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Nizatidin

Izvor: Wikipedija
Nizatidin
(IUPAC) ime
N-(2-[(2-[(dimetilamino)metil]tiazol-4-il)metiltio]etil)-N-metil-2-nitroeten-1,1-diamin
Klinički podaci
Robne marke Aksid
AHFS/Drugs.com Monografija
MedlinePlus a694030
Identifikatori
CAS broj 76963-41-2
ATC kod A02BA04
PubChem[1][2] 3033637
DrugBank DB00585
ChemSpider[3] 2298266
UNII P41PML4GHR DaY
KEGG[4] D00440 DaY
ChEMBL[5] CHEMBL653 DaY
Hemijski podaci
Formula C12H21N5O2S2 
Mol. masa 331,46 g/mol
SMILES eMolekuli & PubHem
Farmakokinetički podaci
Bioraspoloživost >70%
Vezivanje za proteine plazme 35%
Metabolizam Hepatički
Poluvreme eliminacije 1-2 sata
Izlučivanje Renalno
Farmakoinformacioni podaci
Licenca

US FDA:link

Trudnoća B3(AU)
Pravni status Samo na recept (S4) (AU) POM (UK) OTC (SAD)
Način primene Oralno

Nizatidin je histaminski antagonist H2 receptora koji inhibira produkciju želudačne kiseline, i često se koristi za tretiranje želudačnih čireva i gastroezofagealne refluksne bolesti. Ovaj lek je razvila kompanija Eli Lili. U prodaji je pod imenima Tazak i Aksid.

Klinička upotreba

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Glavni članak: Antagonist H2-receptora

Pojedini preparati nizatidina su dostupni na slobodno u raznim zemljama. Nizatidina je eksperimentalno korišćen za kontrolu dodatne telesne težine stečene upotrebom pojedinih antipsihotičkih lekova.[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. Atmaca M, Kuloglu M, Tezcan E, Ustundag B, Kilic N (January 2004). „Nizatidine for the treatment of patients with quetiapine-induced weight gain”. Hum Psychopharmacol 19 (1): 37–40. DOI:10.1002/hup.477. PMID 14716710. 

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