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Metirozin

Izvor: Wikipedija
Metirosin
(IUPAC) ime
(2S)-2-amino- 3-(4-hidroksifenil)- 2-metilpropanoinska kiselina
Klinički podaci
Robne marke Demser
AHFS/Drugs.com Potrošačka informacije o leku
Identifikatori
CAS broj 672-87-7
ATC kod C02KB01
PubChem[1][2] 10123
DrugBank DB00765
ChemSpider[3] 390103
UNII DOQ0J0TPF7 DaY
KEGG[4] D00762 DaY
ChEMBL[5] CHEMBL1200862 DaY
Hemijski podaci
Formula C10H13NO3 
Mol. masa 195,215 g/mol
SMILES eMolekuli & PubHem
Farmakokinetički podaci
Poluvreme eliminacije 3,4–3,7 sata
Farmakoinformacioni podaci
Trudnoća ?
Pravni status

Metirozin (α-Metiltirozin, Metirozin, AMPT) je antihipertenzivni lek. On inhibira enzim tirozinska hidroksilaza i, stoga sintezu kateholamina. Posledica toga je snižavanje nivoa kateholamina dopamina, adrenalina i noradrenalina u telu.

Clinical use

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Metirozin je korišten u tretmanu feohromocitoma.[6]

On se relativno retko koristi kao lek i prvenstveno nalazi primenu u naučnim istraživanjima čiji je cilj utvrđivanje uticaja iscrpljivanja kateholamina na ponašanje.[7]

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. Green KN, Larsson SK, Beevers DG, Bevan PG, Hayes B (August 1982). „Alpha-methyltyrosine in the management of phaeochromocytoma”. Thorax 37 (8): 632–3. DOI:10.1136/thx.37.8.632. PMC 459390. PMID 7179194. 
  7. O'Leary OF, Bechtholt AJ, Crowley JJ, Hill TE, Page ME, Lucki I. Depletion of serotonin and catecholamines block the acute behavioral response to different classes of antidepressant drugs in the mouse tail suspension test. Psychopharmacology (Berlin). 2007 Jun;192(3):357-71. PMID 17318507

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