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Of all the synthesized compounds, the most active compound displayed inhibitory activities with an IC50 value of 5.99 μmol/L.
Among the extracts, Ttriptolide is the most active compound, which has strong immunosuppressive activity.
The most active compound d4 was analyzed for heme binding activity using UV spectrophotometer.
Also in case of antifungal activity the tetrafluoro pyridine derivative 4a was the most active compound.
The most active compound was 6f which registered the highest radical scavenging activity.
The most active compound in the second screen was resveratrol.
The most active compound has IC50 value of 2.5 μM.
The most active compound identified was AZQ (diaziquone).
The most active compound carries methoxy group at 2-position of the phenyl ring.
The enzyme kinetic study of the most active compound 4 indicated uncompetitive AChE inhibition.
The kinetic studies of the most active compound 3a revealed competitive type of AChE inhibition.
More suggestions(15)
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