401915-55-7

Usage

Uses

Used in Peptide Synthesis:
(s)-3-(fmoc-amino)-n-trityl-adipic acid 6-amide is used as a protecting group in peptide synthesis for the amine group. It ensures the selective protection of the amine during the synthesis process, preventing unwanted side reactions and facilitating the stepwise assembly of peptide chains.
Used in Organic Chemistry:
In the field of organic chemistry, (s)-3-(fmoc-amino)-n-trityl-adipic acid 6-amide is used as a protecting group for hydroxyl groups. The trityl group provides a stable and easily removable protection, allowing chemists to carry out reactions on other functional groups without affecting the hydroxyl groups.
Used in Drug Development:
(s)-3-(fmoc-amino)-n-trityl-adipic acid 6-amide can be employed in the development of pharmaceutical compounds, particularly in the synthesis of peptide-based drugs. Its role in peptide synthesis allows for the creation of complex and biologically active molecules with potential therapeutic applications.
Used in Research and Development:
In the research and development sector, (s)-3-(fmoc-amino)-n-trityl-adipic acid 6-amide is utilized for the synthesis and study of novel compounds with potential applications in various industries, including pharmaceuticals, materials science, and biotechnology. Its versatility as a protecting group and its stability make it a valuable tool for exploring new chemical reactions and syntheses.

Upstream product

• 132327-80-1 Fmoc-L-Gln(Trt)-OH 

Relevant academic research and scientific papers

Selective binding of TAR RNA by a Tat-derived β-peptide

(Equation presented) The interaction between the HIV-1 Tat protein and the TAR RNA element in the nascent viral genomic transcript is required for viral replication. An 11-residue β-peptide (1), an all-β homologue of the Arg-rich region Tat 47-57, binds T