In situ click chemistry: a powerful means for lead discovery.
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Biotin Protein Ligase Is a Target for New AntibacterialsCRISPR-Cas9: A Revolutionary Tool for Cancer ModellingClick chemistry in peptide-based drug designA virtual screen discovers novel, fragment-sized inhibitors of Mycobacterium tuberculosis InhARapid preparation of triazolyl substituted NH-heterocyclic kinase inhibitors via one-pot Sonogashira coupling-TMS-deprotection-CuAAC sequenceOptimization of Benzoxazole-Based Inhibitors of Cryptosporidium parvum Inosine 5′-Monophosphate DehydrogenaseBcl-XL-templated assembly of its own protein-protein interaction modulator from fragments decorated with thio acids and sulfonyl azides.Triazole inhibitors of Cryptosporidium parvum inosine 5'-monophosphate dehydrogenaseIn situ click chemistry generation of cyclooxygenase-2 inhibitors.Screening of protein-protein interaction modulators via sulfo-click kinetic target-guided synthesisRecent development of two chitinase inhibitors, Argifin and Argadin, produced by soil microorganisms.Protein-Templated Fragment Ligations-From Molecular Recognition to Drug Discovery.The growing applications of click chemistry.Quick assembly of 1,4-diphenyltriazoles as probes targeting beta-amyloid aggregates in Alzheimer's disease.A new application of click chemistry in situ: development of fluorescent probe for specific G-quadruplex topologyOne-pot, two-step cascade synthesis of quinazolinotriazolobenzodiazepinesCyclopropenone-caged Sondheimer diyne (dibenzo[a,e]cyclooctadiyne): a photoactivatable linchpin for efficient SPAAC crosslinking.Scalable synthesis of Fmoc-protected GalNAc-threonine amino acid and T(N) antigen via nickel catalysis.Click chemistry, a powerful tool for pharmaceutical sciences.Benzyne click chemistry: synthesis of benzotriazoles from benzynes and azides.Ribosome-Templated Azide-Alkyne Cycloadditions: Synthesis of Potent Macrolide Antibiotics by In Situ Click Chemistry.Facile diverted synthesis of pyrrolidinyl triazoles using organotrifluoroborate: discovery of potential mPTP blockers.Protein-Templated Formation of an Inhibitor of the Blood Coagulation Factor Xa through a Background-Free Amidation Reaction.Alkyne-azide cycloadditions with copper powder in a high-pressure continuous-flow reactor: high-temperature conditions versus the role of additives.Coupling reaction of thioamides with sulfonyl azides: an efficient catalyst-free click-type ligation under mild conditions.Reaction site-driven regioselective synthesis of AChE inhibitors.MOF-Derived Cu@Cu₂O Nanocatalyst for Oxygen Reduction Reaction and Cycloaddition Reaction.15N NMR spectroscopic and theoretical GIAO-DFT studies for the unambiguous characterization of disubstituted 1,2,3-triazolesSynthesis of 1,4,6,10-tetraazaadamantane quaternary derivatives
P2860
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P2860
In situ click chemistry: a powerful means for lead discovery.
description
2006 nî lūn-bûn
@nan
2006 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
In situ click chemistry: a powerful means for lead discovery.
@ast
In situ click chemistry: a powerful means for lead discovery.
@en
In situ click chemistry: a powerful means for lead discovery.
@nl
type
label
In situ click chemistry: a powerful means for lead discovery.
@ast
In situ click chemistry: a powerful means for lead discovery.
@en
In situ click chemistry: a powerful means for lead discovery.
@nl
prefLabel
In situ click chemistry: a powerful means for lead discovery.
@ast
In situ click chemistry: a powerful means for lead discovery.
@en
In situ click chemistry: a powerful means for lead discovery.
@nl
P2860
P356
P1476
In situ click chemistry: a powerful means for lead discovery.
@en
P2093
Roman Manetsch
P2860
P304
P356
10.1517/17460441.1.6.525
P407
P577
2006-11-01T00:00:00Z