Amines

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Applications (S)-(+)-Z-4-Amino-2-hydroxybutyric Acid is used in the synthesis of aminoglycoside antibiotics. References Rai, R. et al.: Org. Lett., 8, 887 (2006); Li, Jie. et al.: J. org. Chem., 72, 4055 (2007);

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Please enquire for more information about {[1-(2-Methoxyethyl)-1H-imidazol-5-yl]methyl}amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

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2-[[(Heptadecafluorooctyl)Sulphonyl]Propylamino]Ethyl Methacrylate is a sulfonate that is used as a crosslinker in various chemical substances. It is also used to connect substances together, such as chemicals. 2-[[(Heptadecafluorooctyl)Sulphonyl]Propylamino]Ethyl Methacrylate has the chemical formula CH2=CFCF2CF(OCH2CH2)SO3H. 2-[[(Heptadecafluorooctyl)Sulphonyl]Propylamino]Ethyl Methacrylate is an oily liquid that is colorless and odorless.

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(2R)-2-Aminopropanamide is a chemical compound that is classified as an amide. It has been shown to inhibit bacterial growth and induce apoptosis in mammalian cells, but not in bacteria. This drug has a number of hydrogen bonding interactions with the carbonyl group and amide functional groups and can bind to affinity ligands with hydrogen bonding interactions. (2R)-2-Aminopropanamide inhibits the activity of enzymes that are involved in the synthesis of d-alanine, which is a precursor for protein synthesis. It also inhibits the enzyme glutamine synthase, which plays a key role in building up nitrogen reserves in bacteria. The drug binds to DNA by forming hydrogen bonds with the phosphate backbone and intercalates into double-stranded DNA by forming van der Waals interactions with base pairs.

3-Hydroxyacetaminophen is a reactive metabolite of acetaminophen. It is produced by the bacterial strain Acinetobacter calcoaceticus, which was found to produce 3-hydroxyacetaminophen in the presence of oxygen and nitrate. The production process can be optimized by using surface methodology and kinetic studies. In vitro assays showed that 3-hydroxyacetaminophen has a higher cytotoxicity than acetaminophen, as well as an inhibitory effect on tyrosinase activity. This may be due to the deuterium isotope effect, which causes a substitution of hydrogen with deuterium atoms. The reaction intermediates are not known, but they are thought to be generated by chemical reactions involving the substrate or other reactants.

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