Loxtidine

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Loxtidine
File:Loxtidine structure.png
Systematic (IUPAC) name
[1-methyl-5-({3-[3-(piperidin-1-ylmethyl)phenoxy]propyl}amino)-1H-1,2,4-triazol-3-yl]methanol
Clinical data
Routes of
administration
Oral
Legal status
Legal status
  • Uncontrolled
Identifiers
CAS Number 76956-02-0
ATC code none
PubChem CID 55473
ChemSpider 50093
Chemical data
Formula C19H29N5O2
Molar mass 359.47 g/mol[[Script error: No such module "String".]]
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Loxtidine (INN), also known as lavoltidine (USAN, BAN) or AH-23,844, is a highly potent and selective H2 receptor antagonist which was under development as a treatment for gastroesophageal reflux disease but was discontinued due to the discovery that it produced gastric carcinoid tumors in rodents.[1][2]

Synthesis

450px[3]

See also

References

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  1. Washington, Neena (1991). Antacids and anti-reflux agents. Boca Raton: CRC Press. ISBN 0-8493-5444-7. 
  2. Dictionary of organic compounds. London: Chapman & Hall. 1996. ISBN 0-412-54090-8. 
  3. Cliterow, J. W.; Bradshaw, J.; Price, B. J.; Martin-Smith, M.; Mackinon, J. W. M.; Judd, D. B.; Hayes, R.; Carey, L.; 1983, EP 0016565 .