Açúcares e Nucleobases da Espinha Dorsal

Please enquire for more information about N1-(Pivaloyloxy)methyl-N2-(dimethylamino)methylene 9-deazaguanine including the price, delivery time and more detailed product information at the technical inquiry form on this page

5-Acetamido-6-amino-3-methyluracil hydrate (AAU) is a drug that is used as an analytical reagent in the determination of caffeine, 5-hydroxytryptophan, and other compounds. It can be used to assess interactions between drugs and enzyme activities. AAU has been shown to be a suitable substrate for many enzymes, including alcohol dehydrogenase, acetylcholinesterase, catalase, and glucose oxidase. The sample preparation procedure is performed by dissolving the compound in water or ethanol. The sample is then filtered before it is analyzed using high performance liquid chromatography (HPLC). The chemical properties of AAU are such that it can be easily transported from one place to another without undergoing significant changes in physical properties. AAU has been shown to have no effect on biological samples when exposed to radiation. AAU has been widely studied for its use as a monoclon

2-Mercaptopurine (2MP) is a thiopurine drug that is used to treat bowel disease. 2MP inhibits the activity of methyltransferase, which is an enzyme that converts 6-mercaptopurine to 6-thioguanine. This process prevents the conversion of 6-thioguanine into 6-thiouric acid, which is an intermediate in the synthesis of thymine nucleotides. 2MP also inhibits the binding of atp-binding cassette transporter proteins to DNA and blocks the incorporation of purines into RNA and DNA. The drug has been shown to be effective in treating squamous cell carcinoma and other diseases with a high level of activity. 2MP has been shown to be metabolized by erythrocyte polymerase chain reaction and can be detected in biological samples.

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8-Aminopurine is an aminopurine that is used as a research tool in magnetic resonance spectroscopy. The proton magnetic resonance spectrum of 8-aminopurine shows two characteristic peaks at 3.0 and 4.2 ppm, which are assigned to the aminopurine tautomers (3-HPA, 4-HPA). The kinetic stability of 8-aminopurine in water is pH dependent and has been shown to be strongly dependent on the presence of aldehyde oxidase (AO) activity. AO activity can be inhibited by the addition of dimethylformamide or other non-specific inhibitors such as 2,6-dichloroisonicotinic acid.

Applications Protected Guanine. References Hakimelahi, G., et al.: J. Med. Chem., 44, 3710 (2001),

1-(2'-Tetrahydrothienyl)-5-Fluorouracil-1'-Oxide is a particle that is used as a contrast agent. It has been shown to bind to mesenchymal markers, such as transcription-polymerase chain and epidermal growth factor receptor. The acidic form of the drug is eliminated through dialysis. This active form of 1-(2'-Tetrahydrothienyl)-5-Fluorouracil-1'-Oxide has been shown to be effective in treating chronic pulmonary infections and infectious diseases, including angiogenic factors and body mass index. The mouse tumor model has shown that this drug inhibits malonic acid production by inhibiting the activity of enzymes such as pyruvate carboxylase, which converts malic acid into oxaloacetate. This leads to an accumulation of malonic acid in the tumor cells, eventually leading to cell death.