Chloramphenicol: Difference between revisions

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'''Chloramphenicol''' was the first broad-spectrum [[antibiotic]] discovered, in 1947, from ''[[Streptomyces venequelae]]'' cultures.  Although it is active against a wide variety of organisms including [[tetracycline]]-resistant [[vibrio]]s, toxicity and safety concerns, such as bone marrow damage and anemia, typically limits its use to only the treatment of very serious infections, such as cholera and typhoid fever.  The antibiotic works by binding to bacterial ribosome 50S subunits and inhibiting bacterial protein synthesis.
'''Chloramphenicol''' was the first broad-spectrum [[antibiotic]] discovered, in 1947, from ''[[Streptomyces venequelae]]'' cultures.  Although it is active against a wide variety of organisms including [[tetracycline]]-resistant [[vibrio]]s, toxicity and safety concerns, such as bone marrow damage and anemia, typically limits its systemic use to only the treatment of very serious infections, such as [[cholera]] and [[typhoid fever]].  The antibiotic works by binding to bacterial ribosome 50S subunits and inhibiting bacterial protein synthesis.


{| " style="border: solid; center; width:450px;"
!align=left colspan=3 style="background:#{{{color}}}"| "Therapy with chloramphenicol must be limited to infections for which the benefits of the drug outweigh the risks of the potential toxicities. When other antimicrobial drugs are available that are equally effective and potentially less toxic than chloramphenicol, they should be used." <ref>{{citation
| title = Goodman & Gilman's The Pharmacological Basis of Therapeutics
| edition = 9th Edition
| publisher =McGraw-Hill
}}, p. 1133</ref>
|-
|}
== Chemistry ==
== Chemistry ==
Chloroamphenicol, or 2,2-dichloro-N-[1,3-dihydroxy-1-(4-nitrophenyl)propan-2-yl]acetamide, has molecular formula C<sub>11</sub>H<sub>12</sub>Cl<sub>2</sub>N<sub>2</sub>O<sub>5</sub> and molecular mass 323.1294 g/mol.  The drug is referred to by several names, including CAF, CAM, CAP, chloramphenicole, chloramfenikol, chloroamphenicol, cloroamfenicolo, CPh, D-Chloramphenicol.
Chloroamphenicol, or 2,2-dichloro-N-[1,3-dihydroxy-1-(4-nitrophenyl)propan-2-yl]acetamide, has molecular formula C<sub>11</sub>H<sub>12</sub>Cl<sub>2</sub>N<sub>2</sub>O<sub>5</sub> and molecular mass 323.1294 g/mol.  The drug is referred to by several names, including CAF, CAM, CAP, chloramphenicole, chloramfenikol, chloroamphenicol, cloroamfenicolo, CPh, D-Chloramphenicol.


== References ==
== References ==
{{reflist}}
{{CZMed}}
{{CZMed}}

Revision as of 18:21, 23 August 2010

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Chloramphenicol.jpg
chloramphenicol
IUPAC name: see chemistry section
Synonyms: see below
Formula: C11H12Cl2N2O5

 Uses: antibiotic

 Properties:

 Hazards: toxicity

Mass (g/mol): CAS #:
323.1294 56-75-7


Chloramphenicol was the first broad-spectrum antibiotic discovered, in 1947, from Streptomyces venequelae cultures. Although it is active against a wide variety of organisms including tetracycline-resistant vibrios, toxicity and safety concerns, such as bone marrow damage and anemia, typically limits its systemic use to only the treatment of very serious infections, such as cholera and typhoid fever. The antibiotic works by binding to bacterial ribosome 50S subunits and inhibiting bacterial protein synthesis.

"Therapy with chloramphenicol must be limited to infections for which the benefits of the drug outweigh the risks of the potential toxicities. When other antimicrobial drugs are available that are equally effective and potentially less toxic than chloramphenicol, they should be used." [1]

Chemistry

Chloroamphenicol, or 2,2-dichloro-N-[1,3-dihydroxy-1-(4-nitrophenyl)propan-2-yl]acetamide, has molecular formula C11H12Cl2N2O5 and molecular mass 323.1294 g/mol. The drug is referred to by several names, including CAF, CAM, CAP, chloramphenicole, chloramfenikol, chloroamphenicol, cloroamfenicolo, CPh, D-Chloramphenicol.

References

  1. Goodman & Gilman's The Pharmacological Basis of Therapeutics (9th Edition ed.), McGraw-Hill, p. 1133

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