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N-2 Surface Impoundment Schematic

N-2-alkylated pyridazin-3-ones.

N-21 The model assumed in ordinary OLR.The x2 values are Gaussian distributed around the line with constant standard deviation over the analytical measurement range.The x values are assumed to be without random error. 021 is shown.

N-3 Manipulation of a noxious solid

N-3H-acetylmannosamine was injected into the left eye of chickens and the radioactivity of ganglioside and TCA soluble substances was measured in the contralateral and ipsilateral tectum.

N-4-amino cytosine

N-9 Arylation of 2,4-dichloropurines.

N-a-methoxylation of carbamates and diastereoselective substitution of the methoxy group.

N-a-methoxylation of carbamates and further conversion of the methoxy products.

N-a-rrethoxylation in peptides by anodic decarboxylation.

N-acetyiation in vivo.

N-Acetyl derivatives of monosaccharides.

N-Acetyl homocysteine thiolactone spontaneously reacts with amine groups on proteins to create sulfhydryl groups.

N-acetyl N -methyl alanine amide. Identification of the 4 torsional angles.

N-acetyl phenylalanyl tyrosine in the crystal and minimized

N-acetyl-bisalanine-methylester.

N-acetyl-D-glucosamine functionalised calixarene

N-Acetyl-Valyl-Statyl-Alanyl-Statine inhibition of peptic activity at various pH values with APDT substrate. Extrapolation to zero velocity gives the inhibitor concentration for total inhibition. The pepsin concentration was 1 x 10 M. Other experimental conditions and Ej Cl3 ratios for total inhibition for the various lines are

N-Acetylalanyl N -methylamide.

N-Acetylation of isoniazid.

N-acetylation of lysine. Lysine attacks the acetyl group of acetyl-CoA generating an acetylated protein and CoA.

N-Acetylgalactosamine . intramolecular

N-Acetylglucosamine . intramolecular

N-acetylglucosamine-peptide disulfide selected from a disulfide DCL targeting wheat germ agglutinin.

N-Acetylhomocysteinethiolactone spontaneously reacts with amine groups on proteins to create sulfhydryl groups.



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