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Fig 1.

Schematic diagram for synthesis of ester derivatives of 3-((5-(dimethylcarbamoyl) pyrrolidin-3-yl) thio)-6-(1-hydroxyethyl)-4-methyl-7-oxo-1-azabicyclo[3.2.0] heptane-2-carboxylic acid.

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Fig 1 Expand

Fig 2.

Chemical structures of Meropenem and its synthesized derivatives M1-M8.

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Fig 2 Expand

Table 1.

The results of antibacterial studies were determined and tabulated against gram-positive and gram-negative bacterial strains.

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Table 1 Expand

Table 2.

The results of urease inhibition assay of meropenem and its derivatives.

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Table 2 Expand

Table 3.

DPPH radical scavenging activity of meropenem, its derivatives (M1-M8) and ascorbic acid.

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Table 3 Expand

Table 4.

The results of In-silico molecular docking of the parent molecule and its structural analogues.

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Table 4 Expand

Table 5.

Predicted ADME properties of derivatives of 3-((5-(dimethylcarbamoyl)pyrrolidin-3-yl)thio)-6-(1-hydroxyethyl)-4-methyl-7-oxo-1-azabicyclo[3.2.0]heptane-2-carboxylic acid.

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Table 5 Expand

Fig 3.

In-silico molecular docking of ligands with urease (4H9M).

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Fig 3 Expand

Fig 4.

In-silico molecular docking of ligand with alpha amylase (5E0F).

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Fig 4 Expand

Fig 5.

Egg plot "a correlation between antibacterial activity and ADME parameter.

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Fig 5 Expand