Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
46594
CAS Number:
1451181-13-7
Fmoc-Met-Thr(Psi(Me,Me)pro)-OH
Antibiotic
Documents
$75.50 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Fmoc-Met-Thr(Psi(Me,Me)pro)-OH is a specialized amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is crucial for the selective protection of amines during the synthesis process. Its unique structure, including the Psi(Me,Me)pro configuration, enhances its stability and compatibility with various coupling reactions, making it an ideal choice for researchers focused on synthesizing complex peptides and proteins.

In practical applications, Fmoc-Met-Thr(Psi(Me,Me)pro)-OH is particularly valuable in the pharmaceutical industry for the development of therapeutic peptides, where precision and efficiency are paramount. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups allows for the creation of high-purity products. Additionally, this compound is instrumental in the study of protein interactions and the design of novel biomolecules, providing researchers with a powerful tool for advancing their work in biochemistry and molecular biology.

CAS Number
1451181-13-7
Molecular Formula
C27H32N2O6S
Molecular Weight
512.2
MDL Number
MFCD32202312
Appearance
Liquid
Conditions
Store at 2 - 8 °C
General Information
CAS Number
1451181-13-7
Molecular Formula
C27H32N2O6S
Molecular Weight
512.2
MDL Number
MFCD32202312
Appearance
Liquid
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
Yes
DEA-regulated
No
Warnings
-
Applications

Fmoc-Met-Thr(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, particularly for creating complex structures with specific functionalities. Its Fmoc (fluorenylmethyloxycarbonyl) protection group allows for selective deprotection, facilitating the stepwise assembly of peptides.
  • Drug Development: In pharmaceutical research, it is used to develop peptide-based drugs. The unique properties of this compound can enhance the bioactivity and stability of therapeutic peptides, making it a valuable asset in drug formulation.
  • Bioconjugation: The compound can be employed in bioconjugation processes, where it helps attach peptides to other biomolecules, such as antibodies or nanoparticles, enhancing targeted drug delivery systems.
  • Protein Engineering: Researchers utilize this chemical in the engineering of proteins with modified properties. Its ability to introduce specific amino acid sequences allows for the design of proteins with improved stability or activity.
  • Analytical Chemistry: This compound is also used in analytical techniques, such as mass spectrometry, to study peptide interactions and modifications, providing insights into protein function and dynamics.

Citations