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  2. 2-Pyrrolidone - Wikipedia

    en.wikipedia.org/wiki/2-Pyrrolidone

    2-Pyrrolidone, also known as 2-pyrrolidinone or butyrolactam, is an organic compound consisting of a 5-membered lactam, making it the simplest γ-lactam. It is a colorless liquid that is miscible with water and most common organic solvents.

  3. N-Methyl-2-pyrrolidone - Wikipedia

    en.wikipedia.org/wiki/N-Methyl-2-pyrrolidone

    N-Methyl-2-pyrrolidone (NMP) is an organic compound consisting of a 5-membered lactam. It is a colorless liquid, although impure samples can appear yellow. It is miscible with water and with most common organic solvents. It also belongs to the class of dipolar aprotic solvents such as dimethylformamide and dimethyl sulfoxide.

  4. N1-Acetyl-N2-formyl-5-methoxykynuramine - Wikipedia

    en.wikipedia.org/wiki/N1-Acetyl-N2-formyl-5-meth...

    N 1-Acetyl-N 2-formyl-5-methoxykynuramine (AMFK) is a metabolite of melatonin and an antioxidant. [1] References

  5. N-Formylmethionine - Wikipedia

    en.wikipedia.org/wiki/N-Formylmethionine

    N-Formylmethionine (fMet, [2] HCO-Met, [3] For-Met [3]) is a derivative of the amino acid methionine in which a formyl group has been added to the amino group. It is specifically used for initiation of protein synthesis from bacterial and organellar genes, and may be removed post-translationally.

  6. 2-Acetyl-1-pyrroline - Wikipedia

    en.wikipedia.org/wiki/2-acetyl-1-pyrroline

    2-Acetyl-1-pyrroline (2AP) is an aroma compound and flavor that gives freshly baked bread, jasmine rice and basmati rice, the herb pandan (Pandanus amaryllifolius), and bread flowers (Vallaris glabra) their customary smell. [1]

  7. Purine metabolism - Wikipedia

    en.wikipedia.org/wiki/Purine_metabolism

    Formyl groups build carbon-2 and carbon-8 in the purine ring system, which are the ones acting as bridges between two nitrogen atoms. A key regulatory step is the production of 5-phospho-α- D -ribosyl 1-pyrophosphate ( PRPP ) by ribose-phosphate diphosphokinase , which is activated by inorganic phosphate and inactivated by purine ribonucleotides.

  8. Phosphoribosylglycinamide formyltransferase - Wikipedia

    en.wikipedia.org/wiki/Phosphoribosylglycinamide...

    Phosphoribosylglycinamide formyltransferase (EC 2.1.2.2), also known as glycinamide ribonucleotide transformylase (GAR Tfase), [1] is an enzyme with systematic name 10-formyltetrahydrofolate:5'-phosphoribosylglycinamide N-formyltransferase. [2] [3] [4] This enzyme catalyses the following chemical reaction

  9. Acyl-CoA - Wikipedia

    en.wikipedia.org/wiki/Acyl-CoA

    1. Acyl-CoA dehydrogenase catalyzes dehydrogenation of the acyl-CoA, creating a double bond between the alpha and beta carbons. [6] FAD is the hydrogen acceptor, yielding FADH2. [7] 2. Enoyl-CoA hydrase catalyzes the addition of water across the newly formed double bond to make an alcohol. [5] [6] 3.