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In-Silico Design & Synthesis of MurB Inhibitors as Antibacterial Agent (Paperback)
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In-Silico Design & Synthesis of MurB Inhibitors as Antibacterial Agent (Paperback)
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Heterobicyclic oxazolo pyrimidinone are important class of
compounds. They may become promising candidates for exploiting more
useful therapeutically active molecules. The compounds having
oxazolo pyrimidinone moiety are associated with interesting wide
spectrum biological activities, such as antibacterial, kinase
inhibition, adenosine receptor antagonism, tumour growth inhibition
and some show to inhibit the ability of ricin to inactivate the
ribosomes etc. The intermediate azlactones are also useful
precursors for the synthesis of amino acids, peptides,
heterocycles, biosensors and antitumor or antimicrobial compounds.
In the present study, it was proposed to synthesize lead molecules
of oxazolo pyrimidinone skeleton, apt for binding to the target
enzyme, bacterial MurB based on the rational approach and to study
their docking simulations using ArgusLab 4.0.1 and AutoDock 4.2
softwares. The synthesized test compounds were then characterized
by TLC, melting point determination, UV, IR, 1H-NMR and mass
spectral studies and tested for their antibacterial activity and
compare with the standard drug.
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