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Catalog Number:
31988
CAS Number:
1926163-86-1
Fmoc-D-Ala(α-cyclopropyl)-OH·H2O
Purity:
≥ 99% (HPLC)
Documents
$127.79 /25MG
Pack Size Availability Price
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Product Information

Fmoc-D-Ala(a-cyclopropyl)-OH·H2O is a valuable compound in the field of peptide synthesis and medicinal chemistry. This derivative of D-Alanine features a cyclopropyl group, which enhances its structural diversity and can influence biological activity. The Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for selective deprotection, making it an ideal choice for solid-phase peptide synthesis. Researchers appreciate its utility in developing peptides with specific functionalities, particularly in drug design and development. The compound's unique cyclopropyl moiety can contribute to improved binding affinities and altered pharmacokinetic properties, making it a promising candidate for further exploration in therapeutic applications.

In addition to its role in peptide synthesis, Fmoc-D-Ala(a-cyclopropyl)-OH·H2O can be utilized in the study of enzyme interactions and receptor binding, providing insights into molecular mechanisms. Its stability and ease of handling make it suitable for various laboratory settings, ensuring reliable results in research and development projects. This compound stands out for its potential to enhance the efficacy of peptide-based drugs, offering researchers a powerful tool in their quest for innovative therapeutic solutions.

CAS Number
1926163-86-1
Purity
≥ 99% (HPLC)
Molecular Formula
C21H21NO4·H2O
Molecular Weight
369.42
MDL Number
MFCD30748659
PubChem ID
139600626
Appearance
White powder
Conditions
Store at -15 to -25 °C
General Information
CAS Number
1926163-86-1
Purity
≥ 99% (HPLC)
Molecular Formula
C21H21NO4·H2O
Molecular Weight
369.42
MDL Number
MFCD30748659
PubChem ID
139600626
Appearance
White powder
Conditions
Store at -15 to -25 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-D-Ala(a-cyclopropyl)-OH·H2O is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a crucial building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing researchers to create complex peptide sequences efficiently.
  • Drug Development: Its unique structural properties make it valuable in the design of novel pharmaceuticals, especially for targeting specific biological pathways, enhancing the potential for effective drug candidates.
  • Bioconjugation: The compound can be used in bioconjugation techniques, facilitating the attachment of peptides to various biomolecules, which is essential in developing targeted therapies and diagnostics.
  • Research in Neuroscience: Due to its ability to mimic natural amino acids, it is applied in studies related to neurotransmitter function and receptor interactions, contributing to advancements in understanding neurological disorders.
  • Material Science: Its properties are leveraged in creating functionalized materials for applications in nanotechnology, where precise molecular interactions are critical for developing new materials with tailored functionalities.

Citations