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Adenosine 3 -thio-, preparation

In order to increase the chemical stability of ATP derivatives that possess long thioether tethers, the 1-thiotriphosphate analogues (86) have been prepared from 2-thio-adenosine. These compounds were fourfold more stable to pig pancreas type I ATPDase than ATP. They were also more potent than ATP at stimulating intracellular response and were established as new insulin secreta-... [Pg.141]

There has been a further report on the introduction of the [[2-(methylthio)phenyl]thio] methyl (MPTM) protecting group into the 2 -position of adenosine, guanosine and cytidine building blocks for oligonucleotide synthesis (See Vol. 25, p. 270).300 Some thioacetals and dithioorthoesters at 0-5 of FdU, such as 213 have been prepared and subjected to y-radiolysis.30i... [Pg.254]


See other pages where Adenosine 3 -thio-, preparation is mentioned: [Pg.388]    [Pg.154]    [Pg.158]    [Pg.348]    [Pg.599]    [Pg.189]    [Pg.301]    [Pg.40]    [Pg.40]    [Pg.36]    [Pg.375]    [Pg.269]    [Pg.172]    [Pg.176]    [Pg.192]    [Pg.346]    [Pg.175]    [Pg.249]    [Pg.40]   
See also in sourсe #XX -- [ Pg.6 ]




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2 -thio-, preparation

Adenosine preparation

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