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Usage

Uses

Used in Pharmaceutical Production:
Heptanedioic acid, 2-amino-, (2S)is used as a key component in the synthesis of various pharmaceuticals, leveraging its role in protein synthesis and its potential therapeutic effects.
Used in Medical Research:
In the field of medical research, Heptanedioic acid, 2-amino-, (2S)is employed as a research reagent to study biological processes and explore its potential applications in treating conditions such as diabetes, obesity, and neurological disorders. Its involvement in lysine biosynthesis makes it a valuable tool for understanding the underlying mechanisms of these conditions.
Used in Nutritional Supplements:
Given its presence in protein-rich food sources and its role in protein synthesis, Heptanedioic acid, 2-amino-, (2S)may be used as an ingredient in nutritional supplements to support muscle growth and overall protein synthesis in the body.
Used in Food Industry:
As a naturally occurring amino acid found in various food sources, Heptanedioic acid, 2-amino-, (2S)could be utilized in the food industry to enhance the nutritional content of products or to improve specific characteristics such as taste or texture.

Upstream product

• 627-76-9 alpha-aminopimelic acid 
• 109276-71-3 (S)-2-tert-Butoxycarbonylamino-pentanedioic acid 1-benzyl ester 5-(2-thioxo-2H-pyridin-1-yl) ester 
• 87174-84-3 (S)-2-tert-Butoxycarbonylamino-5-(2,2-dimethyl-4,6-dioxo-[1,3]dioxan-5-ylidene)-5-hydroxy-pentanoic acid benzyl ester 
• 30924-93-7 Boc-Glu-OBn 
• 156386-97-9 (1Z)-α-Ethyl ω-methyl 2-acetamido-2,3-didehydropimelate 
• 156386-98-0 (1E)-α-Ethyl ω-methyl 2-acetamido-2,3-didehydropimelate 
• 1501-26-4 methyl 4-(chlorocarbonyl)butyrate 
• 6026-86-4 methyl 4-formylbutanoate 
• 47312-26-5 (S)-2-Benzyloxycarbonylamino-heptanedioic acid 7-methyl ester 
• 87174-85-4 benzyl 2-<(tert-butyloxycarbonyl)amino>-5-<5-(2,2-dimethyl-4,6-dioxo-1,3-dioxanyl)>pentanoate 
• 115573-33-6 2-L-N-Boc aminopimelic acid 
• 115573-04-1 (S)-2-tert-Butoxycarbonylamino-6-(pyridin-2-ylsulfanyl)-heptanedioic acid 1-benzyl ester 7-methyl ester 
• 834898-11-2 (2S,4S)-2-(1,1-dimethylethyl)-4-(methoxycarbonylbutyl)-5-oxo-3-oxazolidinecarboxylic acid phenylmethyl ester 
• 156387-02-9 (2RS)-α-Ethyl ω-methyl 2-(N-acetylamino)pimelate 

Downstream Products

• 726201-87-2 N-(p-nitrobenzyloxycarbonyl)glycyl-L-α-aminopimelic acid 

Relevant academic research and scientific papers

Practical and efficient enantioselective synthesis of α-amino acids in aqueous media

Enantiomerically pure natural and unnatural α-amino acids have been synthesized from a chiral melhyleneoxazolidinone by means of a highly diastereoselective 1,4-conjugate addition of alkyl iodides in aqueous media. The zinc-copper conjugate addition reaction exhibits high chemoselectivity, with the possibility of using functionalized iodides, to afford a single diastereomer in short reaction times and with good yields.

Peptides of 2-aminopimelic acid: Antibacterial agents that inhibit diaminopimelic acid biosynthesis

Succinyl-CoA:tetrahydrodipicolinate-N-succinyltransferase is a key enzyme in the biosynthesis of diaminopimelic acid (DAP), a component of the cell wall peptidoglycan of nearly all bacteria. This enzyme converts the cyclic precursor tetrahydrodipicolinic

Methotrexate analogues. 20. Replacement of glutamate by longer-chain amino diacids: Effects on dihydrofolate reductase inhibition, cytotoxicity, and in vivo antitumor activity

Chain-extended analogues of methotrexate were synthesized by condensation of 4-amino-4-deoxy-N10-methylpteroic acid with esters of L-α-aminoadipic, L-α-aminopimelic, and L-α-aminosuberic acids, followed by ester hydrolysis with acid or base. Co