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Editorial:Spotlight on Japan - chemical sciences 2023.
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- Frontiers in Chemistry, 2024, p. 1, doi. 10.3389/fchem.2024.1461284
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- Article
Chemical and Chemoenzymatic Synthesis of Peptide and Protein Therapeutics Conjugated with Human N‐Glycans.
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- ChemMedChem, 2024, v. 19, n. 13, p. 1, doi. 10.1002/cmdc.202300692
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- Article
Better Peptides via Chemical Glycosylation: Somatostatin Analogues Having a Human Complex‐Type N‐Glycan with Improved Drug Properties.
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- Chemistry - A European Journal, 2023, v. 29, n. 31, p. 1, doi. 10.1002/chem.202300111
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- Article
A Novel Prodrug of a γ‐Glutamylcyclotransferase Inhibitor Suppresses Cancer Cell Proliferation in vitro and Inhibits Tumor Growth in a Xenograft Mouse Model of Prostate Cancer.
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- ChemMedChem, 2018, v. 13, n. 2, p. 155, doi. 10.1002/cmdc.201700660
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- Article
Development of a sufficiently reactive thioalkylester involving the side-chain thiol of cysteine applicable for kinetically controlled ligation.
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- Biopolymers, 2016, v. 106, n. 4, p. 503, doi. 10.1002/bip.22783
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- Article
Ordered self-assembly of the collagenous domain of adiponectin with noncovalent interactions via glycosylated lysine residues.
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- FEBS Letters, 2016, v. 590, n. 2, p. 195, doi. 10.1002/1873-3468.12034
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- Article
O-Acyl isopeptide method: development of an O-acyl isodipeptide unit for Boc SPPS and its application to the synthesis of A β1-42 isopeptide.
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- Journal of Peptide Science, 2014, v. 20, n. 9, p. 669, doi. 10.1002/psc.2662
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- Article
Evaluation of acid-labile S-protecting groups to prevent Cys racemization in Fmoc solid-phase peptide synthesis.
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- Journal of Peptide Science, 2014, v. 20, n. 1, p. 30, doi. 10.1002/psc.2585
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- Article
A Fluorogenic Probe for γ-Glutamyl Cyclotransferase: Application of an Enzyme-Triggered O-to-N Acyl Migration-Type Reaction.
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- ChemBioChem, 2013, v. 14, n. 16, p. 2110, doi. 10.1002/cbic.201300481
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- Article
Synthesis and application of N<sup>α</sup>-Fmoc- N<sup>π</sup>-4-methoxybenzyloxymethylhistidine in solid phase peptide synthesis.
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- Journal of Peptide Science, 2012, v. 18, n. 12, p. 763, doi. 10.1002/psc.2464
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- Article
Role of the Backbone Conformation at Position 7 in the Structure and Activity of Marinostatin, an Ester-Linked Serine Protease Inhibitor.
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- ChemBioChem, 2012, v. 13, n. 13, p. 1895, doi. 10.1002/cbic.201200315
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- Article
PHD finger of the SUMO ligase Siz/PIAS family in rice reveals specific binding for methylated histone H3 at lysine 4 and arginine 2
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- FEBS Letters, 2012, v. 586, n. 13, p. 1783, doi. 10.1016/j.febslet.2012.04.063
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- Article
The triple helical structure and stability of collagen model peptide with 4( s)-hydroxyprolyl-pro-gly units.
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- Biopolymers, 2012, v. 98, n. 2, p. 111, doi. 10.1002/bip.21730
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- Article
Crystal structure of basic 7S globulin, a xyloglucan-specific endo-β-1,4-glucanase inhibitor protein-like protein from soybean lacking inhibitory activity against endo-β-glucanase.
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- FEBS Journal, 2011, v. 278, n. 11, p. 1944, doi. 10.1111/j.1742-4658.2011.08111.x
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Generation of novel cationic antimicrobial peptides from natural non-antimicrobial sequences by acid-amide substitution.
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- Annals of Clinical Microbiology & Antimicrobials, 2011, v. 10, n. 1, p. 11, doi. 10.1186/1476-0711-10-11
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Structure-activity relationship of marinostatin, a serine protease inhibitor isolated from a marine organism.
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- Journal of Peptide Science, 2010, v. 16, n. 7, p. 329, doi. 10.1002/psc.1244
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- Article
Transient role of CD4+CD25+ regulatory T cells in mycobacterial infection in mice.
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- International Immunology, 2010, v. 22, n. 3, p. 179, doi. 10.1093/intimm/dxp126
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- Article
Quantitative analysis of helix-coil transition of block copolypeptide, Glu<sub>12</sub>-Ala<sub>12</sub>, by combined use of CD and NMR spectroscopy.
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- Biopolymers, 2005, v. 80, n. 2/3, p. 225, doi. 10.1002/bip.20206
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- Article
Collagen-like triple helix formation of synthetic (Pro-Pro-Gly)<sub>10</sub> analogues: (4( S)-hydroxyprolyl-4( R)-hydroxyprolyl-Gly)<sub>10</sub>, (4( R)-hydroxyprolyl-4( R)-hydroxyprolyl-Gly)<sub>10</sub> and (4( S)-fluoroprolyl-4( R)-fluoroprolyl-Gly)<sub>10</sub>
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- Journal of Peptide Science, 2005, v. 11, n. 10, p. 609, doi. 10.1002/psc.671
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- Article
Amino acid deletion products resulting from incomplete deprotection of the Boc group from N<sup>π</sup>-benzyloxymethylhistidine residues during solid-phase peptide synthesis.
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- Journal of Peptide Science, 2005, v. 11, n. 8, p. 512, doi. 10.1002/psc.657
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Structural basis for the biological activity of dendrotoxin-I, a potent potassium channel blocker.
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- Biopolymers, 2000, v. 54, n. 1, p. 44, doi. 10.1002/(SICI)1097-0282(200007)54:1<44::AID-BIP50>3.0.CO;2-Z
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Combined solid-phase and solution approach for the synthesis of large peptides or proteins.
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- Journal of Peptide Science, 2000, v. 6, n. 2, p. 84, doi. 10.1002/(SICI)1099-1387(200002)6:2<84::AID-PSC246>3.0.CO;2-P
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Anti-nociceptive responses produced by human putative counterpart of nocistatin.
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- British Journal of Pharmacology, 1998, v. 124, n. 6, p. 1016, doi. 10.1038/sj.bjp.0701995
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Nocistatin, a peptide that blocks nociceptin action in pain transmission.
- Published in:
- Nature, 1998, v. 392, n. 6673, p. 286, doi. 10.1038/32660
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- Article