Mizolastine

Chemical compound
  • R06AX25 (WHO)
Legal statusLegal status
  • UK: POM (Prescription only)
Identifiers
  • 2-[{1-[1-(4-Fluorobenzyl)-1H-benzimidazol-2-yl]piperidin-4-yl}(methyl)amino]pyrimidin-4(1H)-one
CAS Number
  • 108612-45-9 checkY
PubChem CID
  • 65906
ChemSpider
  • 59315 ☒N
UNII
  • 244O1F90NA
KEGG
  • D01117 checkY
ChEMBL
  • ChEMBL94454 ☒N
CompTox Dashboard (EPA)
  • DTXSID5046801 Edit this at Wikidata
ECHA InfoCard100.149.406 Edit this at WikidataChemical and physical dataFormulaC24H25FN6OMolar mass432.503 g·mol−13D model (JSmol)
  • Interactive image
  • CN(C1CCN(CC1)C2=NC3=CC=CC=C3N2CC4=CC=C(C=C4)F)C5=NC=CC(=O)N5
InChI
  • InChI=1S/C24H25FN6O/c1-29(23-26-13-10-22(32)28-23)19-11-14-30(15-12-19)24-27-20-4-2-3-5-21(20)31(24)16-17-6-8-18(25)9-7-17/h2-10,13,19H,11-12,14-16H2,1H3,(H,26,28,32) ☒N
  • Key:PVLJETXTTWAYEW-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Mizolastine (Mizollen) is a once-daily, non-sedating antihistamine. It blocks H1 receptors and is commonly fast-acting.[1] It does not prevent the actual release of histamine from mast cells, it only prevents histamine from binding to receptors. Side effects can include dry mouth and throat.[2]

References

  1. ^ Simons FE (March 1999). "Mizolastine: antihistaminic activity from preclinical data to clinical evaluation". Clinical and Experimental Allergy. 29 (Suppl 1): 3–8. doi:10.1046/j.1365-2222.1999.00002.x. PMID 10209699. S2CID 616333.
  2. ^ "MIZOLASTINE: British National Formulary". Retrieved 2010-02-01.
  • v
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Antihistamines (R06)
Benzimidazoles (*)DiarylmethanesEthylenediaminesTricyclicsOthers
For topical use
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H1
Agonists
Antagonists
  • Unknown/unsorted: Azanator
  • Belarizine
  • Elbanizine
  • Flotrenizine
  • GSK1004723
  • Napactadine
  • Tagorizine
  • Trelnarizine
  • Trenizine
H2
Agonists
Antagonists
H3
Agonists
Antagonists
H4
Agonists
Antagonists
See also
Receptor/signaling modulators
Monoamine metabolism modulators
Monoamine reuptake inhibitors


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