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The synthesis of fluorotelomer alcohols requires a varying number of tetrafluoroethylene monomers that form an oligomer with a pentafluoroethyl iodide telogen. The fluorinated iodide then undergoes an addition with ethylene to form an organoiodine compound with increased synthesis possibilities. [ 1 ]
Collection of reported fluorescent D-amino acids and their structures.. FDAA consists of a D-amino acid and a fluorophore (coupled through the amino acid side chain).The D-amino acid backbone is required for its incorporation into the bacterial peptidoglycan through the activity of DD-transpeptidases. [3]
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2-Fluoroethanol was originally synthesized by treating 2-chloroethanol with potassium fluoride, in a simple Finkelstein reaction. [5] The product has a lower boiling point that the starting material and may be conveniently isolated by distillation.
The [18 F]FDG-6-phosphate formed when [18 F]FDG enters the cell cannot exit the cell before radioactive decay. As a result, the distribution of [18 F]FDG is a good reflection of the distribution of glucose uptake and phosphorylation by cells in the body. [citation needed] The fluorine in [18 F]FDG decays radioactively via beta-decay to 18 O −.
Lipid II is a precursor molecule in the synthesis of the cell wall of bacteria. It is a peptidoglycan, which is amphipathic and named for its bactoprenol hydrocarbon chain, which acts as a lipid anchor, embedding itself in the bacterial cell membrane. Lipid II must translocate across the cell membrane to deliver and incorporate its disaccharide ...
The location of this enzyme in animal cells is within the mitochondria. [3] Since the enzyme appears to be located near its source of succinyl-CoA and the end of the heme pathway indicates that the starting and end points of heme biosynthesis serves as feedback for ALA synthase. [3] ALA synthase is also inhibited by hemin and glucose. [9] Heme ...
It is classified as a hard Lewis acid and its acceptor properties are discussed in the ECW model yielding E A = 2.07 and C A = 1.06. TFE can be used in biochemical experiments to stabilize alpha helix. [7] [8] There are also stable beta sheets in TFE, suggesting that TFE stabilizes the secondary structure the sequence has a preference for. [8]