BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 32333711)

  • 1. Efficient Chemical Protein Synthesis using Fmoc-Masked N-Terminal Cysteine in Peptide Thioester Segments.
    Kar A; Mannuthodikayil J; Singh S; Biswas A; Dubey P; Das A; Mandal K
    Angew Chem Int Ed Engl; 2020 Aug; 59(35):14796-14801. PubMed ID: 32333711
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Native Chemical Ligation via N-Acylurea Thioester Surrogates Obtained by Fmoc Solid-Phase Peptide Synthesis.
    Palà-Pujadas J; Blanco-Canosa JB
    Methods Mol Biol; 2020; 2133():141-161. PubMed ID: 32144666
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Preparation of protected peptidyl thioester intermediates for native chemical ligation by Nalpha-9-fluorenylmethoxycarbonyl (Fmoc) chemistry: considerations of side-chain and backbone anchoring strategies, and compatible protection for N-terminal cysteine.
    Gross CM; Lelièvre D; Woodward CK; Barany G
    J Pept Res; 2005 Mar; 65(3):395-410. PubMed ID: 15787970
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Automated Fmoc-based solid-phase synthesis of peptide thioesters with self-purification effect and application in the construction of immobilized SH3 domains.
    Mende F; Beisswenger M; Seitz O
    J Am Chem Soc; 2010 Aug; 132(32):11110-8. PubMed ID: 20662535
    [TBL] [Abstract][Full Text] [Related]  

  • 5. One-pot/sequential native chemical ligation using N-sulfanylethylanilide peptide.
    Otaka A; Sato K; Ding H; Shigenaga A
    Chem Rec; 2012 Oct; 12(5):479-90. PubMed ID: 22927228
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An efficient solid-phase synthesis of peptidyl-N-acetylguanidines for use in native chemical ligation.
    Okamoto R; Isoe M; Izumi M; Kajihara Y
    J Pept Sci; 2016 May; 22(5):343-51. PubMed ID: 27005965
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The phenacyl group as an efficient thiol protecting group in a peptide condensation reaction by the thioester method.
    Katayama H; Hojo H
    Org Biomol Chem; 2013 Jul; 11(26):4405-13. PubMed ID: 23715434
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Synthetic procedure for N-Fmoc amino acyl-N-sulfanylethylaniline linker as crypto-peptide thioester precursor with application to native chemical ligation.
    Sakamoto K; Sato K; Shigenaga A; Tsuji K; Tsuda S; Hibino H; Nishiuchi Y; Otaka A
    J Org Chem; 2012 Aug; 77(16):6948-58. PubMed ID: 22816612
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Native Chemical Ligation Strategy to Overcome Side Reactions during Fmoc-Based Synthesis of C-Terminal Cysteine-Containing Peptides.
    Lelièvre D; Terrier VP; Delmas AF; Aucagne V
    Org Lett; 2016 Mar; 18(5):920-3. PubMed ID: 26878883
    [TBL] [Abstract][Full Text] [Related]  

  • 10. N-methyl-phenacyloxycarbamidomethyl (Pocam) group: a novel thiol protecting group for solid-phase peptide synthesis and peptide condensation reactions.
    Katayama H; Nakahara Y; Hojo H
    Org Biomol Chem; 2011 Jun; 9(12):4653-61. PubMed ID: 21537511
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Biomimetic synthesis of cyclic peptides using novel thioester surrogates.
    Hemu X; Taichi M; Qiu Y; Liu DX; Tam JP
    Biopolymers; 2013 Sep; 100(5):492-501. PubMed ID: 23893856
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Towards biomolecular assembly employing extended native chemical ligation in combination with thioester synthesis using an N-->S acyl shift.
    Ackrill T; Anderson DW; Macmillan D
    Biopolymers; 2010; 94(4):495-503. PubMed ID: 20593460
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Making Ends Meet: Microwave-Accelerated Synthesis of Cyclic and Disulfide Rich Proteins Via In Situ Thioesterification and Native Chemical Ligation.
    Gunasekera S; Aboye TL; Madian WA; El-Seedi HR; Göransson U
    Int J Pept Res Ther; 2013 Mar; 19(1):43-54. PubMed ID: 23504256
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Peptide thioester preparation by Fmoc solid phase peptide synthesis for use in native chemical ligation.
    Clippingdale AB; Barrow CJ; Wade JD
    J Pept Sci; 2000 May; 6(5):225-34. PubMed ID: 10823491
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Safety-catch linkers for Fmoc solid-phase synthesis of peptide thioesters and hydrazides by amide-to-imide activation.
    Paprocki MP; Rasmussen JE; Sørensen KK; Jensen KJ
    J Pept Sci; 2021 Dec; 27(12):e3364. PubMed ID: 34505745
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chemical Protein Synthesis with the α-Ketoacid-Hydroxylamine Ligation.
    Bode JW
    Acc Chem Res; 2017 Sep; 50(9):2104-2115. PubMed ID: 28849903
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Investigation of peptide thioester formation via N→Se acyl transfer.
    Adams AL; Macmillan D
    J Pept Sci; 2013 Feb; 19(2):65-73. PubMed ID: 23297044
    [TBL] [Abstract][Full Text] [Related]  

  • 18. On-resin native chemical ligation for cyclic peptide synthesis.
    Tulla-Puche J; Barany G
    J Org Chem; 2004 Jun; 69(12):4101-7. PubMed ID: 15176835
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Serine promoted synthesis of peptide thioester-precursor on solid support for native chemical ligation.
    Elashal HE; Sim YE; Raj M
    Chem Sci; 2017 Jan; 8(1):117-123. PubMed ID: 28451155
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A reversible protection strategy to improve Fmoc-SPPS of peptide thioesters by the N-Acylurea approach.
    Mahto SK; Howard CJ; Shimko JC; Ottesen JJ
    Chembiochem; 2011 Nov; 12(16):2488-94. PubMed ID: 21910203
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.