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  2. Etoposide - Wikipedia

    en.wikipedia.org/wiki/Etoposide

    Etoposide was first synthesized in 1966 and U.S. Food and Drug Administration approval was granted in 1983. [ 6 ] The nickname VP-16 likely comes from a compounding of the last name of one of the chemists who performed early work on the drug (von Wartburg) and podophyllotoxin. [ 12 ]

  3. Topoisomerase inhibitor - Wikipedia

    en.wikipedia.org/wiki/Topoisomerase_inhibitor

    Etoposide, a semi-synthetic derivative of epipodophyllotoxin is commonly used to study this apoptotic mechanism and include: Etoposide; Teniposide; Both etoposide and teniposide are naturally occurring semi-synthetic derivatives of podophyllotoxins and are important anti-cancer drugs that function to inhibit TopII activity. [67]

  4. 20-Hydroxyecdysone - Wikipedia

    en.wikipedia.org/wiki/20-Hydroxyecdysone

    This occurs by a mechanism similar to steroid synthesis in vertebrates. Ecdysone and 20-hydroxyecdysone regulate larval molts, onset of puparium formation, and metamorphosis. As these hormones are hydrophobic, they traverse lipid membranes and permeate the tissues of an organism. Indeed, the ecdysone receptor is an intracellular protein.

  5. Type II topoisomerase - Wikipedia

    en.wikipedia.org/wiki/Type_II_topoisomerase

    Type II topoisomerases increase or decrease the linking number of a DNA loop by 2 units, and it promotes chromosome disentanglement. For example, DNA gyrase, a type II topoisomerase observed in E. coli and most other prokaryotes, introduces negative supercoils and decreases the linking number by 2.

  6. Hsp90 inhibitor - Wikipedia

    en.wikipedia.org/wiki/Hsp90_inhibitor

    An Hsp90 inhibitor is a substance that inhibits that activity of the Hsp90 heat shock protein.Since Hsp90 stabilizes a variety of proteins required for survival of cancer cells, these substances may have therapeutic benefit in the treatment of various types of malignancies. [2]

  7. Polypeptide antibiotic - Wikipedia

    en.wikipedia.org/wiki/Polypeptide_antibiotic

    Bacitracin is a polypeptide antibiotic derived from a bacterium, Bacillus subtilis, and acts against bacteria through the inhibition of cell wall synthesis. [6] It does this by inhibiting the removal of phosphate from lipid compounds, thus deactivating its function to transport peptidoglycan; the main component of bacterial cell membranes, to the microbial cell wall.

  8. Metalloprotease inhibitor - Wikipedia

    en.wikipedia.org/wiki/Metalloprotease_inhibitor

    Examples of diseases are periodontitis, hepatitis, glomerulonephritis, atherosclerosis, emphysema, asthma, autoimmune disorders of skin and dermal photoaging, rheumatoid arthritis, osteoarthritis, multiple sclerosis, Alzheimer's disease, chronic ulcerations, uterine involution, corneal epithelial defects, bone resorption and tumor progression ...

  9. Topoisomerase - Wikipedia

    en.wikipedia.org/wiki/Topoisomerase

    This mechanism is distinct from that of the type IA enzymes, and the two groups of enzymes are structurally and evolutionarily unrelated. Examples of type IB topoisomerases include eukaryotic nuclear and mitochondrial topo I in addition to viral topo I, though they have been identified in all three domains of life.

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