Amino Acids

  1. New: Oxazole expanded Glycines

    Visit our Glycine section and find a series of amino acid derivatives, where oxazole is the characteristic structural element carrying carboxy and amino function.

    Read more
  2. New: Oligo Glycine – Linker

    Oligo-glycines are either flexible linkers or form well defined rigid substructures. We offer a variety of oligo-glycines as building blocks which can easily be introduced into any molecule.

    Read more
  3. New: Cysteine-Pseudoproline

    Pseudoprolines derived from Serine and Threonine have developed to standard building blocks for peptide synthesis since their invention. Now this technology is also available with Cysteine residues, as the corresponding 2,4-dimethoxyphenyl-pseudothiaproline is compatible with standard Fmoc/tBu protocols.

    Read more
  4. Photocleavable Cys Protecting Group

    This oNv (2-Nitroveratryl) is the latest addition to our repertoire of cysteine protecting groups. It opens new possibilities of orthogonality to the existing strategies for disulfide bridge formation.

    Read more
  5. Stable Conjugation with Thiols

    Maleimide (MAL) reacts rather specific with free thiol groups and forms appropriate conjugates. However, this reaction is slightly reversible, resulting in loss of the conjugation partner.

    Amino functions open the maleimido ring structure through hydrolysis with nucleophilc neighboring effect and thus inhibit the undesired release reaction.

    Read more
  6. Structural Element: Aminoisobutyric Acid and Homologues

    Aminoisobutyric acid (Aib) and its homologues are a strong helix promoters in peptide mimetics. Aib-containing model peptides are already used in cancer treatment, antimicrobial peptides and cell penetrating peptides (CPP).

    We offer Aib and its homologues positioning the dimethyl fragment either close to the N- or to the C-terminus.

    Read more
  7. Polar Amino Acids for Increased Solubilization

    alpha-Sulfo-beta-Alanine has been used to couple to hydrophobic molecules and peptides and increase solubility. Attachment can be carried out by conventional Fmoc/tBu protocols.

    Read more
  8. Custom Synthesis of Alkyne Amino Acids Analogues for Click Conjugation

    1,4-substituted 1,2,3-triazole are isosteric to peptide bonds and result in peptide mimetics which even retain activity e.g. in case of certain tyrosinease inhibitors.

    We offer custom synthesis of Alkyne Amino Acid Analogues as building blocks for triazol formation via Click conjugation. Side chains can represent all natural amino acids or unusual residues. In combination with our alpha-azido acids we can offer the whole range of building blocks to design Click-peptide bond analogues for every proteinogenic amino acid.

    Read more
  9. Custom Synthesis of Click-able compounds for Cu-free Click Conjugation

    The presence of catalytic copper, limits the in vivo application of the Click this reaction for several reasons.

    We offer custom synthesis of Strained Cyclooctynes and Substituted 1,2,4,5- Tetrazines as building blocks for fast Click reactions in the absence of any catalyst.

    Read more
  10. Custom Synthesis of beta & gamma Amino Acids including Statine Analogues

    GABA is a neurotransmitter in the central nervous system of mammals and its deficiency is associated with severe neurological disorders. Statine, a GABA analogue, occurs in several peptide APIs.

    Derivatives of gamma-amino acid analogues are of continued vital interest for a variety of applications in medicinal chemistry.

    We have a tool box available to offer a broad range of substituted gamma-amino acids and statines on custom synthesis basis.

    Read more
  11. Items 101-110 of 123
    Show per page