Bifonazole

Summary

Bifonazole (trade name Canespor among others[1]) is an imidazole antifungal drug used in form of ointments.

Bifonazole
Clinical data
Trade namesCanespor, many others
AHFS/Drugs.comInternational Drug Names
Routes of
administration
Topical
ATC code
Legal status
Legal status
Identifiers
  • (RS)-1-[Phenyl(4-phenylphenyl)methyl]-1H-imidazole
CAS Number
  • 60628-96-8 checkY
PubChem CID
  • 2378
DrugBank
  • DB04794 checkY
ChemSpider
  • 2287 checkY
UNII
  • QYJ305Z91O
KEGG
  • D01775 checkY
ChEBI
  • CHEBI:31286 ☒N
ChEMBL
  • ChEMBL277535 checkY
CompTox Dashboard (EPA)
  • DTXSID9045631 Edit this at Wikidata
ECHA InfoCard100.056.651 Edit this at Wikidata
Chemical and physical data
FormulaC22H18N2
Molar mass310.400 g·mol−1
3D model (JSmol)
  • Interactive image
ChiralityRacemic mixture
  • n1ccn(c1)C(c3ccc(c2ccccc2)cc3)c4ccccc4
  • InChI=1S/C22H18N2/c1-3-7-18(8-4-1)19-11-13-21(14-12-19)22(24-16-15-23-17-24)20-9-5-2-6-10-20/h1-17,22H checkY
  • Key:OCAPBUJLXMYKEJ-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

It was patented in 1974 and approved for medical use in 1983.[2] There are also combinations with carbamide for the treatment of onychomycosis.

Adverse effects edit

The most common side effect is a burning sensation at the application site. Other reactions, such as itching, eczema or skin dryness, are rare.[3] Bifonazole is a potent aromatase inhibitor in vitro.[4][5]

Pharmacology edit

Mechanism of action edit

Bifonazole has a dual mode of action. It inhibits fungal ergosterol biosynthesis at two points, via transformation of 24-methylendihydrolanosterol to desmethylsterol, together with inhibition of HMG-CoA. This enables fungicidal properties against dermatophytes and distinguishes bifonazole from other antifungal drugs.[3][6]

Pharmacokinetics edit

Six hours after application, bifonazole concentrations range from 1000 μg/cm3 in the stratum corneum to 5 μg/cm3 in the papillary dermis.[3]

References edit

  1. ^ International Drug Names: Bifonazole.
  2. ^ Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 502. ISBN 9783527607495.
  3. ^ a b c Haberfeld H, ed. (2015). Austria-Codex (in German). Vienna: Österreichischer Apothekerverlag. Canesten Bifonazol-Creme.
  4. ^ Trösken ER, Fischer K, Völkel W, Lutz WK (February 2006). "Inhibition of human CYP19 by azoles used as antifungal agents and aromatase inhibitors, using a new LC-MS/MS method for the analysis of estradiol product formation". Toxicology. 219 (1–3): 33–40. doi:10.1016/j.tox.2005.10.020. PMID 16330141.
  5. ^ Egbuta C, Lo J, Ghosh D (December 2014). "Mechanism of inhibition of estrogen biosynthesis by azole fungicides". Endocrinology. 155 (12): 4622–4628. doi:10.1210/en.2014-1561. PMC 4239419. PMID 25243857.
  6. ^ Berg D, Regel E, Harenberg HE, Plempel M (1984). "Bifonazole and clotrimazole. Their mode of action and the possible reason for the fungicidal behaviour of bifonazole". Arzneimittel-Forschung. 34 (2): 139–146. PMID 6372801.

Further reading edit

  • Lackner TE, Clissold SP (August 1989). "Bifonazole. A review of its antimicrobial activity and therapeutic use in superficial mycoses". Drugs. 38 (2): 204–225. doi:10.2165/00003495-198938020-00004. PMID 2670516. S2CID 195697559.