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Lavoltidine
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Clinical data | |
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Routes of administration |
Oral |
ATC code |
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Formula | C19H29N5O2 |
Molar mass | 359.474 g·mol−1 |
3D model (JSmol) | |
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Lavoltidine (INN,USAN, BAN; previously known as loxtidine, code name AH-23,844) is a highly potent and selective H2 receptor antagonist which was under development by Glaxo Wellcome (now GlaxoSmithKline) as a treatment for gastroesophageal reflux disease but was discontinued due to the discovery that it produced gastric carcinoid tumors in rodents.
See also
- H2 receptor antagonist
- Sufotidine (analogous sequence in which sulfone replaces the hydroxyl group)
H2 antagonists ("-tidine") | |
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Prostaglandins (E)/ analogues ("-prost-") |
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Proton-pump inhibitors ("-prazole") |
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Potassium-competitive acid blockers ("-prazan") |
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