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pyruvic
pyruvic, a. Chem. (paɪˈruːvɪk) [ad. mod.L. pyruvicus, in acidum pyruvicum pyruvic acid (J. J. Berzelius 1835, in Ann. der Physik u. Chem. XXXVI. 5), f. pyro- 3 a + L. uva grape + -ic.] In pyruvic acid, C3H4O3 = CH3.CO.CO2H, also called pyroracemic acid, produced by the dry distillation of racemic or...
Oxford English Dictionary
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Pyruvic acid
Pyruvic acid is a colorless liquid with a smell similar to that of acetic acid and is miscible with water. Environmental chemistry
Pyruvic acid is an abundant carboxylic acid in secondary organic aerosols.
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Methyl pyruvate
This colorless liquid is the methyl ester of pyruvic acid. It has attracted interest as a prochiral precursor to alanine and lactic acid. It is prepared by esterification of pyruvic acid.
References
Methyl esters
Ketoesters
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Pyruvate dehydrogenase (quinone)
Pyruvate dehydrogenase (quinone) (, pyruvate dehydrogenase, pyruvic dehydrogenase, pyruvic (cytochrome b1) dehydrogenase, pyruvate:ubiquinone-8-oxidoreductase
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Pyruvate dehydrogenase (cytochrome)
Other names in common use include pyruvate dehydrogenase, pyruvic dehydrogenase, pyruvic (cytochrome b1) dehydrogenase, pyruvate:ubiquinone-8-oxidoreductase
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Glutamic--pyruvic transaminase 2
Glutamic--pyruvic transaminase 2 is a protein that in humans is encoded by the GPT2 gene.
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Bromopyruvic acid
This colorless solid is the brominated derivative of pyruvic acid. It bears structural similarity to lactic acid and pyruvic acid.
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Pyr
franchise
Pyr (publisher)
Pyridine
Pyridoxine, vitamin B6
Pyrrolidonyl-β-naphthylamide, used in microbiology to distinguish certain Streptococcal organisms
Pyruvic
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Pyranoanthocyanin
nm)
Delphinidin-3-O-glucoside-pyruvic acid (533 - 507 nm)
Delphinidin-3-O-acetylglucoside-pyruvic acid (575 - 509 nm)
Delphinidin-3-O-coumaroylglucoside-pyruvic acid (679 - 511 nm)
Peonidin-3-O-glucoside-pyruvic acid (531 - 509 nm)
Peonidin-3-O-acetylglucoside-pyruvic acid (573 - 510 nm)
Peonidin-3-O-coumaroylglucoside-pyruvic
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Octopine
Octopine is formed by reductive condensation of pyruvic acid and arginine through the action of the NADH-dependent enzyme octopine dehydrogenase (ODH). The reaction is reversible so that pyruvic acid and arginine can be regenerated.
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Uvitonic acid
Preparation
Uvitonic acid is obtained by the action of ammonia on pyruvic acid.
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Doebner reaction
The Doebner reaction is the chemical reaction of an aniline with an aldehyde and pyruvic acid to form quinoline-4-carboxylic acids. One possibility is at first an aldol condensation, starting from the enol form of the pyruvic acid (1) and the aldehyde, forming an β,γ-unsaturated α-ketocarboxylic
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Methyl red
All enterics initially produce pyruvic acid from glucose metabolism. Other enterics subsequently use the butylene glycol pathway to metabolize pyruvic acid to neutral end products.
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Agaropectin
Agaropectin is one of the two main components of agar and mainly consists of D-glucuronic acid and pyruvic acid. Pyruvic acid is possibly attached in an acetal form to the D-galactose residues of the agarobiose skeleton.
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Acetolactic acid
α-Acetolactic acid is a precursor in the biosynthesis of the branched chain amino acids valine and leucine. α-Acetolactic acid is produced from two molecules of pyruvic
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