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Bioactive and model peptides characterized by the helicogenic (αMe)Phe residue
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title
Bioactive and model peptides characterized by the helicogenic (αMe)Phe residue
(English)
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author name string
Claudio Toniolo
series ordinal
1
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Fernando Formaggio
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2
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Marco Crisma
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3
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Giovanni Valle
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4
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Wilhelmus H.J. Boesten
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5
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Hans E. Schoemaker
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6
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Johan Kamphuis
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7
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Piero A. Temussi
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8
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Elmer L. Becker
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9
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Gilles Précigoux
series ordinal
10
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publication date
March 1993
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published in
Tetrahedron
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volume
49
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issue
17
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page(s)
3641-3653
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cites work
Peptaibol antibiotics: a study on the helical structure of the 2-9 sequence of emerimicins III and IV.
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Paracelsin, a peptide antibiotic containing alpha-aminoisobutyric acid, isolated from Trichoderma reesei Simmons. Part A
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Linear oligopeptides. Part 147. Chemical and crystallographic study of the reaction between benzyloxycarbonyl chloride and α-aminoisobutyric acid
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Crystallographic characterization of the conformation of the 1-aminocyclohexane-1-carboxylic acid residue in simple derivatives and peptides
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Bioorganic stereochemistry. A study of the peptide oxazolones from Z-(Aib)n-OH (n = 2-4) in the solid state
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Linear oligopeptides. 188.Crystallographic characterization of the conformation of the 1-aminocyclopentane-1-carboxylic acid residue in simple derivatives
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Crystallographic characterization of conformation of 1-aminocyclopropane-1-carboxylic acid residue (Ac3c) in simple derivatives and peptides
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Structural versatility of peptides from C?,?-disubstituted glycines: Preferred conformation of the C?,?-diphenylglycine residue
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X-Ray diffraction structure determination of a novel peptide oxazol-5(4H)-one with a chiral carbon atom in the heterocyclic moiety
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Crystal and molecular structures of two N-carboxy anhydrides of Cα,α-disubstituted glycines*
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A molecular mechanical study of the structure of poly(alpha-aminoisobutyric acid).
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Structural characteristics of alpha-helical peptide molecules containing Aib residues
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Emerging approaches in the molecular design of receptor-selective peptide ligands: conformational, topographical and dynamic considerations
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Structure of conformationally constrained peptides: from model compounds to bioactive peptides
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Conformationally restricted peptides through short-range cyclizations.
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Sweet taste receptor: evidence of separate specific sites for COO- and NO2/CN groups in sweeteners
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Structure-taste relationships of some dipeptides
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New aspartame-like sweeteners containing L-(αMe)Phe
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IUPAC-IUB Commission on Biochemical Nomenclature. Abbreviations and symbols for the description of the conformation of polypeptide chains. Tentative rules (1969)
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Molecular Theory of Sweet Taste
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Intramolecularly Hydrogen-Bonded Peptide Conformation
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Turns in peptides and proteins
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Efficient preparation of N alpha-formylamino acid tert-butyl esters
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Identifiers
DOI
10.1016/S0040-4020(01)90220-0
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