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1 IC(50)s = 100-700 nm) the binding of (125)I-[alpha-aminoisobutyric acid(1,3),M]PTH(1-15) and were sev
2 ]PTH(1-15) inhibited the agonist actions of [alpha-aminoisobutyric acid(1,3)]PTH(1-34) and [M]PTH(1-1
5 pha-proton of an alanine residue to generate alpha-aminoisobutyric acid (Aib) in alanine-based oligop
6 ally hindered and helix-promoting amino acid alpha-aminoisobutyric acid (Aib) in N-terminal PTH oligo
7 To meet this need, an iterative synthesis of alpha-aminoisobutyric acid (Aib) oligomers was used to c
8 f conformationally constrained residues like alpha-aminoisobutyric acid (Aib) or DPro that nucleate h
11 from the Ala series with the helix promoter alpha-aminoisobutyric acid (Aib) produced similar result
14 acement of (125)I-PTH-(1-34) binding by rat [alpha-aminoisobutyric acid (Aib)(1,3),Nle(8),Gln(10),Har
15 vely increased the transport of radiolabeled alpha-aminoisobutyric acid and dextran into brain tumors
16 ing aspartic acid, serine, glycine, alanine, alpha-aminoisobutyric acid, and valine were optimized by
17 a class of antibiotics known for their high alpha-aminoisobutyric acid content and their synthesis a
18 ement of the fully conserved Pro residues by alpha-aminoisobutyric acid leads to a large increase in
19 e-Val-Aib-D-Val15 -Leu-Phe-Val-Val-OMe (Aib, alpha-aminoisobutyric acid; OMe, methyl ester) was inten
20 tion, motility, Na(+)-dependent transport of alpha-aminoisobutyric acid, or H(+)-dependent synthesis
21 ucture by replacing alanine with glycine and alpha-aminoisobutyric acid resulted in analogues with ac
23 heless, dipeptides 6a and 6c (D-penicillamyl-alpha-aminoisobutyric acid) were able to reduce this AcH
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