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rufinamide

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rufinamide
Clinical data
Trade namesBanzel, Inovelon
AHFS/Drugs.comMonograph
MedlinePlusa609001
License data
Pregnancy
category
  • AU: B3
Routes of
administration
By mouth
ATC code
Legal status
Legal status
  • BR: Class C1 (Other controlled substances)[1]
  • UK: POM (Prescription only)
  • US: ℞-only[2]
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Bioavailability85% (under fed conditions); tmax = 4–6 hours
Protein binding34%
MetabolismCarboxylesterase-mediated hydrolysis (CYP not involved)
MetabolitesInactive
Elimination half-life6–10 hours
ExcretionUrine (85%)[2]
Identifiers
  • 1-(2,6-Difluorobenzyl)-1H-1,2,3-triazole-4-carboxamide
CAS Number
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
KEGG
ChEMBL
Chemical and physical data
FormulaC10H8F2N4O
Molar mass238.197806326 g·mol−1
3D model (JSmol)
  • O=C(c1nnn(c1)Cc2c(F)cccc2F)N
  • InChI=1S/C10H8F2N4O/c11-7-2-1-3-8(12)6(7)4-16-5-9(10(13)17)14-15-16/h1-3,5H,4H2,(H2,13,17) checkY
  • Key:POGQSBRIGCQNEG-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)


Főnév

rufinamide (tsz. rufinamides)

  1. (gyógyszertan) rufinamid
  1. Anvisa: RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial (brazíliai portugál nyelven). Diário Oficial da União, 2023. március 31. [2023. augusztus 3-i dátummal az eredetiből archiválva].
  2. 1 2 Banzel- rufinamide tablet, film coated Banzel- rufinamide suspension. DailyMed , 2020. április 15.