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Sku CI12239_5_G
Chem Impex
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Product Information

Product Name
Z-DL-norleucine
Brand Name
Chem Impex
Product Number
12239
CAS
15027-13-1
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
263476
IUPAC Name
2-(phenylmethoxycarbonylamino)hexanoic acid
InChI Key
NMYWMOZOCYAHNC-UHFFFAOYSA-N
SMILES
CCCCC(C(=O)O)NC(=O)OCC1=CC=CC=C1

Description

Z-DL-norleucine is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, allowing researchers to create specific sequences for various applications in drug development and biochemistry.

Protein Engineering: It is used in the design of modified proteins, enhancing their stability and functionality, which is crucial in fields like biotechnology and pharmaceuticals.

Biochemical Research: Z-DL-norleucine is valuable in studying enzyme activity and protein interactions, helping scientists understand biological processes and develop new therapeutic strategies.

Pharmaceutical Development: The compound is explored for its potential in creating new drugs, particularly in targeting specific diseases where modified amino acids can improve efficacy.

Food Industry: It can be used as a flavor enhancer or nutritional supplement, providing benefits in food formulation and enhancing the overall quality of food products.

References Data Source From Pubchem

Chromatographic Retention and Enantioseparation of Amino Acid Derivatives on Aminated β-Cyclodextrin as Functions of the Hydrophobicity of Adsorbates

Publication Name: Journal of Analytical Chemistry
Publication Date: 2003-05
DOI: 10.1023/a:1024030231261

Use of Unmodified and Aminated β-Cyclodextrins for the Separation of Enantiomers of Amino Acid Derivatives by High-Performance Liquid Chromatography

Publication Name: Journal of Analytical Chemistry
Publication Date: 2002-04
DOI: 10.1023/a:1014954415590

Synthetic Ligands for Lectins

Publication Name: Lectins and Glycobiology
Publication Date: 1993
DOI: 10.1007/978-3-642-77944-2_2