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Catalog Number:
48151
CAS Number:
1359754-16-7
Fmoc-Asp(OtBu)-Cys(Psi(Dmp,H)pro)-OH
Purity:
≥ 95% (HPLC)
Synonym(s):
Na-Fmoc-b-tert-butyl-L-aspartyl-2-(2,4-dimethoxphenyl)thiazolidine-4-carboxylicacid, Fmoc-Asp(OtBu)-2,4-dimethoxybenzyl-pseudothiaproline
Antibiotic
Documents
$70.00 /100MG
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Product Information

Fmoc-Asp(OtBu)-Cys(Psi(Dmp,H)pro)-OH is a sophisticated amino acid derivative that plays a pivotal role in peptide synthesis and drug development. This compound is particularly valued in the field of medicinal chemistry for its ability to facilitate the creation of complex peptide structures, which are essential for the development of therapeutic agents. Its unique thiazolidine ring structure enhances stability and solubility, making it an ideal candidate for researchers focused on synthesizing bioactive peptides and proteins.

The Fmoc protecting group allows for easy manipulation during synthesis, while the presence of the t-butyl ester provides additional protection for the carboxylic acid functionality. This compound is widely utilized in the pharmaceutical industry for the development of peptide-based drugs, as well as in academic research for studying protein interactions and functions. Its versatility and effectiveness in various applications make it a valuable addition to any laboratory focused on peptide chemistry.

Synonyms
Na-Fmoc-b-tert-butyl-L-aspartyl-2-(2,4-dimethoxphenyl)thiazolidine-4-carboxylicacid, Fmoc-Asp(OtBu)-2,4-dimethoxybenzyl-pseudothiaproline
CAS Number
1359754-16-7
Purity
≥ 95% (HPLC)
Molecular Formula
C35H38N2O9S
Molecular Weight
662.75
MDL Number
MFCD32263117
Appearance
White to off-white powder
Conditions
Store at ≤ -10 °C
General Information
Synonyms
Na-Fmoc-b-tert-butyl-L-aspartyl-2-(2,4-dimethoxphenyl)thiazolidine-4-carboxylicacid, Fmoc-Asp(OtBu)-2,4-dimethoxybenzyl-pseudothiaproline
CAS Number
1359754-16-7
Purity
≥ 95% (HPLC)
Molecular Formula
C35H38N2O9S
Molecular Weight
662.75
MDL Number
MFCD32263117
Appearance
White to off-white powder
Conditions
Store at ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
Yes
DEA-regulated
No
Warnings
-
Applications

Fmoc-Asp(OtBu)-Cys(Psi(Dmp,H)pro) is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures for various applications in biochemistry and molecular biology.
  • Drug Development: It plays a crucial role in the development of new pharmaceuticals, particularly in designing peptide-based drugs that can target specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation techniques, enabling the attachment of biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.
  • Protein Engineering: It aids in the modification of proteins, enhancing their stability and functionality, which is vital for creating more effective enzymes and therapeutic proteins.
  • Research in Cancer Therapeutics: This chemical is being explored for its potential in developing targeted cancer therapies, providing a pathway for more effective treatment options with fewer side effects.

Citations