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Chymotrypsin mimetics

Furthermore, phenyl ester are also suitable substrate mimetics for chymotrypsin-catalyzed peptide synthesis, as was established by Bordusa s group and will demonstrated by sophisticated fragment condensations in Sect. 12.5.3.7. [Pg.850]

Figure 12.5-28. Chymotrypsin-catalyzed (8+16) segment synthesis ofthe Ht 31 (493-515) peptide via substrate mimetic strategy12331. Figure 12.5-28. Chymotrypsin-catalyzed (8+16) segment synthesis ofthe Ht 31 (493-515) peptide via substrate mimetic strategy12331.
Chymotrypsin and V8 peptidase, members of the trypsin family of serine proteases, as well as an engineered trypsin variant (D189K/K60E), were employed for the N-terminal introduction of 2-aminobenzoyl- and 3-(4-hydroxy-phenyl)-propionyl groups, and biotin in the form of substrate mimetics into peptides [115]. [Pg.415]


See other pages where Chymotrypsin mimetics is mentioned: [Pg.392]    [Pg.392]    [Pg.394]    [Pg.291]    [Pg.657]    [Pg.658]    [Pg.660]    [Pg.849]    [Pg.850]    [Pg.857]    [Pg.539]    [Pg.359]    [Pg.262]    [Pg.269]    [Pg.404]   
See also in sourсe #XX -- [ Pg.444 ]




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