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The EDX results showed that the chemical compositions for both compounds were very close to the designed compositions.
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In vitro, both compounds are very potent α-glucosidase inhibitors.
In the study target compounds were very potent inhibitors of AChE and BChE.
It was found that the compounds were very sensitive to the presence of an acid yielding metal-free phthalocyanines irreversibly.
Determination of the selective indexes indicated that 50% of the active compounds were very toxic for HepG2 cells.
Also the remaining compounds were very active, although their MIC and PI were in general lower than those of their parent 2-methyl analogues.
However, the geometric standard deviations of the most and the least common compounds were very similar, indicating an overall low variability of the concentrations.
In flowers, all of the identified compounds were very found to be present at high levels.
Alkaloid compounds were very susceptible fungus probably because they act on mucopolysacharide capsule of fungal strains.
Laboratory blank concentrations of organic compounds were very low, and show that contamination associated with laboratory methods, for example, extraction and rotoevaporation, was negligible.
As laboratory blank concentrations of organic compounds were very low, the phthalate esters represent contamination of the coal prior to processing in the laboratory.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com