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Platinum-protein interactions, models

Glutathione readily replaces the GSMe on platinum in the reaction with [Pt(dien)(GSMe)]2+ (GSMe = S-methylglutathione) - this system is claimed to be an effective model for cisplatin-protein interaction 224). Rate constants and activation parameters have been... [Pg.101]

Freeman, H. C., and Golomb, M. L. (1970). Model compounds for metal-protein interaction Crystal structure of three platinum(Il) complexes of l- and DL-methionine and glycyl-L-methionine. Chem. Commun. pp. 1523-1524. [Pg.69]

So, in principle, we have to consider three types of species, all competing for cisplatin, namely, the rescue agents, the peptides and proteins, and the DNA. Although, at present, much highly relevant information is available about Pt-DNA binding, information of other aspects of in vivo platinum chemistry has become recently available [18-20], A review devoted towards the interaction of (new, active, and some relevant inactive) platinum compounds (in model fluids in vitro and in vivo) with cellular components (DNA peptides) and additives (rescue agents) is highly relevant and timely, and the most important results available will be discussed below. [Pg.342]


See other pages where Platinum-protein interactions, models is mentioned: [Pg.335]    [Pg.79]    [Pg.757]    [Pg.59]    [Pg.5459]    [Pg.363]    [Pg.757]    [Pg.255]    [Pg.5458]    [Pg.6902]    [Pg.39]    [Pg.4]    [Pg.283]    [Pg.388]   
See also in sourсe #XX -- [ Pg.196 ]




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