Identification of substrate-analog trypsin inhibitors through the screening of synthetic peptide combinatorial libraries.
about
Versatile C(3)-symmetric scaffolds and their use for covalent stabilization of the foldon trimerSolid phase synthesis of mixture-based acyclic and heterocyclic small molecule combinatorial libraries from resin-bound polyamides.Arginine-based structures are specific inhibitors of cathepsin C. Application of peptide combinatorial libraries.Inhibiting viral proteases: challenges and opportunities.Identification of inhibitors of prohormone convertases 1 and 2 using a peptide combinatorial library.In vitro and direct in vivo testing of mixture-based combinatorial libraries for the identification of highly active and specific opiate ligands.Combinatorial strategies for targeting protein families: application to the proteases.Chemical models of peptide formation in translation.Inhibitors of human heart chymase based on a peptide library.A mimotope from a solid-phase peptide library induces a measles virus-neutralizing and protective antibody response."Libraries from libraries": chemical transformation of combinatorial libraries to extend the range and repertoire of chemical diversity.Recursive deconvolution of combinatorial chemical librariesInvestigation of antigen-antibody interactions using a soluble, non-support-bound synthetic decapeptide library composed of four trillion (4 x 10(12) sequences.Identification of antimicrobial peptides by using combinatorial libraries made up of unnatural amino acidsIdentification of the peptides that stimulate the phosphoinositide hydrolysis in lymphocyte cell lines from peptide libraries.Identification of inhibitors of melittin using nonsupport-bound combinatorial libraries.All D-amino acid hexapeptide inhibitors of melittin's cytolytic activity derived from synthetic combinatorial libraries.Selection of potent inhibitors of farnesyl-protein transferase from a synthetic tetrapeptide combinatorial library.The effect of prime-site occupancy on the hepatitis C virus NS3 protease structure.Revisiting catalysis by chymotrypsin family serine proteases using peptide substrates and inhibitors with unnatural main chains.Identification of novel peptide inhibitors for human trypsins.Gel-phase 19F NMR spectral quality for resins commonly used in solid-phase organic synthesis; a study of peptide solid-phase glycosylations.Virtual screening for compounds that mimic protein-protein interface epitopes.
P2860
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P2860
Identification of substrate-analog trypsin inhibitors through the screening of synthetic peptide combinatorial libraries.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
Identification of substrate-an ...... ptide combinatorial libraries.
@en
type
label
Identification of substrate-an ...... ptide combinatorial libraries.
@en
prefLabel
Identification of substrate-an ...... ptide combinatorial libraries.
@en
P356
P1433
P1476
Identification of substrate-an ...... ptide combinatorial libraries.
@en
P2093
Houghten RA
P304
11035-11041
P356
10.1021/BI00092A013
P407
P577
1993-10-01T00:00:00Z