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

Catalog Number:
29715
Ácido (2 S , 4 S )-Fmoc-4-( N '-Pbf-guanidino)-pirrolidina-2-carboxílico
Purity:
≥ 97 % (HPLC)
Documents
$154.93 /25 mg
Tamaño
Request Bulk Quote
Product Information

The compound (2S, 4S)-Fmoc-4-(N'-Pbf-guanidino)-pyrrolidine-2-carboxylic acid is a specialized amino acid derivative widely utilized in peptide synthesis and drug development. This compound features the Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure, incorporating a guanidino group, enhances its potential as a building block for bioactive peptides, particularly in the design of inhibitors and therapeutic agents targeting various biological pathways.

Researchers and industry professionals can leverage this compound for its high stability and compatibility with standard coupling reagents, making it an ideal choice for solid-phase peptide synthesis. Additionally, its guanidino functionality can improve the binding affinity of peptides to their targets, offering significant advantages in drug design and development. This compound is particularly relevant in the fields of medicinal chemistry and biochemistry, where the synthesis of complex peptides is crucial for advancing therapeutic research.

Purity
≥ 97 % (HPLC)
Molecular Formula
C34H38N4O7S
Molecular Weight
646.76
MDL Number
MFCD18782850
Appearance
Polvo blanco
Optical Rotation
[a]20/D = - 18 ± 2 º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Purity
≥ 97 % (HPLC)
Molecular Formula
C34H38N4O7S
Molecular Weight
646.76
MDL Number
MFCD18782850
Appearance
Polvo blanco
Optical Rotation
[a]20/D = - 18 ± 2 º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(2S, 4S)-Fmoc-4-(N'-Pbf-guanidino)-pyrrolidine-2-carboxylic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of therapeutic agents. Its unique structure allows for the introduction of guanidino groups, enhancing the biological activity of the resulting peptides.
  • Drug Development: Researchers leverage this compound in the design of novel drugs, especially in the field of oncology. Its ability to modify peptide sequences can lead to improved efficacy and selectivity of cancer treatments.
  • Bioconjugation: The compound is employed in bioconjugation processes, where it helps attach biomolecules to drugs or imaging agents. This enhances the targeting capabilities of therapeutic compounds, making treatments more effective.
  • Research in Molecular Biology: It is used in various molecular biology applications, including the study of protein interactions and functions. The ability to modify proteins with this compound allows for deeper insights into biological processes.
  • Custom Synthesis: Laboratories often utilize this compound for custom synthesis projects, providing tailored solutions for specific research needs. Its versatility makes it a preferred choice for chemists looking to innovate.

Citas