Примеры использования Reductase на Английском языке и их переводы на Русский язык
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HMG-CoA reductase is an important developmental enzyme.
Satins are pharmacuetical drugs that work by restricting the enzyme HMG CoA reductase.
Including ribonucleotide reductase, which is involved in the synthesis of DNA.
The enzyme that converts protochlorophyllide to chlorophyllide is protochlorophyllide reductase, EC 1.3.1.33.
Key words: methylenetetrahydrofolate reductase, gene polymorphisms, colorectal cancer.
At 0.5 mM it inhibits the synthesis of fatty acids andsterols and inactivates HMG-CoA reductase in rat hepatocytes.
Ferredoxin-nitrite reductase Hydrogensulfite reductase Nitrite reductase(NAD(P)H) Matthew J. Murphy; et al. 1974.
This flexibility is possible because different oxidases and reductases use the same ubiquinone pool.
Transcription of the reductase gene is enhanced by the sterol regulatory element binding protein SREBP.
Cytochrome f is the largest subunit of cytochrome b6f complex plastoquinol-plastocyanin reductase; EC 1.10.99.1.
Dutasteride(trademark name Avodart)is a dual 5-a reductase inhibitor that inhibits conversion of testosterone to dihydrotestosterone(DHT).
The absolute bioavailability of the medication is about 14%, but the systemic availability for HMG-CoA reductase activity is approximately 30.
Key words: superoxide anion-radical,NADPH-cytochrome P -450 reductase, cytochrome P -450, monooxygenase system, microsomal fraction, liver, Guerin's carcinoma.
The vitamin K epoxide is in turn recycled back to vitamin K andvitamin K hydroquinone by another enzyme, the vitamin K epoxide reductase VKOR.
Approximately 70% of circulating inhibitory activity for HMG-CoA reductase is attributed to active metabolites.
Ferredoxin: NADP+ reductase then transfers an electron from each of two ferredoxin molecules to a single molecule of the two electron carrier NADPH.
This radical then reacts with NADH, to produce adducts that are very potent inhibitors of the enzymes enoyl-acyl carrier protein reductase, and dihydrofolate reductase. .
A decreased aldehyde reductase activity and some alterations in blood aldo-keto reductase spectrum have been observed in late puberty in adolescents with neuroendocrine obesity.
Electron flow in these organisms is similar to those in electron transport, ending in oxygen or nitrate,except that in ferric iron-reducing organisms the final enzyme in this system is a ferric iron reductase.
An additional condition shown to be related to hyperlysinemia is dienoyl-CoA reductase deficiency, though this is a relatively recent discovery and there are not many publications supporting this.
Alpha reductase inhibitors, such as Finasteride, are not very effective because the 5-aplha reductase enzyme does not metabolize trenbolone, and related inhibitors will have very little effect.
We review the results of modern studies of statins confirming the positive effect of HMG-CoA reductase inhibitors on mortality from cardiovascular complications, with good tolerability and relative safety of these drugs.
Warfarin inhibits epoxide reductase(specifically the VKORC1 subunit), thereby diminishing available vitamin K and vitamin K hydroquinone in the tissues, which inhibits the carboxylation activity of the glutamyl carboxylase.
Reference: Ivanov A.V., Kopylov A.T., Zgoda V.G., Toropygin I.Yu., Khrjapova E.V.,Ivanov Yu.D., Mass-spectrometric identification of interaction sites for cytochrome P450 2b4/nadph cytochrome P450 reductase, Biomeditsinskaya khimiya, 2010, vol: 56(1), 40-54.
Generation of superoxide anion-radical(O 2•-) in reductase and oxygenase electron-transport chains in the liver monooxygenase system was investigated in tumor-bearing rats exposed to preliminary irradiation.
The crystallins of different groups of organisms are related to a large number of different proteins, with those from birds and reptiles related to lactate dehydrogenase and argininosuccinate lyase,those of mammals to alcohol dehydrogenase and quinone reductase, and those of cephalopods to glutathione S-transferase and aldehyde dehydrogenase.
Investigation of aldehyde-reductase activity and blood aldo-keto reductase spectrum has been performed in 13-15 and 16-18-years old adolescents with obesity to clear up the mechanisms of neuroendocrine obesity at the age of puberty.
Pharmacology: Hydroxyurea is a nucleoside diphosphate reductase inhibitor, can prevent the nucleotidereduced to deoxy nucleotides, purine and pyrimidine bases interfere with the biosynthesis, selectively impede DNA synthesis, RNA and protein synthesis on the role of non-blocking.