Cargando…

CuAAC-ensembled 1,2,3-triazole-linked isosteres as pharmacophores in drug discovery: review

The review lays emphasis on the significance of 1,2,3-triazoles synthesized via CuAAC reaction having potential to act as anti-microbial, anti-cancer, anti-viral, anti-inflammatory, anti-tuberculosis, anti-diabetic, and anti-Alzheimer drugs. The importance of click chemistry is due to its ‘quicker’...

Descripción completa

Detalles Bibliográficos
Autores principales:	Rani, Alisha, Singh, Gurjaspreet, Singh, Akshpreet, Maqbool, Ubair, Kaur, Gurpreet, Singh, Jandeep
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Royal Society of Chemistry 2020
Materias:	Chemistry
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9049420/ https://www.ncbi.nlm.nih.gov/pubmed/35497465 http://dx.doi.org/10.1039/c9ra09510a

Ejemplares similares

CuAAC ensembled 1,2,3-triazole linked nanogels for targeted drug delivery: a review
por: Singh, Gurleen, et al.
Publicado: (2023)

CuAAC-Derived Selective Fluorescent Probe as a Recognition Agent for Pb(II) and Hg(II): DFT and Docking Studies
por: Singh, Gurleen, et al.
Publicado: (2022)

CuAAC-inspired synthesis of 1,2,3-triazole-bridged porphyrin conjugates: an overview
por: Singh, Dileep Kumar
Publicado: (2023)

Cu(i)-catalysed 1,2,3-triazole stitched chalcomer assembly as Pb(ii) and Cu(ii) ion sensor: DFT and docking scrutiny
por: Singh, Riddima, et al.
Publicado: (2023)

Copper-catalyzed CuAAC/intramolecular C–H arylation sequence: Synthesis of annulated 1,2,3-triazoles
por: Jeyachandran, Rajkumar, et al.
Publicado: (2012)

A CuAAC–Hydrazone–CuAAC Trifunctional Scaffold for the Solid-Phase Synthesis of Trimodal Compounds: Possibilities and Limitations
por: Fabre, Benjamin, et al.
Publicado: (2015)

AT-CuAAC Synthesis of Mechanically Interlocked Oligonucleotides
por: Acevedo-Jake, Amanda, et al.
Publicado: (2020)

Molecular keypad controlled circuit for Ce(iii) and NO(3)(−) ions recognition by μw synthesized silicon-embedded organic luminescent sensor
por: Kaur, Navpreet, et al.
Publicado: (2018)

Peptide Conjugation via CuAAC ‘Click’ Chemistry
por: Ahmad Fuaad, Abdullah A. H., et al.
Publicado: (2013)

A flow platform for degradation-free CuAAC bioconjugation
por: Hatit, Marine Z. C., et al.
Publicado: (2018)

Synthesis and Characterization of Polystyrene-Supported Piperazine-Substituted Triazoles by CuAAC and First Evaluation for Metal Ion Extraction
por: Slimi, Riadh, et al.
Publicado: (2016)

Synthesis of a novel resorcin[4]arene–glucose conjugate and its catalysis of the CuAAC reaction for the synthesis of 1,4-disubstituted 1,2,3-triazoles in water
por: Husain, Ali A., et al.
Publicado: (2019)

Synthesis and Operating Optimization of the PEG Conjugate via CuAAC in scCO(2)
por: López, Sonia, et al.
Publicado: (2021)

Recent Advances in Recoverable Systems for the Copper-Catalyzed Azide-Alkyne Cycloaddition Reaction (CuAAC)
por: Mandoli, Alessandro
Publicado: (2016)

Development and Applications of the Copper-Catalyzed Azide-Alkyne Cycloaddition (CuAAC) as a Bioorthogonal Reaction
por: Li, Li, et al.
Publicado: (2016)

CuAAC click chemistry for the enhanced detection of novel alkyne-based natural product toxins
por: Hems, Edward S., et al.
Publicado: (2018)

Polylactic-Containing Hyperbranched Polymers through the CuAAC Polymerization of Aromatic AB(2) Monomers
por: Pacini, Aurora, et al.
Publicado: (2023)

Mild and efficient synthesis of benzothiazolopyrimidine derivatives via CuAAC/ring cleavage/cyclization reaction
por: Yang, Weiguang, et al.
Publicado: (2023)

Synthesis of self-curable polysulfone containing pendant benzoxazine units via CuAAC click chemistry
por: Dizman, Cemil, et al.
Publicado: (2016)

Synthesis of Tris-Heterocycles via a Cascade IMCR/Aza Diels-Alder + CuAAC Strategy
por: Rentería-Gómez, Manuel A., et al.
Publicado: (2019)

First Class of Phosphorus Dendritic Compounds Containing β-Cyclodextrin Units in the Periphery Prepared by CuAAC
por: Sorroza-Martínez, Kendra, et al.
Publicado: (2020)

Functionalization of boron-doped diamond with a push–pull chromophore via Sonogashira and CuAAC chemistry
por: Raymakers, Jorne, et al.
Publicado: (2018)

Correction: CuAAC click chemistry for the enhanced detection of novel alkyne-based natural product toxins
por: Hems, Edward S., et al.
Publicado: (2018)

CuAAC Click Chemistry Accelerates the Discovery of Novel Chemical Scaffolds as Promising Protein Tyrosine Phosphatases Inhibitors
por: He, X.-P., et al.
Publicado: (2012)

Distinct Sustainable Carbon Nanodots Enable Free Radical Photopolymerization, Photo‐ATRP and Photo‐CuAAC Chemistry
por: Kütahya, Ceren, et al.
Publicado: (2021)

Competitive formation of homocircuit [3]rotaxanes in synthetically useful yields in the bipyridine-mediated active template CuAAC reaction
por: Neal, Edward A., et al.
Publicado: (2015)

Biotin-Conjugated Cellulose Nanofibers Prepared via Copper-Catalyzed Alkyne-Azide Cycloaddition (CuAAC) “Click” Chemistry
por: Goodge, Katarina, et al.
Publicado: (2020)

Molecular Brushes with a Polyimide Backbone and Poly(ε-Caprolactone) Side Chains by the Combination of ATRP, ROP, and CuAAC
por: Kashina, Anna V., et al.
Publicado: (2021)

Scope of tetrazolo[1,5-a]quinoxalines in CuAAC reactions for the synthesis of triazoloquinoxalines, imidazoloquinoxalines, and rhenium complexes thereof
por: Holzhauer, Laura, et al.
Publicado: (2022)

Copper-Catalyzed Azide–Alkyne Cycloaddition (CuAAC) by Functionalized NHC-Based Polynuclear Catalysts: Scope and Mechanistic Insights
por: González-Lainez, Miguel, et al.
Publicado: (2022)

New poly-imidazolium–triazole particles by CuAAC cross-linking of calix[4]arene bis-azide/alkyne amphiphiles – a prospective support for Pd in the Mizoroki–Heck reaction
por: Burilov, Vladimir, et al.
Publicado: (2020)

Recent Progress of Cu-Catalyzed Azide-Alkyne Cycloaddition Reactions (CuAAC) in Sustainable Solvents: Glycerol, Deep Eutectic Solvents, and Aqueous Media
por: Nebra, Noel, et al.
Publicado: (2020)

Design, synthesis, and anticancer activity of novel berberine derivatives prepared via CuAAC “click” chemistry as potential anticancer agents
por: Jin, Xin, et al.
Publicado: (2014)

A synthetic approach to ‘click’ neoglycoprotein analogues of EPO employing one-pot native chemical ligation and CuAAC chemistry
por: Lee, D. J., et al.
Publicado: (2018)

Synthesis of Polyheterocyclic Dimers Containing Restricted and Constrained Peptidomimetics via IMCR-Based Domino/Double CuAAC Click Strategy
por: Pharande, Shrikant G., et al.
Publicado: (2020)

Exfoliated black phosphorous-mediated CuAAC chemistry for organic and macromolecular synthesis under white LED and near-IR irradiation
por: Kocaarslan, Azra, et al.
Publicado: (2021)

Efficient modification of PAMAM G1 dendrimer surface with β-cyclodextrin units by CuAAC: impact on the water solubility and cytotoxicity
por: Sorroza-Martínez, Kendra, et al.
Publicado: (2020)

Copper(I)-Catalyzed Alkyne–Azide Cycloaddition (CuAAC) “Click” Reaction: A Powerful Tool for Functionalizing Polyhydroxylated Platforms
por: Pineda-Castañeda, Héctor Manuel, et al.
Publicado: (2023)

An Oxidant-Free and Mild Strategy for Quinazolin-4(3H)-One Synthesis via CuAAC/Ring Cleavage Reaction
por: He, Yueling, et al.
Publicado: (2023)

A mesoporous metal–organic framework used to sustainably release copper(ii) into reducing aqueous media to promote the CuAAC click reaction
por: Hoffmann, Pascal, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_1lb2k6la1hae4da6hvrf6jadum