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2-amino-6-heptenoic acid amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

790199-96-1

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790199-96-1 Usage

Chemical Class

Fatty acid amide

Biological Activities

Anti-inflammatory: Helps reduce inflammation in the body.
Anti-cancer: Shows potential in combating cancer cells.
Neuroprotective: Protects nerve cells from damage or degeneration.

Potential Medical Applications

Therapeutic Agent for Neurodegenerative Diseases: Investigated for treating conditions like Alzheimer's and Parkinson's diseases.
Anti-aging Compound: Studied for its ability to mitigate aging-related processes.

Natural Occurrence

Found naturally in certain biological systems.

Ongoing Research

Continuous investigation to uncover additional pharmacological effects and medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 790199-96-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,0,1,9 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 790199-96:
(8*7)+(7*9)+(6*0)+(5*1)+(4*9)+(3*9)+(2*9)+(1*6)=211
211 % 10 = 1
So 790199-96-1 is a valid CAS Registry Number.

790199-96-1Upstream product

790199-96-1Downstream Products

790199-96-1Relevant academic research and scientific papers

A Biocatalytic Route to Enantiomerically Pure Unsaturated α-H-α-Amino Acids

Wolf, Larissa B.,Sonke, Theo,Tjen, Kim C. M. F.,Kaptein, Bernard,Broxterman, Quirinus B.,Schoemaker, Hans E.,Rutjes, Floris P. J. T.

, p. 662 - 674 (2007/10/03)

A set of both enantiomeric forms of non-proteinogenic, unsaturated α-H-α-amino acids was efficiently synthesized using a biocatalytic pathway. This route involved the straightforward synthesis of the required unsaturated amino acid amides, followed by resolution with an aminopeptidase present in Pseudomonas putida ATCC 12633 and/or a genetically modified organism, leading to the (S)-acids and (R)-amides. Undesired amino acid racemase activity was identified in the wild-type strain, which was absent in the newly developed organism. The (R)-amides were hydrolyzed under mild conditions using an amidase present in whole cells from Rhodococcus erythropolis NCIMB 11540 to the (R)-acids. The viability of this procedure was demonstrated with the multi-gram synthesis of a variety of unsaturated amino acids in excellent enantiopurity.

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