Fenobarbital je derivat barbituratne kiseline, koji deluje kao neselektivni depresant centralnog nervnog sistema. On promoviše vezivanje za inhibitorni tip receptora gama-aminobuterine kiseline, i moduliše protok hlorida kroz receptorske kanale. On snažno inhibira glutamatom indukovane depolarizacije.[1][2][3][4][5][6][7]

Fenobarbital
IUPAC ime
5-etil-5-phenil-1,3-diazinan-2,4,6-trion
Klinički podaci
Prodajno imeAdonal, Aephenal, Agrypnal, Amylofene
Drugs.comMonografija
Način primeneOralno; Intramaskularno; Oralno;
Farmakokinetički podaci
Poluvreme eliminacije53 do 118 sati
Identifikatori
CAS broj50-06-6 ДаY
ATC kodN03AA01 (WHO), N03AA02
PubChemCID 4763
IUPHAR/BPS2804
DrugBankDB01174 ДаY
ChemSpider4599 ДаY
KEGGC07434 ДаY
ChEMBLCHEMBL8069 ДаY
Hemijski podaci
FormulaC12H12N2O3
Molarna masa232.2353
  • CCC1(C(=O)NC(=O)NC1=O)C1=CC=CC=C1
  • InChI=1S/C12H12N2O3/c1-2-12(8-6-4-3-5-7-8)9(15)13-11(17)14-10(12)16/h3-7H,2H2,1H3,(H2,13,14,15,16,17) ДаY
  • Key:DDBREPKUVSBGFI-UHFFFAOYSA-N ДаY
Fizički podaci
Tačka topljenja174 °C (345 °F)

Reference уреди

  1. ^ Kwan P, Brodie MJ: Phenobarbital for the treatment of epilepsy in the 21st century: a critical review. Epilepsia. 2004 Sep;45(9):1141-9. PMID 15329080
  2. ^ Taylor S, Tudur Smith C, Williamson PR, Marson AG: Phenobarbitone versus phenytoin monotherapy for partial onset seizures and generalized onset tonic-clonic seizures. Cochrane Database Syst Rev. 2001;(4):CD002217. PMID 11687150
  3. ^ Tudur Smith C, Marson AG, Williamson PR: Carbamazepine versus phenobarbitone monotherapy for epilepsy. Cochrane Database Syst Rev. 2003;(1):CD001904. PMID 12535420
  4. ^ Kalviainen R, Eriksson K, Parviainen I: Refractory generalised convulsive status epilepticus : a guide to treatment. CNS Drugs. 2005;19(9):759-68. PMID 16142991
  5. ^ Booth D, Evans DJ: Anticonvulsants for neonates with seizures. Cochrane Database Syst Rev. 2004 Oct 18;(4):CD004218. PMID 15495087
  6. ^ Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS (2011). „DrugBank 3.0: a comprehensive resource for omics research on drugs”. Nucleic Acids Res. 39 (Database issue): D1035—41. PMID 21059682. 
  7. ^ Wishart DS, Knox C, Guo AC, Cheng D, Shrivastava S, Tzur D, Gautam B, Hassanali M (Nucleic Acids Res) (2008). „DrugBank: a knowledgebase for drugs, drug actions and drug targets”. 36 (Database issue): D901—6. PMID 18048412. 

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