Eletriptan (Relpaks, Relert) je član druge generacije triptanski lekova namenjenih tretmanu migrenske glavobolje. On se korist kao blokiranje migrenskih napada koji su već u toku.

Eletriptan
(IUPAC) ime
(R)-3-[(-1-metilprolidin-2-il)metil]-5-(2-fenilsulfoniletil)- 1H-indol
Klinički podaci
Robne marke Relpax
AHFS/Drugs.com Monografija
MedlinePlus a603029
Identifikatori
CAS broj 143322-58-1
ATC kod N02CC06
PubChem[1][2] 77993
DrugBank DB00216
ChemSpider[3] 70379
UNII 22QOO9B8KI DaY
KEGG[4] D01973 DaY
ChEBI CHEBI:50922 DaY
ChEMBL[5] CHEMBL1510 DaY
Hemijski podaci
Formula C22H26N2O2S 
Mol. masa 382,52 g/mol
SMILES eMolekuli & PubHem
Farmakokinetički podaci
Bioraspoloživost 50%
Metabolizam CYP3A4
Poluvreme eliminacije 4 sata
Farmakoinformacioni podaci
Trudnoća C(US)
Pravni status Prescription only
Način primene oralnot

FDA je odobrila eletriptan 2002 za akutni tretman migrene kod odraslih.[6] On je dostupan samo na recept u SAD-u k Kanadi. On nije namenjen za profilaktičku terapiju migrene ili za upotrebu u kontroli hemiplegične ili bazilarne migrene. Eletriptan je pokriven SAD patent 5545644[6][7] and SAD patent 6110940;[6][8] the FDA lists the patents as scheduled for expiration on December 26, 2016, and August 29, 2017, respectively.[6]

Reference

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  1. Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519.  edit
  2. Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1. 
  3. Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846.  edit
  4. Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H. 
  5. Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594.  edit
  6. 6,0 6,1 6,2 6,3 FDA AccessData entry for Eletriptan Hydrobromide, accessed March 10, 2010.
  7. SAD patent 5545644, John E. Macor & Martin J. Wythes, Indole Derivatives, August 13, 1996.
  8. SAD patent 6110940, Valerie Denise Harding, et al., Salts of an anti-migraine indole derivative, August 29, 2000.

Spoljašnje veze

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