about
Studying epigenetic complexes and their inhibitors with the proteomics toolboxFocal Targeting of the Bacterial Envelope by Antimicrobial PeptidesBiosynthetic Polymers as Functional MaterialsBioconjugation and stabilisation of biomolecules in biosensorsClick chemistry in complex mixtures: bioorthogonal bioconjugationIn-gel activity-based protein profiling of a clickable covalent ERK1/2 inhibitorChemical proteomics approaches for identifying the cellular targets of natural productsDevelopment and Applications of the Copper-Catalyzed Azide-Alkyne Cycloaddition (CuAAC) as a Bioorthogonal ReactionProgrammable polyproteams built using twin peptide supergluesA clickable UTP analog for the posttranscriptional chemical labeling and imaging of RNAVirus outbreaks in chemical and biological sensorsDiazo Compounds: Versatile Tools for Chemical BiologyDecreasing Distortion Energies without Strain: Diazo-Selective 1,3-Dipolar Cycloadditions1,3-Dipolar Cycloadditions of Diazo Compounds in the Presence of AzidesA Minimal, Unstrained S-Allyl Handle for Pre-Targeting Diels-Alder Bioorthogonal Labeling in Live CellsVinylboronic Acids as Fast Reacting, Synthetically Accessible, and Stable Bioorthogonal Reactants in the Carboni-Lindsey ReactionChemical Proteomic Profiling of Human Methyltransferases4R- and 4S-iodophenyl hydroxyproline, 4R-pentynoyl hydroxyproline, and S-propargyl-4-thiolphenylalanine: conformationally biased and tunable amino acids for bioorthogonal reactions."Shine & Click" Photo-Induced Interfacial Unmasking of Strained Alkynes on Small Water-Soluble Gold Nanoparticles.Bio-Orthogonal Mediated Nucleic Acid Transfection of Cells via Cell Surface Engineering.Palladium: a future key player in the nanomedical field?Tetrazine ligation for chemical proteomics.Opportunities for merging chemical and biological synthesisDialdehydes lead to exceptionally fast bioconjugations at neutral pH by virtue of a cyclic intermediate.A Bioorthogonal Chemical Reporter of Viral Infection.New organocatalyst scaffolds with high activity in promoting hydrazone and oxime formation at neutral pH.Chemical methods for the proteome-wide identification of posttranslationally modified proteinsSite-specific antibody-drug conjugates: the nexus of bioorthogonal chemistry, protein engineering, and drug developmentDiazo groups endure metabolism and enable chemoselectivity in cellulo.Using non-enzymatic chemistry to influence microbial metabolismThinking big with small molecules.Bioorthogonal Labeling, Bioimaging, and Photocytotoxicity Studies of Phosphorescent Ruthenium(II) Polypyridine Dibenzocyclooctyne Complexes.Conformationally Strained trans-Cyclooctene with Improved Stability and Excellent Reactivity in Tetrazine Ligation.Reconstitution of Formylglycine-generating Enzyme with Copper(II) for Aldehyde Tag Conversion.Convenient analysis of protein modification by chemical blotting with fluorogenic "click" reagents.Fused Bicyclic Caspase-1 Inhibitors Assembled by Copper-Free Strain-Promoted Alkyne-Azide Cycloaddition (SPAAC).Systemic Fluorescence Imaging of Zebrafish Glycans with Bioorthogonal Chemistry.Fluorogenic Strain-Promoted Alkyne-Diazo Cycloadditions.Discovery of new mutually orthogonal bioorthogonal cycloaddition pairs through computational screeningConformationally Strained trans-Cyclooctene (sTCO) Enables the Rapid Construction of (18)F-PET Probes via Tetrazine Ligation
P2860
Q26738885-7D360EF7-5B6C-4E9E-ABAC-BDF351578429Q26744785-00CD638F-D0A3-46A8-9306-5E58BF8908CEQ26745443-CA0DA36D-1727-4F70-A083-842BA046272EQ26745867-1F1965A2-F1EF-46BE-B8BB-CC65F5C6EB8BQ26828895-3DED8D44-4F7D-4796-8ABE-6007CBD66C88Q27716899-A0228FB9-3E51-462D-9868-030E2EC4049AQ28072634-ABC232F2-E232-41E0-BFB8-768B442BDB73Q28079295-517C5B96-0B41-47D8-AAB3-AB77B06E95E8Q28272295-1387D9B0-4C37-4B61-8C80-7EE5483C1F00Q28315272-E8388A50-DE94-4747-A79D-D21A7290743EQ28395028-5923027F-7FE5-4D82-917F-822594449161Q28817199-EAB65A6C-7624-43B1-971D-292765639576Q28817848-F41875B8-BD71-4FF0-842C-434C4071AD69Q28817850-F0B29596-0393-471B-8343-B0E975D82796Q28818184-D6FEE45D-336E-4EE9-908B-84D9036AC76AQ28821205-05B9924C-D37A-4AAB-8CF7-87427E6C1217Q28821490-CCFFFA63-C993-44BA-9557-C884CAB6BEB0Q31039611-8850BB2A-906E-4E3F-A49C-84A8EA93BC45Q31136098-9E3624DE-A18F-4091-811F-F04BBB77CB8BQ33731143-3E21ABB7-D073-4C68-B95F-0D088DC24FA9Q33837025-E3643D4C-B760-41CE-9070-368C73A98686Q33837728-CC3D9392-C4A8-4514-A856-0F371D2676B0Q34353527-1504797D-5183-4BB2-B022-E1131334B59CQ34435511-FC6FBF50-0C7C-491C-841D-EF5A09A34D58Q34476370-106DB751-F5B8-4771-B357-1BE4C52AD593Q34992460-7B0D414F-FBDC-4159-9034-1665A9833284Q35019528-81C4967E-805E-40DC-886A-5BFCC5970E9DQ35105725-F523562B-E13C-4F30-9919-B9F030865028Q35213301-13157214-CA06-4E74-B043-33C225DF5865Q35235881-03EFBA96-A948-4064-8063-B824CA2162D4Q35394706-6395C084-E4E0-4545-9380-CF9BFCC09072Q35669944-B91A17ED-8C0A-4084-9273-69553E92C827Q35768570-8E0A6B3A-A63B-4093-A175-CFCD8A3A4AD9Q35860701-4072DD47-D4EC-4A9D-9C88-043D91731859Q36161926-45C68433-0373-4FB1-8EEE-B8D66ED1C4F3Q36203227-23FAFF4E-E494-41D8-9184-CA1668BD77AEQ36412554-973D406E-CD4D-484E-8B6F-7F52572207C2Q36462219-8F316129-8FF5-4AC9-A420-4694293BEFF1Q36608101-C4496162-5D0B-4634-AE0F-079E9FE3C26BQ36882982-EAB87CFF-66BB-40B4-A78C-DDBA90FA116E
P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Finding the right (bioorthogonal) chemistry.
@en
type
label
Finding the right (bioorthogonal) chemistry.
@en
prefLabel
Finding the right (bioorthogonal) chemistry.
@en
P356
P1433
P1476
Finding the right (bioorthogonal) chemistry
@en
P2093
David M Patterson
P304
P356
10.1021/CB400828A
P577
2014-01-30T00:00:00Z