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1 imultaneous determination of lactic acid and pyruvic acid.
2 eriments of solutions containing alanine and pyruvic acid.
3 of 3-bromopyruvate, a halogenated analog of pyruvic acid.
4 this procedure on a sample of [1,2-(13)C(2)]pyruvic acid.
5 nt role in determining their reactivity with pyruvic acid.
6 emperature (laboratory) reaction products of pyruvic acid.
7 is dependent upon the asorption geometry of pyruvic acid.
8 ple derivative of the endogenous metabolite, pyruvic acid.
9 t of key small-molecule metabolites: 1-(13)C-pyruvic acid, 1-(13)C-sodium lactate, and 1-(13)C-acetic
10 acid (IAA) from tryptophan through indole-3-pyruvic acid (3-IPA) in response to vegetational shade.
11 oselective acyloin reaction between indole-3-pyruvic acid (4) and p-hydroxyphenylpyruvic acid (5) is
12 t alpha-keto acids (alpha-ketoglutaric acid, pyruvic acid, 4-hydroxyphenylpyruvic acid, 3-methyl-2-ox
13 catalase for the deamination of D-alanine to pyruvic acid (a conversion unique to D-alanine), we were
14 tification and quantitation of acetaldehyde, pyruvic acid, acetoin, methylglyoxal, and alpha-ketoglut
16 3H-benzofuran-2-one, 5, easily obtained from pyruvic acid and 1,4-cyclohexanedione, was used as a sta
17 al, glyoxal; the alpha-keto-carboxylic acids pyruvic acid and glyoxylic acid; and the dicarboxylic ac
18 y reported classes of compounds: keto acids (pyruvic acid and homologs), hydroxy tricarboxylic acids
20 ve condensation between O(18)-labeled phenyl pyruvic acid and N-hydroxyphenethylamine oxalate salt re
22 alpha-ketoglutaric acid; (S)-lactic acid and pyruvic acid; and 1-hydroxy-1,3,4,6-hexanetetracarboxyli
25 c accelerated the transamination of indole-3-pyruvic acid by a factor of 4 million relative to the ra
26 actants demonstrate that one compound alone, pyruvic acid, can produce several (nonenzymatic) members
27 bes the rapid microplate method to determine pyruvic acid content in different varieties of onions.
29 cumulation of IAA and changes in the indol-3-pyruvic acid-dependent IAA biosynthesis and IAA conjugat
30 action of the respective hydroxylamines with pyruvic acid derivatives generated the desired amides in
31 e, our laboratory formulated a derivative of pyruvic acid, ethyl pyruvate, in a calcium- and potassiu
32 ate preference for two molecules of indole-3-pyruvic acid imine, necessitating a net two-electron oxi
33 to D-alanine), we were able to identify [14C]pyruvic acid in a [14C]alanine-labeled preparation of pu
34 PSIS1 (TAA1), which converts Trp to indole-3-pyruvic acid in one of four hypothesized Trp-dependent a
35 -(4-nitrophenyl)hydroxylamine and 2 equiv of pyruvic acid in the presence of other nucleophiles such
36 dergo a Norrish Type II reaction to generate pyruvic acid, increasing the diversity of observed photo
37 sed auxin biosynthetic intermediate indole-3-pyruvic acid (IPA) and indole-3-acetic acid rescues the
38 l, yet genetically uncharacterized, indole-3-pyruvic acid (IPA) branch of the auxin biosynthetic path
39 Step one converts tryptophan to indole-3-pyruvic acid (IPA) by tryptophan aminotransferases follo
40 hat TAA1 catalyzes the formation of indole-3-pyruvic acid (IPA) from L-tryptophan (L-Trp), the first
41 are required for the production of indole-3-pyruvic acid (IPyA) from Trp, whereas YUCs are likely to
42 me for catalyzing the conversion of indole-3-pyruvic acid (IPyA) to indole-3-acetic acid (IAA), actin
43 stance, namely the glucose metabolic product pyruvic acid, it is possible to generate a concentration
44 structure of Iso-4 was elucidated as a novel pyruvic acid ketimine derivative of the N-terminal cyste
45 onment, including SO2, methanesulfinic acid, pyruvic acid, lactic acid, ethanesulfinic acid, propanes
46 umulated an intracellular pool of lactic and pyruvic acids, magnified by the MCT1 inhibitor decreasin
48 ted; however, approximately six molecules of pyruvic acid/molecule were found on 98% of the oligosacc
51 proline derivative and a substituted indole pyruvic acid SEM enol ether, followed by a cationic doub
53 1.5) of HCCA and trans-o-hydroxybenzylidene pyruvic acid (tHBPA) in the naphthalene catabolic pathwa
54 uding the formation of oxalic, glyoxilic and pyruvic acids, the oxidation of methyl vinyl ketone (MVK
55 e were used as enzyme mimics to transaminate pyruvic acid to alanine, phenylpyruvic acid to phenylala
56 the sequential conversion of Trp to indole-3-pyruvic acid to IAA However, the pathway leading to a le
58 which are used to elucidate the reduction of pyruvic acid to lactic acid by direct hydrogenation over
59 lpyruvic acid to phenylalanine, and indole-3-pyruvic acid to tryptophan in water at pH 7.5 and 20 deg
60 (2-Hydroxypropanoic acid) is generated from pyruvic acid under anaerobic condition in skeletal muscl
64 via the novel intermediate 4-chloroindole-3-pyruvic acid, which is produced from 4-chlorotryptophan
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