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Peptidomimetics oligomeric

The oligomeric peptidomimetics such as peptoids are particularly interesting compounds since they provide access to an enormous molecular diversity by variation of the building blocks. Peptoids represent a class of polymers that are not found in nature. They differ from the peptides in the manner of side-chain attachment and thus can be considered as peptide mimetics in which the side chain has been shifted from the chiral a-carbon atom in a peptide to the achiral... [Pg.238]

A further amide bond modification, which has been introduced some years ago, is the alkylation of the amide nitrogens all along the peptide backbone [21]. This approach permits the construction of oligomeric peptidomimetics comparable to peptomers, in which the N-substituted glycines are replaced by N-substituted a-amino acids (Fig. 7.3). We could define these oligomers Ca-branched peptoids. [Pg.261]

Peptoids [22] form a particular promising class of oligomeric peptidomimetics, which consists of A-substituted-glycine derivatives. Thus, the concepts to translate a particular peptide sequence, in this case CAAX to a corresponding peptoid sequence is a perfectly suitable approach to obtain potential famesyl inhibitors. This approach was adopted by... [Pg.369]

Kinetically controlled peptide synthesis synthesis ot bioactive peptides in organic solvent (dermorphin, enkephalin) amino acid oligomerization [22] di- and tripeptide synthesis with peptidomimetic leaving group [23-27]... [Pg.400]


See other pages where Peptidomimetics oligomeric is mentioned: [Pg.273]    [Pg.208]    [Pg.464]    [Pg.693]    [Pg.192]    [Pg.120]    [Pg.182]    [Pg.45]    [Pg.304]    [Pg.406]    [Pg.145]    [Pg.999]    [Pg.148]    [Pg.152]    [Pg.209]    [Pg.274]    [Pg.32]    [Pg.511]    [Pg.119]    [Pg.120]    [Pg.119]    [Pg.449]   
See also in sourсe #XX -- [ Pg.369 ]




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Peptidomimetics

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