N6877
L-Norleucine
≥98% (TLC)
Synonym(s):
(S)-(+)-2-Aminohexanoic acid, (S)-2-Aminocaproic acid
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About This Item
Recommended Products
Quality Level
Assay
≥98% (TLC)
form
powder
color
white
mp
>300 °C (lit.)
application(s)
detection
SMILES string
CCCC[C@H](N)C(O)=O
InChI
1S/C6H13NO2/c1-2-3-4-5(7)6(8)9/h5H,2-4,7H2,1H3,(H,8,9)/t5-/m0/s1
InChI key
LRQKBLKVPFOOQJ-YFKPBYRVSA-N
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Application
- l-norleucine on high glucose-induced insulin sensitivity and mitochondrial function in skeletal muscle cells. This study explores the beneficial effects of L-Norleucine on insulin sensitivity and mitochondrial function, underlining its potential in metabolic pathway research and its application in managing diabetes through targeted amino acid therapy (Ding et al., 2024).
Biochem/physiol Actions
L-Norleucine is a synthetic amino acid commonly used as an internal standard.
Other Notes
Non-essential amino acid.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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A short, concise synthesis of enantiopure, side chain-modified α-amino acids such as 4-oxo-L-norvaline, 6-oxo-L-homonorleucine, and 5-cis-alkyl prolines is described. Knoevenagel condensation of l-aminocarboxylate-derived β-ketoesters with aldehydes followed by reductive decarboxylation results in unnatural α-amino acids in good yield. A fluorescent
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