about
Click chemistry in peptide-based drug designAlkyne-azide "click" chemistry in designing nanocarriers for applications in biologyLarge Scale Chemical Cross-linking Mass Spectrometry Perspectives.Optimization of the anti-cancer activity of phosphatidylinositol-3 kinase pathway inhibitor PITENIN-1: switching a thiourea with 1,2,3-triazoleClick Chemistry in Lead Optimization of Boronic Acids as β-Lactamase Inhibitors.Synthesis of 1,2,3-triazol-1-yl-methaneboronic acids via click chemistry: an easy access to a new potential scaffold for protease inhibitors.Combinatorial Synthesis of Structurally Diverse Triazole-Bridged Flavonoid Dimers and Trimers.Synthesis of enantiopure 1,2-azido and 1,2-amino alcohols via regio- and stereoselective ring-opening of enantiopure epoxides by sodium azide in hot water.Monitoring mRNA Translation in Neuronal Processes Using Fluorescent Non-Canonical Amino Acid Tagging.Efficient continuous-flow synthesis of novel 1,2,3-triazole-substituted β-aminocyclohexanecarboxylic acid derivatives with gram-scale productionDesign and development of stable, water-soluble, human Toll-like receptor 2 specific monoacyl lipopeptides as candidate vaccine adjuvants.Peptide conjugation via CuAAC 'click' chemistry.Effect of amide-triazole linkers on the electrochemical and biological properties of ferrocene-carbohydrate conjugates.Identification of gallic acid based glycoconjugates as a novel tubulin polymerization inhibitors.N-2-Aryl-1,2,3-Triazoles: A Novel Class of Blue Emitting Fluorophores-Synthesis, Photophysical Properties Study and DFT Computations.Replacement of the CysA7-CysB7 disulfide bond with a 1,2,3-triazole linker causes unfolding in insulin glargine.Modular assembly of dimeric HIV fusion inhibitor peptides with enhanced antiviral potency.A clickable neurosteroid photolabel reveals selective Golgi compartmentalization with preferential impact on proximal inhibitionBase-catalyzed electrophilic trifluoromethylthiolation of terminal alkynes.Alkyne-azide cycloadditions with copper powder in a high-pressure continuous-flow reactor: high-temperature conditions versus the role of additives.Solvent-free copper-catalyzed click chemistry for the synthesis of N-heterocyclic hybrids based on quinoline and 1,2,3-triazole.Synthesis, In Vitro α-Glucosidase Inhibitory Activity and Molecular Docking Studies of Novel Benzothiazole-Triazole Derivatives.Triazolyl-Based Molecular Gels as Ligands for Autocatalytic 'Click' Reactions.Clickable 4-Oxo-β-lactam-Based Selective Probing for Human Neutrophil Elastase Related Proteomes.Antitubercular activity of 1,2,3-triazolyl fatty acid derivatives.α-Haloacrylates as acceptors in the [3 + 2] cycloaddition reaction with NaN3: an expedient approach to N-unsubstituted 1,2,3-triazole-4-carboxylates.Highly N2-selective coupling of 1,2,3-triazoles with indole and pyrrole.Screening of bromotyramine analogues as antifouling compounds against marine bacteria.An eccentric rod-like linear connection of two heterocycles: synthesis of pyridine trans-tetrafluoro-λ6-sulfanyl triazoles.Biological Evaluation and Docking Studies of Synthetic Oleanane-type TriterpenoidsClick chemistry inspired synthesis of piperazine-triazole derivatives and evaluation of their antimicrobial activitiesOn the investigation of hybrid quinones: synthesis, electrochemical studies and evaluation of trypanocidal activityTandem Catalysis of an Aldol-‘Click’ Reaction System within a Molecular Hydrogel
P2860
Q26853053-619C6AA1-E092-4410-A684-79B316184DE6Q26995503-0CB26F61-3898-4FEB-A0FE-CC00C50E9ABCQ30364926-3887EB8A-2355-4DC0-A3E9-452FE6DEF8BAQ34653200-CA179FBF-6A40-4D96-8697-2125943D3DF6Q35671797-7D108DA8-93BC-4DD9-A50B-F36F4D5C91F8Q35924628-F42B0B57-F76D-4769-B4BD-657C9193C5F4Q36138308-4191EC32-63CC-4DF1-96E9-231DC335FBCEQ36523681-950E4A62-EEAE-4FEF-8B85-C2A1308DD732Q36852438-5D249F8A-6080-401F-8ED6-711370122842Q37088102-136DE573-0A93-4FCA-9AFE-B3DE0049E9A7Q37352073-8CF67057-80EA-4ED9-ADDB-3E1BB9BA2282Q38166894-94D11AA8-4DAD-4061-AE48-986FAA732ED2Q39251297-8D51D428-5EE7-4CDC-A3E7-9EBD39000F12Q40219453-D67283B2-5314-4C37-8324-2CC513810130Q40938328-8B0FF2DF-07A7-4C66-86DE-68F4CC6318C3Q41322679-53433CC0-9E64-4B8C-85C1-892771FBE528Q41841736-D6C5BD58-B337-49E1-82AD-DFD6668C509BQ42072055-AAAE4C00-5454-4487-A2D3-C993FF8EEE49Q43433859-6C6A91C3-4313-4DAA-A498-A6408501CC1FQ44511325-96387CE9-5BDB-4E1F-8FD5-7BEE63184194Q46253119-D2CC8CA6-E182-4E61-9EE2-760D954B45C3Q47671042-41D5EFE8-DCE8-437B-A131-E341A15CA7EEQ47829453-C2668762-EDD5-48DF-B2C1-4BA60E157FDBQ48139537-44CD14B5-EEED-46A8-A2F3-D8F063912745Q49915173-17968D17-6791-4B4A-9069-2FFC7003C736Q53293304-732EEBC9-4CDB-4332-9FF8-CEF4B5FFADF5Q54388547-D49E2982-3C20-44F3-A417-840235FEF901Q54578106-A2BE54D0-AC13-49A4-9C7B-EC09F7DAFFF4Q55399917-5A50DD1A-4D47-46FC-9714-3FE8F7846271Q57489641-5391514E-B8F0-48EB-BD62-A936E651ABE1Q58200639-4D25B8C3-E1D6-481E-AF87-4D4E825EF541Q58856160-2C1767FB-D7D7-49C2-BA41-D894F0115551Q59260500-34779B53-E5A5-4CAF-A88E-AC227315E8CC
P2860
description
2012 nî lūn-bûn
@nan
2012 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
The impact of click chemistry in medicinal chemistry.
@ast
The impact of click chemistry in medicinal chemistry.
@en
The impact of click chemistry in medicinal chemistry.
@nl
type
label
The impact of click chemistry in medicinal chemistry.
@ast
The impact of click chemistry in medicinal chemistry.
@en
The impact of click chemistry in medicinal chemistry.
@nl
prefLabel
The impact of click chemistry in medicinal chemistry.
@ast
The impact of click chemistry in medicinal chemistry.
@en
The impact of click chemistry in medicinal chemistry.
@nl
P2093
P2860
P1476
The impact of click chemistry in medicinal chemistry.
@en
P2093
Guilong Zhao
Jingli Hou
Peng George Wang
Xifang Liu
P2860
P304
P356
10.1517/17460441.2012.682725
P407
P577
2012-05-19T00:00:00Z