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Nicotinamide adenine dinucleotide Subject

The biological applications of tetrazolium salts are the subject of a textbook.96 Kuhn and Jerchel74 were the first to recognize the utility of tetrazolium salts as indicators in redox enzyme activity, particularly those of the various dehydrogenases. It has been recognized449 that this particular utility of tetrazolium salts is related to the proximity of their redox potentials to those of the hydride transfer systems in biology450 such as nicotinamide adenine dinucleotide, NAD, and its phosphate analogue, NADP. [Pg.274]

Working at 3.0T with proton decoupling, Sevastianova et al. partially resolved the resonance of nicotinamide adenine dinucleotide phosphate (NADPH) from that of a-NTP. ° NADPH was higher in subjects with nonalcoholic steatohepatitis and cirrhosis than in healthy controls and correlated with disease severity. Solga et al. investigated the reliability of both and P MRS at 1.5 T in cohorts of obese diabetic subjects and healthy con-trols. ° Whereas hepatic fat could be reliably measured with relative ease, hepatic ATP proved difficult with obese subjects due to reduced P SNR. [Pg.143]

An enzyme reactor with immobilized 3 -hydroxysteroid dehydrogenase has been successfully used for the analysis of residues of 17 -methyltestosterone in trout by high-performance liquid chromatography (HPLC) (269). Following their separation by reversed-phase chromatography, the major tissue metabolites of 17 -methyltestosterone, namely 5 -androstane-17 -methyl-3, 17 -diol, and 5 -androstane-17 -methyl-3, 17 -diol, were enzymatically modified in the presence of a coreactant, nicotinamide-adenine dinucleotide (NAD), to the corresponding ketone. The position at 3 was enzymatically oxidized, and NADH, the reduced form of NAD, was produced as a coproduct and subjected to fluorescence detection. Reoxidation of NADH to NAD provides the possibility for electrochemical detection. [Pg.651]

Human populations that have experienced health effects from exposure to 2-nitrophenol or 4-nitrophenol have not been identified, but little research has been conducted on this subject. Based on results from animal studies, as described in Section 2.6, it is possible that individuals who consume ethanol may have slower rates of clearance of 4-nitrophenol. This subpopulation, if exposed to 4- nitrophenol, may be considered potentially susceptible. Furthermore, newborn infants utilize fetal hemoglobin, which has reduced oxygen-carrying capacity, and also have low levels of nicotinamide adenine dinucleotide diaphorase, which continuously reduces methemoglobin therefore, infants (as well as individuals congenitally deficient in this enzyme) may represent... [Pg.48]

Figure 1 The mitochondrial respiratory chain. Electron transfer (brown arrows) between the three major membrane-bound complexes (I, III, and IV) is mediated by ubiquinone (Q/QH2) and the peripheral protein c)dochrome c (c). Transfer of protons hnked to the redox chemistry is shown by blue arrows red arrows denote proton translocation. NAD+ nicotinamide adenine dinucleotide, FMN flavin mononucleotide, Fe/S iron-sulfur center bH,bi, and c are the heme centers in the cytochrome bc complex (Complex III). Note the bifurcation of the electron transfer path on oxidation of QH2 by the heme bL - Fe/S center. Complex IV is the subject of this review. N and P denote the negatively and positively charged sides of the membrane, respectively... Figure 1 The mitochondrial respiratory chain. Electron transfer (brown arrows) between the three major membrane-bound complexes (I, III, and IV) is mediated by ubiquinone (Q/QH2) and the peripheral protein c)dochrome c (c). Transfer of protons hnked to the redox chemistry is shown by blue arrows red arrows denote proton translocation. NAD+ nicotinamide adenine dinucleotide, FMN flavin mononucleotide, Fe/S iron-sulfur center bH,bi, and c are the heme centers in the cytochrome bc complex (Complex III). Note the bifurcation of the electron transfer path on oxidation of QH2 by the heme bL - Fe/S center. Complex IV is the subject of this review. N and P denote the negatively and positively charged sides of the membrane, respectively...
Nicotinamide (34) and structurally related 51 compounds were subjected to the halting activity bioassay to elucidate the structure-activity relationships [105]. The highest activity was recorded in thionicotinamide (35) followed by pyrazinamide (36) and nicotinamide (34). Nicotinamide adenine dinucleotide (NAD) (oxidized form), nicotinamide adenine dinucleotide phosphate (NADP) (oxidized form), (3-nicotinamide mononucleotide (oxidized form) showed halting activity at ca. 10"7 M... [Pg.1097]

In biological systems, alcohols are metabolized by oxidation to carbonyl compounds. For example, ethanol is converted into acetaldehyde by the cationic oxidizing agent nicotinamide adenine dinucleotide (abbreviated as NAD see Real Life 25-2). The process is catalyzed by the enzyme alcohol dehydrogenase. (This enzyme also catalyzes the reverse process, reduction of aldehydes and ketones to alcohols see Problems 58 and 59 at the end of this chapter.) When the two enantiomers of 1-deuterioethanol are subjected... [Pg.290]


See other pages where Nicotinamide adenine dinucleotide Subject is mentioned: [Pg.315]    [Pg.544]    [Pg.367]    [Pg.30]    [Pg.58]    [Pg.56]    [Pg.678]    [Pg.89]    [Pg.49]    [Pg.813]    [Pg.180]    [Pg.49]    [Pg.545]   


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Dinucleotide

Nicotinamide adenine

Nicotinamide adenine dinucleotid

Nicotinamide adenine dinucleotide

Nicotinamide adenine dinucleotides

Nicotinamide dinucleotide

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