You Searched For: Fmoc-O-trityl-L-serine


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Supplier: Bachem Americas
Description: Fmoc-Leu-Gly can self-assemble forming ultrathin hydrogel membranes.

Catalog Number: (76707-506)
Supplier: AFG Bioscience
Description: Human Serine/Threonine Protein Phosphatase 2A 65 kDa Regulatory Subunit A alpha Isoform (PP2A) ELISA Kit


Supplier: Thermo Scientific
Description: Thermo Scientific Serine Hydrolase Probes are ActivX™ Fluorophosphonate (FP) and other tagged phosphonate probes to purify or assay serine hydrolase active sites using fluorescence, biotin-affinity, or mass spectrometry.
Supplier: AFG Bioscience
Description: Fmoc-L-Ser((Ac)3-β-D-GlcNAc)-OH

Supplier: AFG Bioscience
Description: Fmoc-L-Thr (β-D-GalNAc(Ac)3)-OH

New Product

Supplier: Bachem Americas
Description: Sequence: Fmoc-β-cyclohexyl-Ala-OH

Supplier: Bachem Americas
Description: Please see also the corresponding amino acid derivatives Fmoc-(Dmb)Ala-OH (B-4175), Fmoc-(Dmb)Gly-OH (B-4170), Fmoc-(Hmb)Gly-OH (B-3490), and Fmoc-(Dmb)Leu-OH (B-4165).

Supplier: Thermo Scientific Chemicals
Description: N-Fmoc-3-cyclohexyl-L-alanine, 98%

SDS

Supplier: Bachem Americas
Description: Sequence: Fmoc-α-amino-D-Gly(Boc)-OH

Supplier: Thermo Scientific Chemicals
Description: 2-(Fmoc-amino)benzoic acid, 98%
Supplier: Thermo Scientific Chemicals
Description: 1-Boc-N-Fmoc-L-tryptophan, Purity: 97%, CAS number: 143824-78-6, Molecular Formula: C31H30N2O6, Color: white, Form: solid, Synonym: Fmoc-Trp(Boc)-OH, Size: 25G
Catalog Number: (B-3540.0005BA)
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.


Catalog Number: (B-3910.0005BA)
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.


Catalog Number: (B-3440.0005BA)
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.


Catalog Number: (B-3545.0005BA)
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: For Fmoc-dipeptides Fmoc-Xaa-Gly-OH and Fmoc-Xaa-Pro-OH, which can be used as building blocks in Fmoc-SPPS, please see also the subfamily 'Fmoc-Dipeptide Building Blocks' in the 'Amino Acid Derivatives' section. Pseudoproline dipeptides and isoacyl dipeptides can be found in this section as well. In case of a strong tendency towards diketopiperazine formation during Fmoc-SPPS, Fmoc-dipeptides have been coupled even at the risk of a some epimerization.

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