CAS 15893-47-7
:H-D-LEU-NH2
Description:
H-D-LEU-NH2, also known as D-Leucine amide, is a derivative of the amino acid leucine, characterized by the presence of an amide functional group. This compound is part of the class of amino acids and is specifically the D-enantiomer of leucine, which is one of the essential branched-chain amino acids (BCAAs) important for protein synthesis and metabolic processes. The presence of the amide group (NH2) indicates that it can participate in various biochemical reactions, potentially influencing protein structure and function. H-D-LEU-NH2 is often utilized in peptide synthesis and research applications, particularly in studies related to protein folding, enzyme activity, and metabolic pathways. Its unique stereochemistry may also affect its biological activity and interactions with other biomolecules. As with many amino acid derivatives, it is important to handle H-D-LEU-NH2 with care in laboratory settings, adhering to safety protocols to ensure proper handling and disposal.
Formula:C6H14N2O
Synonyms:- D-Leucine Amide
- D-Leucine-Nh2
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Found 4 products.
Pentanamide, 2-amino-4-methyl-, (2R)-
CAS:Formula:C6H14N2OPurity:98%Color and Shape:SolidMolecular weight:130.1882(R)-2-Amino-4-methylpentanamide
CAS:(R)-2-Amino-4-methylpentanamidePurity:98%Molecular weight:130.19g/mol(R)-2-Amino-4-methylpentanamide
CAS:Formula:C6H14N2OPurity:95.0%Color and Shape:SolidMolecular weight:130.191D-Leucine amide
CAS:<p>D-Leucine amide is a hydrophobic, carboxyamide amino acid that is found in the fungus Ochrobactrum anthropi. D-Leucine amide has been shown to catalyze the formation of tripeptides, such as d-alanine and d-tryptophan, from their monomers. The presence of this compound enhances the expression of genes encoding proteins involved in the synthesis of these amino acids. This compound also has been shown to enhance gene analysis by increasing the stability of DNA and RNA molecules.</p>Formula:C6H14N2OPurity:Min. 95%Molecular weight:130.19 g/mol




