Ketoconazole: Difference between revisions

From Citizendium
Jump to navigation Jump to search
imported>David E. Volk
mNo edit summary
imported>David E. Volk
(→‎Synonyms: Brand names too)
Line 29: Line 29:
* orifungal M
* orifungal M
* panfungol
* panfungol
== Brand names ==
* Extina®
* Fungarest®
* Fungoral®
* Ketocanazole®
* Ketoconazol®
* Ketoconazol®
* Ketoconazole®
* Ketoconazolum®
* Ketoderm®
* Ketoisdin®
* Ketozole®
* Nizoral®
* Nizoral Cream®
* Nizoral Shampoo®
* Nizoral a-D®
* Nizoral a-D Shampoo®
* Orifungal®
* Orifungal M®
* Panfungol®


== External links ==
== External links ==

Revision as of 15:58, 3 March 2008

This article has a Citable Version.
Main Article
Discussion
Related Articles  [?]
Bibliography  [?]
External Links  [?]
Citable Version  [?]
 
This editable Main Article has an approved citable version (see its Citable Version subpage). While we have done conscientious work, we cannot guarantee that this Main Article, or its citable version, is wholly free of mistakes. By helping to improve this editable Main Article, you will help the process of generating a new, improved citable version.
(CC) Image: David E. Volk
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 second-line of defense systemic 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

Brand names

  • Extina®
  • Fungarest®
  • Fungoral®
  • Ketocanazole®
  • Ketoconazol®
  • Ketoconazol®
  • Ketoconazole®
  • Ketoconazolum®
  • Ketoderm®
  • Ketoisdin®
  • Ketozole®
  • Nizoral®
  • Nizoral Cream®
  • Nizoral Shampoo®
  • Nizoral a-D®
  • Nizoral a-D Shampoo®
  • Orifungal®
  • 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.