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Sku CI32567_1_G
Chem Impex
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Product Information

Product Name
Boc-Thr(Val-Fmoc)-OH
Brand Name
Chem Impex
Product Number
32567
CAS
887707-95-1
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
11649564
IUPAC Name
(2S,3R)-3-(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-methylbutanoyloxy-2-(2-methylpropan-2-yl)oxycarbonylaminobutanoic acid
InChI Key
KFMYXFZGGHKJMR-CQLNOVPUSA-N
SMILES
CC@H(C@@H(C(=O)O)NC(=O)OC(C)(C)C)OC(=O)C@H(C(C)C)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13

Description

Boc-Thr(Val-Fmoc)-OH is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis. Its protective groups facilitate the selective addition of amino acids, allowing for complex peptide structures to be constructed efficiently.

Drug Development: In pharmaceutical research, Boc-Thr(Val-Fmoc)-OH is used to develop peptide-based drugs. Its unique structure can enhance the bioactivity and stability of therapeutic peptides, making it valuable in designing new medications.

Bioconjugation: The compound is employed in bioconjugation processes where it helps in attaching peptides to various biomolecules. This application is crucial in creating targeted drug delivery systems and improving the efficacy of therapeutic agents.

Protein Engineering: Researchers use this chemical in protein engineering to modify protein structures. By incorporating it into proteins, scientists can study the effects of specific amino acid changes on protein function and stability.

Academic Research: In academic settings, Boc-Thr(Val-Fmoc)-OH is frequently utilized in studies related to protein interactions and enzymatic functions. Its role in facilitating peptide synthesis makes it a staple in many biochemical laboratories.