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The compound demonstrated significant diuretic activity in this model.
This compound demonstrated comparable antimicrobial activity to that of clinically used antimicrobial agents against selected microorganisms.
A selected PDKA compound demonstrated efficacy in a mouse model of tuberculosis.
The compound demonstrated favorable in vitro metabolic and robust mice pharmacokinetic properties.
This compound demonstrated an improved margin to RARα-mediated adverse effects.
This compound demonstrated activation on GOT and GPT activities, inhibitory effects on the γ-GT activity.
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This compound demonstrates anti-convulsant actions in several animal models of epilepsy.
The designed compound demonstrates highly potential to detect explosive in aqueous suspension because of its special steric structure.
Multiple carbons are labeled for each compound, demonstrating a cycling RuMP pathway for methanol assimilation to support growth.
For effective chemoprevention, it is desirable that the candidate compound demonstrates clear differential growth inhibitory effect against cancer cells.
This compound demonstrates various biological activities such as antioxidant [ 6], anticarcinogenic [ 7– 9], and hypoglycemic or hypolipidemic [ 10, 11].
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