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Aza-Amino Acid Scan for Rapid Identification of Secondary Structure Based on the Application of N-Boc-Aza1-Dipeptides in Peptide Synthesis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Synthesis and Biological Evaluation of a Cyclo--tetrapeptide as a Somatostatin Analogue
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Opportunities for New Chemical Libraries: Unnatural Biopolymers and Diversomers
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Solid‐Phase Syntheses of Unnatural Biopolymers Containing Repeating Urea Units
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Crystal state conformation of three azapeptides containing the Azaproline residue, a β‐turn regulator
inferredcites →https://doi.org/10.1002/jctb.280500205openalex-snapshot
Inhibition of trypsin by t‐Butyloxycarbonyl‐α‐aza‐(4‐aminophenyl)alanine phenyl ester
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Hydrazinverbindungen als Heterobestandteile in Peptiden. XVI. Synthese von 9‐Hydrazinoessigsäure‐, 9‐Azaglycin‐ und 5‐α‐Azaasparagin‐Oxytocin
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Color test for detection of free terminal amino groups in the solid-phase synthesis of peptides
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Synthesis and evaluation of diacylhydrazines as inhibitors of the interleukin-1β converting enzyme (ICE)
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An active-site titrant for chymotrypsin, and evidence that azapeptide esters are less susceptible to nucleophilic attack than ordinary esters
inferredcites →https://doi.org/10.1016/s0040-4020(00)00885-1openalex-snapshot
Ring-Closing Metathesis Strategies to Cyclic Sulfamide Peptidomimetics
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A hierarchical approach to peptidomimetic design
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Design and synthesis of conformationally constrained amino acids as versatile scaffolds and peptide mimetics
inferredcites →https://doi.org/10.1016/s0040-4039(00)00534-7openalex-snapshot
Solid phase synthesis of azapeptides utilising reversible amide bond protection to prevent hydantoin formation
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The couple Pro/AzaPro : A means of β-turn formation control synthesis and conformation of two AzaPro-containing dipeptides
inferredcites →https://doi.org/10.1016/s0040-4039(01)00917-0openalex-snapshot
Synthesis and conformational preferences in solution and crystalline states of an aza-tripeptide
inferredcites →https://doi.org/10.1016/s0166-1280(98)00567-3openalex-snapshot
Conformational properties of azapeptides
inferredcites →https://doi.org/10.1016/s0960-894x(00)80516-8openalex-snapshot
Synthesis and evaluation of azapeptide-derived inhibitors of serine and cysteine proteases
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Synthesis and biological activity of P2–P4 azapeptidomimetic P1-argininal and P1-ketoargininamide derivatives: a novel class of serine protease inhibitors
inferredcites →https://doi.org/10.1016/s0960-894x(97)10198-6openalex-snapshot
Investigations of azapeptides as mimetics of Leu-enkephalin
inferredcites →https://doi.org/10.1021/bi00216a036openalex-snapshot
Solution structure of human calcitonin gene-related peptide by proton NMR and distance geometry with restrained molecular dynamics
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Turn Structures in CGRP C-Terminal Analogues Promote Stable Arrangements of Key Residue Side Chains
inferredcites →https://doi.org/10.1021/cc000022hopenalex-snapshot
An Improved Procedure for N- to C-Directed (Inverse) Solid-Phase Peptide Synthesis
inferredcites →https://doi.org/10.1021/ja00042a052openalex-snapshot
Vinylogous polypeptides: an alternative peptide backbone
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Pro-D-NMe-Amino Acid and D-Pro-NMe-Amino Acid: Simple, Efficient Reverse-Turn Constraints
inferredcites →https://doi.org/10.1021/ja00907a036openalex-snapshot
N- [2-Isopropyl-3-(L-aspartyl-L-arginyl)-carbazoyl]-L- tyrosyl-L-valyl-L-histidyl-L-prolyl-L-phenylalanine,1 an Isostere of Bovine Angiotensin II
inferredcites →https://doi.org/10.1021/ja01520a048openalex-snapshot
Central Stimulants. Chemistry and Structure-Activity Relationship of Aralkyl Hydrazines
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Impact of Azaproline on Amide Cis−Trans Isomerism: Conformational Analyses and NMR Studies of Model Peptides Including TRH Analogues
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Azatides: Solution and Liquid Phase Syntheses of a New Peptidomimetic
inferredcites →https://doi.org/10.1021/ja9635443openalex-snapshot
Site-Selective N-Methylation of Peptides on Solid Support
inferredcites →https://doi.org/10.1021/ja970855kopenalex-snapshot
Conformational Analysis of Reverse-Turn Constraints by N-Methylation and N-Hydroxylation of Amide Bonds in Peptides and Non-Peptide Mimetics
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Cysteine protease inhibition by azapeptide esters
inferredcites →https://doi.org/10.1021/jm00195a025openalex-snapshot
Synthesis of angiotensin II analogs by incorporating .beta.-homotyrosine or .beta.-homoisoleucine residues
inferredcites →https://doi.org/10.1021/jm00208a004openalex-snapshot
Synthesis and biological activity of highly active .alpha.-aza analogs of luliberin
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Designing Non-Peptide Peptidomimetics in the 21st Century: Inhibitors Targeting Conformational Ensembles
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Azapeptides as Inhibitors and Active Site Titrants for Cysteine Proteinases
inferredcites →https://doi.org/10.1021/jo000225sopenalex-snapshot
New Synthesis of 1,1-Substituted Hydrazines by Alkylation of N-Acyl- or N-alkyloxycarbonylaminophthalimide Using the Mitsunobu Protocol
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An improved method for the synthesis of enantiomerically pure amino acid ester isocyanates
inferredcites →https://doi.org/10.1021/jo000759topenalex-snapshot
Synthesis of Cyclic Peptides by Ring-Closing Metathesis
inferredcites →https://doi.org/10.1021/jo01295a026openalex-snapshot
Polymer-bound oxime esters as supports for solid-phase peptide synthesis. The preparation of protected peptide fragments
inferredcites →https://doi.org/10.1021/ol0160856openalex-snapshot
Combination of tert-Butoxycarbonyl and Triphenylphosphonium Protecting Groups in the Synthesis of Substituted Hydrazines
inferredcites →https://doi.org/10.1034/j.1399-3011.2000.00686.xopenalex-snapshot
Structural features of thePip/AzPip couple in the crystalline state: influence of the relative AzPip location in an azadipeptide sequence upon the induced chirality and conformational characteristics
inferredcites →https://doi.org/10.1034/j.1399-3011.2000.00717.xopenalex-snapshot
Role of azaamino acid residue in β‐turn formation and stability in designed peptide
inferredcites →https://doi.org/10.1039/b009651mopenalex-snapshot
The energetically favorable cis peptide bond for the azaglycine-containing peptide: For-AzGly-NH2 model
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Synthetic methodology for alkyl substituted hydrazines
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Polypeptides. Part XIII. Preparation of α-aza-amino-acid (carbazic acid) derivatives and intermediates for the preparation of α-aza-peptides
inferredcites →https://doi.org/10.1039/p19930002843openalex-snapshot
Synthesis of azapeptides by the Fmoc/tert-butyl/polyamide technique
inferredcites →https://doi.org/10.1055/s-1991-26511openalex-snapshot
Sodium Cyanoborohydride Reduction of (Benzyloxycarbonyl)- and (tert-Butoxycarbonyl)hydrazones
inferredcites →https://doi.org/10.1111/j.1399-3011.1991.tb01547.xopenalex-snapshot
Evidence for a β‐turn in an azadipeptide sequence
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Incorporation of azaglutamine residues into peptides synthesised by the ultra‐high load solid (gel)‐phase technique
inferredcites →https://doi.org/10.1111/j.1399-3011.1997.tb01163.xopenalex-snapshot
Aza‐peptides II. X‐Ray structures of aza‐alanine and aza‐asparagine‐containing peptides
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Aza‐peptides. III. Experimental structural analysis of aza‐alanme and aza‐asparagine‐containing peptides
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Azaproline as a β‐turn‐inducer residue opposed to proline
inferredcites →https://doi.org/10.2174/0929867003374499openalex-snapshot
Conformational and Topographical Considerations in Designing Agonist Peptidomimetics from Peptide Leads
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Molecular Modeling in the Design of Peptidomimetics and Peptide Surrogates
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β-Amino Acids: Versatile Peptidomimetics
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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A Single Stereodynamic Center Modulates the Rate of Self‐Assembly in a Biomolecular System
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A Single Stereodynamic Center Modulates the Rate of Self‐Assembly in a Biomolecular System
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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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Benzophenone semicarbazone protection strategy for synthesis of aza‐glycine containing aza‐peptides
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Solid‐Phase Synthesis of Hybrid Urea Oligomers Containing Conservative Thiourea Mutations
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Impact of Cα‐Chirality on Supramolecular Self‐Assembly in Cyclo‐2:1‐[α/aza]‐Hexamers ( d / l ‐Phe‐azaPhe‐Ala)2
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Selective cleavage of an azaGly peptide bond by copper(II). Long‐range effect of histidine residue
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Solution‐phase submonomer diversification of aza‐dipeptide building blocks and their application in aza‐peptide and aza‐DKP synthesis
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Solid‐phase synthesis of C‐terminal azapeptides
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Automation of the Azapeptide Submonomer Synthesis Method
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Positional Scanning for Peptide Secondary Structure by Solid Phase Synthesis with Aza-Amino Acids and Freidinger Lactams
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Aza-peptides with Multiple Aza-amino Acids, Synthesis and Preliminary Conformational Analysis of Glu-azaAla-Ala-azaAla-Leu-azaAla-Lys-azaAla-NH2
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Polymeric prodrug for bio-controllable gene and drug co-delivery
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Peptide and Protein Drugs: Issues and Solutions
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Novel small molecule bradykinin B1 receptor antagonists. Part 1: Benzamides and semicarbazides
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Submonomer synthesis of azapeptide ligands of the Insulin Receptor Tyrosine Kinase domain
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A general strategy for the synthesis of azapeptidomimetic lactams
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Original and efficient synthesis of 2:1-[α/aza]-oligomer precursors
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Unsymmetrical N,N'-functionalization of hydrazine by insertion into Morita–Baylis–Hillman ketones
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Steric impact of aza-amino acid on solid-phase aza-peptide bond synthesis
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Azapeptide Atropisomers From Late-Stage N -Alkylations
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Inter- vs Intramolecular Aldehyde–Alkyne–Amine A 3 -Reaction in the Solution-Phase Synthesis of a Potent Macrocyclic Azapeptide CD36 Modulator
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Fluorescence turn-on detection of Sn 2+ in live eukaryotic and prokaryotic cells
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Aza-proline effectively mimics l -proline stereochemistry in triple helical collagen
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Rules for the design of aza-glycine stabilized triple-helical collagen peptides
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One-Pot Synthesis of Protected Benzylhydrazines from Acetals
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Peptide Scanning for Studying Structure‐Activity Relationships in Drug Discovery
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Aza‐scanning of the Potent Melanocortin Receptor Agonist Ac‐His‐ d ‐Phe‐Arg‐Trp‐NH2
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Metabolic Stability of Peptidomimetics: N‐Methyl and Aza Heptapeptide Analogs of a PKB/Akt Inhibitor
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Synthesis of azabicycloalkanone amino acid and azapeptide mimics and their application as modulators of the prostaglandin F2α receptor for delaying preterm birth
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Synthesis of hydrazine and azapeptide derivatives by alkylation of carbazates and semicarbazones
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A Review on Azapeptides: The Promising Peptidomimetics
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Azapeptides -A History of Synthetic Milestones and Key Examples
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Azapeptides as an Efficient Tool to Improve the Activity of Biologically Effective Peptides
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Development of Cyclic Hydrazine and Hydrazide Type Organocatalyst ⎯ Mechanistic Aspects of Cyclic Hydrazine/Hydrazide-Catalyzed Diels-Αlder Reactions
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Azapeptides and Their Therapeutic Potential
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Synthesis, structural and supramolecular studies of linear and cyclic 2 1-[α/aza]-oligomers
inferred← citeshttps://doi.org/10.70675/ef4d861bz58b4z46a0z9d14z193d71cfe8a7openalex-snapshot
Synthèse et étude conformationnelle d’α-hydrazinopeptides linéaires et cycliques
inferred← citeshttps://doi.org/10.70675/fc87812bzec63z4f0bzb65ez169effd4a004openalex-snapshot
Synthèse et études structurales de nouveaux [α/aza]-oligomères et cyclooligomères, vers de nouveaux foldamères
inferred← citeshttps://doi.org/10.71781/31707openalex-snapshot
Assemblage oligomérique des récepteurs couplés aux protéines G avec les RAMPs
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