Lavoltidin (INN, USAN; AH-23,844, lokstidin) je veoma potentan i selektivan antagonist H2 receptora, koji je bio u razvoju za tretman gastroesofagealne refluksne bolesti, ali je razvoj prekinut zbog otkrića da on proizvodi gastrične karcinoidne tumore kod glodara.[4][5]
Lavoltidin
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(IUPAC) ime
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[1-metil-5-({3-[3-(piperidin-1-ilmetil)fenoksi]propil}amino)-1H-1,2,4-triazol-3-il]metanol
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Klinički podaci
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Identifikatori
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CAS broj
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76956-02-0
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ATC kod
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nije dodeljen
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PubChem[1][2]
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55473
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ChemSpider[3]
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50093
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UNII
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X16K5179V5
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Hemijski podaci
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Formula
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C19H29N5O2
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Mol. masa
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359,47 g/mol
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SMILES
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eMolekuli & PubHem
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InChI |
InChI=1S/C19H29N5O2/c1-23-19(21-18(15-25)22-23)20-9-6-12-26-17-8-5-7-16(13-17)14-24-10-3-2-4-11-24/h5,7-8,13,25H,2-4,6,9-12,14-15H2,1H3,(H,20,21,22) Y Key: VTLNPNNUIJHJQB-UHFFFAOYSA-N Y |
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Farmakoinformacioni podaci
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Trudnoća
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?
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Pravni status
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Uncontrolled
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Način primene
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Oralno
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- ↑ 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
- ↑ 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.
- ↑ 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
- ↑ Washington, Neena (1991). Antacids and anti-reflux agents. Boca Raton: CRC Press. ISBN 0-8493-5444-7.
- ↑ Dictionary of organic compounds. London: Chapman & Hall. 1996. ISBN 0-412-54090-8.