Loxtidine
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Revision as of 06:29, 14 April 2010 by حسن علي البط (Talk) (Adding category Category:Phenol ethers (using HotCat))
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 |
|
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".]] |
Script error: No such module "collapsible list". |
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
See also
References
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- ↑ 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.
- ↑ 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.
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