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  2. Propionate fermentation - Wikipedia

    en.wikipedia.org/wiki/Propionate_fermentation

    Propionate fermentation is a form of fermentation with propionic acid as one of the products. This process is done through the fermentation pathway of bacteria. It is used in a variety of industrial, food-making, and medical applications.

  3. Oxaprozin - Wikipedia

    en.wikipedia.org/wiki/Oxaprozin

    Oxaprozin, also known as oxaprozinum, is a nonsteroidal anti-inflammatory drug (NSAID), [2] used to relieve the inflammation, swelling, stiffness, and joint pain associated with osteoarthritis and rheumatoid arthritis. Chemically, it is a propionic acid derivative. Safety and efficacy has been established in children over 6 years with juvenile ...

  4. Ketoprofen - Wikipedia

    en.wikipedia.org/wiki/Ketoprofen

    Ketoprofen is one of the propionic acid class of nonsteroidal anti-inflammatory drugs (NSAID) with analgesic and antipyretic effects. [3] It acts by inhibiting the body's production of prostaglandin. It was patented in 1967 and approved for medical use in 1980. [4]

  5. Loxoprofen - Wikipedia

    en.wikipedia.org/wiki/Loxoprofen

    Download as PDF; Printable version; ... in the propionic acid derivatives group, ... It was patented in 1977 and approved for medical use in 1986. [2]

  6. Propionic acid - Wikipedia

    en.wikipedia.org/wiki/Propionic_acid

    Propionic acid inhibits the growth of mold and some bacteria at levels between 0.1 and 1% by weight. As a result, some propionic acid produced is consumed as a preservative for both animal feed and food for human consumption. For animal feed, it is used either directly or as its ammonium salt. This application accounts for about half of the ...

  7. Flurbiprofen - Wikipedia

    en.wikipedia.org/wiki/Flurbiprofen

    It was derived from propionic acid by the research arm of Boots UK during the 1960s, a period which also included the discovery of ibuprofen, indometacin, diclofenac, naproxen, ketoprofen, and sulindac. [3] [4]: 34 It was patented in 1964 by Boots UK and approved for medical use in 1987. [5]

  8. Uroporphyrinogen III - Wikipedia

    en.wikipedia.org/wiki/Uroporphyrinogen_III

    Medical significance [ edit ] If uroporphyrinogen-III synthase is not present or inactive, the hydroxymethylbilane will spontaneously cyclise into the structural isomer uroporphyrinogen I , which differs from the III isomer in that the acetic acid ("A") and propionic acid ("P") groups are arranged in a rotationally symmetric order, AP-AP-AP-AP.

  9. Category:Propionic acids - Wikipedia

    en.wikipedia.org/wiki/Category:Propionic_acids

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