| P50 | author | Thomas Kodadek | Q88137481 |
| P2093 | author name string | Patrick J McEnaney | |
| P2860 | cites work | Activation of apoptosis in vivo by a hydrocarbon-stapled BH3 helix | Q24537504 |
| | Encoded combinatorial chemistry | Q24561374 |
| | Identification of candidate IgG biomarkers for Alzheimer's disease via combinatorial library screening | Q24630334 |
| | RNA-peptide fusions for the in vitro selection of peptides and proteins | Q24652859 |
| | Design, synthesis and selection of DNA-encoded small-molecule libraries | Q27656839 |
| | The role of the proteasomal ATPases and activator monoubiquitylation in regulating Gal4 binding to promoters | Q27936877 |
| | The 19S regulatory particle of the proteasome is required for efficient transcription elongation by RNA polymerase II. | Q27939755 |
| | Target-oriented and diversity-oriented organic synthesis in drug discovery | Q28138837 |
| | Phage Display | Q28201864 |
| | Chronic lymphocytic leukemia | Q28236621 |
| | Selecting chemicals: the emerging utility of DNA-encoded libraries | Q30156918 |
| | A combinatorial peptoid library for the identification of novel MSH and GRP/bombesin receptor ligands | Q30653973 |
| | Peptides selected to bind the Gal80 repressor are potent transcriptional activation domains in yeast | Q30870486 |
| | Isolation of protein ligands from large peptoid libraries | Q31023429 |
| | Attenuation of thermal nociception and hyperalgesia by VR1 blockers | Q31039264 |
| | A novel peptide-based encoding system for "one-bead one-compound" peptidomimetic and small molecule combinatorial libraries | Q31087756 |
| | Transformation of low-affinity lead compounds into high-affinity protein capture agents | Q31107567 |
| | Photolithographic synthesis of cyclic peptide arrays using a differential deprotection strategy | Q31143638 |
| | Design and synthesis of an optimized positional scanning library of peptoids: identification of novel multidrug resistance reversal agents | Q31149588 |
| | A positional scanning combinatorial library of peptoids as a source of biological active molecules: identification of antimicrobials | Q31156104 |
| | Peptoids: a modular approach to drug discovery. | Q33191665 |
| | Quantum dots as a visual aid for screening bead-bound combinatorial libraries | Q33194959 |
| | Peptoids as source of compounds eliciting antibacterial activity | Q33215050 |
| | A high-throughput assay for assessing the cell permeability of combinatorial libraries | Q33215569 |
| | A reversible and highly selective inhibitor of the proteasomal ubiquitin receptor rpn13 is toxic to multiple myeloma cells | Q38444221 |
| | Discovery of native autoantigens via antigen surrogate technology: application to type 1 diabetes | Q38446485 |
| | Rapid development of a potent photo-triggered inhibitor of the serine hydrolase RBBP9 | Q38457319 |
| | Beta-peptidic peptidomimetics | Q38572449 |
| | Skeletally diverse small molecules using a build/couple/pair strategy | Q39996265 |
| | Expedient synthesis and design strategies for new peptoid construction | Q40432225 |
| | Peptide folding induces high and selective affinity of a linear and small beta-peptide to the human somatostatin receptor 4. | Q40793260 |
| | On-bead screens sample narrower affinity ranges of protein-ligand interactions compared to equivalent solution assays. | Q34350779 |
| | The direct organocatalytic asymmetric mannich reaction: unmodified aldehydes as nucleophiles | Q34543659 |
| | Aβ42-binding peptoids as amyloid aggregation inhibitors and detection ligands | Q34594159 |
| | Discovery of peptoid ligands for anti-aquaporin 4 antibodies | Q34632417 |
| | Synthesis and screening of stereochemically diverse combinatorial libraries of peptide tertiary amides | Q34632423 |
| | Decoding split and pool combinatorial libraries with electron-transfer dissociation tandem mass spectrometry | Q34699482 |
| | Screening bicyclic peptide libraries for protein-protein interaction inhibitors: discovery of a tumor necrosis factor-α antagonist | Q34832185 |
| | Awakening guardian angels: drugging the p53 pathway | Q35014385 |
| | Discovery Of An Orexin Receptor Positive Potentiator | Q35084855 |
| | Rational design of topographical helix mimics as potent inhibitors of protein-protein interactions | Q35157579 |
| | Direct comparison of linear and macrocyclic compound libraries as a source of protein ligands | Q35166727 |
| | Solid-phase synthesis of peptoid-like oligomers containing diverse diketopiperazine units | Q35197285 |
| | Chemical tools to monitor and manipulate the adaptive immune system | Q35264291 |
| | Design, solid-phase synthesis, and evaluation of a phenyl-piperazine-triazine scaffold as α-helix mimetics | Q35357192 |
| | Rapid lead discovery through iterative screening of one bead one compound libraries | Q35461662 |
| | Robust Suzuki-Miyaura cross-coupling on DNA-linked substrates | Q35473276 |
| | Synthesis and screening of small-molecule α-helix mimetic libraries targeting protein-protein interactions | Q35476105 |
| | Recognition of antigen-specific B-cell receptors from chronic lymphocytic leukemia patients by synthetic antigen surrogates | Q35482083 |
| | Phage selection of bicyclic peptides based on two disulfide bridges | Q35548188 |
| | Solid-phase synthesis of diverse peptide tertiary amides by reductive amination | Q35563845 |
| | Synthesis of a large library of macrocyclic peptides containing multiple and diverse N-alkylated residues | Q35661360 |
| | High affinity binding of conformationally constrained synthetic oligomers to an antigen-specific antibody: Discovery of a diagnostically useful synthetic ligand for murine Type 1 diabetes autoantibodies. | Q35661419 |
| | Optimization of the Magnetic Recovery of Hits from One-Bead-One-Compound Library Screens | Q35722392 |
| | DNA-Encoded Solid-Phase Synthesis: Encoding Language Design and Complex Oligomer Library Synthesis | Q35750869 |
| | Reliable diagnosis of murine type 1 diabetes using a panel of autoantigens and "antigen surrogates" mounted onto a liquid array. | Q35782179 |
| | Extended peptoids: a new class of oligomers based on aromatic building blocks | Q35839051 |
| | Development of proteasome inhibitors as research tools and cancer drugs | Q36389262 |
| | Sequence-specific polypeptoids: a diverse family of heteropolymers with stable secondary structure | Q36470658 |
| | NMR determination of the major solution conformation of a peptoid pentamer with chiral side chains | Q36470879 |
| | Keeping transcriptional activators under control | Q36630626 |
| | Discovery of nanomolar ligands for 7-transmembrane G-protein-coupled receptors from a diverse N-(substituted)glycine peptoid library | Q36737683 |
| | Synthesis of N-substituted glycine peptoid libraries | Q36811754 |
| | The flexizyme system: a highly flexible tRNA aminoacylation tool for the translation apparatus | Q36947740 |
| | Synthesis at the interface of chemistry and biology | Q37581575 |
| | A threaded loop conformation adopted by a family of peptoid nonamers | Q42090247 |
| | Synthesis of natural-product-like molecules with over eighty distinct scaffolds | Q42114290 |
| | Synthesis of functionalised aromatic oligamide rods | Q43131638 |
| | Recruitment of a 19S proteasome subcomplex to an activated promoter | Q43966343 |
| | Development of a potent Bcl-x(L) antagonist based on alpha-helix mimicry | Q44162861 |
| | Structural and Spectroscopic Studies of Peptoid Oligomers with α-Chiral Aliphatic Side Chains | Q44635074 |
| | A new type of synthetic peptide library for identifying ligand-binding activity | Q45106336 |
| | Oligo(N-aryl glycines): a new twist on structured peptoids. | Q46219066 |
| | High-throughput screening for methionyl-tRNA synthetases that enable residue-specific incorporation of noncanonical amino acids into recombinant proteins in bacterial cells | Q46431031 |
| | Practical Proline-catalyzed asymmetric Mannich reaction of aldehydes with N-Boc-imines. | Q52682286 |
| | Controlling curvature in a family of oligoamide alpha-helix mimetics. | Q53686611 |
| | Efficient method for the preparation of peptoids [oligo(N-substituted glycines)] by submonomer solid-phase synthesis | Q56454343 |
| | Activity and stability of human kallikrein-2-specific linear and cyclic peptide inhibitors | Q56894313 |
| | Proteolytic studies of homologous peptide and N-substituted glycine peptoid oligomers | Q57074589 |
| | Residue-based control of helix shape in β-peptide oligomers | Q59090060 |
| | Chiral N-substituted glycines can form stable helical conformations | Q74030961 |
| | Total synthesis of the nematicidal cyclododecapeptide omphalotin A by using racemization-free triphosgene-mediated couplings in the solid phase | Q74689839 |
| | Tuning peptoid secondary structure with pentafluoroaromatic functionality: a new design paradigm for the construction of discretely folded peptoid structures | Q79318907 |
| | Cyclic peptoids | Q79834703 |
| | Local and tunable n-->pi* interactions regulate amide isomerism in the peptoid backbone | Q80561863 |
| | Writing the macrocycle manual: new computational and biochemical tools and informatic rules should spur research on a relatively underexplored class of molecules | Q85656352 |
| | Drug discovery: tools and rules for macrocycles | Q87413192 |
| | Advancing chemistry and biology through diversity-oriented synthesis of natural product-like libraries | Q33216557 |
| | Efficient synthesis of a beta-peptide combinatorial library with microwave irradiation. | Q33223636 |
| | A rapid library screen for tailoring beta-peptide structure and function | Q33225409 |
| | Anti-Tat and anti-HIV activities of trimers of n-alkylglycines. | Q33231378 |
| | Cleavable hydrophilic linker for one-bead-one-compound sequencing of oligomer libraries by tandem mass spectrometry | Q33242440 |
| | Generation and use of synthetic peptide combinatorial libraries for basic research and drug discovery | Q33267847 |
| | Isolation and characterization of coactivator-binding peptoids from a combinatorial library | Q33268849 |
| | Smallest peptoids with antiproliferative activity on human neoplastic cells. | Q33282036 |
| | Design and synthesis of a cell-permeable synthetic transcription factor mimic | Q33285862 |
| | Identification of a peptoid inhibitor of the proteasome 19S regulatory particle | Q33286169 |
| | Reprogramming the translation initiation for the synthesis of physiologically stable cyclic peptides | Q33316151 |
| | Exploration of structure--activity relationships among foldamer ligands for a specific protein binding site via parallel and split-and-mix library synthesis | Q33319872 |
| | A peptoid "antibody surrogate" that antagonizes VEGF receptor 2 activity | Q33326872 |
| | Peptoid architectures: elaboration, actuation, and application | Q33368939 |
| | Design, synthesis, and evaluation of an alpha-helix mimetic library targeting protein-protein interactions | Q33424678 |
| | Selective toxin sequestrants for the treatment of bacterial infections | Q33427560 |
| | Phage-encoded combinatorial chemical libraries based on bicyclic peptides | Q33456683 |
| | Single bead labeling method for combining confocal fluorescence on-bead screening and solution validation of tagged one-bead one-compound libraries | Q33487526 |
| | New strategies for the design of folded peptoids revealed by a survey of noncovalent interactions in model systems | Q33512972 |
| | Isolation of antagonists of antigen-specific autoimmune T cell proliferation | Q33516724 |
| | DNA-encoded chemical libraries: a tool for drug discovery and for chemical biology | Q33555410 |
| | No Splicing, no dicing: non-proteolytic roles of the ubiquitin-proteasome system in transcription | Q33593805 |
| | In vivo modulation of hypoxia-inducible signaling by topographical helix mimetics | Q33694597 |
| | Utility of redundant combinatorial libraries in distinguishing high and low quality screening hits | Q33739175 |
| | Novel pyrrolopyrimidine-based α-helix mimetics: cell-permeable inhibitors of protein−protein interactions | Q33775959 |
| | The rise, fall and reinvention of combinatorial chemistry | Q33942110 |
| | The growing impact of click chemistry on drug discovery | Q33974618 |
| | A biomimetic polyketide-inspired approach to small-molecule ligand discovery | Q34136632 |
| | Incorporation of heterocycles into the backbone of peptoids to generate diverse peptoid-inspired one bead one compound libraries | Q34154966 |
| | Structurally diverse cyclisation linkers impose different backbone conformations in bicyclic peptides. | Q34227953 |
| | Complex synthetic chemical libraries indexed with molecular tags | Q34290628 |
| | A Cleavable Scaffold Strategy for the Synthesis of One-Bead One-Compound Cyclic Peptoid Libraries That Can Be Sequenced By Tandem Mass Spectrometry | Q34318128 |
| | Synthesis of libraries of peptidomimetic compounds containing a 2-oxopiperazine unit in the main chain | Q34328018 |
| P433 | issue | 36 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 6038-6059 | |
| P577 | publication date | 2016-03-21 | |
| P1433 | published in | Chemical Communications | Q426303 |
| P1476 | title | Towards vast libraries of scaffold-diverse, conformationally constrained oligomers | |
| P478 | volume | 52 | |