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Second messenger definition

This empirical approach would predict, in the absence of any data related to interactions with a molecular target, that because j3-adre-noceptor antagonists lower blood pressure, then any compound that lowers blood pressure is by definition a j3-adrenoceptor antagonist, an absurd conclusion, but one that happened nonetheless. The 1960s saw the development of a number of in vitro biochemical screens that moved the measurement of the RL interaction a little closer to the molecular level. Nonetheless, the major challenge was to develop assays that measured the RL interaction independently of "downstream" events such as enzyme activation and second and third messenger systems. By such means, the ability of a compound to bind to a receptor could be determined on the basis of the SAR and thus provide the chemist with a more direct means to model the RL interaction. [Pg.340]


See other pages where Second messenger definition is mentioned: [Pg.1384]    [Pg.78]    [Pg.241]    [Pg.248]    [Pg.30]    [Pg.36]    [Pg.125]    [Pg.214]    [Pg.132]    [Pg.1134]    [Pg.355]    [Pg.83]    [Pg.896]    [Pg.205]    [Pg.55]    [Pg.319]    [Pg.387]   
See also in sourсe #XX -- [ Pg.101 ]




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