1188-24-5

Basic information

• Product Name: H-ARG-LEU-OH ACETATE SALT
• Synonyms: H-ARG-LEU-OH ACETATE SALT;H-ARG-LEU-OH ACOH;L-ARG-LEU CH3COOH;L-ARGINYL-L-LEUCINE ACETATE;H-Arg-Leu-OH;Arg-Leu-OH;L-Arg-L-Leu-OH;N-(L-Arginyl)-L-leucine
• CAS NO: 1188-24-5
• Molecular Formula: C₁₂H₂₅N₅O₃
• Molecular Weight: 347.41
• Mol File: 1188-24-5.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Density: 1.33
• Storage Temp.: 2-8°C
• CAS DataBase Reference: H-ARG-LEU-OH ACETATE SALT(CAS DataBase Reference)
• NIST Chemistry Reference: H-ARG-LEU-OH ACETATE SALT(1188-24-5)
• EPA Substance Registry System: H-ARG-LEU-OH ACETATE SALT(1188-24-5)

Safety Data

• Hazardous Substances Data: 1188-24-5(Hazardous Substances Data)

Usage

General Description

H-ARG-LEU-OH ACETATE SALT is a chemical compound that consists of the amino acids arginine (H-ARG) and leucine (LEU) linked together with an amide bond. The addition of the acetate salt modifies the compound, making it more stable and soluble in water. H-ARG-LEU-OH ACETATE SALT has potential applications in pharmaceutical research and development, particularly in the study of peptide interactions and drug delivery systems. Additionally, it may also be used in biochemistry research to study protein-protein interactions and enzyme activity. The acetate salt form of H-ARG-LEU-OH may offer distinct advantages over other forms of the compound in certain experimental applications due to its improved solubility and stability properties.

Upstream product

• 61-90-5 L-leucine 
• 1234-35-1 Z-Arg-OH 
• 74-79-3 L-arginine 
• 2304-98-5 N^α-benzyloxycarbonyl-N^g-nitro-L-arginine 
• 7517-19-3 methyl (L)-leucinate hydrochloride 
• 5289-88-3 N^α-Benzyloxycarbonyl-N^ω-nitro-arginyl-L-leucin-methylester 
• 2304-98-5 N₅-[imino(nitroamino)methyl]-N₂-[(phenylmethoxy)carbonyl]-L-ornithine 
• 5289-88-3 N-(N^α-benzyloxycarbonyl-N^ω-nitro-L-arginyl)-L-leucine methyl ester 
• 1738-69-8 L-Leucine benzyl ester 
• 2666-93-5 (S)-Leu-OMe 
• 14611-34-8 N^α,N^δ,N^ω-tris(benzyloxycarbonyl)-L-arginine 
• 30611-61-1 N^α-Benzyloxycarbonyl-N^ω-nitro-arginyl-L-leucin 
• 2418-78-2 N^ω-Nitro-L-arginyl-L-leucin 
• 121234-76-2 N-(N^α,N^δ,N^ω-tris-benzyloxycarbonyl-L-arginyl)-L-leucine benzyl ester 

Relevant articles and documents

A novel L-amino acid ligase from Bacillus subtilis NBRC3134, a microorganism producing peptide-antibiotic rhizocticin

L-Amino acid ligase catalyzes the formation of an α-peptide bond from unprotected L-amino acids in an ATP-dependent manner, and this enzyme is very useful in efficient peptide production. We performed enzyme purification to obtain a novel L-amino acid lig

DPP4 INHIBITOR AND PHARMACEUTICAL APPLICATION THEREOF

The present invention provides a Dpp4 inhibitor which comprises a leucine derivative of the following formula (1) or a methionine derivative of the following formula (2): wherein each R1 and R3 represents a hydrogen atom (H) and an L-amino acid residue; R2 represents a hydroxyl group (OH), alkoxy group having 1 to 6 carbon atoms, amino group (NH2), alkylamino group having 1 to 6 carbon atoms, glycine residue, β-alanine residue, L-amino acid (except for proline, alanine and phenylalanine) residue or L-amino-acid amide (except for proline amide, alanine amide and phenylalanine amide) residue; and R4 represents a hydroxyl group (OH), alkoxy group having 1 to 6 carbon atoms, amino group (NH2), alkylamino group having 1 to 6 carbon atoms, glycine residue, β-alanine residue, L-amino acid (except for proline and alanine) residue or L-amino-acid amide (except for proline amide and alanine amide) residue. These derivatives also act as autophagy regulators.

AMINO-ACIDS AND PEPTIDES. XXI. REMOVAL OF THE NITRO-GROUP FROM

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