumarol and warfarin and lessen the effects of some oral contraceptives including ethinyl estradiol and mestranol. Tetracycline and its derivatives doxycycline, demeclocycline, methacycline, minocycline, oxytetracycline, and rolitetracycline may decrease the effectiveness of penicillin. The effects and toxicity of methotrexate increases when used with penicillins.

Brand names

  1. Abbocillin®
  2. Ayercillin®
  3. Benzopenicillin®
  4. Benzylpenicillin®
  5. Benzylpenicillin G®
  6. Benzylpenicillinic Acid®
  7. Bicillin®
  8. Bicillin L-A®
  9. Cillora®
  10. Cilloral®
  11. Cilopen®
  12. Compocillin G®
  13. Cosmopen®
  14. Crysticillin 300 A.S.®

  1. Dropcillin®
  2. Free Benzylpenicillin®
  3. Free Penicillin G®
  4. Free Penicillin Ii®
  5. Galofak®
  6. Gelacillin®
  7. Liquacillin®
  8. Megacillin®
  9. Pencillin G®
  10. Penicillin®
  11. Penicillin G Potassium®
  12. Penicillin G Potassium in Plastic Container®
  13. Penicillin G Sodium®
  14. Penicillin-G Potassium®

  1. Penicillinic Acid, Benzyl-®
  2. Pentids®
  3. Pentids '200'®
  4. Permapen®
  5. Pfizerpen®
  6. Pfizerpen G®
  7. Pharmacillin®
  8. Phenylacetamidopenicillanic Acid®
  9. Pradupen®
  10. Specilline G®
  11. Ursopen®
  12. Wycillin®

External links

The most up-to-date information about Penicillin G and other drugs can be found at the following sites.