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  2. Cimetidine - Wikipedia

    en.wikipedia.org/wiki/Cimetidine

    Cimetidine, sold under the brand name Tagamet among others, is a histamine H 2 receptor antagonist that inhibits stomach acid production. [ 1 ] [ 9 ] [ 10 ] It is mainly used in the treatment of heartburn and peptic ulcers .

  3. CUSP9 - Wikipedia

    en.wikipedia.org/wiki/CUSP9

    The CLOVA Regimen uses cimetidine, lithium, olanzapine, and valproate with temozolomide in treating glioblastoma. [9] The ReDO project [10] and many others [11] [12] also follow this line of thought as in CUSP9, repurposing older drugs for their anti-cancer effect with simultaneous use of several of them, in cancer treatment. The drug ...

  4. Zantac settlements - Wikipedia

    en.wikipedia.org/wiki/Zantac_settlements

    The product's problem was described by The New York Times as being "that a potential cancer-causing contaminant can build up in the drug when stored for long periods." [ 6 ] Heavy marketing expenditures resulted in Zantac being consumed by those who might have satisficed with less harmful alternatives. [ 9 ]

  5. H2 receptor antagonist - Wikipedia

    en.wikipedia.org/wiki/H2_receptor_antagonist

    Cimetidine was the prototypical histamine H 2 receptor antagonist from which later drugs were developed. Cimetidine was the culmination of a project at Smith, Kline & French (SK&F; now GlaxoSmithKline) by James W. Black, C. Robin Ganellin, and others to develop a histamine receptor antagonist that would suppress stomach acid secretion.

  6. Timeline of peptic ulcer disease and Helicobacter pylori

    en.wikipedia.org/wiki/Timeline_of_peptic_ulcer...

    Krienitz finds bacteria in the stomach of people with gastric cancer. [2] Turck feeds dogs Bacillus coli and produces ulcers. [7] 1907 Berkley Moynihan suggests that acid is a cause of ulcers. [1] 1910 Schwartz publishes the excess acid theory of the ulcer, coining the famous phrase "no acid, no ulcer." [2]

  7. Ranitidine - Wikipedia

    en.wikipedia.org/wiki/Ranitidine

    Ranitidine has 10% of the affinity that cimetidine has to CYP450, so it causes fewer side effects, but other H 2 blockers famotidine and nizatidine have no CYP450 significant interactions. [ 131 ] Ranitidine was introduced in 1981, and was the world's biggest-selling prescription drug by 1987. [ 132 ]

  8. Equine melanoma - Wikipedia

    en.wikipedia.org/wiki/Equine_Melanoma

    Cimetidine works by slowing tumor growth; it is a histamine blocker that maintains the body's immune response which aids in the killing of tumor cells. Cimetidine has not been proven to efficiently resolve tumors completely.

  9. Drug discovery - Wikipedia

    en.wikipedia.org/wiki/Drug_discovery

    In the fields of medicine, biotechnology, and pharmacology, drug discovery is the process by which new candidate medications are discovered. [1]Historically, drugs were discovered by identifying the active ingredient from traditional remedies or by serendipitous discovery, as with penicillin.