about
Kinetic target-guided synthesis in drug discovery and chemical biology: a comprehensive facts and figures surveyIn silico study of peptide inhibitors against BACE 1.Dual-purpose linker for alpha helix stabilization and imaging agent conjugation to glucagon-like peptide-1 receptor ligands.Inhibiting EGFR dimerization using triazolyl-bridged dimerization arm mimicsBinaphthyl-1,2,3-triazole peptidomimetics with activity against Clostridium difficile and other pathogenic bacteria.Click 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.Enhancing Intracranial Delivery of Clinically Relevant Non-viral Gene Vectors.Click Chemistry and Radiochemistry: The First 10 YearsTherapeutic conotoxins: a US patent literature survey.Hypervalent-Iodine(III)-Mediated Oxidative Methodology for the Synthesis of Fused Triazoles.Developing HIV-1 Protease Inhibitors through Stereospecific Reactions in Protein Crystals.Bovine and human lactoferricin peptides: chimeras and new cyclic analogs.1,2,3-Triazole Rings as a Disulfide Bond Mimetic in Chimeric AGRP-Melanocortin Peptides: Design, Synthesis, and Functional Characterization.Click and Click-Inspired Chemistry for the Design of Sequence-Controlled Polymers.Strained alkynes derived from 2,2'-dihydroxy-1,1'-biaryls; synthesis and copper-free cycloaddition with azides.Diversity-Oriented Syntheses by Combining CuAAC and Stereoselective INCIC Reactions with Peptides.Urotensin-II peptidomimetic incorporating a non-reducible 1,5-triazole disulfide bond reveals a pseudo-irreversible covalent binding mechanism to the urotensin G-protein coupled receptor.On the design principles of peptide-drug conjugates for targeted drug delivery to the malignant tumor site.
P2860
Q28072198-C56632E6-051F-4A23-A39F-FD9BB078E516Q30374668-C2D907A0-F2D5-4DA8-9EE7-03BE94D4E4F3Q30379845-02CC36B4-952E-419C-9312-A8C375DAC20DQ35195881-0FDEE509-561F-458A-8BAA-82F4CAA1A7F2Q35611260-2D1BC5BC-442F-44F9-8D63-5A3E1465B5A0Q35671797-814BDA82-5AF1-480D-8A82-C7A20C2BFE14Q35924628-1DD63E47-E43C-47E5-A013-FD655297A4EBQ37249326-8E0735BA-F29A-4FE8-85AA-E438A30074BCQ37540109-850790F4-8062-4460-B920-07A0C7B8E7EDQ38525254-BB0CBFF4-E0CF-44FC-85C4-050AC188D615Q38819718-89EC418A-F8CD-4107-B49C-C3A83929ECF8Q40467926-A5E66CC4-31AD-4CEC-92EA-43E410A5F35CQ46881407-C463101F-470E-475A-9890-0B47FD0C2947Q47275234-020F9D19-AD8A-414B-948B-1D7B4E45AAADQ47909208-05243270-106B-4BA2-861B-F51FB8D57D17Q48132440-5E1C076E-D003-496B-9833-9E92BDB4BA95Q48191164-F4081C9A-500A-458D-9DF1-A7287B5CF014Q50992476-9DAF5E11-0424-4E10-9A23-EF6520683393Q55054276-6245D5E9-6996-4AA1-922E-3BD8B3586F69
P2860
description
2013 nî lūn-bûn
@nan
2013 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Click chemistry in peptide-based drug design
@ast
Click chemistry in peptide-based drug design
@en
Click chemistry in peptide-based drug design
@nl
type
label
Click chemistry in peptide-based drug design
@ast
Click chemistry in peptide-based drug design
@en
Click chemistry in peptide-based drug design
@nl
prefLabel
Click chemistry in peptide-based drug design
@ast
Click chemistry in peptide-based drug design
@en
Click chemistry in peptide-based drug design
@nl
P2093
P2860
P1433
P1476
Click chemistry in peptide-based drug design
@en
P2093
Huiyuan Li
Irwin Chaiken
Rachna Aneja
P2860
P304
P356
10.3390/MOLECULES18089797
P407
P577
2013-08-16T00:00:00Z