BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

230 related articles for article (PubMed ID: 16957334)

  • 1. Design and synthesis of beta-peptides with biological activity.
    Koyack MJ; Cheng RP
    Methods Mol Biol; 2006; 340():95-109. PubMed ID: 16957334
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Solid-phase synthesis of "mixed" peptidomimetics using Fmoc-protected aza-beta3-amino acids and alpha-amino acids.
    Busnel O; Bi L; Dali H; Cheguillaume A; Chevance S; Bondon A; Muller S; Baudy-Floc'h M
    J Org Chem; 2005 Dec; 70(26):10701-8. PubMed ID: 16355988
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The world of beta- and gamma-peptides comprised of homologated proteinogenic amino acids and other components.
    Seebach D; Beck AK; Bierbaum DJ
    Chem Biodivers; 2004 Aug; 1(8):1111-239. PubMed ID: 17191902
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Aza-amino acid scanning of secondary structure suited for solid-phase peptide synthesis with fmoc chemistry and aza-amino acids with heteroatomic side chains.
    Boeglin D; Lubell WD
    J Comb Chem; 2005; 7(6):864-78. PubMed ID: 16283795
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Quaternary β
    Yu JS; Noda H; Shibasaki M
    Angew Chem Int Ed Engl; 2018 Jan; 57(3):818-822. PubMed ID: 29168280
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A one-pot procedure for the preparation of N-9-fluorenylmethyloxycarbonyl-α-amino diazoketones from α-amino acids.
    Siciliano C; De Marco R; Guidi LE; Spinella M; Liguori A
    J Org Chem; 2012 Dec; 77(23):10575-82. PubMed ID: 23146162
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Synthesis of C-terminal peptide thioesters using Fmoc-based solid-phase peptide chemistry.
    Shelton PT; Jensen KJ
    Methods Mol Biol; 2013; 1047():119-29. PubMed ID: 23943482
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chemical Synthesis of Antimicrobial Peptides.
    Münzker L; Oddo A; Hansen PR
    Methods Mol Biol; 2017; 1548():35-49. PubMed ID: 28013495
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Design and synthesis of Fmoc-Thr[PO(OH)(OPOM)] for the preparation of peptide prodrugs containing phosphothreonine in fully protected form.
    Qian WJ; Lai CC; Kelley JA; Burke TR
    Chem Biodivers; 2014 May; 11(5):784-91. PubMed ID: 24827688
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Peptidomimetics: Fmoc solid-phase pseudopeptide synthesis.
    Cudic P; Stawikowski M
    Methods Mol Biol; 2008; 494():223-46. PubMed ID: 18726577
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Handles for Fmoc solid-phase synthesis of protected peptides.
    Góngora-Benítez M; Tulla-Puche J; Albericio F
    ACS Comb Sci; 2013 May; 15(5):217-28. PubMed ID: 23573835
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Solid-phase synthesis of N-nosyl- and N-Fmoc-N-methyl-alpha-amino acids.
    Di Gioia ML; Leggio A; Liguori A; Perri F
    J Org Chem; 2007 May; 72(10):3723-8. PubMed ID: 17439178
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Convenient synthesis of N-methylamino acids compatible with Fmoc solid-phase peptide synthesis.
    Biron E; Kessler H
    J Org Chem; 2005 Jun; 70(13):5183-9. PubMed ID: 15960522
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Solid-phase guanidinylation of peptidyl amines compatible with standard Fmoc-chemistry: formation of monosubstituted guanidines.
    Bionda N; Cudic P
    Methods Mol Biol; 2013; 1081():151-65. PubMed ID: 24014439
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fmoc Solid-Phase Peptide Synthesis.
    Hansen PR; Oddo A
    Methods Mol Biol; 2015; 1348():33-50. PubMed ID: 26424261
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Synthetic strategy for side chain mono-N-alkylation of Fmoc-amino acids promoted by molecular sieves.
    Monfregola L; De Luca S
    Amino Acids; 2011 Oct; 41(4):981-90. PubMed ID: 21069398
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Problem of aspartimide formation in Fmoc-based solid-phase peptide synthesis using Dmab group to protect side chain of aspartic acid.
    Ruczyński J; Lewandowska B; Mucha P; Rekowski P
    J Pept Sci; 2008 Mar; 14(3):335-41. PubMed ID: 17975850
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Microwave-assisted solid-phase peptide synthesis based on the Fmoc protecting group strategy (CEM).
    Vanier GS
    Methods Mol Biol; 2013; 1047():235-49. PubMed ID: 23943491
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new environment-sensitive fluorescent amino acid for Fmoc-based solid phase peptide synthesis.
    Eugenio Vazquez M; Rothman DM; Imperiali B
    Org Biomol Chem; 2004 Jul; 2(14):1965-6. PubMed ID: 15254619
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.