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Impact of Azaproline on Peptide Conformation
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Pseudoprolines: Targeting acis Conformation in a Mimetic of the gp120 V3 Loop of HIV-1
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A Triangular Mixed-Valent CuIICuICuI Cluster Supported by the Tripod Ligand 2-Quinolyl-2,2′-dipyrrolylmethane
inferredcites →https://doi.org/10.1002/1097-0282(2001)60:3<246::aid-bip10044>3.0.co;2-vopenalex-snapshot
Peptide interactions with G-protein coupled receptors
inferredcites →https://doi.org/10.1002/1521-3773(20010917)40:18<3364::aid-anie3364>3.0.co;2-sopenalex-snapshot
Atomic Force Microscope Studies on Condensation of Plasmid DNA with Functionalized Fullerenes
inferredcites →https://doi.org/10.1002/bip.1968.360061006openalex-snapshot
Stereochemical criteria for polypeptides and proteins. V. Conformation of a system of three linked peptide units
inferredcites →https://doi.org/10.1002/bip.360280118openalex-snapshot
Cyclo( D ‐Pro‐ L ‐Pro‐ D ‐Pro‐ L ‐Pro): Structural properties and cis/trans isomerization of the cyclotetrapeptide backbone
inferredcites →https://doi.org/10.1002/bip.360330707openalex-snapshot
Crystal state conformation of three azapeptides containing the Azaproline residue, a β‐turn regulator
inferredcites →https://doi.org/10.1002/bip.360360207openalex-snapshot
Conformational mimicry: Synthesis and solution conformation of a cyclic somatostatin hexapeptide containing a tetrazole cis amide bond surrogate
inferredcites →https://doi.org/10.1002/hlca.19950780614openalex-snapshot
Synthesis of a Type‐VIβ‐Turn Peptide Mimetic and Its Incorporation into a High‐Affinity Somatostatin Receptor Ligand
inferredcites →https://doi.org/10.1002/jcc.540070216openalex-snapshot
An all atom force field for simulations of proteins and nucleic acids
inferredcites →https://doi.org/10.1002/jcc.540110311openalex-snapshot
Determining atom‐centered monopoles from molecular electrostatic potentials. The need for high sampling density in formamide conformational analysis
inferredcites →https://doi.org/10.1002/jcc.540110405openalex-snapshot
Macromodel—an integrated software system for modeling organic and bioorganic molecules using molecular mechanics
inferredcites →https://doi.org/10.1002/jcc.540151111openalex-snapshot
A rapidly convergent simulation method: Mixed Monte Carlo/stochastic dynamics
inferredcites →https://doi.org/10.1002/prac.19723140509openalex-snapshot
Hydrazinverbindungen als Heterobestandteile in Peptiden. XVI. Synthese von 9‐Hydrazinoessigsäure‐, 9‐Azaglycin‐ und 5‐α‐Azaasparagin‐Oxytocin
inferredcites →https://doi.org/10.1002/pro.5560050719openalex-snapshot
Experimentally observed conformation‐dependent geometry and hidden strain in proteins
inferredcites →https://doi.org/10.1002/psc.297openalex-snapshot
Influence of N‐terminal residue stereochemistry on the prolyl amide geometry and the conformation of 5‐tert‐butylproline type VI β‐turn mimics
inferredcites →https://doi.org/10.1002/psc.310010307openalex-snapshot
Synthesis and properties of the first all‐aza analogue of a biologically active peptide
inferredcites →https://doi.org/10.1006/jmbi.1998.1770openalex-snapshot
Side-chain effects on peptidyl-prolyl cis/trans isomerisation
inferredcites →https://doi.org/10.1007/978-94-011-0683-2_226openalex-snapshot
Chimeric amino acids in cyclic GnRH antagonists
inferredcites →https://doi.org/10.1007/978-94-011-0683-2_227openalex-snapshot
Chimeric amino acids in cyclic bradykinin analogs: Evidence for receptor-bound turn conformation
inferredcites →https://doi.org/10.1007/978-94-011-1474-5_139openalex-snapshot
Chimeric amino acids as tools in conformational analysis: Bradykinin and angiotensin II
inferredcites →https://doi.org/10.1007/bf01930392openalex-snapshot
Retarded enzymatic degradation of heterologous eledoisin sequences
inferredcites →https://doi.org/10.1016/0006-291x(78)91544-9openalex-snapshot
Potent agonist and antagonist analogues of luliberin containing an azaglycine residue in position 10
inferredcites →https://doi.org/10.1016/0022-2836(90)90159-jopenalex-snapshot
Occurrence and role ofcis peptide bonds in protein structures
inferredcites →https://doi.org/10.1016/0040-4039(93)85081-7openalex-snapshot
A Convenient synthesis of the, conformationally constrained amino acid 5,5-dimethylproline
inferredcites →https://doi.org/10.1016/0301-0104(81)85090-2openalex-snapshot
Electrostatic interaction of a solute with a continuum. A direct utilizaion of AB initio molecular potentials for the prevision of solvent effects
inferredcites →https://doi.org/10.1016/0959-440x(92)90117-popenalex-snapshot
Three-dimensional structure of peptide—protein complexes: implications for recognition
inferredcites →https://doi.org/10.1016/s0006-291x(84)80103-5openalex-snapshot
Azapeptides: A new class of angiotensin-converting enzyme inhibitors
inferredcites →https://doi.org/10.1016/s0040-4020(01)87955-2openalex-snapshot
The conformation of cyclo-[(R)-cysteinyl-(R)-cysteine] in solution
inferredcites →https://doi.org/10.1016/s0040-4020(01)90206-6openalex-snapshot
Approaches to peptidomimetics which serve as surrogates for the cis amide bond: novel disulfide-constrained bicyclic hexapeptide analogs of somatostatic.
inferredcites →https://doi.org/10.1016/s0040-4020(01)91222-0openalex-snapshot
The synthesis and conformational analysis of a pair of diastereomeric, conformationally constrained peptides with opposite amide bond geometries
inferredcites →https://doi.org/10.1016/s0040-4039(00)75983-1openalex-snapshot
Design and synthesis of a cis-gly-pro, type-VI turn, dipeptide mimetic and its use in fmoc-solid phase peptide synthesis
inferredcites →https://doi.org/10.1016/s0040-4039(00)76740-2openalex-snapshot
Design, synthesis and evaluation of a novel bicyclic lactam as a gly-pro type vi beta-turn mimic
inferredcites →https://doi.org/10.1016/s0960-894x(99)00049-9openalex-snapshot
Design, synthesis, and evaluation of azapeptides as substrates and inhibitors for human rhinovirus 3C protease
inferredcites →https://doi.org/10.1021/bi00693a026openalex-snapshot
Consideration of the possibility that the slow step in protein denaturation reactions is due to cis-trans isomerism of proline residues
inferredcites →https://doi.org/10.1021/cr0104375openalex-snapshot
Cis−Trans Isomerization of Organic Molecules and Biomolecules: Implications and Applications
inferredcites →https://doi.org/10.1021/ja00002a067openalex-snapshot
A molecular constraint that generates a cis peptide bond
inferredcites →https://doi.org/10.1021/ja00002a068openalex-snapshot
Structures of the efrapeptins: potent inhibitors of mitochondrial ATPase from the fungus Tolypocladium niveum
inferredcites →https://doi.org/10.1021/ja00172a038openalex-snapshot
Semianalytical treatment of solvation for molecular mechanics and dynamics
inferredcites →https://doi.org/10.1021/ja00172a039openalex-snapshot
Surface concentrations and residence times of intermediates on samarium oxide during the oxidative coupling of methane
inferredcites →https://doi.org/10.1021/ja00225a045openalex-snapshot
Conformational mimicry. 1. 1,5-Disubstituted tetrazole ring as a surrogate for the cis amide bond
inferredcites →https://doi.org/10.1021/ja00225a046openalex-snapshot
Preparation and characterization of two His-59 ruthenium-modified algal plastocyanins and an unusually small rate constant for ruthenium(II) .fwdarw. copper(II) intramolecular electron transfer over.apprx.12 .ANG.
inferredcites →https://doi.org/10.1021/ja00315a052openalex-snapshot
Biosynthetic origin of the carbon skeleton and oxygen atoms of nargenicin A1
inferredcites →https://doi.org/10.1021/ja00907a037openalex-snapshot
Geminal Proton-Proton Coupling Constants in CH2[UNK]N-- Systems
inferredcites →https://doi.org/10.1021/ja012442wopenalex-snapshot
Effect of Sequence on Peptide Geometry in 5-tert-Butylprolyl Type VI β-Turn Mimics
inferredcites →https://doi.org/10.1021/ja960214+openalex-snapshot
Theoretical Study of the Structure and Rotational Flexibility of Diacylhydrazines: Implications for the Structure of Nonsteroidal Ecdysone Agonists and Azapeptides
inferredcites →https://doi.org/10.1021/ja9621760openalex-snapshot
Development and Testing of the OPLS All-Atom Force Field on Conformational Energetics and Properties of Organic Liquids
inferredcites →https://doi.org/10.1021/ja962780aopenalex-snapshot
Pseudo-Prolines as a Molecular Hinge: Reversible Induction ofcisAmide Bonds into Peptide Backbones
inferredcites →https://doi.org/10.1021/jm00001a019openalex-snapshot
Ac-[3- and 4-Alkylthioproline31]-CCK4 Analogs: Synthesis and Implications for the CCK-B Receptor-Bound Conformation
inferredcites →https://doi.org/10.1021/jm000332eopenalex-snapshot
Pseudoproline-Containing Analogues of Morphiceptin and Endomorphin-2: Evidence for aCisTyr−Pro Amide Bond in the Bioactive Conformation
inferredcites →https://doi.org/10.1021/jm0004953openalex-snapshot
Solid-Phase Synthesis of a Nonpeptide RGD Mimetic Library: New Selective αvβ3 Integrin Antagonists
inferredcites →https://doi.org/10.1021/jm00065a013openalex-snapshot
Multiple binding modes for the receptor-bound conformations of cyclic AII agonists
inferredcites →https://doi.org/10.1021/jm00101a004openalex-snapshot
Cysteine protease inhibition by azapeptide esters
inferredcites →https://doi.org/10.1021/jm00208a004openalex-snapshot
Synthesis and biological activity of highly active .alpha.-aza analogs of luliberin
inferredcites →https://doi.org/10.1021/jm970802dopenalex-snapshot
Azapeptides as Inhibitors and Active Site Titrants for Cysteine Proteinases
inferredcites →https://doi.org/10.1021/jo00027a038openalex-snapshot
Conformational mimicry. 3. Synthesis and incorporation of 1,5-disubstituted tetrazole dipeptide analogs into peptides with preservation of chiral integrity: bradykinin
inferredcites →https://doi.org/10.1021/jo010904iopenalex-snapshot
AcisAmide Bond Surrogate Incorporating 1,2,4-Triazole
inferredcites →https://doi.org/10.1021/jo951788kopenalex-snapshot
Molecular Mechanics Parameters and Conformational Free Energies of Proline-Containing Peptides
inferredcites →https://doi.org/10.1021/jo990294aopenalex-snapshot
Use of Steric Interactions To Control Peptide Turn Geometry. Synthesis of Type VI β-Turn Mimics with 5-tert-Butylproline
inferredcites →https://doi.org/10.1021/jo9906173openalex-snapshot
Novel Solid-Phase Synthesis of Azapeptides and Azapeptoides via Fmoc-Strategy and Its Application in the Synthesis of RGD-Mimetics
inferredcites →https://doi.org/10.1021/jp971959kopenalex-snapshot
Evaluation of Solvent Effects in Isotropic and Anisotropic Dielectrics and in Ionic Solutions with a Unified Integral Equation Method: Theoretical Bases, Computational Implementation, and Numerical Applications
inferredcites →https://doi.org/10.1021/ma60051a005openalex-snapshot
Stability of Cis, Trans, and Nonplanar Peptide Groups
inferredcites →https://doi.org/10.1063/1.472902openalex-snapshot
How does basis set superposition error change the potential surfaces for hydrogen-bonded dimers?
inferredcites →https://doi.org/10.1063/1.473558openalex-snapshot
Continuum solvation models: A new approach to the problem of solute’s charge distribution and cavity boundaries
inferredcites →https://doi.org/10.1063/1.474659openalex-snapshot
A new integral equation formalism for the polarizable continuum model: Theoretical background and applications to isotropic and anisotropic dielectrics
inferredcites →https://doi.org/10.1111/j.1399-3011.1991.tb00270.xopenalex-snapshot
Conformational mimicry II. An obligatory cis amide bond in a small linear pep tide
inferredcites →https://doi.org/10.1111/j.1399-3011.1992.tb00315.xopenalex-snapshot
Conformational studies on β‐bend containing a cis peptide unit
inferredcites →https://doi.org/10.1111/j.1399-3011.1996.tb00841.xopenalex-snapshot
Stereoselective syntheses of 3‐mercaptoproline derivatives protected for solid phase peptide synthesis
inferredcites →https://doi.org/10.1111/j.1399-3011.1997.tb01208.xopenalex-snapshot
X‐ray structures of aza‐proline‐containing peptides
inferredcites →https://doi.org/10.1111/j.1399-3011.1998.tb00648.xopenalex-snapshot
Azaproline as a β‐turn‐inducer residue opposed to proline
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Theoretical Structure Determination of a Class of Heterocyclic Compounds: The Pyrazolidines
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Konformationseigenschaften des 4‐Mercaptoprolins und verwandter Derivate
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A Single Stereodynamic Center Modulates the Rate of Self‐Assembly in a Biomolecular System
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Conformational Properties of 4‐Mercaptoproline and Related Derivatives
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A Single Stereodynamic Center Modulates the Rate of Self‐Assembly in a Biomolecular System
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Influence of Proline Chirality on Neighbouring Azaproline Residue Stereodynamic Nitrogen Preorganization
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Effects of i and i+3 residue identity on Cis–Trans isomerism of the aromatici+1–prolyli+2 amide bond: Implications for type VI β‐turn formation
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Impact of Cis‐proline analogs on peptide conformation
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Limiting Assumptions in the Design of Peptidomimetics
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Fructose‐Based Proline Analogues: Exploring the Prolyl trans / cis ‐Amide Rotamer Population in Model Peptides
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1,2‐Diazetidines − Structure, Synthesis, and Functionalization
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Chemogenomics with Protein Secondary-Structure Mimetics
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Development of small molecules designed to modulate protein–protein interactions
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Synthesis of diazetidines
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β-Turn editing in Gramicidin S: Activity impact on replacing proline α-carbon with stereodynamic nitrogen
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The β-turn scaffold of tripeptide containing an azaphenylalanine residue
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Theoretical structure determination of a class of heterocyclic compounds: The pyrazolidines
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Design, synthesis, and biological evaluation of stable β 6.3 -Helices: Discovery of non-hemolytic antibacterial peptides
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A general strategy for the synthesis of azapeptidomimetic lactams
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Synthesis of cyclic α-hydrazino acids
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Efficient synthesis of enantiomerically pure (S)-δ-azaproline starting from (R)-α-hydroxy-γ-butyrolactone via the Mitsunobu reaction
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Divergent amine-catalyzed [2+2] annulation of allenoates with azodicarboxylates: facile synthesis of 1,2-diazetidines
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Multigram Synthesis of 3,3-Spiro-α-prolines
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Cis–Trans Conformational Analysis of δ-Azaproline in Peptides
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Solid-Phase Azopeptide Diels–Alder Chemistry for Aza-pipecolyl Residue Synthesis To Study Peptide Conformation
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Synthesis of Enantiopure ε-Oxapipecolic Acid
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δ-Azaproline and Its Oxidized Variants
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Enantiopure 5-CF3–Proline: Synthesis, Incorporation in Peptides, and Tuning of the Peptide Bond Geometry
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Late-Stage N-Alkylation of Azapeptides
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Phage Display and Peptide Mapping of an Immunoglobulin Light Chain Fibril-Related Conformational Epitope
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Engineering Cyclic Tetrapeptides Containing Chimeric Amino Acids as Preferred Reverse-Turn Scaffolds
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Benzyl 2-Cyano-3,3-Dimethyl-1-pyrrolidinecarboxylate, a Versatile Intermediate for the Synthesis of 3,3-Dimethylproline Derivatives
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Intramolecular Hydrogen Bond-Controlled Prolyl Amide Isomerization in Glucosyl 3′(S)-Hydroxy-5′-hydroxymethylproline Hybrids: Influence of a C-5′-Hydroxymethyl Substituent on the Thermodynamics and Kinetics of Prolyl Amide Cis/Trans Isomerization
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Origin of Rotational Barriers of the N−N Bond in Hydrazine: NBO Analysis
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Conformational Preferences and cis−trans Isomerization of Azaproline Residue
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Intramolecular Hydrogen Bond-Controlled Prolyl Amide Isomerization in Glucosyl 3(S)-Hydroxy-5-hydroxymethylproline Hybrids: A Computational Study
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Aza-proline effectively mimics l -proline stereochemistry in triple helical collagen
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Conformational preferences of aza-proline residues and their impact on the relative stability of polyproline structures
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Stereoselective synthesis of ( R )- and ( S )-1,2-diazetidine-3-carboxylic acid derivatives for peptidomimetics
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Recent Developments in the Synthesis and Applications of Pyrazolidines. A Review
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Azapeptides and Their Therapeutic Potential
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