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  2. Solid-phase synthesis - Wikipedia

    en.wikipedia.org/wiki/Solid-phase_synthesis

    The solid phase now bears a dipeptide. This cycle is repeated to form the desired peptide chain. After all reactions are complete, the synthesised peptide is cleaved from the bead. The protecting groups for the amino groups mostly used in the peptide synthesis are 9-fluorenylmethyloxycarbonyl group and t-butyloxycarbonyl . A number of amino ...

  3. Peptide synthesis - Wikipedia

    en.wikipedia.org/wiki/Peptide_synthesis

    The chemical synthesis of peptides can be carried out using classical solution-phase techniques, although these have been replaced in most research and development settings by solid-phase methods (see below). [3] Solution-phase synthesis retains its usefulness in large-scale production of peptides for industrial purposes moreover.

  4. Custom peptide synthesis - Wikipedia

    en.wikipedia.org/wiki/Custom_peptide_synthesis

    In general, peptides shorter than 8 amino acids are prepared more economically by solution chemistry. Peptides larger than 8 residues are generally assembled by solid phase chemistry. Solid phase peptide synthesis (SPPS) can be carried out either manually or in a fully automated fashion. Manual synthesis for short peptides is advantageous as it ...

  5. Split and pool synthesis - Wikipedia

    en.wikipedia.org/wiki/Split_and_pool_synthesis

    Manual split and pool synthesizer. The device is an aluminum tube mounted on a laboratory shaker and evacuated by a water pump. The split and pool synthesis was first applied to prepare peptide libraries on solid support. The synthesis was realized in a home-made manual device shown in the figure.

  6. Peptide library - Wikipedia

    en.wikipedia.org/wiki/Peptide_library

    A peptide library is a tool for studying proteins.Peptide libraries typically contain a large number of peptides that have a systematic combination of amino acids.Usually, solid phase synthesis, e.g. resin as a flat surface or beads, is used for peptide library generation.

  7. Native chemical ligation - Wikipedia

    en.wikipedia.org/wiki/Native_chemical_ligation

    Peptide-thioesters can be directly prepared by Boc chemistry SPPS; however, thioester-containing peptides are not stable to treatment with a nucleophilic base, thus preventing direct synthesis of peptide thioesters by Fmoc chemistry SPPS. Fmoc chemistry solid phase peptide synthesis techniques for generating peptide-thioesters are based on the ...

  8. Category:Solid-phase synthesis - Wikipedia

    en.wikipedia.org/wiki/Category:Solid-phase_synthesis

    In chemistry, solid-phase synthesis is a method in which molecules are bound on a bead and synthesized step-by-step in a reactant solution; compared with normal synthesis in a liquid state, it is easier to remove excess reactant or byproduct from the product.

  9. Bailey peptide synthesis - Wikipedia

    en.wikipedia.org/wiki/Bailey_peptide_synthesis

    The Bailey peptide synthesis is a name reaction in organic chemistry developed 1949 by J. L. Bailey. [1] [2] It is a method for the synthesis of a peptide from α-amino acid-N-carboxylic acid anhydrides (NCAs) and amino acids or peptide esters. [2] [3] The reaction is characterized by short reaction times and a high yield of the target peptide. [2]

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