N'-Formylkynurenine

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A chemical compound related to tryptophan metabolism


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N'-Formylkynurenine is an intermediate in the metabolism of the essential amino acid tryptophan. It is formed by the action of the enzyme indoleamine 2,3-dioxygenase (IDO) or tryptophan 2,3-dioxygenase (TDO) on tryptophan, leading to the production of kynurenine pathway metabolites.

Biological Role[edit | edit source]

N'-Formylkynurenine plays a crucial role in the kynurenine pathway, which is the primary route of tryptophan catabolism in mammals. This pathway is involved in the production of several bioactive metabolites, including kynurenic acid, quinolinic acid, and nicotinamide adenine dinucleotide (NAD+).

Enzymatic Conversion[edit | edit source]

The conversion of tryptophan to N'-formylkynurenine is catalyzed by the enzymes IDO and TDO. These enzymes incorporate molecular oxygen into the indole ring of tryptophan, resulting in the formation of N'-formylkynurenine. This reaction is the first and rate-limiting step in the kynurenine pathway.

Clinical Significance[edit | edit source]

Alterations in the kynurenine pathway, including changes in the levels of N'-formylkynurenine, have been associated with various diseases, such as neurodegenerative disorders, cancer, and immune system dysfunctions. The pathway's metabolites can influence neurotransmission, immune response, and cellular energy metabolism.

Research and Applications[edit | edit source]

Research into N'-formylkynurenine and the kynurenine pathway is ongoing, with potential applications in developing therapeutic strategies for diseases linked to tryptophan metabolism. Modulating the activity of IDO and TDO, and thereby altering the levels of N'-formylkynurenine and other kynurenine pathway metabolites, is a promising area of study.

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References[edit | edit source]

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Contributors: Prab R. Tumpati, MD