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  2. Manganese(II) sulfate - Wikipedia

    en.wikipedia.org/wiki/Manganese(II)_sulfate

    mno 2 + so 2 + h 2 o → mnso 4 (h 2 o) It can also be made by mixing potassium permanganate with sodium hydrogen sulfate and hydrogen peroxide . Manganese sulfate is a by-product of various industrially significant oxidations that use manganese dioxide, including the manufacture of hydroquinone and anisaldehyde .

  3. Anatomical Therapeutic Chemical Classification System

    en.wikipedia.org/wiki/Anatomical_Therapeutic...

    This means that one drug can have more than one code, for example acetylsalicylic acid (aspirin) has A01AD05 as a drug for local oral treatment, B01AC06 as a platelet inhibitor, and N02BA01 as an analgesic and antipyretic; as well as one code can represent more than one active ingredient, for example C09BB04 is the combination of perindopril ...

  4. ATC code M04 - Wikipedia

    en.wikipedia.org/wiki/ATC_code_M04

    ATC code M04 Antigout preparations is a therapeutic subgroup of the Anatomical Therapeutic Chemical Classification System, a system of alphanumeric codes developed by the World Health Organization (WHO) for the classification of drugs and other medical products. [1] [2] [3] Subgroup M04 is part of the anatomical group M Musculo-skeletal system. [4]

  5. Aspirin - Wikipedia

    en.wikipedia.org/wiki/Aspirin

    By 1899, Bayer had dubbed this drug Aspirin and was selling it globally. [15]: 27 The word Aspirin was Bayer's brand name, rather than the generic name of the drug; however, Bayer's rights to the trademark were lost or sold in many countries. Aspirin's popularity grew over the first half of the 20th century leading to fierce competition with ...

  6. Mechanism of action of aspirin - Wikipedia

    en.wikipedia.org/wiki/Mechanism_of_action_of_aspirin

    This makes aspirin different from other NSAIDs (such as diclofenac and ibuprofen), which are reversible inhibitors; aspirin creates an allosteric change in the structure of the COX enzyme. [2] However, other effects of aspirin, such as uncoupling oxidative phosphorylation in mitochondria, [3] and the modulation of signaling through NF-κB, are ...

  7. Salicin - Wikipedia

    en.wikipedia.org/wiki/Salicin

    Salicin is found in the bark of and leaves of willows, poplars and various other plants. [5] Derivates are found in castoreum.Salicin from meadowsweet was used in the synthesis of aspirin (acetylsalicylic acid), [6] in 1899 by scientists at Bayer.

  8. Acetylsalicylic acid/dipyridamole - Wikipedia

    en.wikipedia.org/wiki/Acetylsalicylic_acid/dipy...

    The combination drug acetylsalicylic acid/dipyridamole (trade names Aggrenox, Asasantin) is a drug combination of: [1] Acetylsalicylic acid (Aspirin) - An extremely common NSAID that has anticoagulant effects; Dipyridamole, a drug that inhibits platelet activation [2] when given chronically and causes vasodilation when given at high doses over ...

  9. Arsphenamine - Wikipedia

    en.wikipedia.org/wiki/Arsphenamine

    Arsphenamine, also known as Salvarsan or compound 606, is an antibiotic drug that was introduced at the beginning of the 1910s as the first effective treatment for the deadly infectious diseases syphilis, relapsing fever, and African trypanosomiasis. [2] [3] This organoarsenic compound was the first modern antimicrobial agent. [4]

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