about
Structural and biological mimicry of protein surface recognition by / -peptide foldamersEvaluation of Diverse α/β-Backbone Patterns for Functional α-Helix Mimicry: Analogues of the Bim BH3 DomainStructure-Guided Rational Design of α/β-Peptide Foldamers with High Affinity for BCL-2 Family Prosurvival ProteinsHighly diastereoselective and enantioselective preparation of homoallylic amines: application for the synthesis of beta-amino acids and gamma-lactams.Structural study of an active analog of EX-4 in solution and micelle associated states.Conformational stability studies of a stapled hexa-β3-peptide library.Peptides and peptidomimetics as immunomodulators.Peptides displayed as high density brush polymers resist proteolysis and retain bioactivity.β-Lysine discrimination by lysyl-tRNA synthetase.A quantum-chemical study of the binding ability of βXaaHisGlyHis towards copper(II) ion.Peptide-based selective inhibitors of matrix metalloproteinase-mediated activitiesSophistication of foldamer form and function in vitro and in vivo.Foldamers with heterogeneous backbones.Peptide-based vaccines for cancer: realizing their potential.Structure-kinetic relationship analysis of the therapeutic complement inhibitor compstatin.Peptidomimetics: modifying peptides in the pursuit of better vaccines.α/β-Peptide foldamers: state of the art.Road to clinical efficacy: challenges and novel strategies for antimicrobial peptide development.Transaminases for the synthesis of enantiopure beta-amino acids.Bacterial β-aminopeptidases: structural insights and applications for biocatalysis.Characterization of signal bias at the GLP-1 receptor induced by backbone modification of GLP-1.Iterative Nonproteinogenic Residue Incorporation Yields α/β-Peptides with a Helix-Loop-Helix Tertiary Structure and High Affinity for VEGF.Organocatalytic Transfer Hydrogenation and Hydrosilylation Reactions.On the terminal homologation of physiologically active peptides as a means of increasing stability in human serum--neurotensin, opiorphin, B27-KK10 epitope, NPY.Synthesis of glycosylated β³-homo-threonine conjugates for mucin-like glycopeptide antigen analogues.Mechanochemical enzymatic resolution of N-benzylated-β3-amino estersExtending foldamer design beyond α-helix mimicry: α/β-peptide inhibitors of vascular endothelial growth factor signaling.α-Helix mimicry with α/β-peptides.Sequence-based design of alpha/beta-peptide foldamers that mimic BH3 domains.Enantioselective catalytic β-amination through proton-coupled electron transfer followed by stereocontrolled radical-radical coupling.Boron-containing peptidomimetics--a novel class of selective anti-tubercular drugs.Antibacterial activity of ultrashort cationic lipo-beta-peptides.Membrane interactions of antimicrobial beta-peptides: the role of amphipathicity versus secondary structure induction.Synthesis of 4-hydroxy-β3-homoprolines and their insertion in α/β/α-tripeptides.Probing the proteolytic stability of beta-peptides containing alpha-fluoro- and alpha-hydroxy-beta-amino acids.β-Amino acid substitution to investigate the recognition of angiotensin II (AngII) by angiotensin converting enzyme 2 (ACE2).Highly efficient synthesis of heterocyclic and alicyclic β2-amino acid derivatives by catalytic asymmetric hydrogenation.Direct chromatographic enantioresolution of fully constrained β-amino acids: exploring the use of high-molecular weight chiral selectors.Efficient Enzymatic Routes for the Synthesis of New Eight-membered Cyclic β-Amino Acid and β-Lactam Enantiomers.One-Pot Lipase-Catalyzed Enantioselective Synthesis of (R)-(-)-N-Benzyl-3-(benzylamino)butanamide: The Effect of Solvent Polarity on Enantioselectivity.
P2860
Q27657158-AC31416B-B53E-4E7F-856A-2123444644F8Q27675317-A84B785A-E7D1-4D64-A651-1CDFECD8850BQ27679468-92BCC862-E3EB-4ACB-94E7-337BDA6B02AEQ30989333-A3B6D6F7-5951-4379-983D-EE91C3EF94DAQ33745444-A8861BBF-FFE6-438C-AB8E-C85C24D10AEDQ34129884-E015C61A-3EDC-4CD0-97DE-445659AE6253Q34359984-658AAE2D-C355-48B1-9179-4110924F2396Q34489488-F11E9F83-1E94-4893-9940-04852AA40451Q35377921-8C1F4507-135E-49B6-B356-96244E070FC8Q35854861-385B47BA-A9A9-47DF-A1E3-641ED163ED49Q36919032-51B30A4D-53A6-4EA3-A8BF-8D0212FA1D66Q36995775-7A273C35-1DAA-4D67-8D69-E7B89C90E24AQ37209830-BD72D9CA-B4AD-4A1C-B1AC-95EC4495AAF1Q37340462-2E9A16CE-3502-4C11-8E31-244A955B7168Q37384384-0DF6862C-F110-4E58-913D-35813698EBB7Q37844539-D110CD0C-5878-429B-92F5-6189003CC9DCQ37861031-982FCD64-E0B1-4CF6-969D-C73DB5313B21Q37894693-68D70379-D8AA-49BF-B4D1-00745C98404DQ37980280-60487FA3-A9AE-4A94-90D0-24FB2C3A108EQ38060668-C33877ED-F9C8-4AB1-AD56-229EBAE61A56Q38864019-C63CA42D-619A-4B53-8431-8BCC246B19B8Q39145905-27437981-2FB4-4473-B5E0-3D34308648CDQ39442487-5FD15291-4578-4807-9CC3-6738BBE25E3FQ39544807-36177EB2-24A4-4743-9579-F3078A36FE8DQ41136648-4C191433-9F22-425B-AE38-7E33BAF4F6A8Q41469023-F6F8C915-62A1-41BE-8664-95AABEEEDC2AQ41916714-36A08632-CE20-4121-836E-B39BE908E172Q41965412-284177E3-127C-4700-9088-766F9E8F350FQ42146826-1D401EF4-6F9E-4B56-9F5A-CD9891DDB67BQ42367444-FE74FE31-3C89-4A68-89EB-CCBF55FE29B4Q42714189-4CBC54F0-74C3-4142-A5CF-415E5F71566AQ43128345-47F03664-C379-4EC5-A592-EB6D202E452EQ43271557-CDBA159C-3AD8-4AF2-92E1-12CB0A829DAAQ43421492-A820E242-C18D-4956-A5AE-16FBE9731351Q44880172-5081B0D2-5C33-43C8-B195-0C5DE20E4E2EQ45918584-145380FE-756C-4D4C-BE2D-F103450A7E77Q46049526-B390A4D6-A8B8-4FD4-81BB-4FB50E1D9611Q47184800-C934EF69-68C5-4DA1-91B2-5531052F338AQ47253869-B8C49E29-91D0-4796-B50B-0C6FBBDE9AF1Q47257380-DD47C604-F40F-44E9-8A82-87053A03BD22
P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Beta-amino acids: versatile peptidomimetics.
@ast
Beta-amino acids: versatile peptidomimetics.
@en
Beta-amino acids: versatile peptidomimetics.
@nl
type
label
Beta-amino acids: versatile peptidomimetics.
@ast
Beta-amino acids: versatile peptidomimetics.
@en
Beta-amino acids: versatile peptidomimetics.
@nl
prefLabel
Beta-amino acids: versatile peptidomimetics.
@ast
Beta-amino acids: versatile peptidomimetics.
@en
Beta-amino acids: versatile peptidomimetics.
@nl
P2093
P356
P1476
Beta-amino acids: versatile peptidomimetics.
@en
P2093
A Ian Smith
David L Steer
Patrick Perlmutter
Rebecca A Lew
P304
P356
10.2174/0929867024606759
P577
2002-04-01T00:00:00Z