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L-Leucine amide hydrochloride|03087|10466-61-2

L-Leucine amide hydrochloride

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Sku CI03087_25_G
Chem Impex
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Product Information

Product Name
L-Leucine amide hydrochloride
Brand Name
Chem Impex
Product Number
03087
CAS
10466-61-2
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
2733199
IUPAC Name
(2S)-2-amino-4-methylpentanamide;hydrochloride
InChI Key
VSPSRRBIXFUMOU-JEDNCBNOSA-N
SMILES
CC(C)CC@@H(C(=O)N)N.Cl

Description

L-Leucine amide hydrochloride is widely utilized in research focused on:

Protein Synthesis: This compound plays a crucial role in stimulating protein synthesis, making it valuable in sports nutrition and muscle recovery formulations.

Pharmaceutical Development: It is used in the formulation of drugs aimed at treating metabolic disorders, enhancing the efficacy of therapeutic agents.

Cell Culture: In laboratory settings, it serves as a supplement in cell culture media, promoting cell growth and viability for various biological studies.

Neuroprotective Research: The compound is investigated for its potential neuroprotective properties, contributing to studies on neurodegenerative diseases.

Cosmetic Applications: It is incorporated into skincare products for its moisturizing properties, helping to improve skin hydration and texture.

References Data Source From Pubchem

The effect of intravenous lipid emulsion (ILE) on the pharmacokinetic/toxicokinetic dispositions of ivermectin and carprofen in rabbits
Publication Name: Naunyn-Schmiedeberg's Archives of Pharmacology
Publication Date: 2023-09-28
DOI: 10.1007/s00210-023-02738-5

Analysis and Enantioseparation of Amino Acids by Liquid Chromatography
Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2019
DOI: 10.1007/978-1-4939-9639-1_17

LAT1 activity of carboxylic acid bioisosteres: Evaluation of hydroxamic acids as substrates
Publication Name: Bioorganic & Medicinal Chemistry Letters
Publication Date: 2016-10-15
DOI: 10.1016/j.bmcl.2016.09.001

Reversed-phase liquid chromatographic resolution of diastereomers of protein and non-protein amino acids prepared with newly synthesized chiral derivatizing reagents based on cyanuric chloride
Publication Name: Amino Acids
Publication Date: 2010-06-18
DOI: 10.1007/s00726-010-0650-z

Chromatographic separation of enantiomers of non-protein α-amino acids after derivatization with Marfey’s reagent and its four variants
Publication Name: Amino Acids
Publication Date: 2008-07-09
DOI: 10.1007/s00726-008-0135-5