Sentence examples similar to methyl as compared from inspiring English sources

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EPCs obtained possessed up to 20 40% higher catalytic efficiency in hydrolysis reactions of Paraoxon and Parathion-methyl as compared with that of the native His6-OPH.

The rigidity in the second hydration shell of Mg2+ may prevent it from readily interacting with threonine, which contains a bulky methyl group, as compared with that of serine.

Bisulfite sequencing of repetitive elements, as performed here for LINE-1 elements, is a quicker and easier method to assess global DNA methylation as compared to genomic 5-methyl cytosine quantification [ 35].

This allows her to explain methyl bromide's reactivity as compared to methyl chloride, and also methyl fluoride, methyl iodide, etc. Insofar as chemists want to explain trends, they make contrastive explanations using chemical concepts.

Finally, these Cu tpa @GO/PES membranes exhibited selective anionic dye rejection of > 80% and > 50% for Congo Red and Methyl Orange respectively as compared to that observed for the cationic dye Methylene Blue at < 20%.

The as-prepared MISCN photocatalysts exhibit improved photocatalytic activity for 4-nitroaniline (4-NA) reduction and methyl orange (MO) degradation as compared with pure MIS nanoplates and pristine CN nanosheets under visible light irradiation.

Such findings can be ascribed to the promptness with which methyl parathion undergoes biotransformation into methyl paraoxon inside liver cells, as compared to other organs.

An increase in the rate from methyl to ethyl is attributed to the greater electron-donating tendency of ethyl (–CH2CH3 of EMA) as compared with methyl group (–CH3 group of MMA) [30].

Increases in the rates from MMA to EMA are attributed to the greater electron-donating power of the ethyl group as compared with methyl.

The increased lipophilicity and often superior metabolic stability as compared to methyl analogues often accounts for an improved activity profile in a medicinal chemistry context.

The presence of two hydroxyl substituent groups probably favors the rapid oxidation of Evans Blue (diazo) by laccase as compared to Methyl Orange (azo), whose redox potential is around +1 V (E0 = +0.961 V vs NHE [ 40]).

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