Ketoconazole: Difference between revisions

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[[Image:Ketoconazole structure.jpg|right|thumb|350px|{{#ifexist:Template:Ketoconazole structure.jpg/credit|{{Ketoconazole structure.jpg/credit}}<br/>|}}Ketoconazole.  The five-membered ring with two nitrogen atoms is an azole.]]  
[[Image:Ketoconazole structure.jpg|right|thumb|350px|{{#ifexist:Template:Ketoconazole structure.jpg/credit|{{Ketoconazole structure.jpg/credit}}<br/>|}}Ketoconazole.  The five-membered ring with two nitrogen atoms is an azole.]]  


'''Ketoconazole''' is one of the [[azole]]-based [[antifungal drug]]s used to treat fungal infections.  Its use has greatly diminished because of the introduction of better treatment alternatives, including the triazoles [[fluconazole]] and [[itraconazole]].
'''Ketoconazole''' is one of the [[azole]]-based [[antifungal drug]]s used to treat fungal infections.  Its use has greatly diminished because of the introduction of better treatment alternatives, including the triazoles [[fluconazole]] and [[itraconazole]].  It is based on [[imidazole]] as are [[clotrimazole]], fluconazole, itraconazole and [[miconazole]]. It is a system, second-line of defense drug use to treat [[candidiasis]], [[candiduria]], [[oral thrush]], [[mucocutaneious candidiasis]], [[blastomycosis]], [[coccidioidomycosis]], [[histoplasmosis]], [[chromomycosis]] and [[paracocccidioidomycosis]].


== Mechanism of action ==
== Mechanism of action ==

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Ketoconazole. The five-membered ring with two nitrogen atoms is an azole.

Ketoconazole is one of the azole-based antifungal drugs used to treat fungal infections. Its use has greatly diminished because of the introduction of better treatment alternatives, including the triazoles fluconazole and itraconazole. It is based on imidazole as are clotrimazole, fluconazole, itraconazole and miconazole. It is a system, second-line of defense drug use to treat candidiasis, candiduria, oral thrush, mucocutaneious candidiasis, blastomycosis, coccidioidomycosis, histoplasmosis, chromomycosis and paracocccidioidomycosis.

Mechanism of action

Azole-based antifungal agents, such as ketoconazole, work by inhibiting the enzyme cytochrome P450 14--demethylase (P45014DM), which is part of the sterol biosynthesis pathway that converts lanosterol to ergosterol[1]. Because ketoconazole has less affinity towards fungal cell membranes than the newer triazole antifungal agents like fluconazole and itraconazole, it is more likely to bind with mammalian cell membranes and induce toxicity[2]. .

Side effects

Becuase ketoconazole disrupts part of the sterol biosynthesis pathway, it may decrease levels of the steroids testosterone and cortisone causing gynecomastia and oligospermia in males and irregular menstration in women. It may also cause anorexia, nausea and vomiting, increased levels of transaminase and liver toxicity.

Chemistry

The IUPAC chemical name for ketoconazole is 1-[4-[4-[[2-(2,4-dichlorophenyl)-2-(imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]piperazin-1-yl]ethanone. It has chemical formula C26H28Cl2N4O4 and registered under CAS Number 79156-75-5.

Synonyms

  • (+-)-cis-1-acetyl-4-(p-((2-(2,4-dichlorophenyl)-2-(imidazol-1-ylmethyl)-1,3-dioxolan-4-yl)methoxy)phenyl)piperazine,
  • 79156-75-5
  • CPD-4503
  • fungarest
  • fungoral,
  • ketoconazol,
  • ketoconazole
  • ketoderm
  • ketoisdin,
  • KW 1414
  • NCI60_002728
  • nizoral
  • NSC317629
  • orifungal M
  • panfungol

External links

  • Doctorfungus [1]

References

  1. (1992) "Systemically administered antifungal agents. A review of the their clinical pharmacology and therapeutic applications". Drugs 44: 9-35.
  2. (1994) "Oral azole drugs as systemic antifungal therapy". N. Engl. J. Med. 330: 263-272.