About: Bicyclic Pyrrolidine-Isoxazoline γ Amino Acid: A Constrained Scaffold for Stabilizing α-Turn Conformation in Isolated Peptides

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About: Bicyclic Pyrrolidine-Isoxazoline γ Amino Acid: A Constrained Scaffold for Stabilizing α-Turn Conformation in Isolated Peptides Goto Sponge NotDistinct Permalink

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article by Francesco Oliva et al published 2019 in Frontiers in Chemistry

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description	wetenschappelijk artikel (nl) article scientifique publié en 2019 (fr) im Jahr 2019 veröffentlichter wissenschaftlicher Artikel (de) наукова стаття, опублікована у 2019 (uk) article by Francesco Oliva et al published 2019 in Frontiers in Chemistry (en)
publication date	wds:Q64079529-CE692200-2B81-4C50-BACB-BC6CBE14C5A9
publication date	2019-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q64079529-6B6DE9A5-2BA4-499A-AD05-5D75B80FF139
language of work or name	English
cites work	wds:Q64079529-0297F226-7538-4A82-AE4B-2121D6094CC3 wds:Q64079529-0445F513-8B84-4A90-9C86-2BB550D65662 wds:Q64079529-05AA127C-51C4-4DC6-9B69-6FC1949723FE wds:Q64079529-0E8699C6-FE2C-4926-9BDA-78A6F985FC89 wds:Q64079529-1EF806FE-8FA3-427F-A531-B8F44BAD18C0 wds:Q64079529-24B5980A-F2E8-44A9-8205-CAE67B2274B8 wds:Q64079529-2D856F59-ACF0-40BD-8EAD-B4CEA1C89DF0 wds:Q64079529-367886BF-6F2E-44ED-8D0C-AC940007711B wds:Q64079529-375E9D33-DDDF-4A17-B485-C43E4B344CF0 wds:Q64079529-49931C35-74A6-48AF-ADF2-50FF0AC1CFF0 wds:Q64079529-4C506C9F-3E62-4652-AE58-134C95C97FE1 wds:Q64079529-4E362743-13A9-4452-A3A6-184A30BB19C2 wds:Q64079529-55801337-9139-4369-9270-3D3E9FDD3BC1 wds:Q64079529-5E3352A0-C764-47DE-B376-02822A36B14C wds:Q64079529-626104FB-2C57-42EA-B439-50322F651996 wds:Q64079529-6BBA1E45-AC0A-4F9A-BE06-4BB7E32C3C72 wds:Q64079529-6D5EA4A5-6BDE-4B62-9BD4-FCF4D6DB81A3 wds:Q64079529-76157515-09C3-44C1-BBB2-6651B43E180F wds:Q64079529-76E53D73-75EA-4A99-9330-80EC81080CF6 wds:Q64079529-7771E64D-41CE-42A9-B18C-F7614B08077D wds:Q64079529-7CEB2052-AB2D-4B83-A337-C51AB204831B wds:Q64079529-8176CA58-869A-44C3-AFE4-CA5000D94DC8 wds:Q64079529-83E6F9EA-A95C-422B-9380-84F6223BA8BE wds:Q64079529-8C9485C3-0FFA-48A2-8AC9-E57BA3064FAD wds:Q64079529-8FC6AD8E-11F7-484D-A938-9559B7498A19 wds:Q64079529-92B94253-53F4-420C-B78E-18CC514EDC24 wds:Q64079529-96477442-A1C0-4D08-B804-B0B71A043731 wds:Q64079529-98E29308-23D7-4E66-B6DB-D65A10DE15FA wds:Q64079529-9AF093E8-78A8-4927-8CDB-9596970C54CF wds:Q64079529-A8892483-830C-4A6D-9556-7C9D0AC253B6 wds:Q64079529-AD19DAA3-B4BD-4BAE-AA71-C64DD8269135 wds:Q64079529-B2B6B884-B896-44CC-8F2E-A28C860D5FC6 wds:Q64079529-B65802BD-FA40-4A4C-8793-76E12017857F wds:Q64079529-B91FAF8C-4CFF-46AF-85A4-06144E830454 wds:Q64079529-BCB4CB1C-136C-4107-A1A2-16F111CD6C2D wds:Q64079529-BCCD21FF-7057-44D9-B9E1-AB681BF351F1 wds:Q64079529-C30D3E4F-F48B-4C3E-98E0-2D3D687C866C wds:Q64079529-C4E14371-1C4D-4C72-8C2A-FC6FC7453E4C wds:Q64079529-CC06A049-AC03-4F2F-A902-AD3408782F9C wds:Q64079529-CCECB6C1-1CB2-47EC-AF8D-3C1477458248 wds:Q64079529-D260A0C6-09CF-43AD-9CEA-12991676C212 wds:Q64079529-D77AE659-61B6-4C08-B889-495D2BDE8664 wds:Q64079529-E7F219A5-B0BF-4A69-8D1B-51370023D9CD wds:Q64079529-F270AAED-FECC-4E87-8D78-63AB59E7DCED
cites work	Fourier transform infrared spectroscopic analysis of protein secondary structures Control of Heme Coordination and Catalytic Activity by Conformational Changes in Peptide-Amphiphile Assemblies Cis-trans amide bond rotamers in β-peptoids and peptoids: evaluation of stereoelectronic effects in backbone and side chains. Expanding the peptide beta-turn in alphagamma hybrid sequences: 12 atom hydrogen bonded helical and hairpin turns Infrared spectroscopy of proteins GROMACS: fast, flexible, and free Canonical sampling through velocity rescaling Furans, thiophenes and related heterocycles in drug discovery. Comparison of multiple Amber force fields and development of improved protein backbone parameters Discovering protein secondary structures: classification and description of isolated alpha-turns Automatic classification and analysis of alpha alpha-turn motifs in proteins. Structural chemistry of peptides containing backbone expanded amino acid residues: conformational features of β, γ, and hybrid peptides New preorganized γ-amino acids as foldamer building blocks Circular dichroism spectra of short, fixed-nucleus alanine helices Alpha-turn mimetics: short peptide alpha-helices composed of cyclic metallopentapeptide modules Foldamers containing γ-amino acid residues or their analogues: structural features and applications Synthesis and biochemical evaluation of δ(2)-isoxazoline derivatives as DNA methyltransferase 1 inhibitors Isoxazoline containing natural products as anticancer agents: a review Peptides in cancer nanomedicine: drug carriers, targeting ligands and protease substrates β-Hairpin mimics containing a piperidine-pyrrolidine scaffold modulate the β-amyloid aggregation process preserving the monomer species. Leucine aminopeptidase. V. Activation, specificity, and mechanism of action Asymmetric Modular Synthesis of a Semirigid Dipeptide Mimetic by Cascade Cycloaddition/Ring Rearrangement and Borohydride Reduction Furan-based locked Z-vinylogous γ-amino acid stabilizing protein α-turn in water-soluble cyclic α3γ tetrapeptides Synthesis and in vitro/in vivo evaluation of the antitrypanosomal activity of 3-bromoacivicin, a potent CTP synthetase inhibitor Dipeptide Nanotubes Containing Unnatural Fluorine-Substituted β(2,3)-Diarylamino Acid and L-Alanine as Candidates for Biomedical Applications Synthesis and characterization of water-soluble macrocyclic peptides stabilizing protein α-turn. Photocyclization of Tetra- and Pentapeptides Containing Adamantylphthalimide and Phenylalanines: Reaction Efficiency and Diastereoselectivity Discovery of covalent inhibitors of glyceraldehyde-3-phosphate dehydrogenase, a target for the treatment of malaria Preorganized Cyclic α,α-Disubstituted α-Amino Acids Bearing Functionalized Side Chains That Act as Peptide-Helix Inducers. Inspired by Nature: The 3-Halo-4,5-dihydroisoxazole Moiety as a Novel Molecular Warhead for the Design of Covalent Inhibitors. Succinct synthesis of beta-amino acids via chiral isoxazolines Bicyclic γ-amino acids as inhibitors of γ-aminobutyrate aminotransferase Protein α-turns recreated in structurally stable small molecules Amphiphilic Peptide Self-Assembly: Expansion to Hybrid Materials. Understanding the conformational analysis of gababutin based hybrid peptides. Tuning optoelectronic and chiroptic properties of peptide-based materials by controlling the pathway complexity. Hydrophobic α,α-Disubstituted Disilylated TESDpg Induces Incipient 310-Helix in Short Tripeptide Sequence. Tetrahydro-4 H-(pyrrolo[3,4- d]isoxazol-3-yl)methanamine: A Bicyclic Diamino Scaffold Stabilizing Parallel Turn Conformations Synthesis of new isoxazoline-based acidic amino acids and investigation of their affinity and selectivity profile at ionotropic glutamate receptors Multicomponent peptide assemblies. Oligomers of enantiopure bicyclic gamma/delta-amino acids (BTAa). 1. Synthesis and conformational analysis of 3-aza-6,8-dioxabicyclo 1H-Azepine-4-amino-4-carboxylic acid: a new α,α-disubstituted ornithine analogue capable of inducing helix conformations in short Ala-Aib pentapeptides 1H-Azepine-2-oxo-5-amino-5-carboxylic Acid: A 310 Helix Inducer and an Effective Tool for Functionalized Gold Nanoparticles Self-assembly of an amphipathic ααβ-tripeptide into cationic spherical particles for intracellular delivery
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