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- Sufotidine abstract "Sufotidine (INN, USAN, codenamed AH25352) is a long-acting competitive H2 receptor antagonist which was under development as an antiulcerant by Glaxo (now GlaxoSmithKline). It was planned to be a follow-up compound to ranitidine (Zantac). When taken in doses of 600 mg twice daily it induced virtually 24-hour gastric anacidity thus closely resembling the antisecretory effect of the proton pump inhibitor omeprazole. Its development was terminated in 1989 from phase III clinical trials based on the appearance of carcinoid tumors in long-term toxicity testing in rodents.".
- Sufotidine atcPrefix "None".
- Sufotidine casNumber "80343-63-1".
- Sufotidine fdaUniiCode "56B0591Y76".
- Sufotidine iupacName "2-methyl-5-(methylsulfonylmethyl)-N-[3-[3-(piperidin-1-ylmethyl)phenoxy]propyl]-1,2,4-triazol-3-amine".
- Sufotidine pubchem "71763".
- Sufotidine thumbnail Sufotidine.svg?width=300.
- Sufotidine wikiPageID "49078162".
- Sufotidine wikiPageLength "4405".
- Sufotidine wikiPageOutDegree "20".
- Sufotidine wikiPageRevisionID "699479020".
- Sufotidine wikiPageWikiLink Category:Abandoned_drugs.
- Sufotidine wikiPageWikiLink Category:Amines.
- Sufotidine wikiPageWikiLink Category:H2_receptor_antagonists.
- Sufotidine wikiPageWikiLink Category:Phenol_ethers.
- Sufotidine wikiPageWikiLink Category:Piperidines.
- Sufotidine wikiPageWikiLink Category:Sulfones.
- Sufotidine wikiPageWikiLink Category:Triazoles.
- Sufotidine wikiPageWikiLink GlaxoSmithKline.
- Sufotidine wikiPageWikiLink Histamine_H2_receptor.
- Sufotidine wikiPageWikiLink International_nonproprietary_name.
- Sufotidine wikiPageWikiLink Lavoltidine.
- Sufotidine wikiPageWikiLink Omeprazole.
- Sufotidine wikiPageWikiLink Peptic_ulcer.
- Sufotidine wikiPageWikiLink Phases_of_clinical_research.
- Sufotidine wikiPageWikiLink Proton-pump_inhibitor.
- Sufotidine wikiPageWikiLink Ranitidine.
- Sufotidine wikiPageWikiLink Receptor_antagonist.
- Sufotidine wikiPageWikiLink Sulfone.
- Sufotidine wikiPageWikiLink United_States_Adopted_Name.
- Sufotidine wikiPageWikiLink File:Sufotidine_synthesis.png.
- Sufotidine wikiPageWikiLinkText "Sufotidine".
- Sufotidine wikiPageWikiLinkText "sufotidine".
- Sufotidine atcPrefix "None".
- Sufotidine c "20".
- Sufotidine casNumber "80343".
- Sufotidine chemspiderid "64802".
- Sufotidine h "31".
- Sufotidine inchi "1".
- Sufotidine inchikey "JEYKZWRXDALMNG-UHFFFAOYSA-N".
- Sufotidine iupacName "2".
- Sufotidine kegg "D05939".
- Sufotidine legalStatus "Development terminated".
- Sufotidine molecularWeight "421.556".
- Sufotidine n "5".
- Sufotidine o "3".
- Sufotidine pubchem "71763".
- Sufotidine routesOfAdministration "Oral".
- Sufotidine s "1".
- Sufotidine smiles "CN1CNCCCOC2=CC=CCCN3CCCCC3".
- Sufotidine unii "56".
- Sufotidine width "300".
- Sufotidine wikiPageUsesTemplate Template:Drugbox.
- Sufotidine wikiPageUsesTemplate Template:H2-receptor_antagonist.
- Sufotidine wikiPageUsesTemplate Template:Histaminergics.
- Sufotidine wikiPageUsesTemplate Template:Reflist.
- Sufotidine subject Category:Abandoned_drugs.
- Sufotidine subject Category:Amines.
- Sufotidine subject Category:H2_receptor_antagonists.
- Sufotidine subject Category:Phenol_ethers.
- Sufotidine subject Category:Piperidines.
- Sufotidine subject Category:Sulfones.
- Sufotidine subject Category:Triazoles.
- Sufotidine hypernym Antagonist.
- Sufotidine type ChemicalSubstance.
- Sufotidine type Drug.
- Sufotidine type ChemicalObject.
- Sufotidine type Thing.
- Sufotidine type Q8386.
- Sufotidine comment "Sufotidine (INN, USAN, codenamed AH25352) is a long-acting competitive H2 receptor antagonist which was under development as an antiulcerant by Glaxo (now GlaxoSmithKline). It was planned to be a follow-up compound to ranitidine (Zantac). When taken in doses of 600 mg twice daily it induced virtually 24-hour gastric anacidity thus closely resembling the antisecretory effect of the proton pump inhibitor omeprazole.".
- Sufotidine label "Sufotidine".
- Sufotidine wasDerivedFrom Sufotidine?oldid=699479020.
- Sufotidine depiction Sufotidine.svg.
- Sufotidine isPrimaryTopicOf Sufotidine.