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  2. Colchicine - Wikipedia

    en.wikipedia.org/wiki/Colchicine

    Colchicine is a medication used to prevent and treat gout, [3] [4] to treat familial Mediterranean fever [5] and Behçet's disease, [6] and to reduce the risk of myocardial infarction. [7] The American College of Rheumatology recommends colchicine, nonsteroidal anti-inflammatory drugs (NSAIDs) or steroids in the treatment of gout.

  3. ATC code M04 - Wikipedia

    en.wikipedia.org/wiki/ATC_code_M04

    [1] [2] [3] Subgroup M04 is part of the anatomical group M Musculo-skeletal system. [4] Codes for veterinary use (ATCvet codes) can be created by placing the letter Q in front of the human ATC code: for example, QM04. [5] National issues of the ATC classification may include additional codes not present in this list, which follows the WHO version.

  4. Colchicaceae - Wikipedia

    en.wikipedia.org/wiki/Colchicaceae

    The APG III system, of 2009 (unchanged from the APG systems, of 1998 and 2003), recognizes this family and places it in the order Liliales, in the clade monocots. [1] It is a group of herbaceous perennials with rhizomes or corms.

  5. Probenecid and colchicine - Wikipedia

    en.wikipedia.org/wiki/Probenecid_and_colchicine

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  6. File:Colchicine.svg - Wikipedia

    en.wikipedia.org/wiki/File:Colchicine.svg

    The following other wikis use this file: Usage on de.wikibooks.org Pharmakologie und Toxikologie; Pharmakologie und Toxikologie: Stoffwechsel; Usage on en.wiktionary.org

  7. Colicin - Wikipedia

    en.wikipedia.org/wiki/Colicin

    A colicin is a type of bacteriocin produced by and toxic to some strains of Escherichia coli. [1] Colicins are released into the environment to reduce competition from other bacterial strains.

  8. Mitotic inhibitor - Wikipedia

    en.wikipedia.org/wiki/Mitotic_inhibitor

    Similarly replacement of the acetyl group at C-16 with L-trp-OC 2 H 5, d-Ala(P)-(OC 2 H 5) 2, L-Ala(P)-(OC 2 H 5) 2 and I-Vla(P)-(OC 2 H 5) 2 gave rise to new analogues having anti- tubulin activity. Also it was found that the vindoline's indole methyl group is a useful position to functionalize potentially and develop new, potent vinblastine ...

  9. Eugene van Tamelen - Wikipedia

    en.wikipedia.org/wiki/Eugene_van_Tamelen

    Eugene Earle van Tamelen (July 20, 1925 – December 12, 2009) was an organic chemist who is especially recognized for his contributions to bioorganic chemistry. [1]van Tamelen published five papers while an undergraduate at Hope College. [2]