Z-D-beta-HAsp(OtBu)-OH DCHA
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Z-D-beta-HAsp(OtBu)-OH DCHA

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Category
β−Amino Acids
Catalog number
BAT-000750
Molecular Formula
C29H46N2O6
Molecular Weight
518.8
Synonyms
N-Z-D-beta-homoaspartic acid gamma t-butyl ester dicyclohexylamine salt; (S)-Z-beta-Glu(OtBu)-OH DCHA; (S)-3-(Z-amino)glutaric acid gamma t-butyl ester dicyclohexylamine salt
Storage
Store at 2-8 °C

Z-D-beta-HAsp(OtBu)-OH DCHA, a versatile chemical compound utilized in peptide synthesis and various biochemical applications, brings numerous advantages to the bioscience arena. Here are four key applications of Z-D-beta-HAsp(OtBu)-OH DCHA:

Peptide Synthesis: Widely employed as a protected amino acid derivative in solid-phase peptide synthesis, Z-D-beta-HAsp(OtBu)-OH DCHA plays a pivotal role in ensuring the purity and yield of synthesized peptides. The t-Butyl (OtBu) group serves as a protective shield for the carboxyl function, while DCHA facilitates seamless peptide coupling, guaranteeing optimal outcomes in peptide chain elongation.

Drug Design: In the realm of medicinal chemistry, Z-D-beta-HAsp(OtBu)-OH DCHA finds its use in enhancing the stability and efficacy of peptide-based drugs. Its unique structural characteristics aid in the creation of novel therapeutic agents tailored to combat diverse diseases. By incorporating this compound, researchers can improve crucial pharmacokinetic properties such as bioavailability and metabolic stability.

Protein Engineering: Delving into the realm of protein modification, Z-D-beta-HAsp(OtBu)-OH DCHA serves as a pivotal component in designing and synthesizing engineered proteins for both research and therapeutic purposes. By substituting traditional amino acids with protected derivatives like Z-D-beta-HAsp(OtBu)-OH DCHA, scientists can delve into the intricacies of protein folding, stability, and functionality.

Bioconjugation: At the forefront of bioconjugate chemistry, Z-D-beta-HAsp(OtBu)-OH DCHA emerges as a key building block for creating linkages between biomolecules. Its distinct properties enable the construction of conjugates where peptides are affixed to diverse carriers such as drugs, nanoparticles, or imaging agents. This innovative approach facilitates the development of targeted delivery systems and aids in the creation of advanced diagnostic tools.

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