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Catalog Number:
14822
CAS Number:
252554-79-3
Fmoc-Ala-Thr[Psi (Yo, Yo) Pro]-OH
Purity:
95 - 105% (Ensayo por titulación)
Synonym(s):
Fmoc-Ala-Thr[ψ(Me,Me)Pro]-OH, (4 S ,5 R )-3-(Fmoc-Ala)-2,2,5-trimetil-oxazolidina-4-ácido carboxílico
Documents
$66.80 /1G
Tamaño
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Product Information

Se utiliza en la síntesis en fase sólida de péptidos que son difíciles de producir.

Synonyms
Fmoc-Ala-Thr[ψ(Me,Me)Pro]-OH, (4 S ,5 R )-3-(Fmoc-Ala)-2,2,5-trimetil-oxazolidina-4-ácido carboxílico
CAS Number
252554-79-3
Purity
95 - 105% (Ensayo por titulación)
Molecular Formula
C25H28N2O6
Molecular Weight
452.51
MDL Number
MFCD03490490
PubChem ID
75627341
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-Ala-Thr[ψ(Me,Me)Pro]-OH, (4 S ,5 R )-3-(Fmoc-Ala)-2,2,5-trimetil-oxazolidina-4-ácido carboxílico
CAS Number
252554-79-3
Purity
95 - 105% (Ensayo por titulación)
Molecular Formula
C25H28N2O6
Molecular Weight
452.51
MDL Number
MFCD03490490
PubChem ID
75627341
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-Ala-Thr[Psi(Me,Me)Pro] is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex peptide sequences efficiently.
  • Drug Development: It plays a significant role in the development of peptide-based therapeutics, providing researchers with a tool to design and optimize drug candidates with enhanced stability and bioactivity.
  • Bioconjugation: The compound can be used in bioconjugation processes, facilitating the attachment of peptides to various biomolecules, which is essential in creating targeted drug delivery systems.
  • Research in Protein Engineering: It aids in the modification of proteins to study structure-function relationships, enabling scientists to explore the effects of specific amino acid substitutions on protein behavior.
  • Diagnostics: Fmoc-Ala-Thr[Psi(Me,Me)Pro] is utilized in the development of diagnostic assays, particularly in the detection of biomarkers through peptide-based methods, enhancing the accuracy of medical diagnostics.