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Supplier: Bachem Americas
Description: The isolation and characterization of cDNAs encoding rat galanin and its precursor peptide reveal that rat galanin is synthesized initially as part of a 124-amino acid precursor that includes a signal peptide, galanin, and a 60-amino acid galanin mRNA-associated peptide. The neuropeptide galanin shows multiple inhibitory actions on neurotransmission and memory. In Alzheimer's disease, increased galanin-containing fibers hyperinnervate cholinergic neurons within the basal forebrain in association with a decline in cognition.

Supplier: Bachem Americas
Description: These peptides correspond to the C-terminus of the 65-residue polypeptide hirudin, a potent thrombin inhibitor found in the saliva of the leech Hirudo medicinalis. Treatment of hirudin with carboxypeptidase Y has shown that the last 5 amino acids are essential for its inhibitory activity.

Supplier: Bachem Americas
Description: approx. ED₅₀ ≤ 0.1 ng/mL Human EGF (urogastrone, nepidermin) is a polypeptide hormone which was first isolated from human urine. It is a potent mitogen for a variety of cultured cells, e.g. fibroblasts. In vivo, urogastrone may have a role in the maintenance of gastrointestinal homeostasis. Furthermore, EGF is used in wound healing.

Supplier: Bachem Americas
Description: For atosiban see H-6722.

Supplier: Bachem Americas
Description: A nanotube-forming dipeptide.

Supplier: Bachem Americas
Description: Sequence: Fmoc-N-Me-Trp-OH

Supplier: Bachem Americas
Description: Sequence: Fmoc-N-Me-Ser(tBu)-OH

Supplier: Bachem Americas
Description: The MePhe-analog of NKB shows high selectivity for NKB receptors.

Supplier: Bachem Americas
Description: Isoacyl dipeptides have been developed as building blocks for preventing aggregation of the growing peptide chains during Fmoc-SPPS. As the isopeptide structure is not affected by the final acidolytic cleavage the solubility of the crude product is improved facilitating the subsequent purification. The depsipeptide will rearrange yielding the desired product in slightly basic solution.

Catalog Number: (B-4055.0005BA)
Supplier: Bachem Americas
Description: These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.


Supplier: Bachem Americas
Description: Isoacyl dipeptides have been developed as building blocks for preventing aggregation of the growing peptide chains during Fmoc-SPPS. As the isopeptide structure is not affected by the final acidolytic cleavage the solubility of the crude product is improved facilitating the subsequent purification. The depsipeptide will rearrange yielding the desired product in slightly basic solution.

Supplier: Bachem Americas
Description: Sequence: Fmoc-Pra-OH
Synonym(s): Fmoc-Propargyl-Gly-OH#(S)-2-(Fmoc-amino)-4-pentynoic acid

Supplier: Bachem Americas
Description: Sequence: Fmoc-cis-4-fluoro-Pro-OH

Supplier: Bachem Americas
Description: Sequence: Fmoc-Asp(OMpe)-OH

Supplier: Bachem Americas
Description: Sequence: Fmoc-Glu-2-phenylisopropyl ester

Catalog Number: (B-3925.0005BA)
Supplier: Bachem Americas
Description: These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
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