1 Our results also show that the active
N-substituted glycines are part of our smaller filtered
2 Peptoids (
N-substituted glycines)
are an important class of biomim
3 omprised of several thousand peptoids (oligo-
N-substituted glycines)
are useful tools for the identif
4 Peptoids, or oligomers of
N-substituted glycine,
are an important class of non-nat
5 Sequence-defined peptoids, or
N-substituted glycines,
are an attractive class of biois
6 ids are biostable, with a protease-resistant
N-substituted glycine backbone, and their sequences are
7 receptor ligands to highly dissimilar active
N-substituted glycine compounds.
8 Peptoids (oligomers of
N-substituted glycines)
demonstrate proteolytic stabilit
9 ly, even the cis-enforcing peptoid residues (
N-substituted glycines)
form stable triple-helices.
10 tified by synthesizing only a portion of the
N-substituted glycine library.
11 oids, which are peptide-mimetics composed of
N-substituted glycine monomers, are less susceptible to
12 corporating peptoids, which are oligomers of
N-substituted glycine monomers, into high-throughput scr
13 Here we describe that
N-substituted glycines (
N-glys), also known as peptoid r
14 The biological activities of
N-substituted glycine oligomers (peptoids) have been the
15 A family of
N-substituted glycine oligomers (peptoids) of defined le
16 ckbone cis- and trans-amides in peptoids, or
N-substituted glycine oligomers, constitutes a significa
17 N-Substituted glycine oligomers, or "peptoids", are a pr
18 N-substituted glycine oligomers, or peptoids, have emerg
19 viously demonstrated the ability of peptoids-
N-substituted glycine oligomers-to stabilize high-oxidat
20 Here we describe a family of
N-substituted glycine or "peptoid" nonamers that folds i
21 The achiral backbone of oligo-
N-substituted glycines or "peptoids" lacks hydrogen-bond
22 Oligomeric
N-substituted glycines or "peptoids" with alpha-chiral,
23 ism (CD) of the helical structures formed by
N-substituted glycine (
or "peptoid") oligomers with alph
24 rcomes these difficulties is the use of poly-
N-substituted glycines,
or peptoids, to mimic SP-C.
25 This report describes a library of synthetic
N-substituted glycine peptoid oligomers that possess "du
26 tegies to enhance conformational ordering of
N-substituted glycine peptoid oligomers.
27 nalysis of the conformational preferences of
N-substituted glycine peptoid oligomers.
28 Antimicrobial
N-substituted glycine (
peptoid) oligomers ("ampetoids")
29 Polymers of
N-substituted glycines ("
peptoids") containing chiral ce
30 finity zinc-binding function into a peptoid (
N-substituted glycine polymer) two-helix bundle.
31 Peptoids are sequence-specific, oligo-
N-substituted glycine polymers designed to mimic the str
32 c 30mer, 45mer, and 60mer peptoid oligomers (
N-substituted glycine polymers) consisting of 15mer unit
33 Peptoids that are oligomers of
N-substituted glycines represent a class of peptide mimi
34 Peptoids, or oligomers of
N-substituted glycine,
represent a versatile class of fo
35 a family of synthetic oligomers composed of
N-substituted glycine units.
36 Cyclic peptoids are macrocyclic oligomers of
N-substituted glycines with specific folding abilities a