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Catalog Number:
30318
CAS Number:
1000164-43-1
Fmoc-Ser(tBu)-Ser[Psi(Me,Me)Pro]-OH
Purity:
95 - 105% (Assay by titration)
Synonym(s):
Fmoc-Ser(tBu)-Ser[Y(Me,Me)Pro]-OH
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Product Information

Fmoc-Ser(tBu)-Ser[Psi(Me,Me)Pro]-OH is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of complex peptides. Its unique structure, incorporating a t-butyl (tBu) side chain and a Psi(Me,Me)Pro configuration, enhances its stability and solubility, making it an ideal choice for researchers focusing on the development of biologically active peptides.

In practical applications, Fmoc-Ser(tBu)-Ser[Psi(Me,Me)Pro]-OH is particularly valuable in the pharmaceutical industry for the synthesis of peptide-based therapeutics, including those targeting specific diseases or conditions. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups allows for the creation of diverse peptide libraries. This compound not only streamlines the synthesis process but also improves yields, making it a preferred choice for researchers aiming to optimize their workflows in peptide chemistry.

Synonyms
Fmoc-Ser(tBu)-Ser[Y(Me,Me)Pro]-OH
CAS Number
1000164-43-1
Purity
95 - 105% (Assay by titration)
Molecular Formula
C28H34N2O7
Molecular Weight
510.58
MDL Number
MFCD11974988
PubChem ID
75103117
Appearance
White to off-white powder
Conditions
Store at ≤ -4 °C
General Information
Synonyms
Fmoc-Ser(tBu)-Ser[Y(Me,Me)Pro]-OH
CAS Number
1000164-43-1
Purity
95 - 105% (Assay by titration)
Molecular Formula
C28H34N2O7
Molecular Weight
510.58
MDL Number
MFCD11974988
PubChem ID
75103117
Appearance
White to off-white powder
Conditions
Store at ≤ -4 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-Ser(tBu)-Ser[Psi(Me,Me)Pro]-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures for drug development and biological studies.
  • Drug Discovery: Its unique properties enable the design of novel therapeutic agents, particularly in the field of cancer research, where specific peptide sequences can target tumor cells effectively.
  • Bioconjugation: The compound is used to attach biomolecules to surfaces or other molecules, enhancing the functionality of drugs and diagnostics in the pharmaceutical industry.
  • Protein Engineering: It aids in the modification of proteins to improve their stability and activity, which is crucial for developing more effective enzymes and therapeutic proteins.
  • Research in Neuroscience: The ability to modify peptide sequences allows for the exploration of neuropeptides, which can lead to advancements in understanding neurological disorders and developing new treatments.

Citations