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N-((9Z,12Z)-octadeca-9,12-dienoyl)-L-phenylalanine, also known as alpha-linolenoyl-L-phenylalanine or ALA, is a naturally occurring conjugated fatty acid and an amino acid derivative. It is formed by the esterification of the essential fatty acid linolenic acid (9Z,12Z-octadecadienoic acid) with the amino acid L-phenylalanine. ALA is an important compound in human metabolism, as it serves as a precursor for the synthesis of other bioactive compounds, such as eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), which are crucial for maintaining proper brain function, reducing inflammation, and supporting cardiovascular health. N-((9Z,12Z)-octadeca-9,12-dienoyl)-L-phenylalanine is found in various plant sources, such as flaxseed oil, and is also present in some animal tissues. Due to its potential health benefits, ALA has been the subject of numerous scientific studies, and it is often used as a dietary supplement to support overall well-being.

2441-64-7

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2441-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2441-64-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,4 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2441-64:
(6*2)+(5*4)+(4*4)+(3*1)+(2*6)+(1*4)=67
67 % 10 = 7
So 2441-64-7 is a valid CAS Registry Number.

2441-64-7Downstream Products

2441-64-7Relevant academic research and scientific papers

CHEMICAL UNCOUPLERS OF RESPIRATION AND METHODS OF USE THEREOF

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Paragraph 0247; 0266; 0267, (2020/11/27)

Uncoupling of respiration is a well-recognized process that increases respiration and heat production in cells. Provided herein are chemical uncouplers of respiration that are compounds of Formula (I). Also provided are methods for preventing or treating metabolic disorders and modulating metabolic processes using compound of Formula (I).

Discovery of Hydrolysis-Resistant Isoindoline N -Acyl Amino Acid Analogues that Stimulate Mitochondrial Respiration

Lin, Hua,Long, Jonathan Z.,Roche, Alexander M.,Svensson, Katrin J.,Dou, Florence Y.,Chang, Mi Ra,Strutzenberg, Timothy,Ruiz, Claudia,Cameron, Michael D.,Novick, Scott J.,Berdan, Charles A.,Louie, Sharon M.,Nomura, Daniel K.,Spiegelman, Bruce M.,Griffin, Patrick R.,Kamenecka, Theodore M.

supporting information, p. 3224 - 3230 (2018/04/23)

N-Acyl amino acids directly bind mitochondria and function as endogenous uncouplers of UCP1-independent respiration. We found that administration of N-acyl amino acids to mice improves glucose homeostasis and increases energy expenditure, indicating that this pathway might be useful for treating obesity and associated disorders. We report the full account of the synthesis and mitochondrial uncoupling bioactivity of lipidated N-acyl amino acids and their unnatural analogues. Unsaturated fatty acid chains of medium length and neutral amino acid head groups are required for optimal uncoupling activity on mammalian cells. A class of unnatural N-acyl amino acid analogues, characterized by isoindoline-1-carboxylate head groups (37), were resistant to enzymatic degradation by PM20D1 and maintained uncoupling bioactivity in cells and in mice.

Improvements in or Relating to Organic Compounds

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, (2016/08/17)

A stock solution comprising a compound of formula (I) Wherein R1 together with the carbonyl group to which it is attached is a residue of a carboxylic acid, and NR2R3, in which R3 is H or together with R2 and the N-atom to which they are attached, a 5-membered ring, is a residue of an amino acid, in particular a proteinogenic amino acid, ornithine, gamma-aminobutyric acid or beta alanine, or a 1-amino cycloalkyl carboxylic acid.

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