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Topoisomerase poisons

Apart from the topoisomerase poisons, other drugs that trap proteins in ternary complexes include Cisplatin, and Et-743. [Pg.175]

Froelich-Ammon, S. J., Osheroff, N. (1995). Topoisomerase poisons Harnessing the dark side of enzyme mechanism. The Journal of Biological Chemistry, 270, 21429-21432. [Pg.446]

Liu LF. DNA topoisomerase poisons as antitumor drugs. Annu Rev Biochem 1989 58 351-75. [Pg.113]

Cardarelli M, Serino G, Campanella L et al (1997) Antimitotic effects of usnic acid on different biological systems. Cell Mol Life Sci 53 667-672 Cheng B, Cao S, Vasquez V et al (2013) Identification of anziaic acid, a lichen depside from Hypotrachyna sp., as a new topoisomerase poison inhibitor. PLoS One 8(4) e60770 Cohen PA, Towers GHN (1995) Anthraquinones and phenanthroperylenequinones from Nephroma laevigatum. J Nat Prod 58 520-526... [Pg.142]

Camptothecin is imique in its mechanism of action. It binds to the cleavable complex of topoisomerase I and covalently attached DNA and stabihzes it (Hsiang et al., 1985). This non-degradable DNA/topoisomerase I complex arrests the rephcation fork and thus kills cells by inhibition of DNA synthesis (Hsiang et al., 1989). Camptothecin and its derivatives are therefore also termed topoisomerase poisons . [Pg.16]


See other pages where Topoisomerase poisons is mentioned: [Pg.37]    [Pg.199]    [Pg.174]    [Pg.174]    [Pg.175]    [Pg.1869]    [Pg.95]    [Pg.97]    [Pg.268]    [Pg.90]    [Pg.432]    [Pg.1832]    [Pg.378]    [Pg.104]    [Pg.110]    [Pg.113]    [Pg.226]    [Pg.16]    [Pg.28]    [Pg.590]    [Pg.591]    [Pg.137]    [Pg.2758]   
See also in sourсe #XX -- [ Pg.590 , Pg.597 ]




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