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Catalog Number:
24276
CAS Number:
1134779-28-4
Boc-D-Thréo-3-(Pyridin-2-Yl)Sérine
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$549.62 /100 mg
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Product Information

Boc-D-Threo-3-(Pyridin-2-Yl)Serine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is characterized by its Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. Its unique structure, featuring a pyridine ring, allows for specific interactions in biological systems, facilitating the design of novel therapeutics and biologically active compounds.

In practical applications, Boc-D-Threo-3-(Pyridin-2-Yl)Serine is often utilized in the synthesis of peptide-based drugs, where it can serve as a building block for creating complex structures with enhanced pharmacological properties. Its ability to mimic natural amino acids while providing additional functional groups makes it particularly valuable in the development of targeted therapies. Researchers appreciate its ease of use in various coupling reactions, which streamlines the synthesis process and improves overall yields. This compound stands out for its potential to contribute to advancements in drug discovery and development, making it a significant asset for professionals in the pharmaceutical industry.

CAS Number
1134779-28-4
Molecular Formula
C13H18N2O5
Molecular Weight
282.29
MDL Number
MFCD03844665
PubChem ID
74315771
Conditions
Conserver à 0-8°C
General Information
CAS Number
1134779-28-4
Molecular Formula
C13H18N2O5
Molecular Weight
282.29
MDL Number
MFCD03844665
PubChem ID
74315771
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-D-Threo-3-(Pyridin-2-Yl)Serine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a crucial building block in the synthesis of peptides, particularly in the development of biologically active compounds. Its protective Boc group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: In medicinal chemistry, it plays a role in designing new pharmaceuticals, especially those targeting neurological disorders, due to its structural similarity to natural amino acids.
  • Bioconjugation: The compound is used in bioconjugation techniques, where it can be linked to other molecules, such as drugs or imaging agents, to improve their delivery and efficacy in therapeutic applications.
  • Research on Enzyme Inhibition: It is employed in studies aimed at understanding enzyme mechanisms, particularly those involving serine residues, providing insights that can lead to the development of enzyme inhibitors.
  • Protein Engineering: The compound is valuable in protein engineering, allowing researchers to modify proteins for enhanced stability and activity, which is essential in various biotechnological applications.

Citations